Aim
Designing and Engineering of Artificial Microbial Consortia (AMC) for Bioprocess trains participants to design, build, and evaluate engineered multi-microbe systems for biomanufacturing and environmental bioprocesses. Learn consortia design logic, metabolic division of labor, stability control, bioreactor integration, and scale-up considerations to develop robust AMC-driven processes.
Program Objectives
- AMC Basics: why consortia outperform monocultures in many bioprocesses.
- Design Approaches: division of labor, cross-feeding, syntrophy, and modular pathway splitting.
- Engineering Tools: strain selection, genetic circuits (intro), control strategies, and safeguards.
- Stability: population dynamics, cheaters, drift, and strategies to maintain function.
- Bioprocess Integration: bioreactor modes, feeding, monitoring, and control.
- Modeling & Analytics: simple design models, omics-informed decisions (overview).
- Application Focus: chemicals, fuels, enzymes, waste-to-value, wastewater, and bioremediation.
- Capstone: design an AMC bioprocess with KPIs and validation plan.
Program Structure
Module 1: Why Artificial Microbial Consortia?
- Monoculture limits: burden, toxicity, pathway length, and robustness issues.
- AMC advantages: modularity, resilience, substrate flexibility, and improved yields.
- Types of consortia: synthetic vs enriched; stable vs dynamic; co-culture formats.
- Key metrics: yield, titer, productivity, stability, and reproducibility.
Module 2: Consortia Design Principles (Division of Labor)
- Pathway splitting: upstream/downstream modules and intermediate handoff.
- Cross-feeding and syntrophy: nutrient, electron, and metabolite exchange.
- Compartmentalization: separating incompatible reactions or toxic steps.
- Design rules: limiting intermediates, balancing flux, minimizing competition.
Module 3: Selecting Strains, Chassis & Compatibility
- Chassis selection: growth rate, tolerance, secretion, and genetic tractability.
- Compatibility checks: pH, temperature, oxygen demand, media requirements.
- Community interactions: competition, mutualism, commensalism (practical view).
- Experimental planning: inoculation ratios and co-culture setup basics.
Module 4: Engineering & Control Strategies
- Genetic tools overview: promoters, sensors, pathway tuning (intro-level).
- Population control: nutrient limitation, auxotrophies, kill-switch concepts (overview).
- Communication: quorum sensing and inducible control concepts.
- Biocontainment and safety considerations (high-level).
Module 5: Stability, Dynamics & Troubleshooting
- Population drift and dominance: why one strain takes over.
- Cheaters and burden: loss of function over time.
- Stabilization methods: periodic resets, selective pressure, spatial separation.
- Diagnostics: plating/qPCR concepts, metabolite tracking, and simple modeling.
Module 6: Bioprocess Integration (From Flask to Bioreactor)
- Bioreactor basics: batch, fed-batch, continuous; co-culture implications.
- Key controls: pH, DO, agitation, feed strategy, and foam management.
- Sampling plans: biomass, strain ratio, substrate/product, byproducts.
- Scale-up risks: oxygen transfer, mixing, gradients, and reproducibility.
Module 7: Monitoring, Analytics & Modeling (Workflow View)
- How to measure consortium composition: markers and quantification concepts.
- Metabolite analytics: HPLC/GC concepts; pathway bottleneck identification.
- Omics overview: using transcriptomics/metabolomics to guide redesign (intro).
- Simple models: growth/flux balance concepts for design decisions.
Module 8: Applications & Scale-Up Pathways
- Industrial chemicals and biopolymers: modular production concepts.
- Biofuels and waste-to-value: mixed substrates and robustness advantages.
- Environmental applications: wastewater, bioremediation, nutrient removal.
- Translation: QA/QC, contamination control, documentation, and regulatory awareness.
Final Project
- Pick a target product or process (chemical, enzyme, waste-to-value, remediation).
- Design the consortium: strains, roles, exchange metabolites, control strategy.
- Define process setup: reactor mode, feeds, monitoring plan, KPIs (Y/T/P).
- Deliverables: AMC design dossier + workflow diagram + risk/stability checklist + KPI table.
Participant Eligibility
- Students/professionals in Biotechnology, Microbiology, Bioprocess Engineering, Synthetic Biology
- PhD scholars working in metabolic engineering, fermentation, systems biology
- Industry professionals in fermentation, biomanufacturing, environmental biotech
- Researchers interested in co-culture design and scale-up planning
Program Outcomes
- Design AMC systems with clear division of labor and control logic.
- Select compatible strains and plan stable co-culture experiments.
- Integrate AMC into bioprocess workflows and define monitoring KPIs.
- Identify stability risks and plan mitigation strategies.
- Deliver an AMC bioprocess proposal as a portfolio project.
Program Deliverables
- e-LMS Access: lessons, case studies, worksheets.
- AMC Toolkit Pack: strain-role matrix, stability checklist, KPI worksheet, monitoring template.
- Capstone Support: feedback on AMC design and process plan.
- Assessment: certification after assignments + capstone submission.
- e-Certification and e-Marksheet: digital credentials on completion.
Future Career Prospects
- Synthetic Biology / Metabolic Engineering Associate
- Bioprocess Development Associate
- Fermentation R&D Associate
- Systems Biology / Microbiome Engineering Research Assistant
Job Opportunities
- Biomanufacturing & Fermentation: co-culture process development, optimization, scale-up support.
- Industrial Biotech: modular pathway engineering and production analytics.
- Environmental Biotech: wastewater and waste-to-value process teams.
- Academic/Research Labs: consortia engineering, microbiome design, systems biology projects.









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