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方法用于遗传操纵野村氏菌。

Methods for the genetic manipulation of Nonomuraea sp. ATCC 39727.

机构信息

Dipartimento di Biotecnologie e Scienze Molecolari, Università degli Studi dell'Insubria, via J. H. Dunant 3, Varese 21100, Italy.

出版信息

J Ind Microbiol Biotechnol. 2010 Oct;37(10):1097-103. doi: 10.1007/s10295-010-0807-5. Epub 2010 Aug 18.

Abstract

Nonomuraea sp. ATCC 39727 belongs to the Streptosporangiaceae family of filamentous actinomycetes. This microorganism produces the teicoplanin-like glycopeptide A40926, which is the starting material for the synthesis of the second-generation glycopeptide dalbavancin. Notwithstanding the strain's pharmaceutical relevance, the lack or poor efficiency of genetic tools to manipulate Nonomuraea sp. ATCC 39727 has hampered strain and product improvement. Here we report the development of gene transfer systems based on protoplast transformation and intergeneric conjugation from Escherichia coli. Efficiency of transformation and conjugation, followed by site specific or homologous recombination with the Nonomuraea sp. genome, were determined using the integrative plasmid pSET152 (5.7 kb), and the Supercos1 derivative cosmid A40ΔY (30 kb). To our knowledge, this is the first report of the transformation of protoplasts of Nonomuraea sp. ATCC 39727, even though the improved procedure for intergeneric conjugation makes it the method of choice for introducing large segments of DNA into Nonomuraea sp. ATCC 39727.

摘要

野野村链霉菌(Nonomuraea sp.)ATCC 39727 属于链霉菌科的丝状放线菌。该微生物产生类似于替考拉宁的糖肽 A40926,这是合成第二代糖肽达巴万星的起始原料。尽管该菌株具有药物相关性,但缺乏或低效的遗传工具来操纵野野村链霉菌(Nonomuraea sp.)ATCC 39727,这阻碍了菌株和产品的改进。在这里,我们报告了基于原生质体转化和大肠杆菌属间接合的基因转移系统的开发。使用整合质粒 pSET152(5.7 kb)和 Supercos1 衍生物 cosmid A40ΔY(30 kb),确定了转化和接合的效率,随后通过与野野村链霉菌基因组的特异性或同源重组进行转化和接合。据我们所知,这是野野村链霉菌(Nonomuraea sp.)ATCC 39727 原生质体转化的首次报道,尽管改进的属间接合程序使其成为将大片段 DNA 引入野野村链霉菌(Nonomuraea sp.)ATCC 39727 的首选方法。

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