聚酮
生物合成
基因簇
生物化学
定向诱变
突变
酶
还原酶
生物
基因
化学
立体化学
突变
突变体
作者
Yang Gao,Yuchun Zhao,Jie Zhou,Maohua Yang,Lin Lin,Wenning Wang,Meifeng Tao,Zixin Deng,Ming Jiang
标识
DOI:10.1002/anie.202110445
摘要
We investigated the biosynthetic pathway of type II polyketide murayaquinone. The murayaquinone biosynthetic cluster contains genes for three putative short-chain dehydrogenase/reductase family enzymes including MrqF and MrqH with known functions and MrqM with unclear function. We report the functional characterization of MrqM for its role in murayaquinone biosynthesis. Our gene deletion experiment and structural elucidation of the accumulated intermediates revealed that MrqM is related with the second polyketide ring cyclization, because the inactivation of mrqM resulted in the accumulation of an off-pathway intermediate SEK43 and disrupted the second and third ring cyclization. Site-directed mutagenesis studies showed that two conserved residues in MrqM and homologous proteins Y151 and K155 are essential for its activity. The previously proposed second/third ring cyclase, MrqD, might instead play another important role in the chain releasing step of the murayaquinone biosynthesis.
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