New insights into substrate folding preference of plant OSCs

文献类型： 外文期刊

第一作者： Ma, Yongshuo

作者： Ma, Yongshuo;Zhou, Yuan;Huang, Sanwen;Shang, Yi;Ovchinnikov, Sergey;Greisen, Per, Jr.;Greisen, Per, Jr.;Huang, Sanwen;Shang, Yi

作者机构：

关键词： Oxidosqualene cyclase;Homology modeling;Residue coevolution;Substrate folding

期刊名称：SCIENCE BULLETIN （ 影响因子：11.78； 五年影响因子：7.658 ）

ISSN： 2095-9273

年卷期： 2016 年 61 卷 18 期

页码：

收录情况： SCI

摘要： Sterols and triterpenes are structurally diverse bioactive molecules generated through cyclization of linear 2,3-oxidosqualene. Based on carbocationic intermediates generated during initial substrate preorganization step, oxidosqualene cyclases (OSCs) are roughly segregated into protosteryl cation group that mainly catalyzes tetracyclic products and dammarenyl cation group which mostly generates pentacyclic products. However, in contrast to well-studied cascade of ring-forming reactions, little is known about the mechanism underlying the initial substrate folding process. Previously, we have identified a cucurbitadienol synthase (Bi) and its null allele bi (C393Y) from cucumber. By integration of homology modeling, residue coevolution and site-directed mutagenesis, we discover that four covarying amino acids including C393 constitute a dynamic domain that may be involved in substrate folding process for Bi. We also reveal a group of co-conserved residues that closely associated with the segregation of plant OSCs. These residues may act collaboratively in choice of specific substrate folding intermediate for OSCs. Thus, our findings open a door to engineer plant OSCs from four-ringed skeleton catalysts into five-ringed producer.

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