Gowrishankar J, Jayashree P, Rajkumari K
J Bacteriol. 1986 Dec;168(3):1197-204. doi: 10.1128/jb.168.3.1197-1204.1986.
The proU locus in Escherichia coli encodes an important osmoregulatory function which mediates the growth-promoting effect of L-proline and glycine betaine in high-osmolarity media. This locus was cloned, in contiguity with a closely linked Tn10 insertion, onto a multicopy plasmid directly from the E. coli chromosome. For a given level of osmotic stress, the magnitude of osmoresponsive induction of a single-copy proU::lac fusion was reduced in strains with multiple copies of the proU+ genes; in comparison with haploid proU+ strains, strains with the multicopy proU+ plasmids also exhibited enhanced osmotolerance in media supplemented with 1 mM L-proline or glycine betaine. Experiments involving subcloning, Tn1000 mutagenesis, and interplasmid complementation in a deletion mutant provided evidence for the presence at this locus of two cistrons, both of which are necessary for the expression of ProU function. We propose the designations proU for the gene originally identified by the proU224::Mu d1(lac Ap) insertion and proV for the gene upstream (that is, counterclockwise) of proU.
大肠杆菌中的proU位点编码一种重要的渗透调节功能,该功能介导L-脯氨酸和甘氨酸甜菜碱在高渗培养基中的促生长作用。该位点与一个紧密连锁的Tn10插入片段相邻,直接从大肠杆菌染色体克隆到一个多拷贝质粒上。对于给定水平的渗透胁迫,在含有多个proU+基因拷贝的菌株中,单拷贝proU::lac融合体的渗透反应诱导幅度降低;与单倍体proU+菌株相比,含有多拷贝proU+质粒的菌株在补充有1 mM L-脯氨酸或甘氨酸甜菜碱的培养基中也表现出增强的渗透压耐受性。在缺失突变体中进行的亚克隆、Tn1000诱变和质粒间互补实验提供了证据,表明该位点存在两个顺反子,这两个顺反子对于ProU功能的表达都是必需的。我们提议将最初由proU224::Mu d1(lac Ap)插入鉴定的基因命名为proU,将proU上游(即逆时针方向)的基因命名为proV。