Kobayashi M, Nishiyama M, Nagasawa T, Horinouchi S, Beppu T, Yamada H
Department of Agricultural Chemistry, Faculty of Agriculture, Kyoto University, Japan.
Biochim Biophys Acta. 1991 Dec 2;1129(1):23-33. doi: 10.1016/0167-4781(91)90208-4.
Rhodococcus rhodochrous J1 produces two kinds of cobalt-containing nitrile hydratases (NHases); one is a high molecular mass-NHase (H-NHase) and the other is a low molecular mass-NHase (L-NHase). Both NHases are composed of two subunits of different sizes (alpha and beta subunits). The H- and L-NHase genes were cloned into Escherichia coli by a DNA-probing method using the NHase gene of Rhodococcus sp. N-774, a ferric ion-containing NHase producing strain, as the hybridization probe and their nucleotide sequences were determined. In each of the H- and L-NHase genes, the open reading frame for the beta subunit was located just upstream of that for the alpha subunit, which probably belongs to the same operon. The amino acid sequences of each subunit of the H- and L-NHases from R. rhodochrous J1 showed generally significant similarities to those from Rhodococcus sp. N-774, but the arrangement of the coding sequences for two subunits is reverse of the order found in the NHase gene of Rhodococcus sp. N-774. Each of the NHase genes was expressed in E. coli cells under the control of lac promoter, only when they were cultured in the medium supplemented with CoCl2.
红平红球菌J1可产生两种含钴腈水合酶(NHases);一种是高分子量腈水合酶(H-NHase),另一种是低分子量腈水合酶(L-NHase)。两种腈水合酶均由大小不同的两个亚基(α和β亚基)组成。利用产含铁离子腈水合酶的红球菌N-774的腈水合酶基因作为杂交探针,通过DNA探针法将H-和L-NHase基因克隆到大肠杆菌中,并测定了它们的核苷酸序列。在H-和L-NHase基因中,β亚基的开放阅读框位于α亚基的开放阅读框的上游,它们可能属于同一个操纵子。红平红球菌J1的H-和L-NHases各亚基的氨基酸序列与红球菌N-774的氨基酸序列总体上有显著相似性,但两个亚基编码序列的排列顺序与红球菌N-774腈水合酶基因中的顺序相反。只有在添加了CoCl2的培养基中培养时,每个腈水合酶基因才会在lac启动子的控制下在大肠杆菌细胞中表达。