首页> 美国卫生研究院文献>Journal of Bacteriology >γ-Butyrolactone-Dependent Expression of the Streptomyces Antibiotic Regulatory Protein Gene srrY Plays a Central Role in the Regulatory Cascade Leading to Lankacidin and Lankamycin Production in Streptomyces rochei
【2h】

γ-Butyrolactone-Dependent Expression of the Streptomyces Antibiotic Regulatory Protein Gene srrY Plays a Central Role in the Regulatory Cascade Leading to Lankacidin and Lankamycin Production in Streptomyces rochei

机译:γ-丁内酯依赖的链霉菌抗生素调节蛋白基因srrY的表达在罗氏链霉菌中产生lancancidin和lankamycin的调控级联中起着核心作用

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Our previous studies revealed that the srrX and srrA genes carried on the large linear plasmid pSLA2-L constitute a γ-butyrolactone-receptor system in Streptomyces rochei. Extensive transcriptional analysis has now showed that the Streptomyces antibiotic regulatory protein gene srrY, which is also carried on pSLA2-L, is a target of the receptor/repressor SrrA and plays a central role in lankacidin and lankamycin production. The srrY gene was expressed in a growth-dependent manner, slightly preceding antibiotic production. The expression of srrY was undetectable in the srrX mutant but was restored in the srrX srrA double mutant. In addition, SrrA was bound specifically to the promoter region of srrY, and this binding was prevented by the addition of the S. rochei γ-butyrolactone fraction, while the W119A mutant receptor SrrA was kept bound even in the presence of S. rochei γ-butyrolactone. Furthermore, the introduction of an intact srrY gene under the control of a foreign promoter into the srrX or srrA(W119A) mutant restored antibiotic production. All of these results confirmed the signaling pathway from srrX through srrA to srrY, leading to lankacidin and lankamycin production.
机译:我们以前的研究表明,携带在大型线性质粒pSLA2-L上的srrX和srrA基因构成了罗氏链霉菌中的γ-丁内酯-受体系统。现在广泛的转录分析表明,链霉菌抗生素调节蛋白基因srrY(也携带在pSLA2-L上)是受体/阻遏物SrrA的靶标,在兰卡霉素和兰卡霉素的生产中起着核心作用。 srrY基因以生长依赖的方式表达,在抗生素生产之前。 srrY的表达在srrX突变体中无法检测到,但在srrX srrA双重突变体中得以恢复。此外,SrrA特异地结合到srrY的启动子区域,并且通过添加罗氏链球菌γ-丁内酯部分来防止这种结合,而W119A突变受体SrrA即使在罗氏链球菌γ存在下也保持结合。 -丁内酯。此外,在外来启动子的控制下将完整的srrY基因引入srrX或srrA(W119A)突变体可恢复抗生素的生产。所有这些结果证实了从 srrX srrA srrY 的信号传导途径,从而导致了兰卡霉素和兰卡霉素的产生。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号