作者: Yanfang Jiang , Rachael M. Morgan-Kiss , John W. Campbell , Chi Ho Chan , John E. Cronan
DOI: 10.1021/BI901890A
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摘要: Although the Escherichia coli fatty acid synthesis (FAS) pathway is best studied type II system, a major experimental limitation has been inability to feed intermediates into in vivo because exogenously supplied free acids are not efficiently converted acyl-acyl carrier protein (ACP) thioesters required by pathway. We report that expression of Vibrio harveyi acyl-ACP synthetase (AasS), soluble cytosolic enzyme ligates ACP form acyl-ACPs, allows exogenous enter E. The incorporated intact and can be elongated or directly complex lipids acyltransferases specific for acyl-ACPs. Moreover, AasS strains supplementation with appropriate restored growth mutant lack essential enzymes. Thus, this strategy provides new tool circumventing loss enzymes FAS function.