Berks B C, Richardson D J, Reilly A, Willis A C, Ferguson S J
Centre for Metalloprotein Spectroscopy and Biology, School of Biological Sciences, University of East Anglia, Norwich, U.K.
Biochem J. 1995 Aug 1;309 ( Pt 3)(Pt 3):983-92. doi: 10.1042/bj3090983.
The napEDABC locus coding for the periplasmic nitrate reductase of Thiosphaera pantotropha has been cloned and sequenced. The large and small subunits of the enzyme are coded by napA and napB. The sequence of NapA indicates that this protein binds the GMP-conjugated form of the molybdopterin cofactor. Cysteine-181 is proposed to ligate the molybdenum atom. It is inferred that the active site of the periplasmic nitrate reductase is structurally related to those of the molybdenum-dependent formate dehydrogenases and bacterial assimilatory nitrate reductases, but is distinct from that of the membrane-bound respiratory nitrate reductases. A four-cysteine motif at the N-terminus of NapA binds a [4Fe-4S] cluster. The DNA- and protein-derived primary sequence of NapB confirm that this protein is a dihaem c-type cytochrome and, together with spectroscopic data, indicate that both NapB haems have bis-histidine ligation. napC is predicted to code for a membrane-anchored tetrahaem c-type cytochrome that shows sequence similarity to the NirT cytochrome c family. NapC may be the direct electron donor to the NapAB complex. napD is predicted to encode a soluble cytoplasmic protein and napE a monotopic integral membrane protein, napDABC genes can be discerned at the aeg-46.5 locus of Escherichia coli K-12, suggesting that this operon encodes a periplasmic nitrate reductase system, while napD and napC are identified adjacent to the napAB genes of Alcaligenes eutrophus H16.
编码嗜糖假单胞菌周质硝酸还原酶的napEDABC基因座已被克隆并测序。该酶的大亚基和小亚基分别由napA和napB编码。NapA的序列表明该蛋白结合钼蝶呤辅因子的GMP缀合形式。推测半胱氨酸-181连接钼原子。据推断,周质硝酸还原酶的活性位点在结构上与钼依赖性甲酸脱氢酶和细菌同化硝酸还原酶的活性位点相关,但与膜结合呼吸硝酸还原酶的活性位点不同。NapA N端的一个四半胱氨酸基序结合一个[4Fe-4S]簇。NapB的DNA和蛋白质衍生的一级序列证实该蛋白是一种双血红素c型细胞色素,并且与光谱数据一起表明两个NapB血红素都有双组氨酸连接。预测napC编码一种膜锚定的四血红素c型细胞色素,其与NirT细胞色素c家族具有序列相似性。NapC可能是NapAB复合物的直接电子供体。预测napD编码一种可溶性细胞质蛋白,napE编码一种单一位点整合膜蛋白,在大肠杆菌K-12的aeg-46.5基因座可识别napDABC基因,这表明该操纵子编码一个周质硝酸还原酶系统,而napD和napC在嗜碱假单胞菌H16的napAB基因附近被鉴定出来。