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恶臭假单胞菌σ⁵⁴ Pu启动子中不同生理调节机制的遗传证据。

Genetic evidence of distinct physiological regulation mechanisms in the sigma(54) Pu promoter of Pseudomonas putida.

作者信息

Cases I, de Lorenzo V

机构信息

Centro Nacional de Biotecnología CSIC, 28049 Madrid, Spain.

出版信息

J Bacteriol. 2000 Feb;182(4):956-60. doi: 10.1128/JB.182.4.956-960.2000.

Abstract

The activity of the toluene-responsive sigma(54) Pu promoter of the pWW0 TOL plasmid of Pseudomonas putida is down-regulated in vivo during exponential growth in rich medium and also by the presence of glucose in the culture. Although the Pu promoter already performs poorly during log growth in minimal medium when amended with casamino acids, the addition of glucose further decreased by two- to threefold the accumulation of beta-galactosidase in a Pu-lacZ reporter P. putida strain. Since Pu was still down-regulated during exponential growth regardless of glucose addition, it appeared that the carbohydrate separately influenced promoter activity. This notion was supported by the growth-dependent induction pattern of Pu in a ptsN mutant of P. putida, the loss of which makes Pu no longer responsive to repression by glucose. On the other hand, overexpression of the sigma factor sigma(54), known to partially alleviate the exponential silencing of the promoter, did not affect glucose inhibition of Pu. These data indicated that exponential silencing and carbon source-dependent repression are two overlapping but genetically distinguishable mechanisms that adapt Pu to the physiological status of the cells and nutrient availability.

摘要

恶臭假单胞菌pWW0 TOL质粒中对甲苯响应的sigma(54) Pu启动子的活性,在丰富培养基中指数生长期间以及培养物中存在葡萄糖时,在体内会下调。尽管在用酪蛋白氨基酸修正的基本培养基中对数生长期间,Pu启动子的表现已经很差,但添加葡萄糖会使Pu-lacZ报告基因恶臭假单胞菌菌株中β-半乳糖苷酶的积累进一步降低两到三倍。由于无论是否添加葡萄糖,Pu在指数生长期间仍会下调,因此似乎碳水化合物分别影响启动子活性。恶臭假单胞菌ptsN突变体中Pu的生长依赖性诱导模式支持了这一观点,ptsN突变体的缺失使Pu不再对葡萄糖的抑制有反应。另一方面,已知部分缓解启动子指数沉默的sigma因子sigma(54)的过表达,并不影响Pu对葡萄糖的抑制。这些数据表明,指数沉默和碳源依赖性阻遏是两种重叠但在遗传上可区分的机制,它们使Pu适应细胞的生理状态和营养可用性。

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