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链霉菌属 ambofaciens 的基因组挖掘。

Genome mining of Streptomyces ambofaciens.

机构信息

Université de Lorraine, Dynamique des Génomes et Adaptation Microbienne, UMR 1128, 54506, Vandœuvre-lès-Nancy, France,

出版信息

J Ind Microbiol Biotechnol. 2014 Feb;41(2):251-63. doi: 10.1007/s10295-013-1379-y. Epub 2013 Nov 21.

DOI:10.1007/s10295-013-1379-y
PMID:24258629
Abstract

Since the discovery of the streptomycin produced by Streptomyces griseus in the middle of the last century, members of this bacterial genus have been largely exploited for the production of secondary metabolites with wide uses in medicine and in agriculture. They have even been recognized as one of the most prolific producers of natural products among microorganisms. With the onset of the genomic era, it became evident that these microorganisms still represent a major source for the discovery of novel secondary metabolites. This was highlighted with the complete genome sequencing of Streptomyces coelicolor A3(2) which revealed an unexpected potential of this organism to synthesize natural products undetected until then by classical screening methods. Since then, analysis of sequenced genomes from numerous Streptomyces species has shown that a single species can carry more than 30 secondary metabolite gene clusters, reinforcing the idea that the biosynthetic potential of this bacterial genus is far from being fully exploited. This review highlights our knowledge on the potential of Streptomyces ambofaciens ATCC 23877 to synthesize natural products. This industrial strain was known for decades to only produce the drug spiramycin and another antibacterial compound, congocidine. Mining of its genome allowed the identification of 23 clusters potentially involved in the production of other secondary metabolites. Studies of some of these clusters resulted in the characterization of novel compounds and of previously known compounds but never characterized in this Streptomyces species. In addition, genome mining revealed that secondary metabolite gene clusters of phylogenetically closely related Streptomyces are mainly species-specific.

摘要

自上个世纪中叶发现灰色链霉菌产生的链霉素以来,该细菌属的成员已被广泛用于生产在医学和农业中有广泛用途的次生代谢产物。它们甚至被认为是微生物中最具生产力的天然产物生产者之一。随着基因组时代的到来,很明显这些微生物仍然是发现新型次生代谢产物的主要来源。这一点在灰色链霉菌 A3(2)的完整基因组测序中得到了强调,该测序揭示了该生物体具有出乎意料的潜在能力,可以合成迄今为止通过经典筛选方法无法检测到的天然产物。此后,对来自许多链霉菌物种的测序基因组进行分析表明,单个物种可以携带 30 多个次生代谢物基因簇,这进一步证实了该细菌属的生物合成潜力远未得到充分利用。

本文重点介绍了我们对灰色链霉菌 ATCC 23877 合成天然产物的潜力的认识。这种工业菌株几十年来只被认为能生产药物螺旋霉素和另一种抗菌化合物康加霉素。对其基因组的挖掘鉴定出了 23 个可能参与其他次生代谢产物生产的簇。对其中一些簇的研究导致了对新型化合物和以前在该链霉菌种中从未表征过的化合物的特征描述。此外,基因组挖掘揭示了系统发育上密切相关的链霉菌的次生代谢物基因簇主要是种特异性的。

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