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锌和铁调节铜绿假单胞菌弹性蛋白酶编码基因的翻译。

Zinc and iron regulate translation of the gene encoding Pseudomonas aeruginosa elastase.

作者信息

Brumlik M J, Storey D G

机构信息

Department of Microbiology and Infectious Diseases, University of Calgary, Alberta, Canada.

出版信息

Mol Microbiol. 1992 Feb;6(3):337-44. doi: 10.1111/j.1365-2958.1992.tb01476.x.

Abstract

A lasB-lacZ translational fusion (pTS400) was used to examine expression of the elastase gene (lasB) in Pseudomonas aeruginosa strain PAO1. Expression from the lasB-lacZ fusion was enhanced when PAO1(pTS400) was grown in a defined medium containing elevated levels of zinc (6.0 micrograms ml-1). Transcript accumulation studies on PAO1(pTS400) and PAO1 showed that the addition of zinc had a slight negative effect on lasB transcription. These results indicated that zinc regulates the expression of elastase at the translational level. A comparison between zinc regulation and iron regulation was also made. Iron has a negative effect on lasB-lacZ expression. When PAO1(pTS400) was grown in a defined medium with a low iron content (0.1 microgram ml-1) the bacteria still responded to zinc. The independent effects of low iron and high zinc concentrations suggest separate control mechanisms for the two factors. Transcript accumulation studies on PAO1 and PAO1 (pTS400) indicated that early in the growth curve iron did not influence transcription of lasB or lasB-lacZ. Later in the growth curve a slight increase in lasB-lacZ transcription was observed only in PAO1(pTS400) grown in low iron. These results suggest that the iron regulation of lasB occurs predominantly at the translational level. Finally, when PAO1(pTS400) was grown in a complex peptone-based medium, a high level of transcript accumulation accounted for elastase expression. Alterations of iron and zinc concentrations of this medium did not affect the expression of elastase. These results suggest that there may be additional environmental cues regulating lasB transcription.

摘要

采用A lasB-lacZ翻译融合体(pTS400)来检测铜绿假单胞菌PAO1菌株中弹性蛋白酶基因(lasB)的表达。当PAO1(pTS400)在含有高水平锌(6.0微克/毫升)的限定培养基中生长时,lasB-lacZ融合体的表达增强。对PAO1(pTS400)和PAO1进行转录本积累研究表明,添加锌对lasB转录有轻微的负面影响。这些结果表明,锌在翻译水平上调节弹性蛋白酶的表达。还对锌调节和铁调节进行了比较。铁对lasB-lacZ表达有负面影响。当PAO1(pTS400)在低铁含量(0.1微克/毫升)的限定培养基中生长时,细菌仍对锌有反应。低铁和高锌浓度的独立作用表明这两种因素有各自独立的控制机制。对PAO1和PAO1(pTS400)的转录本积累研究表明,在生长曲线早期,铁不影响lasB或lasB-lacZ的转录。在生长曲线后期,仅在低铁条件下生长的PAO1(pTS400)中观察到lasB-lacZ转录略有增加。这些结果表明,lasB的铁调节主要发生在翻译水平。最后,当PAO1(pTS400)在基于蛋白胨的复合培养基中生长时,高水平的转录本积累导致了弹性蛋白酶的表达。该培养基中铁和锌浓度的改变不影响弹性蛋白酶的表达。这些结果表明,可能存在其他环境信号调节lasB转录。

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