| Literature DB >> 25461833 |
Mukesh Saini1, Min Hong Chen1, Chung-Jen Chiang2, Yun-Peng Chao3.
Abstract
We proposed a potential production platform of n-butanol in Escherichia coli. First, a butyrate-conversion strain was developed by removal of undesired genes and recruiting endogenous atoDA and Clostridium adhE2. Consequently, this E. coli strain grown on the M9 mineral salt with yeast extract (M9Y) was shown to produce 6.2g/L n-butanol from supplemented butyrate at 36h. The molar conversion yield of n-butanol on butyrate reaches 92%. Moreover, the production platform was advanced by additional inclusion of a butyrate-producing strain. This strain was equipped with a pathway comprising atoDA and heterologous genes for the synthesis of butyrate. Without butyrate, the butyrate-conversion and the butyrate-producing strains were co-cultured in M9Y medium and produced 5.5g/L n-butanol from glucose at 24h. The production yield on glucose accounts for 69% of the theoretical yield. Overall, it indicates a promise of the developed platform for n-butanol production in E. coli.Entities:
Keywords: Butyrate; Co-culturing; Metabolic engineering; n-Butanol
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Year: 2014 PMID: 25461833 DOI: 10.1016/j.ymben.2014.11.001
Source DB: PubMed Journal: Metab Eng ISSN: 1096-7176 Impact factor: 9.783