
Stakeholder Network-Themed Role-Playing Game
Introduction
To deeply analyze the complex interactions and strategic dynamics among stakeholders in the ginseng industry within a synthetic-biology context , the JLU-NBBMS iGEM HP team created an original Stakeholder Network-Themed Role-Playing Game titled “Blame It All on Ginseng” (《都是人参惹的祸》). Centered on immersive role play , the event invites participants from diverse backgrounds—along with team members and special guests—to help players intuitively understand the relational logic among different stakeholders in the ginseng ecosystem .
Record
Set in “Happiness Village” on Changbai Mountain, the murder-mystery unfolds around a central thread—the scramble for the “Thousand-Year Ginseng King.” The core design highlight is six carefully crafted, representative roles drawn from real industry contexts —farmer, student, researcher, entrepreneur, government official, and social-media creator—covering the ginseng sector's key stakeholder groups. Each character's plot arc and decision tendencies closely track their real-world interests , enabling players, through role play, to experience conflicts from different standpoints and grasp the multifaceted social impacts that synthetic biology may bring .
A standout feature of this event is the successful translation of an abstract, complex stakeholder network into tangible, perceptible, and interactive characters and plot conflicts —eschewing traditional lecturing so the public can, through immersive participation, naturally appreciate the multidimensional interplay between technological development and industrial society. This design aligns with public learning habits and serves as both a practice of and a tribute to the iGEM HP ethos , deepening our understanding of stakeholder relationships.
Feedback
According to participant feedback, the core value of this role-playing game was fully realized: most players said that, through role play, they not only clearly understood stakeholder interactions within synthetic-biology projects but also developed genuine empathy for the positions and dilemmas of different groups. According to participants' feedback, the team will extend the “stakeholder role-experience” design to more iGEM events and public-outreach programs, further deepening HP practices in stakeholder engagement and helping more people grasp the relational logic among the industry's diverse groups. For more details, please see Stakeholder Role-Playing Game in the Education section
"Genes & Beliefs" iGEM Asia Virtual Gathering
Introduction
On July 13, the “Genes & Beliefs” Asian Online Exchange, hosted by iGEM VIT, was successfully held. The event aimed to explore the interaction between culture, belief, and synthetic biology , inviting several iGEM teams from across Asia—including iGEM UGM, MITMPL, iGEM IISERBPR, among others—to share their experiences and challenges in engaging with local cultures during their scientific practices. Topics included traditional medicine, religious belief, national identity, and science communication.
Record
The JLU-NBBMS team was invited to participate and delivered a keynote talk titled "Advantages as Challenges: Traditional Chinese Medicinal Materials in the Context of Synthetic Biology." The presentation introduced the applications and challenges of synthetic biology in the development of traditional Chinese medicinal resources, focusing particularly on the synthesis of ginsenoside Ro. It highlighted how the project confronts the dual challenges posed by cultural traditions and public perception.
We observed that ginseng, as an important herb in traditional Chinese medicine, not only possesses diverse pharmacological effects but also carries profound cultural symbolism. However, as a typical modern scientific approach, synthetic biology's method of isolating and replicating single components at the molecular level inevitably raises concerns regarding efficacy, authenticity, and cultural acceptance when contrasted with the Traditional Chinese Medicine (TCM) emphasis on “nature,” “holism,” and “authenticity.”
We sought to propose a strategy of " providing modern interpretations and solutions to traditional concepts. " First, the team attempted to reinterpret TCM notions in scientific language —for instance, understanding qi气 as metabolic reactions arising from specific environmental stresses and root-associated microbial symbiosis, while simulating ginseng's natural accumulation process by adjusting fermentation conditions. Second, starting from the scientific basis of “authenticity” (daodi ), we proposed a new paradigm of “synthetic authenticity ”: by incorporating geo-specific trace elements, simulating climatic rhythms to regulate metabolic pathways, and even introducing medicinal genes with regional cultural identifiers, the synthetic products could be endowed with recognizable and trustworthy "cultural identities." In this way, beyond functional equivalence, they could embody cultural authenticity.
We emphasized that synthetic biology can serve as a pathway for the creative transformation and innovative continuation of traditional wisdom . Technological progress enables traditional medicine to persist and spread in new forms within modern society, while cultural foundations can enhance the social acceptance and shared value of scientific research.
Q & A:
Q: (Kevin Thomas Paul, event organizer): “How does your team view the concept of yin and yang in Chinese traditional medical culture? How does this concept influence the cultural promotion of your project?”
A: The yin-yang concept is an abstract and profound philosophical notion in traditional Chinese culture . On one hand, as rigorous scientific researchers, we must avoid mechanically mapping it onto specific substances or research processes. On the other hand, as researchers conscious of public communication and cultural inheritance, we may use the dynamic interplay of yin and yang—mutual complementarity and the generation of myriad phenomena—as a metaphor for the collaborative relationship between synthetic biology and traditional medicine. In this way, our project's narrative can help the public understand the interaction between science and culture.
Feedback
Through this in-depth exchange with Asian teams, we not only gained deeper insights into how historical and cultural differences influence research acceptance and public communication , but also obtained valuable perspectives for our team's future efforts in international outreach and science communication . Accordingly, during our communication with the Ginseng Task Force of the Jilin Provincial Department of Agriculture and Rural Affairs , we drew on these lessons to better introduce the cultural roots of ginsenoside research to audiences from different cultural backgrounds.
The Second Northeast China iGEM Conference
Introduction
To foster mutual understanding among universities and friendly teams in Northeast China, break down inter-institutional barriers, promote resource sharing and experience exchange , and jointly explore the boundless possibilities of synthetic biology, the Second Northeast China iGEM Conference was convened at Jilin University on May 11, 2025. Co-hosted by our team, the JLU-NBBMS Team from the College Basic Medical Sciences Jilin University, and JLU-CP Team from the School of Computer Science and Technology Jilin University. The event attracted 14 university teams from across the region, including Jilin University, Northeast Normal University, Northeast Forestry University, and Shenyang Pharmaceutical University—along with teams from institutions outside Northeast China such as Lanzhou University, Ocean University of China, Beijing University of Chemical Technology, Zhejiang University of Technology, and Yan'an University. These teams shared and presented their iGEM projects both online and offline.
Record
At the main venue, iGEM teams from various universities delivered project presentations on topics including efficient extraction of ginsenosides, new breast cancer detection technologies, microplastic degradation, Alzheimer's disease, liver cancer, and innovative treatment approaches for diabetic wounds . These discussions collectively explored the intersection of synthetic biology between fundamental scientific research and practical applications. During the roundtable session, our team, serving as moderators, guided in-depth discussions on "Safety Issues in Synthetic Biology" and "Expanding Decentralized Thinking" , delving into research paradigms beyond traditional boundaries.
Feedback
Through this exchange, all participating teams gained fresh insights to advance their projects, further igniting their innovative potential . Whether through project showcases, technical deliberations, or future joint initiatives in human practices and modeling analysis, this regional conference not only facilitated a collision of ideas among universities but also sounded the clarion call for teams to shine on the global stage in Paris this October. Our team, too, feels emboldened to radiate our unique brilliance amid the competition.
iGEM Greater Bay Area Synthetic Biology Industry-Academia-Research Forum
Introduction
The iGEM Greater Bay Area Synthetic Biology Industry-Academia-Research Forum is a region-wide gathering initiated by iGEM teams across the Guangdong-Hong Kong-Macao Greater Bay Area. Designed as a corporate-team exchange platform, it brings together the highest density of iGEM teams and bio-related high-tech industries on the planet. By forging a brand-new cooperation model among iGEM teams and placing university-industry linkage at its core, the Forum converges the two strongest innovation and growth poles—local universities and enterprises—to build bridges among academia, industry and research, and to catalyze cluster-wide development of the Bay Area's bio-economy.
In 2024 the iGBA Synthetic Biology Regional Alliance Council was officially established; it will continue to lead iGBA and the Greater Bay Area iGEM community, engaging ever more iGEMers in building a vibrant SynBio ecosystem in the region.
Record
The three-day itinerary was packed with exhibitions, round-tables and on-site corporate visits. iGEMers from different teams showcased their projects, exchanged ideas and sparked new collaborations.
Day 1 - The University of Hong Kong
After opening remarks by HKU professors, team leaders and liaison teachers—who shared their visions for synthetic biology and their high expectations for iGEMers—participants dove into lively discussions.
JLU-NBBMS members (Zhu Tong, Chai Xinyue, Zhang Jiayi, Jin Mo, Liu Fanfei) introduced their project at their booth, patiently answered questions and attracted crowds with their EDU activities—especially a murder-mystery game they had designed. They gained insights into the research backgrounds and design concepts of other teams, while forging deep friendships with them.
In parallel workshops Jin Mo and Liu Fanfei ran a bingo mini-game and an experimental-skills contest, gaining valuable feedback while handing out creative souvenirs.
Day 2 - Corporate Visits
The second day was devoted to industry exploration. The delegation toured Shenzhen's innovation hubs, witnessing the journey “from bench to bioplant”. Stops included:
·Shenzhen Guangming Engineering Biology Industry Innovation Center
·Salus Medical Technology (founded Oct 2020 by a renowned U.S. professor and three Shenzhen “Peacock Talent” awardees; develops proprietary upstream sequencing platforms and a world-leading super-resolution spatial-omics system for research and clinical translation)
·Shenzhen Synthetic Biology Major Science Facility (equipped with internationally top-tier robotics, high-throughput instruments and AI-driven pipelines for automated design-build-test-learn cycles on biological parts, gene networks and synthetic cells).
The visits prompted JLU-NBBMS members to rethink experimental design in light of real-world manufacturing constraints.
Day 3 - Southern University of Science and Technology
Prof. Wang Zefeng (SUSTech School of Life Sciences) spoke on “Deep Academia, Real-world Impact, Youth Innovation”. A round-table on career planning followed, featuring Prof. Liu Xingyin and other veterans who debated academic vs. industrial paths in synthetic biology.
Corporate booths buzzed with activity as JLU-NBBMS chatted with exhibitors.
Meanwhile, in the Concert Hall of the SUSTech Conference Center, corporate representatives from Synbio Technologies and Lingfu Topright Technology took the stage one after another, bringing two product presentations closely aligned with the industry's cutting edge. Though the two presentations focused on different fields, they jointly outlined clear pathways for the industrialization of synthetic biology. These sessions, which combined depth and practical applicability, not only allowed everyone to witness breakthroughs in synthetic biology at the technical level, but also demonstrated the boundless possibilities for bridging basic research and industrial application.
The day closed with a bio-safety-themed collective painting led by the SUSTech iGEM team.
Feedback
The successful organization of the iGBA Forum and its diverse activities have made it clear that we should seek deeper team-enterprise partnerships with a broader range of synthetic-biology companies.
Conference of China iGEMer Community
Introduction
CCiC (Conference of China iGEMer Community) is a flagship synthetic biology gathering that brings together faculty and students from over 100 universities nationwide. From August 6-8, 2025, CCiC and the Synbiopunk Bio Developers Conference were held concurrently at the Beijing Yuquanshan Conference Center. JLU-NBBMS, carrying its latest research results and forward-looking ideas, actively participated in this exchange, joining young scholars and teams from across the country to explore frontier applications of programming living systems.
Record
During the conference's presentation session, Zongjun Li, the student team leader of JLU-NBBMS took the stage on behalf of the team. Starting from the current state of ginsenoside development in China, he clearly outlined the latest progress in both the dry-lab and wet-lab, highlighting the team's distinctive ideas and innovative breakthroughs in synthetic biology.
Meanwhile, in the poster area , the team engaged face-to-face with attendees from across the country, holding lively discussions on technical roadmaps, application scenarios, and market prospects—cross-disciplinary, cross-background exchanges that sparked ideas and offered valuable insights for further project optimization.
A standout feature was the SynCamp Sessions . Led by JLU-NBBMS, the thematic exchange focused on " Applications of Synthetic Biology in Water Remediation ," with MammothEdu-South, XJTLU-China, and ZJU-China invited to participate. Representatives shared progress in turn: ZJU-China detailed how hardware design and component screening can raise detection precision and safety; XJTLU-China targeted green-tide remediation, combining predictive models with biofilm technologies; MammothEdu-South addressed marine-plastic mitigation, showing how high-salinity environments can be used to screen stress-tolerant strains. JLU-NBBMS also presented its “industrial waste oil → bioactives” route to synthesize the rare ginsenoside Ro. Though varied in emphasis, all talks converged on a core theme: leveraging synthetic biology to tackle complex environmental challenges . The session adopted an " Unconference " format—no fixed agenda, open questions and viewpoints—yielding deeper, more creative discussion.
Feedback
Thanks to its strong presentation and proactive organizing, the JLU-NBBMS team received a special sponsorship from the Changjiang (Yangtze River) 3D Scientific Computing Center : computational resources for 50 molecular-dynamics systems, providing solid support for future research.
The conference yielded gains on multiple fronts. Through talks and poster exchanges, JLU-NBBMS not only experienced the value of cross-team collaboration but also gathered many constructive cross-disciplinary suggestions . The subsequent “Synthetic Biology: Blessing or Disaster?”—iGEM Informal Talk is one such innovative model of cross-field dialogue.
Furthermore, through this conference, our team dedicated to advancing biosafety in biosynthesis has established collaboration and is preparing to begin drafting the Substrate Microorganism Illustration White Paper.
Introduction
To enhance understanding of the iGEM competition and project commercialization, a representative from the JLU-NBBMS Team attended the iGEM Innovation and Industrialization Shanghai Exchange Event on August 24, 2025. Attendees included iGEM Ambassador Zhang Xiaohan , the founder of wave3d.ai, and teams from NACIS Shanghai, Jilin University, Tongji University, South China University of Technology, and South China Agricultural University.
Record
During the event, iGEM Ambassador Zhang Xiaohan provided insights into competition preparation, covering topics such as: Reviewing judging criteria; Time and health management; Presentation skills; Team collaboration; Mental well-being. Subsequently, the founder of wave3d.ai demonstrated the application of their product in synthetic biology, including DNA visualization and related innovations. Teams from NACIS Shanghai, Jilin University, South China University of Technology, South China Agricultural University, and Tongji University then presented their projects across diverse fields and tracks.
Feedback
Key takeaways from the exchange include:
(1) Judging Handbook: Prioritize thorough study of the Judging Handbook as the foundational evaluation metric, while respecting judges' subjective assessments.
(2) Time Management: Address time zone differences and strictly adhere to deadlines, particularly for critical compliance issues (e.g., biosafety protocols, animal use whitelist).
(3) Project Narratives: Beyond technical merits, emphasize storytelling to highlight the project's societal responsibility and global impact.
(4) DBTL Cycle: Integrate the Design-Build-Test-Learn (DBTL) framework rigorously.
(5) Team Culture: Foster transparency, mutual respect, and a focus on resolving issues rather than assigning blame.
(6) Collaborative Mindset: Maintain inclusivity and openness in cross-team interactions.
This event reinforced the importance of balancing technical rigor with strategic communication and ethical responsibility in synthetic biology innovation.
Introduction
To better foster public decision-making through plural dialogue, we partnered with the JLU Zhibo Debate Club and hosted three “Informal Talks” on the theme “Synthetic Biology: Blessing or Disaster?” at Jilin University's Dongrong Building. Students from philosophy, sociology, psychology, clinical medicine, biomedical engineering, and other majors participated.
Record
Each session involved one chair, two invited guest commentators, and six
speakers. Before the discussion, speakers and guests introduced their academic
backgrounds. The chair then posed the topic; speakers stated their views and reasons
in turn, followed by an open discussion where anyone could support, rebut, or
question others. The chair invited the guests to comment on the arguments and deepen
the analysis.
Topics of the three sessions were:
·If gene editing became
as routine as vaccination, would you choose to design a “perfect genome” for your
unborn child?
·Should products made from pollutants via genetic technologies be
labeled for source—even when their composition is indistinguishable from natural
counterparts?
·Do gene-improvement technologies enhance or undermine the
“natural attributes” of traditional Chinese medicinal materials?
These topics touched upon the public's right to know about biological modifications, the impact of gene editing on humanity's future, and the challenges posed by the development of traditional medical resources to conventional philosophical concepts, combining both theoretical depth and practical significance.
To involve the audience, we distributed “attitude cards” (support/oppose). In the Q & A, attendees questioned the speakers, then voted for the session's “Best Speaker,” simulating public democratic deliberation and underscoring responsibility for one's public stance.
Q & A:
Q(first-year sociology student, Jilin University): In parents' use of
gene editing to choose a child's genes, what kind of relationship exists between
parent and child?
A(Chen Yichun, Philosophy, Jilin University): In that
process, parents are in fact exercising power—serving parental expectations or
helping the child compete. This power is often driven by instrumental rationality
and may harm the child. Crucially, the unborn seem to lack independent rights, so
the child becomes a mere recipient of parental power without protection; the
relationship risks being unequal.
Q(Zhang Shuai, Sociology, Jilin University):
By evolution theory, mutations constantly occur and species reach new equilibria.
Does that mean whatever gene editing we do, nature will “solve it,” so we needn't
worry?
A(Xi Yue, Clinical Medicine, Jilin University): No. While mutation is
natural, human gene editing compresses timescales dramatically. Without careful
control, it can have large ecological impacts, such as shifting dominant
populations. Nature may adapt in the long run, but many species could face
catastrophic consequences in the meantime. Human action may be part of “nature”
broadly, but that doesn't absolve us of responsibility.
Feedback
Participants were highly curious about knowledge beyond their own fields —revealing real barriers across disciplines. By simulating public deliberation, the “Informal Talks” enabled speakers to offer cross-disciplinary insights and take clear positions. Characterized by equality, enjoyment, and interactivity —unlike adversarial debates or one-way lectures—this format innovated communication within synthetic biology.
Introduction
During the Conference of China iGEMer Community, we recognized that the safety, ethics, and regulatory issues of chassis microorganisms are shared concerns among society, experts, and the public. As the foundational tools of synthetic biology, chassis microorganisms not only drive scientific and industrial progress but also involve a potential gap in risk perception. To respond to these concerns, we collaborated with BUCT-China, NJTech-China, ZJUT-China, XJTLU-AI-China, and Tsinghua teams to jointly compile the illustrated white paper Synterra (Synthetic + Terra, “land of synthesis”). This white paper is both a popular science resource for the public and a practice of dialogue between our team and society: by clarifying issues of safety, compliance, and application value, we aim to foster rational understanding among the public while providing a reference for future iGEM teams in standardizing and educating about the use of chassis microorganisms.
Record
In compiling the white paper, we ensured its comprehensiveness and credibility through expert consultation, public engagement, and policy review:
Expert consultation: invited professors to discuss chassis selection, safety evaluation, and compliant use;
Public engagement: collected societal concerns through online Q&A, such as “Are chassis microorganisms harmful to humans?” and “Can synthetic biology products be trusted?”;
Policy review: examined relevant regulatory frameworks and international standards to incorporate a compliance perspective into the white paper.
The final white paper covers the concepts, common types, application scenarios, safety risks, and regulatory aspects of chassis microorganisms. By combining illustrations with simple language, it lowers barriers to understanding. We further released selected chapters on WeChat, Rednote (Xiaohongshu), and Instagram to expand reach and allow public participation in discussions.
Feedback
For our team, this white paper is not only a tool for knowledge dissemination, but also a practical outcome of integrating societal concerns into project design. It has helped us continuously reflect on the responsibility and boundaries of scientific research while advancing synthetic biology, and it provides the iGEM community with a sustainable resource that supports future progress in biosafety and public engagement. For more details, please see Illustrated White Paper on Chassis Organisms in the Education section.
Interview with Professor Li Wanying
Introduction
To understand the current status of ginsenoside Ro research, its industrialization progress, and advanced technologies—and to align our project with real industry needs and standards—we visited the Ginseng Engineering Center, Jilin Agricultural University for an exchange with Professor Li Wanying and other experts.
Record
We briefly introduced the project background and core direction. Drawing on the Center's research practice, Professor Li offered guidance from an agricultural perspective:
Multi-dimensional cultivar evaluation
Elite ginseng varieties are assessed with composite criteria encompassing yield, composition (key ginsenoside content and stability), stress resistance, growth cycle, and uniformity. In breeding, the Center routinely uses HPLC to screen for target ginsenoside levels, and in recent years has incorporated marker-assisted selection (MAS) and genome-wide association analysis (GWAS) . By specifically marking genes that regulate ginsenoside biosynthesis, they can predict phenotypes in advance , greatly improving screening efficiency and selection accuracy.
Complementarity with synthetic biology
Synthetic biology is not a threat to traditional cultivation but a complementary force . Microbial fermentation and related methods can rapidly and efficiently produce scarce ginsenosides, easing pressure on wild-resource conservation and the cost/environmental burdens of large-scale planting; meanwhile, field cultivation supplies a rich ginsenoside spectrum, genetic diversity , and natural environmental support for the industry.
Willingness to collaborate
Potential joint work could focus on cloning and functional verification of key biosynthetic enzymes , saponin structural optimization , plant gene editing , and co-culture technologies , aiming for full-chain innovation from gene resources → high-value products through interdisciplinary collaboration.
Q & A:
Q: What are the main criteria for evaluating elite ginseng
cultivars?
A:
Four integrated dimensions: (1)
Yield
—plump roots and high root weight to secure economic
returns; (2)
Composition
—high and stable levels of key ginsenosides to meet
medicinal/processing needs; (3)
Stress resistance
—robust tolerance to pests, low temperature,
and continuous-cropping obstacles to reduce risk; (4)
Growth cycle & uniformity
—appropriate cultivation years and
good plant uniformity to enable mechanization and improve efficiency.
Q: How do you balance “high ginsenoside content” with
“stress tolerance” and “growth stability” during breeding?
A:
The Center applies a
tiered breeding strategy
. First ensure stress tolerance and
environmental adaptability, stabilizing agronomic traits through multi-generation
selection so the variety grows reliably under real conditions. On that basis, select
single plants with
higher ginsenoside content
from the qualified pool for
re-selection, ultimately identifying elite lines that combine
stress resistance
with
high ginsenoside levels
.
Feedback
Professor Li shared that the Center has successfully promoted elite varieties such as Jishen No. 2 , establishing over 2,000 mu (≈ 133 ha ) of demonstration bases across major ginseng-producing areas in Fusong, Ji'an, and Tonghua (Jilin Province), providing farmers with tangible trial models. To address common concerns about planting risk and upfront investment , the Center offers seedling subsidies and technical training , strengthening farmers' confidence. It also maintains close cooperation with local governments and cooperatives, advancing varietal adoption through deep industry-academia-research integration.
Guided by this broadened stakeholder perspective, we subsequently visited the Kuaida Ginseng Market and began designing farmer interviews and government interviews.
Interview with Professor Lu Cong
Introduction
To enable environmentally friendly treatment of industrial waste oil while synthesizing high-value products—and to seek guidance on technical optimization and science-education outreach—we held a meeting with Professor Lu Cong of Jilin University's College of New Energy and Environment on August 6, 2025 .
Record
We presented our dual objective of “waste-oil valorization (carbon-source extraction) + biosynthesis (ginsenoside Ro production)” and our current technical ideas (e.g., aeration-based oil-water separation, a preliminary MBR concept, and a bifunctional material design). Professor Lü offered three sets of professional suggestions:
Recognition of the project's environment-engineering integration
She affirmed the project's “environmental protection × engineering” concept. Single remediation technologies struggle with complex environmental problems; our attempt to achieve “waste-oil treatment + resource utilization” via bioengineering exemplifies the cross-integration of environmental philosophy and life sciences, aligning with future trends.
Optimization of the technical scheme
Theoretical basis. Our analogy-driven design needs reinforcement with domain literature in wastewater treatment . Before extracting glycerol and fatty acids from waste oil, we must determine—by measurement rather than assumption—the source (e.g., industrial machinery oil vs. restaurant grease) and composition (impurity load, fatty-acid chain length), and then build processes on empirical data .
Operational details. In our MBR design and in the anaerobic pretreatment module for waste oil, the core risk is microbial community interactions . Through extensive literature review and bench-scale trials, clarify the relationships between introduced biofilms/inocula and the indigenous microbes in the waste oil to ensure synergy rather than competitive inhibition —this governs pretreatment efficiency and the stability of downstream carbon-source extraction.
Science communication & outreach
For non-specialist audiences, we need to follow the principles of plain language and visualization convey core value via visual tools + everyday examples .
Q & A:
Q:
We plan to engineer
bifunctional
materials
to “adsorb target carbon sources + remove impurities.” Is this
suitable for a bio-centric process?
A:
Such adsorption/separation materials fit
chemical pretreatment
better. Direct use inside the
biosynthesis stage
may interfere with microbial reactions.
Position them as
waste-oil pretreatment tools
—to remove macromolecular
impurities and tune the oil phase—so the subsequent
bio-extraction of glycerol and fatty acids
receives cleaner
feed, forming a
chemical-pretreatment + bio-core
workflow rather than embedding
them in biosynthesis.
Q:
Our original plan used
aeration
for oil-water separation and to increase dissolved oxygen. What
issues exist, and how should we adjust?
A:
Two key misconceptions: (1) Aeration alone does
not
“raise DO to eliminate anaerobes”; establishing an
oxygen-rich milieu requires
dedicated oxygenation equipment
. (2) Oil-water separation must
match
oil type
: use
flotation
for
light oils
, and for
heavy oils
employ
integrated anaerobic pretreatment + MBR
for deeper separation.
First
characterize
the waste-oil type (light/heavy), then select the
appropriate separation process to avoid mismatches.
Feedback
Following the “visual + everyday” outreach approach, we designed a high-school-facing environmental activity— “Feedstock Purification Challenge” —guiding students to use simple setups to simulate waste-oil pretreatment and carbon-source extraction , visibly demonstrating the transformation from turbid to clear liquids.
Interview with Professor Li Quanshun
Introduction
To deepen the project's academic value, optimize the experimental plan, and provide precise guidance for translating theory into practice, we met on August 27, 2025 with Professor Li Quanshun , an expert in enzyme engineering and metabolic regulation at Jilin University's College of Life Sciences.
Record
We presented a comprehensive briefing on our technical framework, current bottlenecks (e.g., R1 intermediate accumulation , product degradation), and analytical methods already in use (e.g., ODE + MCA to quantify modification effects). Professor Li offered expert analysis across five core areas—academic value, bottleneck localization, experimental design, and more—and provided targeted guidance.
He emphasized that the project's academic highlight lies in the cross-innovation of sustainable resource utilization and high-value product synthesis : driving rare ginsenoside Ro biosynthesis with industrial waste-oil-derived carbon sources squarely fits green synthesis and metabolic-engineering trends and is highly persuasive. Practical feasibility, however, depends on balancing the metabolic network and boosting key enzyme efficiencies , especially maintaining stable flux under complex substrate conditions , which will determine real-world deployment.
Q & A:
Q:R1 accumulates substantially. What are the likely causes,
and which in vivo/in vitro tests should we prioritize?
A:
Possible causes include: (1)
kinetic mismatch
between upstream and downstream enzymes; (2)
insufficient cofactor supply/regeneration
; (3)
substrate competition
or
feedback inhibition
by intermediates. Prioritize two
experimental tracks:
in vivo
—metabolic flux analysis and
isotope tracing
to map carbon-flow distribution;
in vitro
—kinetic characterization of
purified enzymes
to determine
kcat/Km
and
cofactor dependencies
. Integrate these data to pinpoint
bottlenecks.
Q:How can we screen Ro-specific hydrolases (esterases)
without disturbing essential cellular metabolism?
A:
Three steps: (1) shortlist candidates via
multi-omics
plus
product-correlation
analyses; (2) assess
Ro specificity
using
structural biology
and
molecular dynamics
; (3) verify
in vitro
that activity is restricted to Ro and does not affect
core metabolites, then proceed to
in vivo knockout/editing
to mitigate risks from esterase
substrate promiscuity
.
Q:In enzyme-engineering design, should we start with in
vivo screening or in vitro characterization—and why?
A:
Prefer
in vitro purified-enzyme characterization
first to quickly
obtain quantitative parameters and substrate scope for decision-making;
in vivo
screening is confounded by cellular complexity and
cannot isolate single-variable effects. Recommended pathway:
“in vitro sets direction; in vivo provides validation.”
Feedback
(1)To address R1 accumulation , we will not prioritize knocking out a putative Ro-specific hydrolase, given the esterase family's frequent substrate promiscuity and the risk of perturbing core metabolism.
(2) When using the ODE framework combined with metabolic control analysis (MCA) , we will proceed cautiously : these models rest on assumptions and are sensitive to parameter accuracy, so we will treat them primarily as directional guides rather than precise predictors.
Interview with Professor Gao Renjun
Introduction
To ensure efficient project delivery within the competition's limited timeline and to resolve feasibility and hands-on issues in pathway optimization, on March 15, 2025 the JLU-NBBMS team held a project exchange with Professor Gao Renjun an expert in enzyme engineering at Jilin University's College of Life Sciences.
Record
We presented the overall design and current optimization framework, focusing on the pathway glycerol → 2,3-OSQ (2,3-oxidosqualene) → oleanolic acid (OA) → ginsenoside Ro , along with preliminary optimization ideas (e.g., remodeling respiratory pathways, suppressing ergosterol biosynthesis, site-directed enzyme mutagenesis). We sought advice on our “four-stage pathway optimization plan.” Professor Gao evaluated feasibility against the competition timeline and offered adjustments for each stage.
Q & A:
Q: We plan to use homologous recombination to remodel
respiration and fermentation pathways to maximize glycerol utilization. Is this
suitable for a short-term project?
A:
Not recommended. It increases plasmid count and
experimental complexity, and the benefit to final product titer is uncertain—poor
cost-effectiveness. In a short timeline, prioritize the organism's
native metabolism
, optimize only
key steps
, and let the rest follow
natural routes
.
Q:We intend to suppress yeast ergosterol biosynthesis to
channel precursors toward the target product. Should we keep this design?
A:
Trim or remove it. With limited time, focus on the
decisive
OA → Ro
conversion rather than early-stage regulation. Dropping
this step avoids metabolic disturbance in yeast and lets you concentrate resources on
the most impactful late steps. If time is tight,
omit it outright
.
Q:We originally planned site-directed mutagenesis on the
key enzyme UGT73P40. How can we improve enzyme performance in the short term?
A:
Abandon the original mutagenesis plan—its workload
exceeds a short project's capacity. Instead,
screen candidate glycosyltransferases from databases
, narrow
the set via
molecular docking
and
molecular dynamics
, then validate activity
experimentally
. This saves time, but simulation results
must
be confirmed in the wet lab, and avoid blind mutations at
the enzyme
active site
.
Feedback
Through this discussion, we clarified feasibility across optimization options and adopted a “ focus on the core under time constraints ” approach. Based on Professor Gao's advice, we made four changes:
(1) For glycerol → 2,3-OSQ , rely on the organism's endogenous pathways to reduce plasmid burden and prevent metabolic disorder.
(2) Shift the project's emphasis to OA → Ro ; do not suppress the ergosterol pathway to avoid compromising yeast viability.
(3) Use a glycosyltransferase database plus MD/docking (and optionally AI ) to screen enzymes efficiently, instead of heavy site-directed mutagenesis.
(4) Because Ro biosynthesis requires multiple glycosylation steps and consumes substantial UDPG (UDP-glucose), enhance the endogenous UDPG pathway .
Professor Gao emphasized tight project scoping , prioritizing the second half of the pathway. For enzyme engineering, he highlighted two higher-feasibility routes: AI-assisted and database-driven screening.
Interview with Professor Zhang Xinmin
Introduction
To ensure smooth progress in the project's later experimental phase, we held a project exchange meeting with Professor Zhang Xinmin from the School of Pharmacy, Jilin University .
Record
We briefed Professor Zhang on the overall design and sought his advice on three key, hands-on questions in the lab: plasmid design and construction , carbon-source selection , and final product verification . Based on his guidance, we finalized the next steps: first complete laboratory training and plasmid preparation , then officially launch the experimental work.
Q & A:
Q: Our project needs to load many key enzyme genes across
multiple plasmids. How should we optimize the design?
A:
2-3 genes
, using a
promoter-terminator concatenation
strategy is more conducive to
efficient protein expression. Focus on two points: (1) choose
different selection conditions/markers
for different plasmids;
(2) consider
plasmid incompatibility
—avoid using the same
origin of replication
wherever possible. Since your current
selections are mostly
antibiotic resistance markers
, you can also consider
auxotrophic (nutritional) selection
to reduce costs.
Q: Our carbon sources are glycerol and fatty acids. Do we
need to remove one of them?
A: No.
Glycerol
is inexpensive and the primary by-product of
biodiesel; many studies already convert glycerol into value-added products. For
fatty acids
, your
compartmentalization
approach—targeting key enzymes to the
peroxisome
to run the
MVA pathway
—is innovative and should be retained.
Q:How should we verify the final product, ginsenoside
Ro?
A:
Validation typically proceeds in
two steps
: first use
thin-layer chromatography (TLC)
for preliminary checks, and
finally confirm with
high-performance liquid chromatography (HPLC)
. Unexpected
results may arise, so different sub-teams often run experiments under varied conditions.
Directly starting with HPLC is time-consuming;
TLC
is faster and can also reveal
intermediate products
. Biosynthetic work should be
stepwise
—even if the final product is not obtained, you can
pinpoint the problematic stage.
Feedback
We adopted the three recommendations above in our experiments and, one month later, visited Professor Zhang's lab again to finalize specific experimental details, discussing carbon-source use in depth. As carbon sources, fatty acids include saturated and unsaturated types, which generally occur as solid and liquid , respectively; therefore, when setting the medium formulation, we must pay special attention to how yeast can effectively utilize fatty acids.
Dialogue with scholars from Oxford University
Introduction
To deepen the scope and breadth of our project research, from August 15 to August 20, 2025, members of the JLU-NBBMS team visited the University of Oxford, where they engaged with professors from the fields of medicine, biology, and ethics. The purpose of this visit was to present our project to international scholars and seek valuable feedback on critical issues such as bioethics, technological risks, and social impacts. At the same time, we aimed to further improve our work and promote traditional Chinese medicine culture abroad.
Record
We briefly presented the core design, technical path and application prospects of the project, followed by in-depth discussions with the professors on technical challenges and ethical considerations. The professors showed great interest in our effort to integrate traditional Chinese medicine wisdom with modern biotechnology and offered valuable insights from multiple perspectives.
Feedback
Our project concept and preliminary outcomes received high recognition. The professors particularly praised the project's unique cross-cultural perspective and commended the team's responsible approach in proactively integrating ethical considerations. This not only highlighted the valuable impact of the previous “Genes & Beliefs” iGEM Asia Virtual Gathering , but also inspired us to organize subsequent informal discussions on synthetic biology ethics . In these sessions, we engaged in in-depth debates around specific cases and conducted multi-perspective analyses and exchanges on the ethical implications of synthetic biology from different disciplinary viewpoints.
Interview with Professor Zhang Zuoming
Introduction
To clarify our project's core strengths, refine our experimental design, and address key bottlenecks in progress, we held an in-depth discussion with Professor Zhang Zuoming from the Department of Bioengineering, College of Life Sciences, Jilin University.
Record
Our team presented a systematic overview of the project, emphasizing the core architecture of three metabolic modules —(1) channeling fatty acids → MVA (mevalonate) to boost MVA supply, (2) converting MVA → ginsenoside Ro , and (3) channeling glycerol → UDP-glucose (UDPG) to increase UDPG availability—as well as our methodological innovation: using AI/ML-guided single-site saturation mutagenesis and rational design of UGT73F3 .
Based on the briefing, Professor Zhang provided expert feedback on highlights, feedstock definitions, troubleshooting and optimization, and toxicity control. He specifically suggested complementing “ opening the source ” (increasing precursor supply) with a “ blocking competing flux ” design: downregulate ERG7 (2,3-oxidosqualene cyclase/lanosterol synthase) to limit flux toward ergosterol, thereby redirecting more precursors to the target product.
Q & A:
Q: What are our project's core highlights?
A:
Twofold: (1) a clear metabolic-pathway
construction—three modules that respectively strengthen MVA and UDPG supply and drive
MVA toward Ro, with well-defined logic for precursor utilization and product synthesis;
(2) strong methodological innovation—AI/ML-assisted single-site saturation mutagenesis
and rational design of UGT73F3, exemplifying tight integration of dry-lab and wet-lab
work.
Q: We describe glycerol and fatty acids as “industrial
waste oil.” Is this accurate? If not, how should we adjust?
A:
Not accurate. Glycerol and fatty acids are
low-value industrial by-products
, not industrial waste oil. In
biodiesel
production (from vegetable/animal oils and methanol), they are residual
co-products
. If you retain the “waste-oil upgrading”
positioning, add an
initial purification
step to ensure feedstock quality;
alternatively, pivot to a
pure synthetic-biology
framing by using by-products from
established biodiesel processes (vegetable
oil, animal fat, or cellulose-derived routes), which sacrifices some “green” messaging
but makes
feedstock cleanliness
easier to guarantee—choose according to
your core aim.
Q: HPLC did not detect the final product Ro with three
sugar moieties. How should we troubleshoot?
A:
Proceed stepwise—
molecule → protein → in vitro
:
(1)Confirm plasmid transformation success (PCR already normal).
(2)Check transcription (RT-PCR) and translation (Western blot).
(3)If translation is confirmed, consider misfolding or hyperglycosylation in yeast causing loss of activity. Then run in-vitro enzyme assays by extracting the enzyme and adding substrate to detect product formation. Because plant proteins are prone to over-glycosylation in yeast, use dry-lab predictions to identify glycosylation sites and perform site-directed mutagenesis .
Q: The synthesized product is toxic to yeast growth. How
can we reduce intracellular accumulation?
A:
Use a standard
“export-on-production” strategy
: localize the terminal enzyme
to the
cell membrane
so the product is directly secreted upon
formation, lowering intracellular buildup. Together with “opening the source” and
“blocking competing flux,” this forms a core optimization triad in synthetic biology.
Feedback
At this stage, our main issue is that HPLC shows, besides the target Ro peak, deglycosylated Ro products (disaccharide ginsenosides) . Based on Ro's biosynthetic route, we suspect intermediate accumulation .
Professor Zhang offered four lines of action that substantially advanced our work:
(1) Determine whether the problem lies in plasmid expression versus a fault in the constructed metabolic pathway .
(2) Verify transformation and expression via PCR and Western blot .
(3) Assess enzyme activity in vitro . He noted that the heterologous genes originate from Panax notoginseng; when expressed in yeast, over-glycosylation can inactivate the enzymes.
(4) Through in-vitro assays , compare conversion efficiencies of the two branches, and—guided by dry-lab analysis—implement “source-opening” and “flux-blocking” adjustments to balance pathway flux.
Interview with Professor Wangfang
Introduction
To further clarify the project's scientific significance and social value—and to seek guidance for subsequent Human Practices (HP) activities—the JLU-NBBMS team held a project exchange with Professor Wang Fang , Dean of the College of Basic Medical Sciences, Jilin University .
Record
We presented a detailed overview of the project. Dean Wang affirmed the design concept and raised three key scientific questions:
1. Advantages of Ro: Compared with its intermediate R1 , how much higher is Ro's bioactivity? What are its concrete advantages? Why not target R1 as the final product?
2. Natural abundance: What are the natural levels of R1 or other ginsenosides in ginseng and related plants?
3. Enzyme choice: Why did we choose a Panax notoginseng-derived, specificity-driven glycosyltransferase rather than enzymes from other plant sources?
After gaining deeper understanding, Dean Wang offered three core recommendations for the team's future direction—especially for HP:
1. Clarify the purpose of HP: Define the ultimate objective so every activity serves a unified, impactful central theme.
2. Refine the role-play game narrative: Strengthen story logic and coherence for an international audience so it's easier for non-Chinese participants to follow.
3. Deepen the project story: Tell it from a broader perspective—first, underscore ginseng's importance to China and the world (e.g., Jilin's pharmaceutical industry, South Korea's beauty industry); then note that, despite the industry's growth, high-value components remain underutilized—hence the government's push for industrial upgrading.
Feedback
Acting on Dean Wang's advice, we further refined the narrative logic of our project website, added missing experimental-display details, and designed a Xinmin Street HP activity.
Interview with Professor Dhan Kalvakolanu
Introduction
To ensure our ginsenoside Ro biosynthesis project is presented with stronger rigor, logic, and international adaptability in global forums, we held an exchange with Professor Dhan Kalvakolanu .
Record
We reported the project by modules— wet lab, dry lab, HP, Education , and Entrepreneurship —and Professor Kalvakolanu offered line-by-line suggestions, followed by overarching guidance on tone and international perspective.
(1) Wet-lab module: standardize expression and tighten structure
In the background, precisely define the graphic: the circles depict aglycones (sapogenins) . Emphasize that our goal is to biosynthesize naturally occurring rare ginsenosides with proven pharmacology , not to invent novel ginsenosides.
Be rigorous in result statements: PCR only evidences successful gene transfer, not expression ; label the control as “positive” ; display different products separately to keep mapping clear.
Close the loop: provide reasonable explanations for negative results and add a brief summary at the end of each part to achieve standardized reporting.
(2) Dry-lab module: format fixes and logic reinforcement
Unify formatting: consistently highlight “pn022859” ; convert all figures to English ; keep gene/protein names (e.g., UGT73F3 ) consistent.
Rebuild the narrative with a “problem → solution” frame, showing how dry-lab work optimizes wet-lab design and underpins experimental choices.
(3) HP (market/industry): improve international fit
Internationalize labels and use English for all trademarks .
Be specific: replace “this industry” with “ginsenoside-extraction industry” or “ginseng-cultivation industry” ; replace “some people” with “ginseng growers” or “pharmaceutical R&D staff” to avoid cross-cultural ambiguity.
(4) Education (science outreach): strengthen coherence
When reporting activities from primary to high school, show progressive linkage (e.g., primary: fun “waste-to-resource” demo; middle: fundamentals of microbial synthesis; high: small-scale simulations), forming a step-by-step outreach system.
Use the standardized term “traditional Chinese medicine (TCM)” accurately.
(5) Entrepreneurship module: affirm and retain
The module clearly presents what / how / why ; no additional changes needed. Keep the current structure and content.
(6) Overall project tone: center on globally legible first principles
Anchor the project's intent around three core themes: (i) environmental cleanliness, (ii) biosynthesis of ginsenoside Ro, (iii) economic impact .
In the background, highlight these three rather than region-specific points like “low ginsenoside yield in Northeast China.” If short-term economic benefits are not yet evident, prioritize environmental and biosynthesis angles.
Ensure each module aligns to this revised core.
Feedback
This exchange provided clear directions on experimental standards, narrative logic, and overall positioning, improving the clarity and international suitability of our presentations.
Dialogue with the Ginseng Task Force
Introduction
To observe the ginseng industry ecosystem from a government-level, macro perspective and use our project to promote system-wide coordinated development, on September 9, 2025 we visited the Jilin Provincial Department of Agriculture and Rural Affairs and held a dialogue with the Jilin Provincial Task Force for Promoting High-Quality Development of the Ginseng Industry(hereinafter referred to as the "Ginseng Task Force") .

Record
During this visit, officials first introduced us to existing ginseng-related products in Jilin Province—such as ginseng coffee and compressed ginseng candies—as well as media placement plans in high-traffic areas like transportation hubs. We then held an in-depth discussion with the Jilin Provincial Task Force for Promoting High-Quality Development of the Ginseng Industry. We learned about the Task Force's mandate, departmental structure, the current state of ginseng development in the province, publicity strategies, and related activities that have recently been held or are forthcoming .


Q & A
Q: How can we encourage consumers to better accept bio-synthetic
ginseng products?
A:Currently, steering consumers toward a specific product is not the government's top
priority. From my personal perspective, for medicines containing ginseng-derived
ingredients, consumers care more about efficacy and price than about the source—i.e.,
whether the ginsenosides are natural or biosynthesized. If we focus on promoting
acceptance of biosynthetic technology but cannot deliver actual products, the discussion
has little value. Artemisinin, artificial bezoar (calculi bovis), and berberine
hydrochloride all moved from whole-herb extraction to synthetic production. Consumers
now recognize that single compounds and raw herbal materials can differ in efficacy, and
they will make choices accordingly.

Feedback
To better showcase our project in international contexts, we closely studied the “Jilin Ginseng at the UN Palais des Nations” campaign plan that the Department of Agriculture and Rural Affairs is slated to launch in Geneva, Switzerland, in October 2025. From a European perspective, we prepared related promotional materials, including a promo video, posters, a pocket guide, and a ginseng brochure
Interview with Ginseng Farmers
Introduction
To gain a more comprehensive understanding of the ginseng industry chain and the genuine needs of its stakeholders—along with the production realities under traditional cultivation, farmers' attitudes amid industry challenges, and their awareness and acceptance of innovative solutions such as synthetic biology—we turned to the source of ginseng cultivation: Baicheng, Jilin Province, where we conducted in-depth interviews with local ginseng farmers.

Record
We held face-to-face conversations with several experienced ginseng farmers, focusing on cultivation costs, environmental impact, market volatility, and technology adoption. Farmers described multiple pressures in traditional cultivation : severe soil degradation, lengthy growth cycles, increasing climate uncertainty, and economic risks from price fluctuations. Many expressed an urgent need for “green cultivation” and “sustainable development,” while candidly noting major hurdles in transitioning due to limited technical support and funding . We also discussed their initial views on “synthetic biology” and “cell-factory production of ginsenosides,” and listened to their authentic perspectives on technology ethics, industry complementarity, and impacts on their livelihoods.
Q & A:
Q: What do you think is the biggest challenge in ginseng cultivation today?
A(a farmer with over 20 years of experience): The biggest issue is still the land.
After growing ginseng, the land can't be reused for many years. The soil fertility drops
severely, and pests and diseases are becoming harder to manage. We want to transition to
ecological farming, but the investment is too high, and the cycle is even longer—we
smallholders can't afford it.

Q: What would you think if a new technology could replace some traditional
cultivation with lab-based methods?
A(a middle-aged farmer) : If it can protect
the land
and provide us with a reasonable income, of course, it would be a good thing. But what I
worry about is whether our skills and land would become useless. It would be best if
it's not a complete replacement but a technology that can develop together with us.
Feedback
Through these interviews, we realized that ginseng farmers place a strong emphasis on soil health and sustainable cultivation but lack the technical and financial support to achieve a transition . They are cautiously open to new technologies and prefer innovation that is “ complementary rather than substitutive .” Most importantly, farmers want to be seen and heard —and to be included in technology-industry discussions.

Visit to the Jilin Province Kuai Da Ginseng Trading Market
Introduction
To comprehensively explore the full ginseng value chain—from cultivation and trading to end consumption—and gather first-hand stakeholder feedback from the front line, we made a dedicated site visit to the Kuaida Ginseng Trading Market in Tonghua, Jilin Province, on the afternoon of August 23, 2025. Warmly guided by Ms. Xiao Lei, a representative of the market's merchants, we conducted on-site field research at this key hub of the ginseng industry.

Record
Led by Ms. Xiao Lei, our team was first struck by the vast scale and modern management of the Kuaida Ginseng Market. We visited trading zones for different product categories in turn, where Ms. Xiao explained in detail how to distinguish various types of ginseng and the relevant processing techniques. From completely unprocessed fresh ginseng to finely sliced medicinal pieces, the market offered an exceptionally rich array of product forms to meet diverse consumer needs. We gained a vivid, first-hand sense of a vibrant ginseng industry ecosystem that blends traditional know-how with modern business models .

Q & A:
Q: What specific changes has the establishment of the National Quality
Inspection Center's service department brought to your business?
A: This impact has been revolutionary. In the past, authenticity and grade were
judged purely by experience, and disputes between buyers and sellers were common. Now,
with authoritative national-level testing, our customers can purchase with greater
confidence, and honest merchants like us have more confidence too—quality goods can
fetch better prices. It has greatly enhanced the brand reputation of Tonghua ginseng and
improved the overall standardization of the market.
Q: In recent years, many deep-processed ginseng products like beverages and
cosmetics have appeared. How do you see their market prospects compared to traditional
whole ginseng roots and slices?
A: Traditional whole-root ginseng and sliced
products have a stable consumer base—especially among middle-aged and older
customers—who trust “all-natural” items they can prepare themselves. Younger consumers,
by contrast, prefer modern products that are convenient and quick to use. As a result,
the traditional market and the new-product market are developing in parallel, each
serving its own clientele.

Feedback
Through face-to-face conversations with merchants at the Kuaida Ginseng Market, we gained a deeper understanding of the project's real-world application scenarios and potential social impacts. For example:
1. Clear Need for Industrial Upgrading: There is strong market demand for standardized, traceable, high-quality ginseng products, indicating that the industry is actively embracing standardization. This creates a logical market entry point for our biomanufactured, high-purity, single-ingredient ginsenosides.
2. Market Segmentation and Coexistence: Traditional ginseng and modern deep-processed products each serve distinct target markets. Our project should not be positioned as a “disruptor” of traditional cultivation, but as an enabler of industry modernization—supplying downstream manufacturers with cost-effective, quality-consistent core ingredients that are difficult to obtain through conventional extraction.
3. Public Acceptance is Key: Merchants widely noted consumers' preference for “natural” and their potential skepticism toward “factory-made” products. This reminds us that success hinges not only on technical breakthroughs, but also on effective science communication and market outreach.
Youth Health Run Questionnaire Survey
Introduction
To further promote our project, raise public awareness about the scientific knowledge related to bio-manufacturing ginseng health components, and gather public views and needs regarding this technology and related products, we participated in Jilin University's Youth Health Run event. We set up checkpoints along the running route to collect electronic questionnaires . The questionnaire covered multiple aspects, including participants' understanding of microbial manufacturing technologies , their willingness to purchase ginseng and related products , and their concerns and suggestions about the application of the technology . In total, we collected 111 valid questionnaires, which provide important data support for the subsequent development of our project.
Record
This Health Run combined exercise with on-site research: while completing the run, participants filled out the “iGEM Ginseng Microbial Factory” survey on site. We set up a dedicated consultation area where we answered questions about the Youth Health Run procedure and the questionnaire to ensure that participants clearly understood the items and completed them accurately.
Survey Findings:
1. Respondent Characteristics & Technology Acceptance: The respondent pool skewed young and relatively well-educated , with 18-30-year-old technicians, university students, physicians, and other knowledge-based groups comprising the majority. In terms of technological awareness, most had previously heard of using microorganisms (e.g., yeast) to manufacture medicines or health products and thus possessed a basic understanding. Attitudinally, support for the specific application of using yeast to produce ginseng health components was very high; only a small minority were unsupportive or uncertain due to unfamiliarity with the underlying principles.
2. Purchase Intent and Concerns: The public already has an existing purchasing base for ginseng and related products (including supplements and cosmetics). As for purchase drivers, ginseng health components with a higher price-performance ratio and produced through more environmentally friendly processes—along with products certified by authoritative institutions and carrying clear safety labels—are more likely to boost most consumers' purchase intentions. At the same time, many respondents voiced notable concerns , focusing on potential health risks (e.g., ingredient safety), environmental risks (e.g., impacts of microbial release), and possible ethical issues. They explicitly indicated a desire for companies or relevant institutions to provide more detailed safety-testing data and explanations to strengthen trust in such products.
3. Social Perception and Information Dissemination: Culturally, the vast majority acknowledge ginseng's special cultural significance . In terms of social impact, many note that this technology may disrupt the livelihoods of traditional ginseng farmers and express concern about its effects on workers in the conventional industry. In terms of means of learning, short videos are the public's most favored way to learn about new technologies , far surpassing lectures or hands-on experiments. In terms of content appeal , most people become more interested when presented with “health-benefit” information. At the science-education level, the public generally supports incorporating new technologies related to microorganisms and health into youth curricula, viewing this as important for improving scientific literacy among young people.
Feedback
Youth Health Run activity clarified the public's support, concerns and worries about the project's technology and related products . These data provide important basis for the subsequent technology research and development, product promotion and publicity strategy formulation of the project.
Subsequently, the wet-lab team further tightened biosafety controls throughout the biosynthetic process and established effective risk-management protocols; the Education team produced engaging short videos and posts for platforms such as Douyin and Xiaohongshu to attract a wider public adopted youth-friendly formats—comics and interactive experiments—to foster young people's interest in synthetic biology.
Street Interview on Xinmin Street
Introduction
To understand consumers' views on pricing, safety, and other aspects of biosynthesized ginseng saponin products—and to foster recognition of synthetic biology's translational potential—we conducted street interviews with the general public on Xinmin Street in Changchun on August 23, 2025. As a key destination in Changchun's cultural and tourism development, this area attracts many residents and visitors. Our interviewees included children, middle-aged, and older adults, comprising students, tourists, and retirees.
Record
We obtained a sales booth on Xinmin Street and displayed conventionally extracted (non-biosynthetic) ginsenoside products sold by company Jizhenshen (吉甄参) —including ginseng beverages, face masks, and hand creams. We interviewed consumers interested in these items and, through our questions, guided their attention to biosynthesized ginsenoside products as a new technological alternative.
In designing the questions, we did not attempt to cram large amounts of scientific knowledge into a brief interaction. Instead, by drawing an analogy between organic and genetically modified (GM) agricultural products and using clear, accessible language, we helped participants quickly grasp how synthetic biology differs from traditional production methods and encouraged them to articulate their concerns when making purchasing decisions.
Q & A:
Q: What advantages might synthetically produced foods and medicines have
compared with purely natural products?
A1: Natural products don't harm the human
body, whereas chemically synthesized ones inevitably contain chemical components that
can be harmful.
A2: Do chemically synthesized products have a longer shelf life?
Still, the anti-aging effects of ginseng may come from a combination of substances
rather than a single one. If biosynthesis produces only one compound, might it overlook
that synergistic effect?
Q: When choosing health products, what factors matter most to you?
A:
Safety first, then efficacy, and lastly cost-effectiveness. I'd rather choose greater
safety than pursue very high efficacy at the risk of more side effects.
Q: If you were willing to buy biosynthesized ginseng saponin products, what
price range would you prefer?
A1: I buy based on efficacy. For example, wild
ginseng is more expensive than cultivated ginseng, but if it works better, I'm willing
to pay more. As technology advances, extraction or synthesis may target different
pharmacological effects, different saponins will lead to different prices. As a
consumer, I weigh many factors—it's hard to judge price by production method
alone.
A2: It depends on your production technology. If your technical level is
high, costs go down, so lab-made products may be cheaper than natural ones. That could
be the broader trend as technology develops.
Feedback
In our research, we found that “safety” remains the primary factor consumers consider when choosing health and pharmaceutical products. The public generally believes that medical/scientific institutions and the government should bear responsibility for ensuring food and drug safety. This became a focal topic in our interview with the Ginseng Task Force (人参专班) of the Jilin Provincial Department of Agriculture and Rural Affairs .
During the interviews, we also found that, given the diverse makeup of Xinmin Street's passersby, some respondents lacked interest in or familiarity with ginseng extracts and related topics, resulting in a relatively high rate of refusals or non-informative responses. Consequently, we shifted our efforts to the Northeast Asia Expo in Changchun—its dedicated ginseng exhibition area draws a more targeted audience, enabling us to identify suitable interviewees with greater precision.
Consumer Interviews at the Northeast Asia Expo
Introduction
To collect feedback more efficiently, deepen our understanding of public awareness of the concept and products of “synthetic biology,” and probe consumers' acceptance and considerations regarding food safety, pricing, and efficacy, we visited the Changchun Northeast Asia International Expo Center on August 27, 2025, and interviewed target audiences in the ginseng exhibition area. These insights provide important public perspectives and data support for the subsequent advancement of our project.

Record
Continuing with an oral Q&A format, we conducted random interviews with attendees of different ages in the ginseng exhibition area at the Northeast Asia Expo.
The results show that most consumers have clear concerns about the safety of biosynthetically produced ginseng saponins. The main reason is their belief that ginseng's efficacy depends on years of natural growth, so they remain cautious about whether laboratory-produced ingredients can deliver comparable efficacy and value. However, after learning that the project is supported by a university research team, many changed their view, expressing a willingness to trust scientific findings and offering support and encouragement for the project.
In addition, many respondents said their purchase intention would rise significantly if biosynthesized ginseng products provided clear traceability labels and third-party safety certification. Regarding product formats, younger groups prefer convenient, easy-to-take modern dosage forms (e.g., capsules or functional beverages), while middle-aged and older groups pay more attention to whether products align with traditional Chinese medicine concepts.

Q & A
Q: If there were a ginseng saponin product manufactured via synthetic
biology, what would you care about most?
A(middle-aged female consumer): Safety,
of course. Traditional ginseng values the
“essence of heaven and earth” and sufficient years of growth. If you make it in a lab,
will the composition and efficacy really match field-grown ginseng? Unless there is
certification from the National Medical Products Administration (NMPA) proving it is as
safe as natural ginseng and has comparable efficacy—perhaps even greater purity—I would
only then consider it.
Q: How should such a product be promoted so that you'd be more willing to
trust or accept it?
A1 (male graduate student) :Universities stand for
noncommercial, rigorous science. If
it's developed by a university and all research data are disclosed—rather than by an
unfamiliar commercial company—I'd be far more receptive. Emphasize the research
background and make the papers and datasets openly accessible; that's more persuasive
than any advertisement.
A2(male health-supplement salesperson): From an industry
perspective, consumers care
most about “safety” and “effectiveness.” If your synthetic saponin can provide
scientific evidence—especially human studies or third-party certification—to dispel
safety concerns, and if it also offers a price advantage, the market should gradually
accept it. I personally support this kind of innovation.

Feedback
Through targeted interviews at the Northeast Asia Expo, we obtained highly valuable first-hand public feedback. These insights not only confirmed parts of our hypotheses but also pointed the way for subsequent project advancement.
We have turned this feedback into concrete actions:
1. We further strengthened safety validation in our experiments and conducted efficacy-comparison studies between biosynthesized saponins and those produced by traditional methods.
2. Leveraging our university affiliation, we will also host The First Lesson in Synthetic Biology, using lab tours and engaging hands-on activities to present our technical principles, safety profile, and application prospects in an accessible way—converting the university's credibility into effective science outreach.
THE PLANET OF ENTERPRISES
Changchun International Pharmaceutical and Health Industry Expo
Introduction
To gain a deeper understanding of the
real-world demands
about the scientific
and
technological frontiers
of the ginseng industry at the
early stage
of our project, on December 9, 2024, the JLU-NBBMS team visited the
Changchun International Pharmaceutical and Health Industry Expo at the Northeast
Asia International Expo Center. Through this field study, we aimed to systematically
grasp the
current state of technological development,
market challenges, and innovation trends
related to ginseng and its
derivative
products, with a particular focus on the potential application
of emerging technologies such as synthetic biology in the field of
traditional medicinal materials.
Record
During the expo, our team conducted
on-site visits and
informal exchanges
with exhibitors and professional visitors, focusing on the following areas:
The technological implementation and market performance of
ginseng
extracts
and high value-added products
(such as rare ginsenosides, functional
beverages,
and anti-aging skincare products).
Application cases and acceptance levels of innovative technologies—such
as synthetic biology
and biomanufacturing—within the field of traditional Chinese medicine.
Industry perspectives and cooperation intentions regarding the
technological
route of “biosynthetic ginsenosides.”
Feedback
hrough exchanges with multiple enterprises, researchers, and industry
participants
at the expo, we gained valuable insights that provided a crucial foundation for
determining the project's early direction and technical roadmap. We found that the
ginseng industry is facing several
pressing challenges
: first,
difficulties in standardizing extracts
, with
significant fluctuations in composition
and obstacles to meeting international quality standards; second,
rare
ginsenosides
involve
highly complex extraction processes with extremely low yields
,
while their separation and
purification remain difficult. As a result, the final products are prohibitively
expensive and struggle to achieve
widespread use in mass health products.
In response, we quickly transformed these insights into concrete actions. We
launched systematic
literature reviews and technical route comparisons, focusing on existing microbial
biosynthesis pathways of
ginsenosides, key enzymes, and chassis organism selection. The current industrial
challenges clearly remind us that
technological innovation
is not merely an option, but an
imperative.
In addition, we
expanded our perspective on human
practices
.
We initiated preliminary engagement with
ginseng farmers
and
enterprise R&D staff
to
continuously gather their practical needs and to explore possible transformations in the
future of the ginseng industry.
Company Visit: Xiuzheng Pharmaceutical
Introduction
To explore ginsenoside technologies and market demand, we visited Xiuzheng
Pharmaceutical
Changchun High-Tech Pharmaceutical Co., Ltd.. As a large enterprise spanning multiple
drug classes, its
R&D center offered a valuable setting for our study. Through expert discussions and an
on-site tour, our
team identified industry pain points, gained insights into cost control and
sustainability, and considered
how synthetic biology might enhance existing production models.
Record
During the visit to Xiuzheng Pharmaceutical, we combined expert roundtables
with a plant
tour to conduct in-depth research on ginsenoside production and enterprise practices,
focusing on:
The technical/process details of Xiuzheng's core production stages
(extraction, purification) for ginsenosides, and the key steps—and bottleneck
breakthroughs—in
translating lab results to industrial-scale manufacturing.
Concrete strategies and practical experience in raw-material screening,
control of
compositional/stability consistency, and cost optimization during R&D of
ginsenoside-related products.
The company's market layout: its logic for positioning consumer demand
and the
mechanisms that align research directions with market needs.
Xiuzheng's views on applying synthetic biology to ginsenoside (e.g., Ro)
production,
along with potential intentions for technical collaboration and industrial translation.
Feedback
The visit to Xiuzheng Pharmaceutical helped us optimize our
technology
roadmap
and
industrial roll-out
with a market-oriented lens: through discussions with R&D
experts and on-site
observations, we clarified gaps between laboratory technology and industrial needs,
identified
pain points in scale-up stability and cost control, and translated the findings into
follow-up actions.
Subsequently, we analyzed ginsenoside production processes and, drawing on
Xiuzheng's experience,
conducted cost modeling and cost-reduction pathway studies to support selecting routes
that balance advancement
with cost controllability. We also expanded our Human Practices work by launching a
multi-stage research across
the industrial chain (covering other companies, farmers, and consumers) to
comprehensively understand needs
and concerns and to promote win-win collaboration between R&D and industry.
Company Visit: Yatai Pharmaceutical
Introduction
To gain an in-depth understanding of the
end-to-end
industrialization pathway
and
key technical bottlenecks
from laboratory research to
commercial products
for rare ginsenosides—and to find practical benchmarks for our startup producing
ginsenoside Ro via
synthetic biology—our team made a dedicated site visit to Jilin Yatai Pharmaceutical
Co., Ltd.
Record
As a high-tech enterprise that successfully achieved
large-scale production
of ginsenoside Rg3
in China and developed the national Class I new drug “Shenyi Capsule”, the
company's comprehensive experience—from
technological breakthroughs and process scale-up to market entry—provides highly
valuable insights for us in exploring the
feasible path of tech entrepreneurship and the translation model of innovation. This
interview not only aimed to understand
the specific challenges of traditional extraction processes, purity control strategies,
and byproduct management, but also
sought, from an entrepreneurial perspective, to explore
the industrial
potential of synthetic
biology in rare ginsenoside production
, the possible commercialization
barriers, and the prospects of building
a sustainable entrepreneurial ecosystem.
Q & A:
Q: What was the core driving force behind your company's successful
development
and industrialization of Shenyi Capsule?
A: Ginsenoside Rg3 is present at extremely low levels in red ginseng (only
0.0003%),
but it has remarkable anti-tumor effects, particularly in inhibiting angiogenesis,
making it highly promising
for drug development. However, due to its scarcity and the difficulties of industrial
extraction, achieving efficient
large-scale production became a major challenge. This has been the core driving force
behind our continued R&D investment.
Q: What were the key technological innovations in improving Rg3
extraction efficiency and purity?
A: At the beginning, extraction efficiency was very low, costs were high, and
byproduct handling was problematic.
By introducing ceramic membrane filtration, biocatalytic directional transformation, and
chiral
compound separation technologies, we greatly improved the extraction yield and achieved
large-scale production of Rg3 with
over 95% purity, breaking through the limitations of traditional extraction methods.
Q: What is the company's future strategic focus in R&D and market expansion?
A: We plan to move from single herbal monomers (like Rg3) to compound components
such as total
ginsenosides, while expanding from the pharmaceutical industry to food and cosmetics,
promoting diversified development.
Q: What is your view on the potential of synthetic biology in rare
ginsenoside production?
A: Synthetic biology is expected to solve the bottlenecks of traditional
extraction, such as strong resource dependence,
low efficiency, and high costs. By constructing microbial cell factories, ginsenosides
can be produced at scale in a sustainable
way, and product structures can be optimized directionally. The application prospects
are broad, and our company attaches great
importance to this field and follows it closely.
Feedback
Yatai's operating experience gave us
a large-enterprise
benchmark to reflect on the
obstacles we may face as a startup
. Their proposed diversification strategies
also prompted us to consider
whether our technology has
the potential to move further downstream
into product manufacturing and sales
.
Company Visit: Yisheng Pharmaceutical
Introduction
To gain a deeper understanding of the ginseng industry's practical needs and
pain points—and to keep
our project closely aligned with the sector's development trajectory—we paid a special
visit on the morning of August 23
to Jilin Province Ji'an Yisheng Pharmaceutical Co., Ltd. (a leading full-value-chain
enterprise). Warmly received by company
representatives, team members from Jilin University's Norman Bethune College of Medicine
toured the modern production
facilities of Yisheng Han-Shen Biotechnology Co., Ltd. and held in-depth discussions
with company leadership.
Record
Company representatives briefed us on Yisheng Pharmaceutical's development
history, industrial layout,
and corporate culture. Yisheng has built a complete value chain covering cultivation,
R&D, processing,
and sales, with businesses spanning pharmaceuticals, health foods, and cosmetics. During
the exchange, both sides
discussed market demand for high-purity ginseng saponins, challenges in raw-material
supply, and the prospects for
applying synthetic biology in the industry, and exchanged views on the coordinated
development of biosynthetic
technologies and traditional cultivation.
Q & A:
Q: Among your product lines, which categories need high-purity ginsenoside Ro
the most? What about its raw material source and cost?
A: The strongest demand comes from high-end cosmetics and functional health foods.
Ro offers antioxidant and
anti-aging effects in cosmetics and shows liver-protective potential in health foods.
Currently, it is mainly extracted
from ginseng berries, which have low yield and batch variation, resulting in high costs
and unstable quality. Hence,
a stable, scalable, and cost-effective Ro source is urgently needed---precisely where
synthetic biology could add value.
Q: Do you think biosynthesized ginsenosides will disrupt traditional ginseng
farming and farmers' livelihoods? What role should they play?
A: This is not a disruption but an industrial upgrade. Consumers strongly value
whole ginseng “from the earth”
in food and traditional health uses, which biosynthesized compounds cannot replace.
Synthetic biology excels at producing
high-purity rare ginsenosides efficiently, meeting pharmaceutical and cosmetic needs.
This can free farmers to focus on
premium cultivation, raising overall industry value. The two are complementary and
mutually beneficial, not zero-sum.
Feedback
From this exchange, we came to understand that the ginseng industry's urgent
needs are
rare ginsenosides with high purity,
low cost, and stable supply
. We also learned that the primary
commercialization bottleneck lies in
downstream purification
costs
. Cosmetics and health foods are the fastest avenues for Ro commercialization, whereas
pharmaceuticals face higher safety requirements and thus longer approval timelines.
Enterprises That Could Not Be Reached
Introduction
Over the past few months, the JLU-NBBMS team has centered its efforts on the
project theme of ginsenosides and the core concept of "decentralization". Through a
combination of online and offline approaches, we proactively reached out to
pharmaceutical companies, biotechnology firms
, and other
relevant enterprises to seek
communication, and learning opportunities. However,
this process was
far from
smooth
—some readily agreed to engage, others canceled midway, and some
outright rejected
our outreach.
Record
Shortly after establishing the team and confirming the project theme, we
began our efforts to contact enterprises
starting in March
. Our
goal was to pursue
on-site visits, online and offline discussions, and knowledge exchanges, aiming to
identify market needs and practical requirements from an enterprise perspective. We
received strong support from major pharmaceutical companies such as
Xiuzheng and Yatai
group
, as well as
government departments
. However,
our potential competitors—
leading
enterprises in ginsenoside production
—largely
either
rejected our visit requests or
interrupted the process midway
. This is not entirely unexpected. As leaders
in the
ginsenoside production field and a current hotspot in synthetic biology,
it is entirely
justified for these enterprises to protect their trade secrets. Of course, it is
also
possible that some simply lacked the time to engage
.
Beyond that,
a number of enterprises remained uncontacted
primarily due to
poor communication channels
. For some businesses, especially small- to
medium-sized
enterprises (SMEs) and emerging startups, they may not even have their own official
websites or WeChat public accounts. Gleaning limited information about them often relies
on third-party platforms like Tianyancha, Qichacha or Aiqicha. Unfortunately, details
provided on such platforms—including phone numbers and email addresses—are frequently
incorrect.
Feedback
Based on these experiences, our approach to seeking contact information now
prioritizes:
1.
Official Channels:
Utilizing enterprise websites,
WeChat public accounts, rednote (xiaohongshu), and integrated media accounts (e.g.,
Bilibili, Weibo, Douyin) to send inquiries through publicly available means.
2.
Bidding & Exhibition Data:
Searching for bidding
information, exhibitor lists, and other public records to trace contact details.
3.
Hierarchical Follow-Up:
For specific departments
or special task forces within enterprises, we start with general contact information and
progressively follow up via phone transfers to reach the targeted units.
4.
Leveraging Networks:
For enterprises that are
urgently needed but impossible to contact through standard channels, we seek assistance
from personal connections or teachers to establish direct communication.
In terms of communication tactics, we first
propose online
discussions or soften the "sharpness" of our initial inquiries by framing questions
more broadly
, making it easier for the other party to accept.
Through these methods, we have generally succeeded in reaching our target
enterprises. This cumbersome and non-transparent information disclosure process has also
made our team realize
the importance of transparency and openness in
business collaboration and enterprise engagement
. Such practices
not only reflect
accountability but also demonstrate our commitment to
fulfilling social responsibilities
.
Changchun International Pharmaceutical and Health Industry Expo
Introduction
To gain a deeper understanding of the real-world demands about the scientific and technological frontiers of the ginseng industry at the early stage of our project, on December 9, 2024, the JLU-NBBMS team visited the Changchun International Pharmaceutical and Health Industry Expo at the Northeast Asia International Expo Center. Through this field study, we aimed to systematically grasp the current state of technological development, market challenges, and innovation trends related to ginseng and its derivative products, with a particular focus on the potential application of emerging technologies such as synthetic biology in the field of traditional medicinal materials.
Record
During the expo, our team conducted on-site visits and informal exchanges with exhibitors and professional visitors, focusing on the following areas:
The technological implementation and market performance of ginseng extracts and high value-added products (such as rare ginsenosides, functional beverages, and anti-aging skincare products).
Application cases and acceptance levels of innovative technologies—such as synthetic biology and biomanufacturing—within the field of traditional Chinese medicine.
Industry perspectives and cooperation intentions regarding the technological route of “biosynthetic ginsenosides.”
Feedback
hrough exchanges with multiple enterprises, researchers, and industry participants at the expo, we gained valuable insights that provided a crucial foundation for determining the project's early direction and technical roadmap. We found that the ginseng industry is facing several pressing challenges : first, difficulties in standardizing extracts , with significant fluctuations in composition and obstacles to meeting international quality standards; second, rare ginsenosides involve highly complex extraction processes with extremely low yields , while their separation and purification remain difficult. As a result, the final products are prohibitively expensive and struggle to achieve widespread use in mass health products.
In response, we quickly transformed these insights into concrete actions. We launched systematic literature reviews and technical route comparisons, focusing on existing microbial biosynthesis pathways of ginsenosides, key enzymes, and chassis organism selection. The current industrial challenges clearly remind us that technological innovation is not merely an option, but an imperative.
In addition, we expanded our perspective on human practices . We initiated preliminary engagement with ginseng farmers and enterprise R&D staff to continuously gather their practical needs and to explore possible transformations in the future of the ginseng industry.
Company Visit: Xiuzheng Pharmaceutical
Introduction
To explore ginsenoside technologies and market demand, we visited Xiuzheng Pharmaceutical Changchun High-Tech Pharmaceutical Co., Ltd.. As a large enterprise spanning multiple drug classes, its R&D center offered a valuable setting for our study. Through expert discussions and an on-site tour, our team identified industry pain points, gained insights into cost control and sustainability, and considered how synthetic biology might enhance existing production models.
Record
During the visit to Xiuzheng Pharmaceutical, we combined expert roundtables with a plant tour to conduct in-depth research on ginsenoside production and enterprise practices, focusing on:
The technical/process details of Xiuzheng's core production stages (extraction, purification) for ginsenosides, and the key steps—and bottleneck breakthroughs—in translating lab results to industrial-scale manufacturing.
Concrete strategies and practical experience in raw-material screening, control of compositional/stability consistency, and cost optimization during R&D of ginsenoside-related products.
The company's market layout: its logic for positioning consumer demand and the mechanisms that align research directions with market needs.
Xiuzheng's views on applying synthetic biology to ginsenoside (e.g., Ro) production, along with potential intentions for technical collaboration and industrial translation.
Feedback
The visit to Xiuzheng Pharmaceutical helped us optimize our technology roadmap and industrial roll-out with a market-oriented lens: through discussions with R&D experts and on-site observations, we clarified gaps between laboratory technology and industrial needs, identified pain points in scale-up stability and cost control, and translated the findings into follow-up actions.
Subsequently, we analyzed ginsenoside production processes and, drawing on Xiuzheng's experience, conducted cost modeling and cost-reduction pathway studies to support selecting routes that balance advancement with cost controllability. We also expanded our Human Practices work by launching a multi-stage research across the industrial chain (covering other companies, farmers, and consumers) to comprehensively understand needs and concerns and to promote win-win collaboration between R&D and industry.
Company Visit: Yatai Pharmaceutical
Introduction
To gain an in-depth understanding of the end-to-end industrialization pathway and key technical bottlenecks from laboratory research to commercial products for rare ginsenosides—and to find practical benchmarks for our startup producing ginsenoside Ro via synthetic biology—our team made a dedicated site visit to Jilin Yatai Pharmaceutical Co., Ltd.
Record
As a high-tech enterprise that successfully achieved large-scale production of ginsenoside Rg3 in China and developed the national Class I new drug “Shenyi Capsule”, the company's comprehensive experience—from technological breakthroughs and process scale-up to market entry—provides highly valuable insights for us in exploring the feasible path of tech entrepreneurship and the translation model of innovation. This interview not only aimed to understand the specific challenges of traditional extraction processes, purity control strategies, and byproduct management, but also sought, from an entrepreneurial perspective, to explore the industrial potential of synthetic biology in rare ginsenoside production , the possible commercialization barriers, and the prospects of building a sustainable entrepreneurial ecosystem.
Q & A:
Q: What was the core driving force behind your company's successful
development
and industrialization of Shenyi Capsule?
A: Ginsenoside Rg3 is present at extremely low levels in red ginseng (only
0.0003%),
but it has remarkable anti-tumor effects, particularly in inhibiting angiogenesis,
making it highly promising
for drug development. However, due to its scarcity and the difficulties of industrial
extraction, achieving efficient
large-scale production became a major challenge. This has been the core driving force
behind our continued R&D investment.
Q: What were the key technological innovations in improving Rg3
extraction efficiency and purity?
A: At the beginning, extraction efficiency was very low, costs were high, and
byproduct handling was problematic.
By introducing ceramic membrane filtration, biocatalytic directional transformation, and
chiral
compound separation technologies, we greatly improved the extraction yield and achieved
large-scale production of Rg3 with
over 95% purity, breaking through the limitations of traditional extraction methods.
Q: What is the company's future strategic focus in R&D and market expansion?
A: We plan to move from single herbal monomers (like Rg3) to compound components
such as total
ginsenosides, while expanding from the pharmaceutical industry to food and cosmetics,
promoting diversified development.
Q: What is your view on the potential of synthetic biology in rare
ginsenoside production?
A: Synthetic biology is expected to solve the bottlenecks of traditional
extraction, such as strong resource dependence,
low efficiency, and high costs. By constructing microbial cell factories, ginsenosides
can be produced at scale in a sustainable
way, and product structures can be optimized directionally. The application prospects
are broad, and our company attaches great
importance to this field and follows it closely.
Feedback
Yatai's operating experience gave us a large-enterprise benchmark to reflect on the obstacles we may face as a startup . Their proposed diversification strategies also prompted us to consider whether our technology has the potential to move further downstream into product manufacturing and sales .
Company Visit: Yisheng Pharmaceutical
Introduction
To gain a deeper understanding of the ginseng industry's practical needs and pain points—and to keep our project closely aligned with the sector's development trajectory—we paid a special visit on the morning of August 23 to Jilin Province Ji'an Yisheng Pharmaceutical Co., Ltd. (a leading full-value-chain enterprise). Warmly received by company representatives, team members from Jilin University's Norman Bethune College of Medicine toured the modern production facilities of Yisheng Han-Shen Biotechnology Co., Ltd. and held in-depth discussions with company leadership.
Record
Company representatives briefed us on Yisheng Pharmaceutical's development history, industrial layout, and corporate culture. Yisheng has built a complete value chain covering cultivation, R&D, processing, and sales, with businesses spanning pharmaceuticals, health foods, and cosmetics. During the exchange, both sides discussed market demand for high-purity ginseng saponins, challenges in raw-material supply, and the prospects for applying synthetic biology in the industry, and exchanged views on the coordinated development of biosynthetic technologies and traditional cultivation.
Q & A:
Q: Among your product lines, which categories need high-purity ginsenoside Ro
the most? What about its raw material source and cost?
A: The strongest demand comes from high-end cosmetics and functional health foods.
Ro offers antioxidant and
anti-aging effects in cosmetics and shows liver-protective potential in health foods.
Currently, it is mainly extracted
from ginseng berries, which have low yield and batch variation, resulting in high costs
and unstable quality. Hence,
a stable, scalable, and cost-effective Ro source is urgently needed---precisely where
synthetic biology could add value.
Q: Do you think biosynthesized ginsenosides will disrupt traditional ginseng
farming and farmers' livelihoods? What role should they play?
A: This is not a disruption but an industrial upgrade. Consumers strongly value
whole ginseng “from the earth”
in food and traditional health uses, which biosynthesized compounds cannot replace.
Synthetic biology excels at producing
high-purity rare ginsenosides efficiently, meeting pharmaceutical and cosmetic needs.
This can free farmers to focus on
premium cultivation, raising overall industry value. The two are complementary and
mutually beneficial, not zero-sum.
Feedback
From this exchange, we came to understand that the ginseng industry's urgent needs are rare ginsenosides with high purity, low cost, and stable supply . We also learned that the primary commercialization bottleneck lies in downstream purification costs . Cosmetics and health foods are the fastest avenues for Ro commercialization, whereas pharmaceuticals face higher safety requirements and thus longer approval timelines.
Enterprises That Could Not Be Reached
Introduction
Over the past few months, the JLU-NBBMS team has centered its efforts on the project theme of ginsenosides and the core concept of "decentralization". Through a combination of online and offline approaches, we proactively reached out to pharmaceutical companies, biotechnology firms , and other relevant enterprises to seek communication, and learning opportunities. However, this process was far from smooth —some readily agreed to engage, others canceled midway, and some outright rejected our outreach.
Record
Shortly after establishing the team and confirming the project theme, we began our efforts to contact enterprises starting in March . Our goal was to pursue on-site visits, online and offline discussions, and knowledge exchanges, aiming to identify market needs and practical requirements from an enterprise perspective. We received strong support from major pharmaceutical companies such as Xiuzheng and Yatai group , as well as government departments . However, our potential competitors— leading enterprises in ginsenoside production —largely either rejected our visit requests or interrupted the process midway . This is not entirely unexpected. As leaders in the ginsenoside production field and a current hotspot in synthetic biology, it is entirely justified for these enterprises to protect their trade secrets. Of course, it is also possible that some simply lacked the time to engage .
Beyond that, a number of enterprises remained uncontacted primarily due to poor communication channels . For some businesses, especially small- to medium-sized enterprises (SMEs) and emerging startups, they may not even have their own official websites or WeChat public accounts. Gleaning limited information about them often relies on third-party platforms like Tianyancha, Qichacha or Aiqicha. Unfortunately, details provided on such platforms—including phone numbers and email addresses—are frequently incorrect.
Feedback
Based on these experiences, our approach to seeking contact information now prioritizes:
1. Official Channels: Utilizing enterprise websites, WeChat public accounts, rednote (xiaohongshu), and integrated media accounts (e.g., Bilibili, Weibo, Douyin) to send inquiries through publicly available means.
2. Bidding & Exhibition Data: Searching for bidding information, exhibitor lists, and other public records to trace contact details.
3. Hierarchical Follow-Up: For specific departments or special task forces within enterprises, we start with general contact information and progressively follow up via phone transfers to reach the targeted units.
4. Leveraging Networks: For enterprises that are urgently needed but impossible to contact through standard channels, we seek assistance from personal connections or teachers to establish direct communication.
In terms of communication tactics, we first propose online discussions or soften the "sharpness" of our initial inquiries by framing questions more broadly , making it easier for the other party to accept.
Through these methods, we have generally succeeded in reaching our target enterprises. This cumbersome and non-transparent information disclosure process has also made our team realize the importance of transparency and openness in business collaboration and enterprise engagement . Such practices not only reflect accountability but also demonstrate our commitment to fulfilling social responsibilities .



