Improvement of butanol production in Clostridium acetobutylicum through enhancement of NAD(P)H availability |
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Authors: | Feng Qi author-information" >,Chandresh Thakker,Fayin Zhu,Matthew Pena,Ka-Yiu San,George N. Bennett |
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Affiliation: | 1.Department of BioSciences,Rice University,Houston,USA;2.Engineering Research Center of Industrial Microbiology of Ministry of Education, College of Life Sciences,Fujian Normal University,Fuzhou,China;3.Department of Bioengineering,Rice University,Houston,USA;4.Department of Chemical and Biomolecular Engineering,Rice University,Houston,USA;5.Provincial University Key Laboratory of Cellular Stress Response and Metabolic Regulation, College of Life Sciences,Fujian Normal University,Fuzhou,China |
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Abstract: | Clostridium acetobutylicum is a natural producer of butanol, butyrate, acetone and ethanol. The pattern of metabolites reflects the partitioning of redox equivalents between hydrogen and carbon metabolites. Here the exogenous genes of ferredoxin-NAD(P)+ oxidoreductase (FdNR) and trans-enoyl-coenzyme reductase (TER) are introduced to three different Clostridium acetobutylicum strains to investigate the distribution of redox equivalents and butanol productivity. The FdNR improves NAD(P)H availability by capturing reducing power from ferredoxin. A butanol production of 9.01 g/L (36.9% higher than the control), and the highest ratios of butanol/acetate (7.02) and C4/C2 (3.17) derived metabolites were obtained in the C acetobutylicum buk- strain expressing FdNR. While the TER functions as an NAD(P)H oxidase, butanol production was decreased in the C. acetobutylicum strains containing TER. The results illustrate that metabolic flux can be significantly changed and directed into butanol or butyrate due to enhancement of NAD(P)H availability by controlling electron flow through the ferredoxin node. |
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