非核糖体肽
酶
化学
肽
立体化学
生物化学
羧酸
生物合成
作者
Elisabeth Hühner,Kristin Öqvist,Shu-Ming Li
出处
期刊:Organic Letters
[American Chemical Society]
日期:2019-01-02
卷期号:21 (2): 498-502
被引量:11
标识
DOI:10.1021/acs.orglett.8b03793
摘要
Nonribosomal peptide synthetase (NRPS)-like enzymes comprising A-T-TE architectures catalyze the dimerization of α-keto carboxylic acids leading to the formation of hydroxybenzoquinones or lactones. Domain change experiments with five enzymes revealed that A and A-T domains of phenyl or 4-hydroxyphenyl pyruvate-using enzymes can be effectively used by the TE domains of other enzymes. Even the A and A-T domains of an indolyl hydroxybenzoquinone synthase were successfully recombined with TE domains of a phenyl and a 4-hydroxyphenyl pyruvate-activating enzyme.
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