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The Actinomycin Biosynthetic Gene Cluster of Streptomyces chrysomallus: a Genetic Hall of Mirrors for Synthesis of a Molecule with Mirror Symmetry ▿

机译:链霉菌的放线菌素生物合成基因簇:用于镜像对称的分子合成的镜像遗传殿▿

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摘要

A gene cluster was identified which contains genes involved in the biosynthesis of actinomycin encompassing 50 kb of contiguous DNA on the chromosome of Streptomyces chrysomallus. It contains 28 genes with biosynthetic functions and is bordered on both sides by IS elements. Unprecedentedly, the cluster consists of two large inverted repeats of 11 and 13 genes, respectively, with four nonribosomal peptide synthetase genes in the middle. Nine genes in each repeat have counterparts in the other, in the same arrangement but in the opposite orientation, suggesting an inverse duplication of one of the arms during the evolution of the gene cluster. All of the genes appear to be organized into operons, each corresponding to a functional section of actinomycin biosynthesis, such as peptide assembly, regulation, resistance, and biosynthesis of the precursor of the actinomycin chromophore 4-methyl-3-hydroxyanthranilic acid (4-MHA). For 4-MHA synthesis, functional analysis revealed genes that encode pathway-specific isoforms of tryptophan dioxygenase, kynurenine formamidase, and hydroxykynureninase, which are distinct from the corresponding enzyme activities of cellular tryptophan catabolism in their regulation and in part in their substrate specificity. Phylogenetic analysis indicates that the pathway-specific tryptophan metabolism in Streptomyces most probably evolved divergently from the normal pathway of tryptophan catabolism to provide an extra or independent supply of building blocks for the synthesis of tryptophan-derived secondary metabolites.
机译:鉴定出一个基因簇,该基因簇包含与放线菌素的生物合成有关的基因,该基因涵盖了黄链霉菌染色体上50 kb的连续DNA。它包含28个具有生物合成功能的基因,并且在两侧均被IS元素接界。前所未有地,该簇由两个分别由11个和13个基因组成的大型反向重复组成,中间有四个非核糖体肽合成酶基因。每个重复序列中的九个基因在相同的排列中却在相反的方向上彼此相对,这表明在基因簇进化过程中一个臂的反向重复。所有基因似乎都组织成操纵子,每个基因都对应于放线菌素生物合成的功能部分,例如放线菌素发色团4-甲基-3-羟基邻氨基苯甲酸(4-的前体的肽组装,调控,抗性和生物合成) MHA)。对于4-MHA合成,功能分析揭示了编码色氨酸双加氧酶,犬尿氨酸甲酰胺酶和羟尿屈烯酶的途径特异性同工型的基因,这些基因在调节和部分底物特异性方面不同于细胞色氨酸分解代谢的相应酶活性。系统发育分析表明,链霉菌中特定于途径的色氨酸代谢很可能与色氨酸分解代谢的正常途径不同,从而为色氨酸衍生的次级代谢产物的合成提供了额外的或独立的结构单元。

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