Emmanuel J. Kokarakis. PhD · Microbiology · Open to industry roles
Biochemistry · Molecular Biology · Microbiology · Synthetic Biology · Cell Factories

Emmanuel (Manos)
Kokarakis, PhD

PhD scientist with 9+ years in biochemistry, microbiology, and chemistry. I work across two parallel tracks: developing and validating analytical methods — LC-MS/MS, flow cytometry, mass spectrometry workflows, and high-throughput screening pipelines — and engineering microorganisms as programmable cell factories. Transitioning from academia to industry, with applications spanning pharmaceutical, biotech, clinical, and biomedical research.

Based in Athens, Greece
Current role QC Analyst, Eurofins (Pharmaceutical) · Greece
Focus Biochemistry · Microbiology · Genetic engineering · Analytical chemistry · Molecular biology
§ 00 — Currently

What I'm doing now

Active role
QC Analyst — Pharmaceutical Sector
Eurofins · Greece
Since March 2026
HPLC ICP-MS LC-MS/MS GC-MS Ion Chromatography LIMS GMP ISO 17025

Working as a QC Analyst in the pharmaceutical division of Eurofins in Greece. Day-to-day, I'm operating across the full analytical-instrument stack — HPLC, ICP-MS, LC-MS/MS, GC-MS, and ion chromatography — running QC analyses under GMP standards and ISO 17025 quality framework, with all results tracked through LIMS.

On the method-development side, I'm currently leading an LC-MS/MS method validation for emamectin benzoate — taking it through specificity, linearity, accuracy, precision, LOD/LOQ, and robustness against ICH-aligned acceptance criteria. It's a clean example of where my doctoral training in mass spectrometry meets the regulated-environment discipline that pharmaceutical QC demands.

This role is sharpening exactly the muscle I want to grow next: rigorous analytical chemistry under regulated frameworks, with direct application to drug quality and patient safety.

§ 01 — Profile

About the work

Emmanuel (Manos) Kokarakis

I'm fascinated by the idea that some of the most consequential tools in modern science came out of microorganisms. DNA polymerase — the enzyme that powers every PCR machine on Earth — was first isolated from a heat-loving bacterium living in a hot spring. CRISPR-Cas9 started as a bacterial immune system before it became a gene-editing revolution. Microbes have been quietly solving problems for billions of years; a lot of what we call biotechnology is really just learning to ask them the right questions.

My own way in was photosynthesis. During my Master's, I was the one in the lab synthesizing and isolating natural products from microalgae and cyanobacteria — slow, manual, hands-on work. At some point it clicked: what if the microbes did the synthesis themselves? Cyanobacteria already harvest sunlight, fix carbon, and build complex molecules for a living. The interesting question isn't how to extract more from them — it's how to program them: turn genes on and off on demand, coordinate populations, divide labor across species, build co-cultures that produce things no single organism could. That's the world I want to help build — one where a bioreactor of engineered microbes can make a drug, a biomaterial, or a delivery system, scalably, without needing constant external inducers or expensive inputs. My PhD in the Ducat Lab at Michigan State was a step in that direction.

Across nine years of grant-funded research at Michigan State, the University of Crete, and a visiting position at the University of Düsseldorf, I've designed and constructed 30+ genetic vectors, developed validated extraction protocols for LC-MS/MS analysis of 2,000+ samples, and trained teams of researchers in advanced analytical techniques. I've co-authored 10 peer-reviewed publications in journals including Metabolic Engineering, ACS Synthetic Biology, and PLOS Computational Biology, and presented at international conferences in the US and Germany.

I'm now looking to bring that disciplined, solutions-oriented mindset into industry — particularly into pharmaceutical companies, clinical research organizations, biotech, and biomedical research environments. I'm at my best embedded in cross-functional teams where rigorous science meets real-world deployment. Greek and US citizen — fully work-authorized across the EU and the United States.

Although my doctoral work centered on microbial systems, the underlying skill set translates directly to clinical and biomedical applications. Method development and validation under strict QC and SOP frameworks, biomarker quantification via flow cytometry and LC-MS/MS, protocol design across thousands of samples with full data traceability, and team training and supervision are exactly the competencies that pharmaceutical R&D, clinical research, medical affairs, and translational biomedical roles depend on. The biological substrate changes; the analytical rigor, regulatory awareness, and project-execution discipline do not.

§ 02 — Competencies

Skills & techniques

Analytical chemistry

  • LC-MS/MS (TQ-XS)
  • LC-MS (Q-Exactive)
  • ICP-MS
  • GC-MS
  • HPLC
  • Ion Chromatography
  • IR Spectroscopy
  • NMR
  • UV-Vis Spectroscopy

Molecular biology

  • Gibson Assembly
  • Restriction enzyme cloning
  • Cloning
  • PCR
  • DNA Sequencing
  • Plasmid & primer design
  • DNA/RNA extraction
  • Genomic engineering

Characterization

  • Flow cytometry (Attune NxT, BD-LSR II)
  • Optical microscopy
  • Fluorescent reporters & viability dyes
  • Enzyme assays
  • ELISA
  • Western blot
  • DNA gel electrophoresis

Microbiology

  • Aseptic technique
  • Media preparation
  • Bacteria & cyanobacteria culture
  • Yeast & microalgae
  • Cancer cell lines (HeLa)
  • Co-culture systems

Engineering & methods

  • Synthetic biology
  • Bioencapsulation (alginate beads)
  • Enzyme engineering
  • Protocol development & validation
  • High-throughput screening
  • Quality control & SOP compliance

Software & languages

  • Benchling
  • OriginLab
  • Minitab
  • FCS Express 7
  • ChemDraw
  • MS Office
  • Greek (Native)
  • English (C2)
§ 03 — Trajectory

Work experience

QC Analyst — Pharmaceutical Sector

Eurofins · Greece

Quality control analyst in the pharmaceutical division, operating across the full analytical-instrument stack under GMP and ISO 17025 frameworks. All workflows tracked through LIMS.

  • Daily operation of HPLC, ICP-MS, LC-MS/MS, GC-MS, and ion chromatography for pharmaceutical QC analyses.
  • Leading LC-MS/MS method validation for emamectin benzoate: specificity, linearity, accuracy, precision, LOD/LOQ, and robustness against ICH-aligned acceptance criteria.
  • Working within ISO 17025-accredited quality management system; full GMP compliance, audit-ready documentation, and electronic data integrity (ALCOA+ principles).
  • End-to-end LIMS use for sample tracking, result entry, and reporting.

Postdoctoral Research Scientist

Ducat Lab, Michigan State University · Michigan, USA · Grant-funded

Led method development and validation work at the intersection of analytical chemistry and microbial co-culture engineering, while managing daily operations of a 10-researcher laboratory.

  • Developed and validated high-throughput LC-MS/MS (TQ-XS) extraction protocols for quantitative analysis of plant hormones in cyanobacteria, achieving a 33% improvement in sample throughput through process redesign and cost reduction.
  • Applied protocols across 500+ samples from two distinct bacterial strains; identified and characterized 2 key specialized metabolites indicative of inter-organism communication.
  • Designed synthetic lichen models to study fungi-cyanobacteria symbiotic interactions; optimized culture conditions, media composition, and environmental parameters to a 90% stable co-culture success rate.
  • Managed laboratory operations for 10 researchers (inventory, technical readiness, resource availability); trained and supervised 7 researchers in advanced analytical techniques.
  • Ensured 100% adherence to institutional safety and quality control standards across all laboratory procedures.

PhD Candidate — Microbiology, Genetics & Immunology

Ducat Lab, Michigan State University · Michigan, USA · NSF- & DOE-funded

Doctoral research engineering quorum-sensing circuits in Synechococcus elongatus PCC 7942, with applications in synthetic microbial consortia and self-inducible expression systems.

  • Designed and constructed 30+ novel genetic vectors via Gibson Assembly and restriction enzyme cloning; 50% of resulting data cited in peer-reviewed publications.
  • Developed, validated, and implemented 3 optimized extraction protocols for isolating lipids and secondary metabolites from cyanobacteria and bacteria using LC-MS (Q-Exactive and TQ-XS).
  • Quantified cell viability and gene expression across 2,000+ sample sets using Attune NxT and BD-LSR II flow cytometry with fluorescent reporters and viability dyes.
  • Co-authored grant writing and renewal applications (NSF, DOE); accountable for milestone delivery and sponsor reporting across 3 concurrent funded projects.
  • Visiting scholar at the University of Düsseldorf, Germany (6–27 May 2024); established international scientific partnerships and contributed to cross-cultural research exchange.
  • Delivered oral and poster presentations at national and international conferences (2021–2025).

Research Assistant

Ghanotakis Lab, Biochemistry Department, University of Crete · Crete, Greece · EU grant-funded

Contributed to EU-funded research on bioactive natural compounds from photosynthetic microorganisms with applications in biofuels, food supplements, and pharmaceuticals.

  • Optimized and implemented 4 novel extraction protocols for natural products from Anabaena, Chlorella, and Botryococcus braunii.
  • Characterized 12+ natural products using GC-MS, HPLC, and IR Spectroscopy with 95% accuracy in compound identification and quantification.
  • Isolated and established cultures for 10+ strains of cyanobacteria, microalgae, and bacteria from diverse environments; maintained aseptic cultures including bacterial strains and HeLa cancer cells.
  • Delivered EU grant deliverables on schedule with full documentation compliance.

Undergraduate Researcher

Ghanotakis Lab, Biochemistry Department, University of Crete · Crete, Greece

Undergraduate thesis research on phenol biodegradation by microalgae, combining bioremediation with photosynthesis assessment.

  • Studied phenol biodegradation by Chlamydomonas reinhardtii and its effects on photosynthesis and growth.
  • Quantified bioremediation of aromatic pollutants via HPLC from spent culture media.
  • Isolated and characterized microalgae strains from contaminated environments.

Lab Analyst — Chemist Intern

Bureau Veritas — Verifuel · Athens, Greece

Foundational experience in a regulated commercial analytical laboratory, including standardized quality documentation, industry reporting practices, and analytical protocol compliance.

  • Assisted in fuel analysis and laboratory testing: flash point, viscosity, pour point, sulfur content, and elemental analysis.
  • Set and oversaw quality assurance guidelines for laboratory work.
§ 04 — Formation

Education

PhD in Microbiology, Molecular Genetics & Immunology

Michigan State University · East Lansing, MI, USA

Thesis: AHL Quorum Sensing Systems Utilization in Synechococcus elongatus PCC 7942 — under Prof. Daniel Ducat.

GPA: 4.0 / 4.0 (coursework)

MSc in Chemistry (Major: Biochemistry)

University of Crete · Heraklion, Greece

Thesis: Isolation and Characterization of Natural Products from Photosynthetic Microorganisms — under Prof. D. Ghanotakis.

GPA: 9.17 / 10 · Top 1% of MSc class

BSc in Chemistry

University of Crete · Heraklion, Greece

Thesis: Phenol Biodegradation by Microalgae Chlamydomonas reinhardtii — under Prof. D. Ghanotakis.

GPA: 8.11 / 10 · Ranked 2nd in a class of 100

§ 05 — Selected work

Featured projects

First-author · Doctoral capstone

Engineering self-inducible quorum-sensing circuits in cyanobacteria

Kokarakis et al. (2025). Metabolic Engineering, Vol. 92, pp. 76–89.
The problem
Cyanobacteria are uniquely promising as sustainable, light-driven cell factories — they harvest sunlight, fix carbon, and can produce a wide range of valuable molecules. But scaling them up has been stubbornly hard. Most strains aren't well adapted to bioreactor conditions, and growth and harvesting at industrial scale need features cyanobacteria mostly don't have. On top of that, most existing gene-induction systems rely on adding chemical inducers like IPTG — fine in a lab flask, expensive and impractical at scale.
The idea
What if the cells could induce themselves? Heterotrophic bacteria coordinate behavior through quorum sensing — they secrete small signaling molecules (acyl-homoserine lactones, or AHLs) that accumulate as the population grows. When the signal hits a threshold, the population acts in concert. I wanted to graft that logic into Synechococcus elongatus PCC 7942 so that gene expression would trigger automatically at high cell density, with no external inducer needed.
What I built
I integrated AHL synthase and receiver modules from Vibrio fischeri (Lux) and Pseudomonas aeruginosa (Las) into cyanobacteria, then characterized them with LC-MS quantification of secreted AHLs and flow cytometry readouts of the downstream response. A hybrid combination — the LasI synthase paired with the LuxR receiver — gave the best on/off ratio and avoided the toxicity seen with some native pairings. Cross-talk between the two systems was a real headache; resolving it took rounds of redesign.
Proof of concept
As a downstream test, I coupled the quorum-sensing circuit to overexpression of cdv3, a cell-division inhibitor. The hypothesis: at high density, cells would stop dividing and instead elongate. Elongated cells, being larger and denser, should sediment under gravity — meaning you could harvest biomass without a centrifuge. It worked. Late-phase cultures elongated, sedimented, and gave improved biomass recovery — a small but real step toward scalable, low-input cyanobacterial bioproduction.
Why it matters
Autoinducible expression is a foundational tool for any future industrial cyanobacterial process — biofuels, pharmaceutical precursors, biomaterials, drug delivery vehicles. Beyond the application, the paper is also one of the first demonstrations of programmable inter-species signaling in a photosynthetic chassis, which opens the door to designed microbial consortia where labor is divided across species.
2022–2025 Synthetic biology · Gibson Assembly · LC-MS · Flow cytometry
First-author · Foundational

Cyanobacterial quorum-sensing toolkits for interspecies coordination

Kokarakis, Rillema, Ducat & Sakkos (2022). ACS Synthetic Biology, 12(1), 265–276.
The problem
Mixed-species microbial communities — say, a sugar-producing cyanobacterium feeding a heterotroph that synthesizes a target molecule — could unlock division of labor in bioproduction. But stable consortia are hard to build: there's no good way to make different species coordinate their behavior. Without communication, populations drift, one species outcompetes the other, productivity collapses.
What we did
We built the first quorum-sensing toolkit for Synechococcus elongatus PCC 7942 — designing, integrating, and characterizing genetic circuits responsive to acyl-homoserine lactones from three different bacterial QS systems (Lux, Tra, Las). All three could sense both exogenous and secreted AHLs. We then demonstrated direct inter-species communication in co-cultivation between cyanobacteria and heterotrophs.
The honest part
Response patterns in cyanobacteria resembled those in E. coli, but with higher background expression and lower induction ratios — there's still genuine work to do on tightening these circuits. That foundation is what the 2025 self-inducible paper directly built on.
Why it matters
This was the first demonstration of QS-based inducible promoters and cross-species gene regulation in cyanobacteria. It's a foundational piece of infrastructure for anyone building light-driven synthetic consortia — applications range from sustainable bioproduction to engineered biofilms to drug-delivery microbiomes.
2022 Synthetic biology · Inter-species signaling · Co-culture
First-author · Natural products

Characterizing an aminosugar-rich exopolysaccharide from Chlorella

Kokarakis et al. (2022). Algal Research, 68, 102881.
The story
A Chlorella strain previously isolated by our group from a Cretan river had an unusual property: it could resist herbicides and antibiotics that should have killed it. The hypothesis was that an extensive extracellular polysaccharide matrix was acting as a shield. This work was about figuring out what that matrix actually was — chemically, structurally, and physically.
What I did
I developed a gentle, low-cost extraction protocol — just successive centrifugation and resuspension, no hazardous solvents — to isolate the exopolysaccharide matrix intact. Then I characterized it using NMR spectroscopy and ESI-MS/MS for structural composition, and DSC and TGA for thermal properties. The polysaccharide turned out to be a heteropolymer with aminosugars (mainly glucosamine and galactosamine) making up over 40% of its molar composition — unusually high for a microalgal EPS.
What was surprising
The matrix showed remarkable thermal stability — well above what's typical for biological polysaccharides — along with measurable antioxidant activity. The aminosugar-rich composition also raised real questions about biosynthesis, since this kind of polymer is more typical of bacterial cell walls than microalgae.
Why it matters
Aminosugar-rich polymers with this thermal profile are candidates for biomedical applications — wound dressings, sustained-release formulations, food-grade coatings — and the paper has since been cited by groups exploring related Chlorella-derived polysaccharides for anti-glucosidase and immunomodulatory activity. It's also a reminder that resilient microorganisms isolated from extreme environments often carry chemistry worth examining closely.
2022 Natural products · NMR · ESI-MS/MS · DSC/TGA
Postdoctoral research

Synthetic lichen co-culture systems

Designed fungi-cyanobacteria symbiotic models from scratch to study inter-organism metabolic communication. Optimized media and culture conditions to a 90% stable co-culture success rate; identified 2 key specialized metabolites indicative of cross-kingdom chemical signaling via LC-MS/MS metabolic profiling.

2025 Co-culture · LC-MS/MS · Optical microscopy
Method development

High-throughput plant hormone analysis

Developed and validated LC-MS/MS (TQ-XS) extraction protocols for quantitative analysis of plant hormones in cyanobacteria. Achieved 33% improvement in sample throughput and preparation time through process redesign; deployed across 500+ samples with full audit-ready documentation.

2025 Analytical chemistry · Method validation · QC
International collaboration

Cyanobacteria–yeast co-culture quantification

Collaboration with the Axmann and Matuszyńska labs (University of Düsseldorf) on protocols for assembling and quantifying co-cultures combining heterotrophic yeast with sugar-secreting cyanobacteria. Visiting scholar at University of Düsseldorf, May 2024. Published in JoVE.

2024 Co-culture · Bioencapsulation · International
Applied science

Bacteria encapsulation in alginate beads

Invited to the MibiNeXt workshop in Düsseldorf/Aachen to demonstrate alginate-based encapsulation of cyanobacteria and bacteria — a method with direct applications in biocontrol, sustained-release formulations, drug delivery systems, and industrial biocatalysis. Recipient of the MSU Research Enhancement Award.

2024 Bioencapsulation · Industrial biotech
Master's research

Natural products from photosynthetic microorganisms

Isolated and characterized bioactive natural compounds from Anabaena, Chlorella, and Botryococcus braunii. Developed 4 novel extraction protocols; characterized 12+ natural products via GC-MS, HPLC, and IR spectroscopy. This is the work that first sparked the question: what if the microbes did the synthesis themselves?

2016–2018 Natural products · GC-MS · HPLC
§ 06 — Bibliography

Publications

  1. 01
    Engineering quorum-sensing circuits in Synechococcus elongatus PCC 7942 towards self-inducible systems
    Kokarakis, E. J., et al.
    Metabolic Engineering, Vol. 92, pp. 76–89 · November 2025
  2. 02
    Plastoquinone redox status influences carboxysome integrity via a RpaA- and reactive oxygen species-dependent regulatory network
    Santos-Merino, M., Nikkanen, L., Kokarakis, E. J., Allahverdiyeva, Y., & Ducat, D. C.
    The Plant Journal · 19 September 2025
  1. 03
    Assembly and quantification of co-cultures combining heterotrophic yeast with phototrophic sugar-secreting cyanobacteria
    Hasenklever, D., Pohlentz, J. C., Berwanger, T., Kokarakis, E. J., Hassan, T., Schipper, K., Matuszyńska, A., Axmann, I. M., & Ducat, D. C.
    Journal of Visualized Experiments (JoVE), 214, e67311
  1. 04
    Predicting partner fitness based on spatial structuring in a light-driven microbial community
    Sakkos, J. K., Santos-Merino, M., Kokarakis, E. J., Li, B., Fuentes-Cabrera, M., Zuliani, P., & Ducat, D. C.
    PLOS Computational Biology, 19(5), e1011045
  2. 05
    Microplastics and their impact on the marine environment
    Kokarakis, J., Kokarakis, E. J., Ladakis, E., & Petrakakos, H.
    SNAME International Symposium on Ship Operations, Management and Economics, D021S006R003
  1. 06
    Developing cyanobacterial quorum sensing toolkits: toward interspecies coordination in mixed autotroph/heterotroph communities
    Kokarakis, E. J., Rillema, R., Ducat, D. C., & Sakkos, J. K.
    ACS Synthetic Biology, 12(1), 265–276
  2. 07
    Structural and physicochemical characterization of an aminosugar-rich exopolysaccharide isolated from a Chlorella sp.
    Kokarakis, E. J., et al.
    Algal Research, 68, 102881
  1. 08
    Characterization of a novel herbicide and antibiotic-resistant Chlorella sp. with an extensive extracellular matrix
    Nazos, T. T., Kokarakis, E. J., Valsami, E.-A., Stratigakis, N.-C., Poloniataki, E. G., Sfendourakis, G. P., & Ghanotakis, D. F.
    Photosynthesis Research, 143, 315–334
  1. 09
    Metabolism of xenobiotics by Chlamydomonas reinhardtii: phenol degradation under conditions affecting photosynthesis
    Nazos, T. T., Kokarakis, E. J., & Ghanotakis, D. F.
    Photosynthesis Research, 131, 31–40
  1. 10
    Challenges associated with the use of low sulphur fuels
    Kokarakis, J. E., Kokarakis, E. J., & Apostolidis, A.
    SNAME Technical Paper
§ 07 — Presence

Conferences & talks

Oral presentation

Autoinduction expression systems by AHL-mediated quorum sensing in Synechococcus elongatus PCC 7942

15th Cyano Workshop
Nashville, Tennessee · June 2025
Invited demonstration

Bacteria encapsulation in alginate beads

MibiNeXt Workshop
Düsseldorf & Aachen, Germany · May 2024
Poster

Application of quorum sensing in Synechococcus elongatus PCC 7942 for harvesting cell biomass

14th International Workshop on Cyanobacteria
Michigan, USA · 2022
Poster · 2nd Prize ★

Stabilizing light-driven synthetic microbial consortia with quorum sensing modules

MSU-DOE Plant Research Laboratory (PRL) Retreat
Michigan State University · 2021
Conference contribution

Bioenergetics as a tool to monitor environment restoration — phenol biodegradation by photosynthetic microalgae

7th European Bioremediation & 11th ISEB Joint Conference
Chania, Greece · June 2018
Conference contribution

Biodegradation of phenolic compounds by photosynthetic microalgae

19th Postgraduates' Conference on Chemistry
Heraklion, Crete · May 2017
§ 08 — Recognition

Honors & awards

2025

Reddy Endowed Award

Department of Microbiology, Genetics & Immunology · Michigan State University

2024

Reddy Endowed Award

Department of Microbiology, Genetics & Immunology · Michigan State University

2024

Research Enhancement Award

Awarded by Michigan State University for participation in the MibiNeXt Workshop (Düsseldorf & Aachen) demonstrating bacteria encapsulation in alginate beads.

2021

2nd Prize — Best Poster

MSU-DOE Plant Research Laboratory (PRL) Retreat · Michigan State University

§ 09 — Influences

Papers that shaped my thinking

Five papers that map the intellectual lineage behind my work. Most are landmark discoveries that started in microbes and became foundational tools across modern biology — the same arc I want to be part of continuing.

  1. 01
    Jinek, Chylinski, Fonfara, Hauer, Doudna & Charpentier · Science · 2012
    A programmable dual-RNA-guided DNA endonuclease in adaptive bacterial immunity

    The CRISPR-Cas9 paper. A discovery rooted in how bacteria defend themselves against viruses turned out to be the most precise gene-editing tool ever built — Nobel-winning, and a textbook example of why basic microbiology keeps producing transformative technology. Every time I design a guide RNA or think about programmable cells, the lineage runs back here.

  2. 02
    Waters & Bassler · Annual Review of Cell and Developmental Biology · 2005
    Quorum sensing: cell-to-cell communication in bacteria

    The canonical synthesis of how bacteria detect their own population density through small molecules and coordinate behavior collectively. This paper — and Bonnie Bassler's broader body of work — is the conceptual foundation underneath my entire PhD. Reading it as a graduate student is what made me ask: if bacteria can synchronize themselves, can I make cyanobacteria do it on demand?

  3. 03
    Saiki et al. · Science · 1988
    Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase

    The paper that introduced Taq polymerase to PCR — an enzyme purified from Thermus aquaticus, a bacterium living in a Yellowstone hot spring. Every PCR run in every lab today (including every single one of mine) depends on this. It's the cleanest possible illustration of the idea that drew me to microbiology in the first place: a tool that quietly rewrote molecular biology came from an organism most people would never have looked twice at.

  4. 04
    Gibson, Young, Chuang, Venter, Hutchison & Smith · Nature Methods · 2009
    Enzymatic assembly of DNA molecules up to several hundred kilobases

    Gibson Assembly — the isothermal cloning method I used to build 30+ genetic vectors during my PhD. Three enzymes acting in concert (a 5′ exonuclease, a DNA polymerase, and a DNA ligase) replaced the multi-step pain of restriction-enzyme cloning. Practical, elegant, and the kind of methodological leap that quietly made the work of an entire generation of synthetic biologists possible.

  5. 05
    Nielsen et al. · Science · 2016
    Genetic circuit design automation

    Christopher Voigt's group built "Cello" — a programming-language-style tool that converts a Verilog-like specification into a functional genetic circuit, automatically. This is where synthetic biology is headed: less hand-crafted construct-by-construct work, more design-and-compile. The quorum-sensing modules I helped develop are the kind of standardized parts a system like Cello needs to scale into photosynthetic and multi-species chassis.

Let's collaborate.

kokomanoschem@gmail.com
Athens, Greece · +30 6975917901 · Available for industry roles & collaboration