1. High ethanol titers from cellulose by using metabolically engineered thermophilic, anaerobic microbes.
- Author
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Argyros DA, Tripathi SA, Barrett TF, Rogers SR, Feinberg LF, Olson DG, Foden JM, Miller BB, Lynd LR, Hogsett DA, and Caiazza NC
- Subjects
- Clostridium thermocellum enzymology, DNA, Bacterial chemistry, DNA, Bacterial genetics, Fermentation, Gene Deletion, Genetic Engineering methods, Molecular Sequence Data, Organisms, Genetically Modified, Plasmids, Recombination, Genetic, Sequence Analysis, DNA, Thermoanaerobacterium enzymology, Thermoanaerobacterium genetics, Bacteria, Anaerobic genetics, Bacteria, Anaerobic metabolism, Cellulose metabolism, Clostridium thermocellum genetics, Clostridium thermocellum metabolism, Ethanol metabolism, Metabolic Networks and Pathways genetics
- Abstract
This work describes novel genetic tools for use in Clostridium thermocellum that allow creation of unmarked mutations while using a replicating plasmid. The strategy employed counter-selections developed from the native C. thermocellum hpt gene and the Thermoanaerobacterium saccharolyticum tdk gene and was used to delete the genes for both lactate dehydrogenase (Ldh) and phosphotransacetylase (Pta). The Δldh Δpta mutant was evolved for 2,000 h, resulting in a stable strain with 40:1 ethanol selectivity and a 4.2-fold increase in ethanol yield over the wild-type strain. Ethanol production from cellulose was investigated with an engineered coculture of organic acid-deficient engineered strains of both C. thermocellum and T. saccharolyticum. Fermentation of 92 g/liter Avicel by this coculture resulted in 38 g/liter ethanol, with acetic and lactic acids below detection limits, in 146 h. These results demonstrate that ethanol production by thermophilic, cellulolytic microbes is amenable to substantial improvement by metabolic engineering.
- Published
- 2011
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