Enhancing Tolerance to Short-Chain Alcohols by Engineering the Escherichia coli AcrB Efflux Pump to Secrete the Non-native Substrate n-Butanol

被引:86
作者
Fisher, Michael A. [1 ]
Boyarskiy, Sergey [1 ,2 ]
Yamada, Masaki R. [3 ]
Kong, Niwen [4 ]
Bauer, Stefan [1 ]
Tullman-Ercek, Danielle [1 ,3 ]
机构
[1] Univ Calif Berkeley, Energy Biosci Inst, Berkeley, CA 94704 USA
[2] Univ Calif Berkeley, Dept Bioengn, Berkeley, CA 94720 USA
[3] Univ Calif Berkeley, Dept Chem & Biomol Engn, Berkeley, CA 94720 USA
[4] Univ Calif Berkeley, Dept Mol & Cell Biol, Berkeley, CA 94720 USA
来源
ACS SYNTHETIC BIOLOGY | 2014年 / 3卷 / 01期
关键词
directed evolution; protein engineering; biofuels; tolerance; efflux pump; transporter; POLYMERASE EXTENSION CLONING; ETHANOL TOLERANCE; DIRECTED EVOLUTION; SOLVENT TOLERANCE; COLI; TRANSPORTER; MECHANISM; IDENTIFICATION; TRANSLOCATION; EXPRESSION;
D O I
10.1021/sb400065q
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The microbial conversion of sugars to fuels is a promising technology, but the byproducts of biomass pretreatment processes and the fuels themselves are often toxic at industrially relevant levels. One promising solution to these problems is to engineer efflux pumps to secrete fuels and inhibitory chemicals from the cell, increasing microbial tolerance and enabling higher fuel titer. Toward that end, we used a directed evolution strategy to generate variants of the Escherichia coli AcrB efflux pump that act on the non-native substrate n-butanol, enhancing growth rates of E. coli in the presence of this biofuel by up to 25%. Furthermore, these variants confer improved tolerance to isobutanol and straight-chain alcohols up to n-heptanol. Single amino acid changes in AcrB responsible for this phenotype were identified. We have also shown that both the chemical and genetic inactivation of pump activity eliminate the tolerance conferred by AcrB pump variants, supporting our assertion that the variants secrete the non-native substrates. This strategy can be applied to create an array of efflux pumps that modulate the intracellular concentrations of small molecules of interest to microbial fuel and chemical production.
引用
收藏
页码:30 / 40
页数:11
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