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色氨酰-tRNA 合成酶样基因位于肠球菌 durans 的酪胺生物合成簇中,其转录受到酪氨酸浓度和细胞外 pH 的调控。

The tyrosyl-tRNA synthetase like gene located in the tyramine biosynthesis cluster of Enterococcus durans is transcriptionally regulated by tyrosine concentration and extracellular pH.

机构信息

Instituto de Productos Lácteos de Asturias (IPLA-CSIC), Spain.

出版信息

BMC Microbiol. 2012 Feb 14;12:23. doi: 10.1186/1471-2180-12-23.

Abstract

BACKGROUND

The tyramine producer Enterococcus durans IPLA655 contains all the necessary genes for tyramine biosynthesis, grouped in the TDC cluster. This cluster includes tyrS, an aminoacyl-tRNA synthetase like gene.

RESULTS

This work shows that tyrS was maximally transcribed in absence of tyrosine at acidic pH, showing a greater than 10-fold induction in mRNA levels over levels occurring in presence of tyrosine. Mapping of the tyrS transcriptional start site revealed an unusually long untranslated leader region of 322 bp, which displays the typical features of the T box transcriptional attenuation mechanism. The tyrosine concentration regulation of tyrS was found to be mediated by a transcription antitermination system, whereas the specific induction at acidic pH was regulated at transcription initiation level.

CONCLUSIONS

The expression of the tyrS gene present in the TDC cluster of E. durans is transcriptionally regulated by tyrosine concentration and extracelular pH. The regulation is mediated by both an antitermination system and the promoter itself.

摘要

背景

产酪胺的肠球菌 E. durans IPLA655 包含 tyramine 生物合成所需的所有基因,这些基因聚集在 TDC 簇中。该簇包括 tyrS,一种类似氨酰-tRNA 合成酶的基因。

结果

这项工作表明,在酸性 pH 值下没有酪氨酸时,tyrS 被最大程度地转录,mRNA 水平比有酪氨酸时的水平高出 10 多倍。tyrS 转录起始位点的定位揭示了一个异常长的 322bp 非翻译前导区,该区域显示了 T 盒转录衰减机制的典型特征。酪氨酸浓度对 tyrS 的调控是通过转录终止抑制系统介导的,而在酸性 pH 值下的特异性诱导则是在转录起始水平上进行调控的。

结论

E. durans TDC 簇中 tyrS 基因的表达受到酪氨酸浓度和细胞外 pH 值的转录调控。这种调控是通过终止抑制系统和启动子本身共同介导的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74cc/3315439/309eec4b867c/1471-2180-12-23-1.jpg

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