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首页> 外文期刊>Current Microbiology: An International Journal >Expression of the heat shock gene hsp16.6 and promoter analysis in the cyanobacterium, Synechocystis sp PCC 6803
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Expression of the heat shock gene hsp16.6 and promoter analysis in the cyanobacterium, Synechocystis sp PCC 6803

机译:热休克基因hsp16.6的表达和启动子分析在蓝细菌Synechocystis sp PCC 6803中

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摘要

hsp16.6 and its upstream region from the cyanobacterium, Synechocystis sp. PCC 6803, have been analyzed. The hsp16.6 transcriptional start point was positioned 44 base pairs (bp) upstream of the ATG translation start codon. A reporter vector was constructed by ligating the 265 bp upstream fragment onto the upstream region of the lacZ coding sequence. beta-galactosidase analysis indicated that the 265 bp region did not induce lacZ gene expression in E. coli; although expression was induced when the Synechocystis groESL promoter was used. In Synechocystis cells, lacZ was expressed when the 265 bp fragment was used as a promoter. Cold stress and ethanol did not induce lacZ expression, while heat shock, salt stress, sorbitol, hydrogen peroxide, and high light induced lacZ, A series of deletions from the 265 bp region demonstrated that a region around -35 was essential for hsp16.6 expression.
机译:hsp16.6及其从蓝细菌,集胞藻属的上游区域。已对PCC 6803进行了分析。 hsp16.6转录起始点位于ATG翻译起始密码子上游44个碱基对(bp)处。通过将265 bp的上游片段连接到lacZ编码序列的上游区域来构建报告载体。 β-半乳糖苷酶分析表明,265 bp的区域不诱导大肠杆菌中lacZ基因的表达。尽管在使用集胞藻groESL启动子时诱导了表达。在集胞藻细胞中,当265 bp片段用作启动子时表达lacZ。冷胁迫和乙醇不会诱导lacZ表达,而热休克,盐胁迫,山梨糖醇,过氧化氢和强光诱导的lacZ,265 bp区域的一系列缺失表明-35左右的区域对于hsp16.6是必不可少的表达。

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