Rubio L M, Flores E, Herrero A
Instituto de Bioquímica Vegetal y Fotosíntesis, Consejo Superior de Investigaciones Científicas-Universidad de Sevilla, Seville, Spain.
J Bacteriol. 1998 Mar;180(5):1200-6. doi: 10.1128/JB.180.5.1200-1206.1998.
The narA locus required for nitrate reduction in Synechococcus sp. strain PCC 7942 is shown to consist of a cluster of genes, namely, moeA, moaC, moaD, moaE, and moaA, involved in molybdenum cofactor biosynthesis. The product of the moaC gene of strain PCC 7942 shows homology in its N-terminal half to MoaC from Escherichia coli and in its C-terminal half to MoaB or Mog. Overexpression of the Synechococcus moaC gene in E. coli resulted in the synthesis of a polypeptide of 36 kDa, a size that would conform to a protein resembling a fusion of the MoaC and MoaB or Mog polypeptides of E. coli. Insertional inactivation of the moeA, moaC, moaE, and moaA genes showed that the moeA-moa gene cluster is required for growth on nitrate and expression of nitrate reductase activity in strain PCC 7942. The moaCDEA genes constitute an operon which is transcribed divergently from the moeA gene. Expression of the moeA gene and the moa operon was little affected by the nitrogen source present in the culture medium.
已证明,聚球藻属菌株PCC 7942中硝酸盐还原所需的narA基因座由一组基因组成,即参与钼辅因子生物合成的moeA、moaC、moaD、moaE和moaA。菌株PCC 7942的moaC基因产物在其N端一半与大肠杆菌的MoaC具有同源性,在其C端一半与MoaB或Mog具有同源性。聚球藻moaC基因在大肠杆菌中的过表达导致合成了一条36 kDa的多肽,该大小与类似于大肠杆菌MoaC和MoaB或Mog多肽融合体的蛋白质相符。moeA、moaC、moaE和moaA基因的插入失活表明,moeA - moa基因簇是菌株PCC 7942在硝酸盐上生长以及硝酸盐还原酶活性表达所必需的。moaCDEA基因构成一个操纵子,其转录方向与moeA基因相反。moeA基因和moa操纵子的表达受培养基中氮源的影响很小。