Suppr超能文献

灰色链霉菌链霉素生物合成基因簇中A因子依赖性启动子的鉴定

Identification of an A-factor-dependent promoter in the streptomycin biosynthetic gene cluster of Streptomyces griseus.

作者信息

Vujaklija D, Ueda K, Hong S K, Beppu T, Horinouchi S

机构信息

Department of Agricultural Chemistry, Faculty of Agriculture, University of Tokyo, Japan.

出版信息

Mol Gen Genet. 1991 Sep;229(1):119-28. doi: 10.1007/BF00264220.

Abstract

A-factor (2-isocapryloyl-3R-hydroxymethyl-gamma-butyrolactone) is a microbial hormone controlling streptomycin (Sm) production, Sm resistance and sporulation in Streptomyces griseus. In order to identify A-factor-dependent promoters in the Sm biosynthetic gene cluster, a new promoter-probe plasmid with a low copy number was constructed by using an extremely thermostable malate dehydrogenase gene as the reporter. Of the three promoters in the Sm production region that includes strR, aphD and strB, only the promoter of strR, which codes for a putative regulatory protein, was found to be directly controlled by A-factor. This was also confirmed by S1 nuclease mapping. The region essential for its A-factor-dependence was determined to be located 430-330 base pairs upstream of the transcriptional start point. Increase in the copy number of the strR promoter region did not lead to a corresponding increase in the total promoter activity, probably due to titration of a putative activator which binds to the enhancer-like region and controls the expression of the strR promoter. This putative activator is apparently distinct from the A-factor-receptor protein. The aphD gene, which encodes the major Sm resistance determinant, Sm-6-phosphotransferase, was transcribed mainly by read-through from the A-factor-dependent strR promoter; this accounts for the prompt induction of Sm resistance by A-factor.

摘要

A因子(2-异辛酰基-3R-羟甲基-γ-丁内酯)是一种微生物激素,可控制灰色链霉菌中链霉素(Sm)的产生、对链霉素的抗性及孢子形成。为了鉴定链霉素生物合成基因簇中依赖A因子的启动子,以一种极其耐热的苹果酸脱氢酶基因作为报告基因,构建了一种低拷贝数的新型启动子探针质粒。在包括strR、aphD和strB的链霉素产生区域中的三个启动子中,只有编码假定调节蛋白的strR启动子被发现直接受A因子控制。这也通过S1核酸酶图谱分析得到了证实。其对A因子依赖性所必需的区域被确定位于转录起始点上游430-330个碱基对处。strR启动子区域拷贝数的增加并未导致总启动子活性相应增加,这可能是由于与增强子样区域结合并控制strR启动子表达的假定激活剂被滴定所致。这种假定激活剂显然不同于A因子受体蛋白。编码主要链霉素抗性决定因素——链霉素-6-磷酸转移酶的aphD基因,主要通过依赖A因子的strR启动子通读进行转录;这就解释了A因子对链霉素抗性的快速诱导作用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验