Yu Xinyan, Chen Min, Jiang Zhen, Hu Yi, Xie Zhixiong
College of Life Sciences, Key Laboratory of Analytical Chemistry for Biology and Medicine (Ministry of Education), State Key Laboratory of Virology, Wuhan University, Wuhan, People's Republic of China Hubei Provincial Cooperative Innovation Center of Industrial Fermentation, Wuhan, People's Republic of China.
College of Life Sciences, Key Laboratory of Analytical Chemistry for Biology and Medicine (Ministry of Education), State Key Laboratory of Virology, Wuhan University, Wuhan, People's Republic of China.
J Bacteriol. 2014 Sep;196(18):3259-70. doi: 10.1128/JB.01756-14. Epub 2014 Jun 30.
Siderophores, which are produced to overcome iron deficiency, are believed to be closely related to the adaptability of bacteria. The high-siderophore-yielding Pseudomonas sp. strain HYS simultaneously secretes the fluorescent siderophore pyoverdine and another nonfluorescent siderophore that is a major contributor to the high siderophore yield. Transposon mutagenesis revealed siderophore-related genes, including the two-component regulators GacS/GacA and a special cluster containing four open reading frames (the nfs cluster). Deletion mutations of these genes abolished nonfluorescent-siderophore production, and expression of the nfs cluster depended on gacA, indicating that gacS-gacA may control the nonfluorescent siderophore through regulation of the nfs cluster. Furthermore, regulation of the nonfluorescent siderophore by GacS/GacA involved the Gac/Rsm pathway. In contrast, inactivation of GacS/GacA led to upregulation of the fluorescent pyoverdine. The two siderophores were secreted under different iron conditions, probably because of differential effects of GacS/GacA. The global GacS/GacA regulatory system may control iron uptake by modulating siderophore production and may enable bacteria to adapt to changing iron environments.
铁载体是为克服缺铁而产生的,被认为与细菌的适应性密切相关。高产铁载体的假单胞菌属菌株HYS同时分泌荧光铁载体绿脓菌素和另一种对高铁载体产量起主要作用的非荧光铁载体。转座子诱变揭示了与铁载体相关的基因,包括双组分调节因子GacS/GacA和一个包含四个开放阅读框的特殊基因簇(nfs基因簇)。这些基因的缺失突变消除了非荧光铁载体的产生,并且nfs基因簇的表达依赖于gacA,这表明gacS-gacA可能通过调节nfs基因簇来控制非荧光铁载体。此外,GacS/GacA对非荧光铁载体的调节涉及Gac/Rsm途径。相反,GacS/GacA的失活导致荧光绿脓菌素上调。这两种铁载体在不同的铁条件下分泌,可能是由于GacS/GacA的不同作用。全局GacS/GacA调节系统可能通过调节铁载体的产生来控制铁的摄取,并可能使细菌适应不断变化的铁环境。