Genetic interrelations in the actinomycin biosynthetic gene clusters of Streptomyces antibioticus IMRU 3720 and Streptomyces chrysomallus ATCC11523, producers of actinomycin X and actinomycin C.

Q2 Biochemistry, Genetics and Molecular Biology
Advances and Applications in Bioinformatics and Chemistry Pub Date : 2017-04-07 eCollection Date: 2017-01-01 DOI:10.2147/AABC.S117707
Ivana Crnovčić, Christian Rückert, Siamak Semsary, Manuel Lang, Jörn Kalinowski, Ullrich Keller
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引用次数: 1

Abstract

Sequencing the actinomycin (acm) biosynthetic gene cluster of Streptomyces antibioticus IMRU 3720, which produces actinomycin X (Acm X), revealed 20 genes organized into a highly similar framework as in the bi-armed acm C biosynthetic gene cluster of Streptomyces chrysomallus but without an attached additional extra arm of orthologues as in the latter. Curiously, the extra arm of the S. chrysomallus gene cluster turned out to perfectly match the single arm of the S. antibioticus gene cluster in the same order of orthologues including the the presence of two pseudogenes, scacmM and scacmN, encoding a cytochrome P450 and its ferredoxin, respectively. Orthologues of the latter genes were both missing in the principal arm of the S. chrysomallus acm C gene cluster. All orthologues of the extra arm showed a G +C-contents different from that of their counterparts in the principal arm. Moreover, the similarities of translation products from the extra arm were all higher to the corresponding translation products of orthologue genes from the S. antibioticus acm X gene cluster than to those encoded by the principal arm of their own gene cluster. This suggests that the duplicated structure of the S. chrysomallus acm C biosynthetic gene cluster evolved from previous fusion between two one-armed acm gene clusters each from a different genetic background. However, while scacmM and scacmN in the extra arm of the S. chrysomallus acm C gene cluster are mutated and therefore are non-functional, their orthologues saacmM and saacmN in the S. antibioticus acm C gene cluster show no defects seemingly encoding active enzymes with functions specific for Acm X biosynthesis. Both acm biosynthetic gene clusters lack a kynurenine-3-monooxygenase gene necessary for biosynthesis of 3-hydroxy-4-methylanthranilic acid, the building block of the Acm chromophore, which suggests participation of a genome-encoded relevant monooxygenase during Acm biosynthesis in both S. chrysomallus and S. antibioticus.

Abstract Image

Abstract Image

Abstract Image

放线菌素X和放线菌素C产生源链霉菌IMRU 3720和链霉菌ATCC11523放线菌素生物合成基因簇的遗传关系
对产生放线菌素X (acm X)的链霉菌(Streptomyces antibiotic) IMRU 3720的放线菌素(acm)生物合成基因簇进行测序,发现20个基因的结构与链霉菌(Streptomyces chrysomallus)的双臂acm C生物合成基因簇高度相似,但没有像后者那样附加额外的同源物臂。奇怪的是,金黄色葡萄球菌基因簇的额外臂被证明与抗生素葡萄球菌基因簇的单臂在相同的同源物序列上完全匹配,包括两个假基因scacmM和scacmN的存在,分别编码细胞色素P450和它的铁氧还蛋白。后一种基因的同源基因在金花葡萄C基因簇的主臂中均缺失。所有额外手臂的同源物显示的G + c含量与主手臂的对应物不同。此外,额外臂的翻译产物与抗菌葡萄球菌acm X基因簇中同源基因对应的翻译产物的相似性均高于其自身基因簇主臂编码的翻译产物。这表明金黄色葡萄球菌(S. chrysomallus) acm C生物合成基因簇的重复结构是由两个来自不同遗传背景的单臂acm基因簇融合而来的。然而,尽管S. chrysomallus acm C基因簇额外臂中的scacmM和scacmN发生了突变,因此没有功能,但它们在S.抗生素acm C基因簇中的同源物saacmM和saacmN似乎没有缺陷,编码具有acm X生物合成特异性功能的活性酶。这两个acm生物合成基因簇都缺乏3-羟基-4-甲基氨基苯酸(acm发色团的组成部分)生物合成所必需的犬尿氨酸-3-单加氧酶基因,这表明在金黄色葡萄球菌和抗生素葡萄球菌的acm生物合成过程中都有基因组编码的相关单加氧酶参与。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Advances and Applications in Bioinformatics and Chemistry
Advances and Applications in Bioinformatics and Chemistry Biochemistry, Genetics and Molecular Biology-Biochemistry, Genetics and Molecular Biology (miscellaneous)
CiteScore
6.50
自引率
0.00%
发文量
7
审稿时长
16 weeks
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