非核糖体肽
腺苷酸化
底物特异性
生物
酶
基质(水族馆)
定向进化
生物化学
化学
计算生物学
肽
蛋白质工程
生物合成
基因
生态学
突变体
作者
Max Crüsemann,Christoph Kohlhaas,Jörn Piel
出处
期刊:Chemical Science
[Royal Society of Chemistry]
日期:2012-11-27
卷期号:4 (3): 1041-1045
被引量:87
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.
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