五角多的生物合成:从贝纳斯和格里索罗丁路径中推断出来的结果
Gerald Lackner1, Angéla Schenk, Zhongli Xu
1Department of Biomolecular Chemistry, Leibniz Institute for Natural Product Research and Infection Biology, Hans-Knöll-Institute, Beutenbergstrasse 11a, Jena, Germany.
Journal of the American Chemical Society
|July 13, 2007
概括
研究人员在参与生产复杂多的actinomycetes中发现了一种新型缩酶 (KR). 这一发现澄清了包括贝纳斯塔丁在内的"五角形"多基基的生物合成.
科学领域:
- 生物化学 生化学
- 分子生物学分子生物学
- 自然产品生物合成 自然产品生物合成
背景情况:
- 动菌体产生各种长链多,如贝纳斯塔丁和灰色丁.
- 它们的生物合成基因集群共享无特征的缩酶 (KR) 基因.
- KR区域特异性通常预测II型多基酸合成酶 (PKS) 系统中的多基酸结构.
研究的目的:
- 描述涉及多生物合成的缩酶 (KRs) 的一个新型类.
- 为了测试这些KRs产生具有扩展角结构的"五角形"多角形的假设.
- 阐明BenL缩酶在贝纳素通路中的特定功能.
主要方法:
- 来自II型PKS系统的降酶的遗传学分析.
- 生产一种突变菌株,产生一个五角通路中间体 (collinone).
- 在贝纳的生物合成途径中对benL的基因失活.
主要成果:
- 发现了一种新型的KRs类,可能负责合成五边形多角.
- 通过collinone生产,证明了贝纳沙丁和格里索罗丁之间的生物遗传联系.
- L的无活化导致了19-基衍生物,证实L在五边形路径中是C-19 KR.
结论:
- 描述的缩酶是五边形多的生物合成中的关键参与者.
- 在这些途径中,BenL 特别起到 C-19 基因减少酶的作用.
- 这项工作为预测基于KR序列的多基基结构提供了一个框架.
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