A synthetic O sub(2)-tolerant butanol pathway exploiting native fatty acid biosynthesis in Escherichia coli
Several synthetic metabolic pathways for butanol synthesis have been reported in Escherichia coli by modification of the native CoA-dependent pathway from selected Clostridium species. These pathways are all dependent on the O sub(2)-sensitive AdhE2 enzyme from Clostridium acetobutylicum that cataly...
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Veröffentlicht in: | Biotechnology and bioengineering 2015-01, Vol.112 (1), p.120-128 |
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Zusammenfassung: | Several synthetic metabolic pathways for butanol synthesis have been reported in Escherichia coli by modification of the native CoA-dependent pathway from selected Clostridium species. These pathways are all dependent on the O sub(2)-sensitive AdhE2 enzyme from Clostridium acetobutylicum that catalyzes the sequential reduction of both butyryl-CoA and butyraldehyde. We constructed an O sub(2)-tolerant butanol pathway based on the activities of an ACP-thioesterase, acting on butyryl-ACP in the native fatty acid biosynthesis pathway, and a promiscuous carboxylic acid reductase. The pathway was genetically optimized by screening a series of bacterial acyl-ACP thioesterases and also by modification of the physical growth parameters. In order to evaluate the potential of the pathway for butanol production, the ACP-dependent butanol pathway was compared with a previously established CoA-dependent pathway. The effect of (1) O sub(2)-availability, (2) media, and (3) co-expression of aldehyde reductases was evaluated systematically demonstrating varying and contrasting functionality between the ACP- and CoA-dependent pathways. The yield of butanol from the ACP-dependent pathway was stimulated by enhanced O sub(2)-availability, in contrast to the CoA-dependent pathway, which did not function well under aerobic conditions. Similarly, whilst the CoA-dependent pathway only performed well in complex media, the ACP-dependent pathway was not influenced by the choice of media except in the absence of O sub(2). A combination of a thioesterase from Bacteroides fragilis and the aldehyde reductase, ahr, from E. coli resulted in the greatest yield of butanol. A product titer of 300mg/L was obtained in 24h under optimal batch growth conditions, in most cases exceeding the performance of the reference CoA-pathway when evaluated under equivalent conditions. Biotechnol. Bioeng. 2015; 112: 120-128. copyright 2014 Wiley Periodicals, Inc. Butanol is an attractive biofuel for which sustainable production systems need to be developed. The authors constructed a novel synthetic pathway for butanol biosynthesis and carried out a systematic evaluation of its performance under varying environmental conditions. The pathway was found to be highly robust with features best suited for implementation in an oxygenic biotechnological host. |
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ISSN: | 0006-3592 1097-0290 |
DOI: | 10.1002/bit.25324 |