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盐对嗜盐嗜碱菌地中海富盐菌气泡基因转录的影响及内源性转录激活基因的鉴定

Influence of salt on the transcription of the gas-vesicle genes of Haloferax mediterranei and identification of the endogenous transcriptional activator gene.

作者信息

Röder R, Pfeifer F

机构信息

Institut für Mikrobiologie, TH Darmstadt, Germany.

出版信息

Microbiology (Reading). 1996 Jul;142 ( Pt 7):1715-23. doi: 10.1099/13500872-142-7-1715.

DOI:10.1099/13500872-142-7-1715
PMID:8757736
Abstract

The transcription of the 14 gvp genes of the gas-vesicle-encoding mc-vac region was investigated, using RNA from 25% and 15% (w/v) salt cultures of the moderately halophilic archaeon Haloferax mediterranei. Transcription occurred only from two promoters, located in front of the mc-gvpA and mc-gvpD genes. In both cultures transcripts spanning the entire mc-gvpDEFGHIJKLM transcription unit were formed only during the exponential growth phase. Amounts of these transcripts were larger in the 25% salt culture, in which the 2.0 kb mc-gvpD transcripts were also synthesized during the stationary phase. The levels of the mc-gvpD transcripts and of the 324 nt mc-gvpA mRNA increased in parallel during the stationary phase of the 25% salt culture. Only under these conditions were mRNAs spanning the entire mc-gvpACNO transcription unit observed, and gas-vesicles were formed. Investigation of the influence of the mc-gvpDE genes on both mc-vac promoters in transformants revealed that by themselves they were nearly inactive. The addition of mc-gvpE, however, resulted in a high level of constitutively produced mc-gvpA and mc-gvpD mRNA, indicating a transcriptional activator function for the mc-gvpE product.

摘要

利用嗜盐古菌地中海富盐菌(Haloferax mediterranei)在25%和15%(w/v)盐浓度培养条件下获得的RNA,对编码气荚膜的mc-vac区域的14个gvp基因的转录情况进行了研究。转录仅发生在位于mc-gvpA和mc-gvpD基因之前的两个启动子处。在两种培养条件下,跨越整个mc-gvpDEFGHIJKLM转录单元的转录本仅在指数生长期形成。这些转录本在25%盐浓度培养条件下的含量更高,在该条件下,2.0 kb的mc-gvpD转录本在稳定期也会合成。在25%盐浓度培养条件的稳定期,mc-gvpD转录本和324 nt的mc-gvpA mRNA的水平平行增加。只有在这些条件下,才观察到跨越整个mc-gvpACNO转录单元的mRNA,并且形成了气荚膜。对转化体中mc-gvpDE基因对两个mc-vac启动子的影响进行研究发现,它们自身几乎没有活性。然而,添加mc-gvpE会导致组成型产生高水平的mc-gvpA和mc-gvpD mRNA,这表明mc-gvpE产物具有转录激活功能。

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