Peng Xiaojing, Ji Junjie, Zhang Xia, Fan Keqiang, Jin Ling, Zhang Yuxiu, Yang Keqian
School of Chemical and Environmental Engineering, China University of Mining and Technology (Beijing), Beijing 100083, China.
Sheng Wu Gong Cheng Xue Bao. 2012 Aug;28(8):950-8.
JadH is a bifunctional hydoxylase/dehydrase involved in jadomycin biosynthesis; it catalyzes a post-PKS modification reaction to convert 2,3-dehydro-UWM6 to dehydrorabelomycin. To identify the key residues involved in substrate-binding and catalysis, structural modeling and multiple sequence alignments of JadH homologs were performed to predict nine residues at the proximity of substrate. Site-directed mutagenesis of the corresponding residues and in vitro evaluation of the activities of the mutant enzymes, indicate these mutations severely reduced JadH activity. Our results indicate these residues are specifically involved in substrate-binding or catalysis in JadH.
JadH是一种参与制霉素生物合成的双功能羟化酶/脱水酶;它催化聚酮合酶后修饰反应,将2,3-脱氢-UWM6转化为脱水制霉素。为了鉴定参与底物结合和催化的关键残基,对JadH同源物进行了结构建模和多序列比对,以预测底物附近的九个残基。对相应残基进行定点诱变并对突变酶的活性进行体外评估,结果表明这些突变严重降低了JadH的活性。我们的结果表明,这些残基在JadH中特异性地参与底物结合或催化。