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枯草芽孢杆菌发育调控型葡萄糖脱氢酶基因的特性分析

Characterization of the developmentally regulated Bacillus subtilis glucose dehydrogenase gene.

作者信息

Lampel K A, Uratani B, Chaudhry G R, Ramaley R F, Rudikoff S

出版信息

J Bacteriol. 1986 Apr;166(1):238-43. doi: 10.1128/jb.166.1.238-243.1986.

Abstract

The DNA sequence of the structural gene for glucose dehydrogenase (EC 1.1.1.47) of Bacillus subtilis was determined and comprises 780 base pairs. The subunit molecular weight of glucose dehydrogenase as deduced from the nucleotide sequence is 28,196, which agrees well with the subunit molecular weight of 31,500 as determined from sodium dodecyl sulfate-polyacrylamide gel electrophoresis. The sequence of the 49 amino acids at the NH2 terminus of glucose dehydrogenase purified from sporulating B. subtilis cells matched the amino acid sequence derived from the DNA sequence. Glucose dehydrogenase was purified from an Escherichia coli strain harboring pEF1, a plasmid that contains the B. subtilis gene encoding glucose dehydrogenase. This enzyme has the identical amino acid sequence at the NH2 terminus as the B. subtilis enzyme. A putative ribosome-binding site, 5'-AGGAGG-3', which is complementary to the 3' end of the 16S rRNA of B. subtilis, was found 6 base pairs preceding the translational start codon of the structural gene of glucose dehydrogenase. No known promoterlike DNA sequences that are recognized by B. subtilis RNA polymerases were present immediately preceding the translational start site of the glucose dehydrogenase structural gene. The glucose dehydrogenase gene was found to be under sporulation control at the trancriptional level. A transcript of 1.6 kilobases hybridized to a DNA fragment within the structural gene of glucose dehydrogenase. This transcript was synthesized 3 h after the cessation of vegetative growth concomitant to the appearance of glucose dehydrogenase.

摘要

测定了枯草芽孢杆菌葡萄糖脱氢酶(EC 1.1.1.47)结构基因的DNA序列,其由780个碱基对组成。根据核苷酸序列推导的葡萄糖脱氢酶亚基分子量为28,196,这与通过十二烷基硫酸钠 - 聚丙烯酰胺凝胶电泳测定的31,500亚基分子量非常吻合。从产孢的枯草芽孢杆菌细胞中纯化的葡萄糖脱氢酶NH2末端49个氨基酸的序列与从DNA序列推导的氨基酸序列相符。葡萄糖脱氢酶是从携带pEF1的大肠杆菌菌株中纯化的,pEF1是一种含有编码葡萄糖脱氢酶的枯草芽孢杆菌基因的质粒。这种酶在NH2末端的氨基酸序列与枯草芽孢杆菌酶相同。在葡萄糖脱氢酶结构基因的翻译起始密码子之前6个碱基对处发现了一个推定的核糖体结合位点5'-AGGAGG-3',它与枯草芽孢杆菌16S rRNA的3'末端互补。在葡萄糖脱氢酶结构基因的翻译起始位点之前没有发现枯草芽孢杆菌RNA聚合酶识别的已知启动子样DNA序列。发现葡萄糖脱氢酶基因在转录水平上受芽孢形成控制。一个1.6千碱基的转录本与葡萄糖脱氢酶结构基因内的一个DNA片段杂交。这个转录本是在营养生长停止3小时后伴随着葡萄糖脱氢酶的出现而合成的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcd8/214582/965eb913fd73/jbacter00209-0249-a.jpg

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