Literature DB >> 25368184

Single gene insertion drives bioalcohol production by a thermophilic archaeon.

Mirko Basen1, Gerrit J Schut1, Diep M Nguyen1, Gina L Lipscomb1, Robert A Benn1, Cameron J Prybol1, Brian J Vaccaro1, Farris L Poole1, Robert M Kelly2, Michael W W Adams3.   

Abstract

Bioethanol production is achieved by only two metabolic pathways and only at moderate temperatures. Herein a fundamentally different synthetic pathway for bioalcohol production at 70 °C was constructed by insertion of the gene for bacterial alcohol dehydrogenase (AdhA) into the archaeon Pyrococcus furiosus. The engineered strain converted glucose to ethanol via acetate and acetaldehyde, catalyzed by the host-encoded aldehyde ferredoxin oxidoreductase (AOR) and heterologously expressed AdhA, in an energy-conserving, redox-balanced pathway. Furthermore, the AOR/AdhA pathway also converted exogenously added aliphatic and aromatic carboxylic acids to the corresponding alcohol using glucose, pyruvate, and/or hydrogen as the source of reductant. By heterologous coexpression of a membrane-bound carbon monoxide dehydrogenase, CO was used as a reductant for converting carboxylic acids to alcohols. Redirecting the fermentative metabolism of P. furiosus through strategic insertion of foreign genes creates unprecedented opportunities for thermophilic bioalcohol production. Moreover, the AOR/AdhA pathway is a potentially game-changing strategy for syngas fermentation, especially in combination with carbon chain elongation pathways.

Entities:  

Keywords:  Archaea; aldehydes; carbon monoxide; hyperthermophile; metabolic engineering

Mesh:

Substances:

Year:  2014        PMID: 25368184      PMCID: PMC4267397          DOI: 10.1073/pnas.1413789111

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  31 in total

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2.  Bioalcohol production by a new synthetic route in a hyperthermophilic archaeon.

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Review 6.  "Hot" acetogenesis.

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10.  Genome Stability in Engineered Strains of the Extremely Thermophilic Lignocellulose-Degrading Bacterium Caldicellulosiruptor bescii.

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