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Increase in furfural tolerance by combinatorial overexpression of NAD salvage pathway enzymes in engineered isobutanol-producing E. coli. | LitMetric

Increase in furfural tolerance by combinatorial overexpression of NAD salvage pathway enzymes in engineered isobutanol-producing E. coli.

Bioresour Technol

Department of Biological Engineering, College of Engineering, Konkuk University, 1 Hwayang-dong, Gwangjin-gu, Seoul 143-701, Republic of Korea; Institute for Ubiquitous Information Technology and Applications, Konkuk University, Seoul 143-701, Republic of Korea. Electronic address:

Published: December 2017

AI Article Synopsis

  • A new method was developed to reduce furfural toxicity in E. coli for biochemical production by supplying NAD(P)H through the nicotinamide salvage pathway.
  • Overexpressing the genes pncB and nadE in E. coli led to increased tolerance to furfural, with the combination of both genes being the most effective.
  • The study suggests that using the nicotinamide salvage pathway can improve isobutanol production and reduce furfural toxicity, and this approach may also be useful for producing other biochemicals.

Article Abstract

To reduce the furfural toxicity for biochemical production in E. coli, a new strategy was successfully applied by supplying NAD(P)H through the nicotine amide salvage pathway. To alleviate the toxicity, nicotinamide salvage pathway genes were overexpressed in recombinant, isobutanol-producing E. coli. Gene expression of pncB and nadE respectively showed increased tolerance to furfural among these pathways. The combined expression of pncB and nadE was the most effective in increasing the tolerance of the cells to toxic aldehydes. By comparing noxE- and fdh-harbouring strains, the form of NADH, rather than NAD, was the major effector of furfural tolerance. Overall, this study is the application of the salvage pathway to isobutanol production in the presence of furfural, and this system seems to be applicable to alleviate furfural toxicity in the production of other biochemical.

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Source
http://dx.doi.org/10.1016/j.biortech.2017.05.197DOI Listing

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