Dila D K, Maloy S R
J Bacteriol. 1986 Nov;168(2):590-4. doi: 10.1128/jb.168.2.590-594.1986.
The putP gene encodes a proline permease required for Salmonella typhimurium LT2 to grow on proline as the sole source of nitrogen. The wild-type strain is sensitive to two toxic proline analogs (azetidine-2-carboxylic acid and 3,4-dehydroproline) also transported by the putP permease. Most mutations in putP prevent transport of all three substrates. Such mutants are unable to grow on proline and are resistant to both of the analogs. To define domains of the putP gene that specify the substrate binding site, we used localized mutagenesis to isolate rare mutants with altered substrate specificity. The position of the mutations in the putP gene was determined by deletion mapping. Most of the mutations are located in three small (approximately 100-base-pair) deletion intervals of the putP gene. The sensitivity of the mutants to the proline analogs was quantitated by radial streaking to determine the affinity of the mutant permeases for the substrates. Some of the mutants showed apparent changes in the kinetics of the substrates transported. These results indicate that the substrate specificity mutations are probably due to amino acid substitutions at or near the active site of proline permease.
putP基因编码一种脯氨酸通透酶,鼠伤寒沙门氏菌LT2在以脯氨酸作为唯一氮源时生长需要该酶。野生型菌株对两种有毒的脯氨酸类似物(氮杂环丁烷-2-羧酸和3,4-脱氢脯氨酸)敏感,这两种类似物也由putP通透酶转运。putP中的大多数突变会阻止所有三种底物的转运。这类突变体无法在脯氨酸上生长,并且对这两种类似物均具有抗性。为了确定putP基因中指定底物结合位点的结构域,我们使用定位诱变来分离具有改变的底物特异性的罕见突变体。通过缺失作图确定putP基因中突变的位置。大多数突变位于putP基因的三个小的(约100个碱基对)缺失区间内。通过径向划线对突变体对脯氨酸类似物的敏感性进行定量,以确定突变通透酶对底物的亲和力。一些突变体在转运底物的动力学上表现出明显变化。这些结果表明,底物特异性突变可能是由于脯氨酸通透酶活性位点处或其附近的氨基酸取代所致。