首页> 外文期刊>Journal of bacteriology >Excretion of alkaline phosphatase by Escherichia coli K-12 pho constitutive mutants transformed with plasmids carrying the alkaline phosphatase structural gene.
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Excretion of alkaline phosphatase by Escherichia coli K-12 pho constitutive mutants transformed with plasmids carrying the alkaline phosphatase structural gene.

机译:用携带碱性磷酸酶结构基因的质粒转化的大肠杆菌K-12 pho组成型突变体分泌碱性磷酸酶。

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Escherichia coli alkaline phosphatase constitutive mutants carrying a pst or a phoS mutation and a plasmid-bearing gene phoA+ excreted into the growth medium up to 50% of the total alkaline phosphatase production. This excretion was pH dependent and did not involve drastic modifications of the cell envelope. Alkaline phosphatase accounted for 80% of total released proteins. Amplification of gene phoA+ was a necessary condition for excretion to occur. When the beta-lactamase structural gene bla+ was coamplified with gene phoA+, both enzymes were excreted. pst-transformed excretory strains did not show the pleiotrophic phenotype previously described for lky mutants.
机译:带有pst或phoS突变和带有质粒的基因phoA +的大肠杆菌碱性磷酸酶组成型突变体分泌到生长培养基中的量最多占碱性磷酸酶总产量的50%。该排泄物是pH依赖性的,并且不涉及细胞包膜的剧烈修饰。碱性磷酸酶占总释放蛋白的80%。 phoA +基因的扩增是排泄发生的必要条件。当将β-内酰胺酶结构基因bla +与phoA +基因共同扩增时,两种酶均被排出。经pst转化的排泄菌株未显示先前针对lky突变体描述的多营养表型。

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