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寻常马杜拉放线菌中流感霉素B1聚酮合酶的序列、克隆及分析

Sequence, cloning, and analysis of the fluvirucin B1 polyketide synthase from Actinomadura vulgaris.

作者信息

Lin Tsung-Yi, Borketey Lawrence S, Prasad Gitanjeli, Waters Stephanie A, Schnarr Nathan A

机构信息

Department of Chemistry, University of Massachusetts , 710 N. Pleasant Street, Amherst, Massachusetts 01003, United States.

出版信息

ACS Synth Biol. 2013 Nov 15;2(11):635-42. doi: 10.1021/sb4000355. Epub 2013 Apr 16.

Abstract

Fluvirucin B1 , produced by Actinomadura vulgaris, is a 14-membered macrolactam active against a variety of infectious fungi as well as influenza A. Despite considerable interest from the synthetic community, very little information is available regarding the biosynthetic origins of the fluvirucins. Herein, we report the identification and initial characterization of the fluvirucin B1 polyketide synthase and related enzymes. The cluster consists of five extender modules flanked by an N-terminal acyl carrier protein and C-terminal thioesterase domain. All but one of the synthase modules contain the full complement of tailoring domains (ketoreductase, dehydratase, and enoyl reductase) as determined by sequence homology with known polyketide synthases. Acitve site analyses of several key components of the cluster are performed to further verify that this gene cluster is associated with production of fluvirucin B1 . This work will both open doors toward a better understanding of macrolactam formation and provide an avenue to genetics-based diversification of fluvirucin structure.

摘要

由普通马杜拉放线菌产生的氟维菌素B1是一种14元大环内酰胺,对多种感染性真菌以及甲型流感病毒具有活性。尽管合成领域对此兴趣浓厚,但关于氟维菌素生物合成起源的信息却非常少。在此,我们报告了氟维菌素B1聚酮合酶及相关酶的鉴定和初步表征。该基因簇由五个延伸模块组成,两侧分别是N端酰基载体蛋白和C端硫酯酶结构域。通过与已知聚酮合酶的序列同源性确定,除一个合酶模块外,所有模块都包含完整的修饰结构域(酮还原酶、脱水酶和烯酰还原酶)。对该基因簇的几个关键组分进行活性位点分析,以进一步验证该基因簇与氟维菌素B1的产生有关。这项工作将为更好地理解大环内酰胺的形成打开大门,并为基于遗传学的氟维菌素结构多样化提供途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e94c/4235520/26eb98fcaa28/nihms639904f1.jpg

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