Evolution-guided engineering of nonribosomal peptide synthetase adenylation domains
化学
氨基酸
肽
蛋白质工程
生物合成
立体化学
作者
Max Crüsemann,Christoph Kohlhaas,Jörn Piel
出处
期刊:Chemical Science [The Royal Society of Chemistry] 日期:2013-01-01卷期号:4 (3): 1041-1045被引量:71
标识
DOI:10.1039/c2sc21722h
摘要
Hormaomycin is a structurally unusual morphogenic and antibiotic peptide biosynthesized by a bacterial nonribosomal peptide synthetase (NRPS). Bioinformatic analysis suggested that parts of the NRPS adenylation (A) domains had recombined during evolution, resulting in a major switch of substrate specificity. This feature inspired us to create A domains with altered substrates based on the putative recombination points. Following characterization of all native hormaomycin A domains, engineered versions were constructed and characterized. Three of the enzymes displayed an almost identical specificity profile to that of native domains recognizing the same substrates. The data support the evolutionary hypothesis regarding the emergence of the hormaomycin pathway and suggest new strategies in NRPS engineering.