首页> 外文期刊>Applied and Environmental Microbiology >Cloning of the citrate permease gene of Lactococcus lactis subsp. lactis biovar diacetylactis and expression in Escherichia coli.
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Cloning of the citrate permease gene of Lactococcus lactis subsp. lactis biovar diacetylactis and expression in Escherichia coli.

机译:乳酸乳球菌亚种柠檬酸盐渗透酶基因的克隆。乳酸生物变种二乙酰基肌动蛋白及其在大肠杆菌中的表达。

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The citrate plasmid (Cit+ plasmid) from Lactococcus lactis subsp. lactis biovar diacetylactis was cloned into the EcoRI site of plasmid pUC18. This recombinant plasmid enabled Escherichia coli K-12 to transport and utilize citrate as a source of energy, indicating expression of the citrate permease from L. lactis biovar diacetylactis. The citrate permease was under the control of the lac promoter of pUC18. Genetic expression of the Cit+ plasmid in maxicells revealed that the plasmid encoded two polypeptides of 47 and 32 kilodaltons, determined by sodium dodecyl sulfate-polyacrylamide gel electrophoresis.
机译:来自乳酸乳球菌亚种的柠檬酸盐质粒(Cit +质粒)。将乳酸菌的生物变二乙酰基克隆到质粒pUC18的EcoRI位点。该重组质粒使大肠杆菌K-12能够运输和利用柠檬酸盐作为能源,表明乳酸乳球菌生物var diacetylactis的柠檬酸盐通透酶表达。柠檬酸盐通透酶在pUC18的lac启动子的控制下。 Cit +质粒在maxicells中的遗传表达表明,该质粒编码了十二个硫酸钠和聚丙烯酰胺凝胶电泳确定的两个多肽,分别为47和32千道尔顿。

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