Blomqvist Trinelise, Steinmoen Hilde, Håvarstein Leiv Sigve
Department of Chemistry, Biotechnology and Food Science, Norwegian University of Life Sciences, P.O.Box 5003, 1432, As, Norway.
Arch Microbiol. 2006 Dec;186(6):465-73. doi: 10.1007/s00203-006-0162-0. Epub 2006 Aug 24.
A locus encoding proteins with high homology to the pneumococcal BlpABCHR quorum-sensing system was identified in Streptococcus thermophilus LMG 18311. The BlpABCHR system regulates bacteriocin production in Streptococcus pneumoniae by monitoring the extracellular concentration of a peptide-pheromone encoded by blpC. The homologous system in S. thermophilus, termed StbABCHR, contains a corresponding gene (stbC) encoding a possible peptide-pheromone (STP) that presumably controls bacteriocin production in S. thermophilus. We synthesized this peptide and found that it activates transcription of a gusA reporter gene placed behind the promoter of the bacteriocin-like gene stbD. Furthermore, deletion mapping and mutational analysis of the stbD promoter region were used to identify a degenerated direct repeat motif required for STP induced GusA expression. Our findings provide strong evidence that STP regulates bacteriocin production in S. thermophilus LMG 18311, and show that the StbABCHR quorum-sensing system can be exploited for inducible expression of recombinant proteins in this bacterial species.
在嗜热链球菌LMG 18311中鉴定出一个与肺炎链球菌BlpABCHR群体感应系统具有高度同源性的蛋白质编码基因座。BlpABCHR系统通过监测由blpC编码的肽信息素的细胞外浓度来调节肺炎链球菌中细菌素的产生。嗜热链球菌中的同源系统,称为StbABCHR,包含一个相应的基因(stbC),该基因编码一种可能的肽信息素(STP),推测其控制嗜热链球菌中细菌素的产生。我们合成了这种肽,发现它能激活置于类细菌素基因stbD启动子下游的gusA报告基因的转录。此外,通过对stbD启动子区域进行缺失定位和突变分析,以鉴定STP诱导GusA表达所需的简并直接重复基序。我们的研究结果提供了强有力的证据,证明STP调节嗜热链球菌LMG 18311中细菌素的产生,并表明StbABCHR群体感应系统可用于在该细菌物种中诱导重组蛋白的表达。