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本文引用的文献

1
Exploring the chemistry and biology of vanadium-dependent haloperoxidases.探索钒依赖性卤过氧化物酶的化学与生物学特性。
J Biol Chem. 2009 Jul 10;284(28):18577-81. doi: 10.1074/jbc.R109.001602. Epub 2009 Apr 10.
2
Vanadium containing bromoperoxidase--insights into the enzymatic mechanism using X-ray crystallography.含钒溴过氧化物酶——利用X射线晶体学对酶促机制的深入研究
J Inorg Biochem. 2009 Apr;103(4):617-21. doi: 10.1016/j.jinorgbio.2009.01.011. Epub 2009 Jan 25.
3
Formation of the pyridazine natural product azamerone by biosynthetic rearrangement of an aryl diazoketone.通过芳基重氮酮的生物合成重排形成哒嗪天然产物氮杂美酮。
Angew Chem Int Ed Engl. 2009;48(4):767-70. doi: 10.1002/anie.200805140.
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Halogenation strategies in natural product biosynthesis.天然产物生物合成中的卤化策略。
Chem Biol. 2008 Feb;15(2):99-109. doi: 10.1016/j.chembiol.2008.01.006.
5
Molecular basis for chloronium-mediated meroterpene cyclization: cloning, sequencing, and heterologous expression of the napyradiomycin biosynthetic gene cluster.氯鎓介导的聚酮萜烯环化反应的分子基础:纳派霉素生物合成基因簇的克隆、测序及异源表达
J Biol Chem. 2007 Jun 1;282(22):16362-8. doi: 10.1074/jbc.M611046200. Epub 2007 Mar 28.
6
Nature's inventory of halogenation catalysts: oxidative strategies predominate.自然界中的卤化催化剂:氧化策略占主导地位。
Chem Rev. 2006 Aug;106(8):3364-78. doi: 10.1021/cr050313i.
7
Bromine is an endogenous component of a vanadium bromoperoxidase.
J Am Chem Soc. 2005 Nov 9;127(44):15340-1. doi: 10.1021/ja053416r.
8
Antibiotic terpenoid chloro-dihydroquinones from a new marine actinomycete.来自一种新型海洋放线菌的抗生素萜类氯代二氢醌。
J Nat Prod. 2005 Jun;68(6):904-10. doi: 10.1021/np058011z.
9
Vanadium bromoperoxidase-catalyzed biosynthesis of halogenated marine natural products.钒溴过氧化物酶催化的卤化海洋天然产物的生物合成。
J Am Chem Soc. 2004 Nov 24;126(46):15060-6. doi: 10.1021/ja047925p.
10
The role of vanadium bromoperoxidase in the biosynthesis of halogenated marine natural products.钒溴过氧化物酶在卤化海洋天然产物生物合成中的作用。
Nat Prod Rep. 2004 Feb;21(1):180-8. doi: 10.1039/b302337k. Epub 2004 Jan 21.

细菌抗生素生物合成中的立体选择性钒依赖型氯化过氧化物酶。

A stereoselective vanadium-dependent chloroperoxidase in bacterial antibiotic biosynthesis.

机构信息

Scripps Institution of Oceanography, University of California, San Diego, California 92093, USA.

出版信息

J Am Chem Soc. 2011 Mar 30;133(12):4268-70. doi: 10.1021/ja201088k. Epub 2011 Mar 8.

DOI:10.1021/ja201088k
PMID:21384874
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3065929/
Abstract

Halogenases catalyze reactions that introduce halogen atoms into electron-rich organic molecules. Vanadium-dependent haloperoxidases are generally considered to be promiscuous halogenating enzymes that have thus far been derived exclusively from eukaryotes, where their cellular function is often disputed. We now report the first biochemical characterization of a bacterial vanadium-dependent chloroperoxidase, NapH1 from Streptomyces sp. CNQ-525, which catalyzes a highly stereoselective chlorination-cyclization reaction in napyradiomycin antibiotic biosynthesis. This finding biochemically links a vanadium chloroperoxidase to microbial natural product biosynthesis.

摘要

卤化酶催化将卤素原子引入富电子有机分子的反应。钒依赖的卤过氧化物酶通常被认为是混杂的卤化酶,迄今为止仅从真核生物中衍生而来,其细胞功能常常存在争议。我们现在报告了第一个细菌钒依赖的氯过氧化物酶的生化特征,即来自链霉菌属 CNQ-525 的 NapH1,它在萘啶抗生素生物合成中催化高度立体选择性的氯化环化反应。这一发现从生物化学上把一种钒氯过氧化物酶与微生物天然产物生物合成联系起来。