首页> 外文期刊>Journal of bacteriology >Molecular basis of isozyme formation of beta-galactosidases in Bacillus stearothermophilus: isolation of two beta-galactosidase genes, bgaA and bgaB.
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Molecular basis of isozyme formation of beta-galactosidases in Bacillus stearothermophilus: isolation of two beta-galactosidase genes, bgaA and bgaB.

机译:嗜热脂肪芽孢杆菌中β-半乳糖苷酶同工酶形成的分子基础:分离两个β-半乳糖苷酶基因bgaA和bgaB。

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Bacillus stearothermophilus IAM11001 produced three beta-galactosidases, beta-galactosidase I, II, and III (beta-gal I, II, and III), which are detectable by polyacrylamide (nondenatured) gel electrophoresis. By connecting restriction fragments of the chromosomal DNA to plasmid vectors, followed by transformation of Escherichia coli, two beta-galactosidase genes (bgaA and bgaB) located close to each other on the chromosome were isolated. Identification of the gene products and Southern hybridization analyses with a 2.7-kilobase-pair EcoRI fragment containing the bgaA gene as probe revealed that a single bgaA gene exists on the genome and that beta-gal II and beta-gal III consist of a common subunit (the bgaA gene product; molecular weight, 120,000), but differ in their assembly (beta-gal II is a dimer, and beta-gal III is a tetramer). The bgaB gene product (molecular weight, 70,000) in Bacillus subtilis harboring pHG5 (a hybrid plasmid consisting of pUB110 and a 2.9-kilobase-pair EcoRI fragment) was estimated to be the beta-gal I protein from its heat stability. Southern hybridization and immunological testing indicated that the two genes have no homology.
机译:嗜热脂肪芽孢杆菌IAM11001产生了三种β-半乳糖苷酶,β-半乳糖苷酶I,II和III(β-galI,II和III),可通过聚丙烯酰胺(未变性)凝胶电泳检测到。通过将染色体DNA的限制性片段连接到质粒载体,然后转化大肠杆菌,分离了位于染色体上彼此靠近的两个β-半乳糖苷酶基因(bgaA和bgaB)。基因产物的鉴定和含有bgaA基因作为探针的2.7碱基对EcoRI片段的Southern杂交分析表明,基因组上存在单个bgaA基因,β-galII和β-galIII由一个共同的亚基组成(bgaA基因产物;分子量为120,000),但其组装方式有所不同(β-galII是二聚体,β-galIII是四聚体)。从枯草芽孢杆菌中携带pHG5(由pUB110和2.9碱基对的EcoRI片段组成的杂交质粒)中的bgaB基因产物(分子量为70000)估计为β-galI蛋白。 Southern杂交和免疫学测试表明这两个基因没有同源性。

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