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鉴定来自卡特利链霉菌的硫霉素基因簇中硫霉素和头孢霉素C生物合成基因的转录激活因子。

Identification of transcriptional activators for thienamycin and cephamycin C biosynthetic genes within the thienamycin gene cluster from Streptomyces cattleya.

作者信息

Rodríguez Miriam, Núñez Luz Elena, Braña Alfredo F, Méndez Carmen, Salas José A, Blanco Gloria

机构信息

Departamento de Biología Funcional e Instituto Universitario de Oncología del Principado de Asturias, Universidad de Oviedo, 33006 Oviedo, Spain.

出版信息

Mol Microbiol. 2008 Aug;69(3):633-45. doi: 10.1111/j.1365-2958.2008.06312.x.

DOI:10.1111/j.1365-2958.2008.06312.x
PMID:19138192
Abstract

Two regulatory genes, thnI and thnU, were identified in the thienamycin (thn) gene cluster from Streptomyces cattleya. ThnI resembles LysR-type transcriptional activators and ThnU belongs to the SARP family of transcriptional activators. Their functional role was established after independent inactivation by gene replacement together with transcriptional analysis involving reverse transcription polymerase chain reaction (RT-PCR). Deletion of thnI abolished thienamycin production showing its involvement in thienamycin biosynthesis. Gene expression analysis applied to the thn gene cluster demonstrated that ThnI is a transcriptional activator essential for thienamycin biosynthesis that regulates the expression of nine genes involved in thienamycin assembly and export (thnH, thnJ, thnK, thnL, thnM, thnN, thnO, thnP and thnQ). Unexpectedly, the thnU disrupted mutant was not affected in thienamycin production but turned out to be essential for cephamycin C biosynthesis. Transcript analysis applied to early and late structural genes for cephamycin C biosynthesis (pcbAB and cmcI), revealed that ThnU is the transcriptional activator of these cephamycin C genes although they are not physically linked to the thn cluster. In addition, it was shown that deletion of thnI has an upregulatory effect on pcbAB and cmcI transcription consistent with a significant increase in cephamycin C biosynthesis in this mutant.

摘要

在来自卡氏链霉菌的硫霉素(thn)基因簇中鉴定出两个调控基因thnI和thnU。ThnI类似于LysR型转录激活因子,而ThnU属于转录激活因子的SARP家族。通过基因置换独立失活并结合逆转录聚合酶链反应(RT-PCR)进行转录分析后,确定了它们的功能作用。thnI的缺失消除了硫霉素的产生,表明其参与硫霉素的生物合成。对thn基因簇进行的基因表达分析表明,ThnI是硫霉素生物合成所必需的转录激活因子,它调节参与硫霉素组装和输出的9个基因(thnH、thnJ、thnK、thnL、thnM、thnN、thnO、thnP和thnQ)的表达。出乎意料的是,thnU破坏突变体在硫霉素产生方面未受影响,但结果表明其对头孢霉素C的生物合成至关重要。对头孢霉素C生物合成的早期和晚期结构基因(pcbAB和cmcI)进行的转录分析表明,ThnU是这些头孢霉素C基因的转录激活因子,尽管它们与thn簇没有物理连接。此外,研究表明thnI的缺失对pcbAB和cmcI转录具有上调作用,这与该突变体中头孢霉素C生物合成的显著增加一致。

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