Kondo H, Shiratsuchi K, Yoshimoto T, Masuda T, Kitazono A, Tsuru D, Anai M, Sekiguchi M, Tanabe T
Faculty of Engineering, Nagasaki University, Japan.
Proc Natl Acad Sci U S A. 1991 Nov 1;88(21):9730-3. doi: 10.1073/pnas.88.21.9730.
Biotin carboxylase [biotin-carboxyl-carrier-protein:carbon-dioxide ligase (ADP-forming), EC 6.3.4.14] is the enzyme mediating the first step of the acetyl-CoA carboxylase [acetyl-CoA:carbon-dioxide ligase (ADP-forming), EC 6.4.1.2] reaction. We screened an Escherichia coli DNA library and a DNA fragment carrying the biotin carboxylase gene fabG, and its flanking regions were cloned. The gene for biotin carboxyl carrier protein was found 13 base pairs upstream of the fabG gene. Nucleotide sequencing of the recombinant plasmids revealed that the fabG codes for a 449-amino acid residue protein with a calculated molecular weight of 49,320, a value in good agreement with that of 51,000 determined by SDS/polyacrylamide gel electrophoresis of the purified enzyme. The deduced amino acid sequence of biotin carboxylase is also consistent with the partial amino acid sequence determined by Edman degradation. The primary structure of this enzyme exhibits a high homology with those of other biotin-dependent enzymes and carbamoyl-phosphate synthetase [carbon-dioxide:L-glutamine amino-ligase (ADP-forming, carbamate-phosphorylating), EC 6.3.5.5]; therefore, all these enzymes probably function through the same mechanism of reaction.
生物素羧化酶[生物素-羧基载体蛋白:二氧化碳连接酶(形成ADP),EC 6.3.4.14]是介导乙酰辅酶A羧化酶[乙酰辅酶A:二氧化碳连接酶(形成ADP),EC 6.4.1.2]反应第一步的酶。我们筛选了一个大肠杆菌DNA文库,并克隆了携带生物素羧化酶基因fabG及其侧翼区域的DNA片段。发现生物素羧基载体蛋白基因位于fabG基因上游13个碱基对处。重组质粒的核苷酸测序表明,fabG编码一个由449个氨基酸残基组成的蛋白质,计算分子量为49320,这一数值与通过纯化酶的SDS/聚丙烯酰胺凝胶电泳测定的51000非常一致。生物素羧化酶推导的氨基酸序列也与通过埃德曼降解法测定的部分氨基酸序列一致。该酶的一级结构与其他生物素依赖性酶和氨甲酰磷酸合成酶[二氧化碳:L-谷氨酰胺氨基连接酶(形成ADP,氨基甲酰磷酸化),EC 6.3.5.5]的一级结构具有高度同源性;因此,所有这些酶可能通过相同的反应机制发挥作用。