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S-腺苷甲硫氨酸(SAM)与抗生素生物合成:SAM 外源添加和 SAM 生物合成基因过表达对链霉菌诺维霉素产量的影响。

S-Adenosylmethionine (SAM) and antibiotic biosynthesis: effect of external addition of SAM and of overexpression of SAM biosynthesis genes on novobiocin production in Streptomyces.

机构信息

Pharmaceutical Institute, Eberhard-Karls-Universität Tübingen, Germany.

出版信息

Arch Microbiol. 2010 Apr;192(4):289-97. doi: 10.1007/s00203-010-0548-x. Epub 2010 Feb 23.

DOI:10.1007/s00203-010-0548-x
PMID:20177662
Abstract

The production of antibiotics in different Streptomyces strains has been reported to be stimulated by the external addition of S-adenosylmethionine (SAM) and by overexpression of the SAM synthetase gene metK. We investigated the influence of SAM addition, and of the expression of SAM biosynthetic genes, on the production of the aminocoumarin antibiotic novobiocin in the heterologous producer strain Streptomyces coelicolor M512 (nov-BG1). External addition of SAM did not influence novobiocin accumulation. However, overexpression of a SAM synthase gene stimulated novobiocin formation, concomitant with an increase of the intracellular SAM concentration. Streptomyces genomes contain orthologs of all genes required for the SAM cycle known from mammals. In contrast, most other bacteria use a different cycle for SAM regeneration. Three secondary metabolic gene clusters, coding for the biosynthesis of structurally very different antibiotics in different Streptomyces strains, were found to contain an operon comprising all five putative genes of the SAM cycle. We cloned one of these operons into an expression plasmid, under control of a strong constitutive promoter. However, transformation of the heterologous novobiocin producer strain with this plasmid did not stimulate novobiocin production, but rather showed a detrimental effect on cell viability in the stationary phase and strongly reduced novobiocin accumulation.

摘要

已有报道称,在不同的链霉菌菌株中,抗生素的生产可通过外加 S-腺苷甲硫氨酸(SAM)和过量表达 SAM 合成酶基因 metK 来刺激。我们研究了 SAM 加合物以及 SAM 生物合成基因表达对异源生产菌株变灰链霉菌 M512(nov-BG1)中氨基香豆素抗生素新生霉素产生的影响。SAM 的外加并不影响新生霉素的积累。然而,SAM 合酶基因的过表达刺激了新生霉素的形成,同时细胞内 SAM 浓度增加。链霉菌基因组包含了哺乳动物中已知的 SAM 循环所需的所有基因的同源物。相比之下,大多数其他细菌使用不同的循环来再生 SAM。三个次级代谢基因簇,编码结构上非常不同的抗生素,在不同的链霉菌菌株中,被发现包含一个操纵子,其中包含 SAM 循环的所有五个假定基因。我们将其中一个操纵子克隆到一个表达质粒中,受强组成型启动子的控制。然而,将这个质粒转化为异源新生霉素生产菌株并没有刺激新生霉素的产生,反而对静止期细胞活力产生了有害影响,并大大降低了新生霉素的积累。

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