Combinatorial use of environmental stresses and genetic engineering to increase ethanol titres in cyanobacteria.

Carbon partitioning Cyanobacteria Environmental stress Ethanol Microbial pathway engineering Synechocystis PCC 6803 Synthetic biology

Journal

Biotechnology for biofuels
ISSN: 1754-6834
Titre abrégé: Biotechnol Biofuels
Pays: England
ID NLM: 101316935

Informations de publication

Date de publication:
17 Dec 2021
Historique:
received: 04 10 2021
accepted: 05 12 2021
entrez: 18 12 2021
pubmed: 19 12 2021
medline: 19 12 2021
Statut: epublish

Résumé

Current industrial bioethanol production by yeast through fermentation generates carbon dioxide. Carbon neutral bioethanol production by cyanobacteria uses biological fixation (photosynthesis) of carbon dioxide or other waste inorganic carbon sources, whilst being sustainable and renewable. The first ethanologenic cyanobacterial process was developed over two decades ago using Synechococcus elongatus PCC 7942, by incorporating the recombinant pdc and adh genes from Zymomonas mobilis. Further engineering has increased bioethanol titres 24-fold, yet current levels are far below what is required for industrial application. At the heart of the problem is that the rate of carbon fixation cannot be drastically accelerated and carbon partitioning towards bioethanol production impacts on cell fitness. Key progress has been achieved by increasing the precursor pyruvate levels intracellularly, upregulating synthetic genes and knocking out pathways competing for pyruvate. Studies have shown that cyanobacteria accumulate high proportions of carbon reserves that are mobilised under specific environmental stresses or through pathway engineering to increase ethanol production. When used in conjunction with specific genetic knockouts, they supply significantly more carbon for ethanol production. This review will discuss the progress in generating ethanologenic cyanobacteria through chassis engineering, and exploring the impact of environmental stresses on increasing carbon flux towards ethanol production.

Identifiants

pubmed: 34920731
doi: 10.1186/s13068-021-02091-w
pii: 10.1186/s13068-021-02091-w
pmc: PMC8684110
doi:

Types de publication

Journal Article Review

Langues

eng

Pagination

240

Subventions

Organisme : Engineering and Physical Sciences Research Council
ID : EP/S01778X/1
Organisme : Office of Naval Research Global
ID : N62909-18-1-2137

Informations de copyright

© 2021. The Author(s).

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Auteurs

Fraser Andrews (F)

EPSRC/BBSRC Future Biomanufacturing Research Hub, BBSRC/EPSRC Synthetic Biology Research Centre SYNBIOCHEM Manchester Institute of Biotechnology and School of Chemistry, The University of Manchester, Manchester, M1 7DN, UK.

Matthew Faulkner (M)

EPSRC/BBSRC Future Biomanufacturing Research Hub, BBSRC/EPSRC Synthetic Biology Research Centre SYNBIOCHEM Manchester Institute of Biotechnology and School of Chemistry, The University of Manchester, Manchester, M1 7DN, UK.

Helen S Toogood (HS)

EPSRC/BBSRC Future Biomanufacturing Research Hub, BBSRC/EPSRC Synthetic Biology Research Centre SYNBIOCHEM Manchester Institute of Biotechnology and School of Chemistry, The University of Manchester, Manchester, M1 7DN, UK.

Nigel S Scrutton (NS)

EPSRC/BBSRC Future Biomanufacturing Research Hub, BBSRC/EPSRC Synthetic Biology Research Centre SYNBIOCHEM Manchester Institute of Biotechnology and School of Chemistry, The University of Manchester, Manchester, M1 7DN, UK. nigel.scrutton@manchester.ac.uk.
C3 Biotechnologies Ltd, 20 Mannin Way, Lancaster Business Park, Caton Road, Lancaster, LA1 3SW, Lancashire, UK. nigel.scrutton@manchester.ac.uk.

Classifications MeSH