Murtif V L, Bahler C R, Samols D
Proc Natl Acad Sci U S A. 1985 Sep;82(17):5617-21. doi: 10.1073/pnas.82.17.5617.
We have cloned the gene coding for the 1.3S biotin-containing subunit of transcarboxylase (EC 2.1.3.1) from Propionibacterium shermanii. Transcarboxylase is a well-characterized enzyme composed of 30 polypeptides of three different types: twelve 1.3S biotinyl subunits, six 5S dimeric outer subunits, and one 12S hexameric central subunit. In propionic acid fermentation, the enzyme catalyzes the transfer of a carboxyl group from methylmalonyl-CoA to pyruvate in two partial reactions. The 1.3S subunit binds the outer and central subunits of the enzyme together, and its biotin serves as carboxyl carrier between subsites on the central and outer subunits where each partial reaction occurs. The cloned gene has been expressed in Escherichia coli, and the 1.3S subunit accumulates to 7% of total cellular protein. The foreign protein is recognized and biotinated by biotin holoenzyme synthetase of E. coli. The identifications of the gene and its product were confirmed by four independent approaches: DNA sequence analysis, immunoprecipitation, incorporation of labeled biotin, and measurement of enzymatic activity in the first partial reaction.
我们已经从谢氏丙酸杆菌中克隆出编码转羧酶(EC 2.1.3.1)含生物素的1.3S亚基的基因。转羧酶是一种特性明确的酶,由三种不同类型的30个多肽组成:十二个1.3S生物素亚基、六个5S二聚体外部亚基和一个12S六聚体中心亚基。在丙酸发酵中,该酶在两个部分反应中催化羧基从甲基丙二酰辅酶A转移到丙酮酸。1.3S亚基将酶的外部和中心亚基结合在一起,其生物素作为每个部分反应发生的中心和外部亚基上亚位点之间的羧基载体。克隆的基因已在大肠杆菌中表达,1.3S亚基积累至总细胞蛋白的7%。外源蛋白被大肠杆菌的生物素全酶合成酶识别并生物素化。通过四种独立的方法证实了该基因及其产物的鉴定:DNA序列分析、免疫沉淀、标记生物素的掺入以及第一个部分反应中酶活性的测定。