首页> 外文OA文献 >Transcriptional Control of the Hydrogen Cyanide Biosynthetic Genes hcnABC by the Anaerobic Regulator ANR and the Quorum-Sensing Regulators LasR and RhlR in Pseudomonas aeruginosa
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Transcriptional Control of the Hydrogen Cyanide Biosynthetic Genes hcnABC by the Anaerobic Regulator ANR and the Quorum-Sensing Regulators LasR and RhlR in Pseudomonas aeruginosa

机译:铜绿假单胞菌中厌氧调节剂ANR和群体敏感调节剂LasR和RhlR对氰化氢生物合成基因hcnABC的转录控制。

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摘要

Virulence factors of Pseudomonas aeruginosa include hydrogen cyanide (HCN). This secondary metabolite is maximally produced at low oxygen tension and high cell densities during the transition from exponential to stationary growth phase. The hcnABC genes encoding HCN synthase were identified on a genomic fragment complementing an HCN-deficient mutant of P. aeruginosa PAO1. The hcnA promoter was found to be controlled by the FNR-like anaerobic regulator ANR and by the quorum-sensing regulators LasR and RhlR. Primer extension analysis revealed two transcription starts, T1 and T2, separated by 29 bp. Their function was confirmed by transcriptional lacZ fusions. The promoter sequence displayed an FNR/ANR box at −42.5 bp upstream of T2 and a lux box centered around −42.5 bp upstream of T1. Expression of the hcn genes was completely abolished when this lux box was deleted or inactivated by two point mutations in conserved nucleotides. The lux box was recognized by both LasR [activated by N-(oxododecanoyl)-homoserine lactone] and RhlR (activated by N-butanoyl-homoserine lactone), as shown by expression experiments performed in quorum-sensing-defective P. aeruginosa mutants and in the N-acyl-homoserine lactone-negative heterologous host P. fluorescens CHA0. A second, less conserved lux box lying 160 bp upstream of T1 seems to account for enhanced quorum-sensing-dependent expression. Without LasR and RhlR, ANR could not activate the hcn promoter. Together, these data indicate that expression of the hcn promoter from T1 can occur under quorum-sensing control alone. Enhanced expression from T2 appears to rely on a synergistic action between LasR, RhlR, and ANR.
机译:铜绿假单胞菌的毒力因子包括氰化氢(HCN)。在从指数生长期到固定生长期的过渡过程中,该次生代谢产物在低氧张力和高细胞密度下产生最大。在与铜绿假单胞菌PAO1的HCN缺陷型突变体互补的基因组片段上鉴定了编码HCN合酶的hcnABC基因。发现hcnA启动子受FNR样厌氧调节剂ANR和群体感应调节剂LasR和RhlR的控制。引物延伸分析显示两个转录起点T1和T2,相距29 bp。通过转录lacZ融合证实了它们的功能。启动子序列在T2上游-42.5 bp处显示FNR / ANR框,在T1上游-42.5 bp处以lux框为中心。当这个lux框被保守核苷酸中的两个点突变删除或失活时,hcn基因的表达被完全消除。如在群体感应缺陷性铜绿假单胞菌突变体和铜绿假单胞菌突变体中进行的表达实验所示,LuxR被LasR [被N-(氧十二烷酰基)-高丝氨酸内酯激活]和RhlR(被N-丁酸-高丝氨酸内酯激活)识别。在N-酰基高丝氨酸内酯阴性的异源宿主荧光假球菌CHA0中。位于T1上游160 bp处的第二个保守性较低的勒克斯盒似乎说明了增强的群体感应依赖性表达。没有LasR和RhlR,ANR无法激活hcn启动子。总之,这些数据表明来自T1的hcn启动子的表达可以仅在群体感应控制下发生。来自T2的增强表达似乎依赖于LasR,RhlR和ANR之间的协同作用。

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