Lauterbach F, Körtner C, Tripier D, Unden G
Eur J Biochem. 1987 Jul 15;166(2):447-52. doi: 10.1111/j.1432-1033.1987.tb13536.x.
The fumarate reductase complex of the anaerobic bacterium Wolinella succinogenes catalyzes the electron transfer from menaquinol to fumarate. Two structural genes coding for subunits of the enzyme have been cloned in Escherichia coli. The genes were isolated from a lambda EMBL3 phage gene bank by immunological screening and subcloned in an expression vector. The genes frdA and frdB, which encode the FAD protein (Frd A, Mr 79,000) and the iron-sulfur protein (Frd B, Mr 31,000) of the fumarate reductase complex, were cloned together with a W. succinogenes promoter. The gene order was promoter-frdA-frdB. The FAD protein and the iron-sulfur protein were expressed in the correct molar mass in E. coli from the clones. The identity of the frdA gene and the suggested polarity were confirmed by comparing the amino-terminal sequence of the Frd A protein with that predicted from the 5'-terminal nucleotide sequence of frdA. The frdA and frdB genes are present only once in the genome. A region downstream of frdB, possibly a gene encoding cytochrome b of the fumarate reductase complex, hybridizes with a second site in the genome.
厌氧细菌琥珀酸沃林氏菌的延胡索酸还原酶复合物催化电子从甲基萘醌转移至延胡索酸。编码该酶亚基的两个结构基因已在大肠杆菌中克隆。这些基因通过免疫筛选从λEMBL3噬菌体基因文库中分离出来,并亚克隆到一个表达载体中。延胡索酸还原酶复合物的编码黄素腺嘌呤二核苷酸(FAD)蛋白(Frd A,分子量79,000)和铁硫蛋白(Frd B,分子量31,000)的基因frdA和frdB与琥珀酸沃林氏菌的一个启动子一起被克隆。基因顺序为启动子 - frdA - frdB。FAD蛋白和铁硫蛋白在大肠杆菌中从这些克隆以正确的分子量表达。通过比较Frd A蛋白的氨基末端序列与从frdA的5'末端核苷酸序列预测的序列,证实了frdA基因的身份和推测的极性。frdA和frdB基因在基因组中仅存在一次。frdB下游的一个区域,可能是编码延胡索酸还原酶复合物细胞色素b的一个基因,与基因组中的第二个位点杂交。