Improving isobutanol production in metabolically engineered Escherichia coli by co-producing ethanol and modulation of pentose phosphate pathway. (1st June 2016)

• Record Type: Journal Article
• Authors: Liu, Zichun; Liu, Pingping; Xiao, Dongguang; Zhang, Xueli
• Is Part Of: Journal of industrial microbiology & biotechnology. Volume 43:Number 6(2016)
• Page Start: 851
• Page End: 860
• Publication Date: 2016-06-01
• Subjects: Isobutanol -- Ethanol -- Co-producing -- Escherichia coli -- NADPH; Industrial microbiology -- Periodicals; 660.62
• DOI: 10.1007/s10295-016-1751-9
• Languages: English
• ISSNs: 1367-5435

Abstract

Abstract: Redox imbalance has been regarded as the key limitation for anaerobic isobutanol production in metabolically engineered Escherichia coli strains. In this work, the ethanol synthetic pathway was recruited to solve the NADH redundant problem while the pentose phosphate pathway was modulated to solve the NADPH deficient problem for anaerobic isobutanol production. Recruiting the ethanol synthetic pathway in strain AS108 decreased isobutanol yield from 0.66 to 0.29 mol/mol glucose. It was found that there was a negative correlation between aldehyde/alcohol dehydrogenase (AdhE) activity and isobutanol production. Decreasing AdhE activity increased isobutanol yield from 0.29 to 0.6 mol/mol. On the other hand, modulation of the glucose 6-phosphate dehydrogenase gene of the pentose phosphate pathway increased isobutanol yield from 0.29 to 0.41 mol/mol. Combination of these two strategies had a synergistic effect on improving isobutanol production. Isobutanol titer and yield of the best strain ZL021 were 53 mM and 0.74 mol/mol, which were 51 % and 12 % higher than the starting strain AS108, respectively. The total alcohol yield of strain ZL021 was 0.81 mol/mol, which was 23 % higher than strain AS108.