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苔藓抑素生物合成途径中聚酮化合物β-分支的化学酶法剖析

Chemoenzymatic Dissection of Polyketide β-Branching in the Bryostatin Pathway.

作者信息

Slocum Samuel T, Lowell Andrew N, Tripathi Ashootosh, Shende Vikram V, Smith Janet L, Sherman David H

机构信息

Life Sciences Institute, University of Michigan, Ann Arbor, MI, United States; Life Sciences Institute, Department of Biological Chemistry, University of Michigan, Ann Arbor, MI, United States.

Life Sciences Institute, University of Michigan, Ann Arbor, MI, United States.

出版信息

Methods Enzymol. 2018;604:207-236. doi: 10.1016/bs.mie.2018.01.034. Epub 2018 Apr 9.

Abstract

β-Branching is an expansion upon canonical polyketide synthase extension that allows for the installation of diverse chemical moieties in several natural products. Several of these moieties are unique among natural products, including the two vinyl methylesters found in the core structure of bryostatins. This family of molecules is derived from an obligate bacterial symbiont of a sessile marine bryozoan, Bugula neritina. Within this family, bryostatin 1 has been investigated as an anticancer, neuroprotective, and immunomodulatory compound. We have turned to the biosynthetic gene cluster within the bacterial symbiont to investigate the biosynthesis of bryostatins. Recent sequencing efforts resulted in the annotation of two missing genes: bryT and bryU. Using novel chemoenzymatic techniques, we have validated these as the missing enoyl-CoA hydratase and donor acyl carrier protein, essential components of the β-branching cassette of the bryostatin pathway. Together, this cassette installs the vinyl methylester moieties essential to the activity of bryostatins.

摘要

β-分支是对经典聚酮合酶延伸的一种扩展,它允许在几种天然产物中安装不同的化学基团。其中一些基团在天然产物中是独特的,包括在苔藓抑素核心结构中发现的两种乙烯基甲酯。这个分子家族来源于一种固着性海洋苔藓虫(苔藓虫属)的专性细菌共生体。在这个家族中,苔藓抑素1已作为一种抗癌、神经保护和免疫调节化合物进行了研究。我们已转向细菌共生体内的生物合成基因簇来研究苔藓抑素的生物合成。最近的测序工作导致注释了两个缺失基因:bryT和bryU。使用新型化学酶技术,我们已证实它们分别是缺失的烯酰辅酶A水合酶和供体酰基载体蛋白,这是苔藓抑素途径β-分支盒的必需组分。这个盒式结构共同安装了对苔藓抑素活性至关重要的乙烯基甲酯基团。

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