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苜蓿中华根瘤菌WSM419菌株的耐酸性涉及一个双组分传感调节系统。

Acid tolerance in Rhizobium meliloti strain WSM419 involves a two-component sensor-regulator system.

作者信息

Tiwari R P, Reeve W G, Dilworth M J, Glenn A R

机构信息

Nitrogen Fixation Research Group, School of Biological and Environmental Sciences, Murdoch University, Australia.

出版信息

Microbiology (Reading). 1996 Jul;142 ( Pt 7):1693-704. doi: 10.1099/13500872-142-7-1693.

Abstract

An acid-sensitive mutant, TG5-46, derived from Rhizobium meliloti WSM419 by Tn5 mutagenesis, fails to grow below pH 6.0 whereas the parent strain grows at pH 5.7. The DNA sequence of a 2.2 kb rhizobial DNA region flanking Tn5 in TG5-46 contains two open reading frames, ORF1 (designated actS) and ORF2 (designated actR), having high similarity to the sensor-regulator pairs of the two-component systems involved in signal transduction in prokaryotes. Insertion of an omega interposon into actS in R. meliloti WSM419 resulted in an acid-sensitive phenotype. A DNA fragment from the wild-type complemented the acid-sensitive phenotype of RT295 (ActS-) and TG5-46 (ActR-), while fragments containing only actR or actS complemented TG5-46 and RT295, respectively. The presence of multiple copies of actR complemented not only TG5-46 but also RT295. Cloning DNA upstream from actR and actS into a broad-host-range lacZ expression vector and measuring beta-galactosidase activities showed that both genes are constitutively expressed regardless of the external pH. Genomic DNA from all strains of R. meliloti, but no other bacteria tested, hybridized with an actRS probe at high stringency. These data implicate a two-component sensor-regulator protein pair in acid tolerance in R. meliloti and suggest their involvement in pH sensing and/or response by these bacteria.

摘要

通过Tn5诱变从苜蓿中华根瘤菌WSM419衍生而来的酸敏感突变体TG5-46,在pH 6.0以下无法生长,而亲本菌株在pH 5.7时能够生长。TG5-46中Tn5侧翼的一个2.2 kb根瘤菌DNA区域的DNA序列包含两个开放阅读框,即ORF1(命名为actS)和ORF2(命名为actR),它们与原核生物信号转导中涉及的双组分系统的传感器-调节子对具有高度相似性。在苜蓿中华根瘤菌WSM419的actS中插入一个ω插入子导致了酸敏感表型。来自野生型的一个DNA片段互补了RT295(ActS-)和TG5-46(ActR-)的酸敏感表型,而仅包含actR或actS的片段分别互补了TG5-46和RT295。actR多拷贝的存在不仅互补了TG5-46,也互补了RT295。将actR和actS上游的DNA克隆到一个广泛宿主范围的lacZ表达载体中并测量β-半乳糖苷酶活性,结果表明这两个基因无论外部pH如何均组成型表达。所有苜蓿中华根瘤菌菌株的基因组DNA,但未检测的其他细菌的基因组DNA,都能与actRS探针在高严谨度下杂交。这些数据表明双组分传感器-调节子蛋白对参与了苜蓿中华根瘤菌的耐酸性,并暗示它们参与了这些细菌对pH的感知和/或响应。

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