Ramaswamy K S, Endley S, Golden J W
Department of Biology, Texas A&M University, College Station, Texas 77843-3258, USA.
J Bacteriol. 1996 Jul;178(13):3893-8. doi: 10.1128/jb.178.13.3893-3898.1996.
Mutants of Anabaena sp. strain PCC 7120 that form heterocysts when grown on nitrate-containing media were isolated following nitrosoguanidine mutagenesis. Six independent mutants were isolated, and the characterization of one mutant, strain AMC260, which forms 6 to 8% heterocysts in the presence of nitrate, is presented. A 1.8-kb chromosomal fragment that complemented the AMC260 mutant was sequenced, and a 1.2-kb open reading frame, named moeA, was identified. The deduced amino acid sequence of the predicted Anabaena sp. strain PCC 7120 MoeA polypeptide shows 37% identity to MoeA from Escherichia coli, which is required for the synthesis of molybdopterin cofactor. Molybdopterin is required by various molybdoenzymes, such as nitrate reductase. Interruption of the moeA gene in Anabaena sp. strain PCC 7120 resulted in a strain, AMC364, that showed a phenotype similar to that of AMC260. We show that AMC260 and AMC364 lack methyl viologen-supported nitrate reductase activity. We conclude that the inability of the moeA mutants to metabolize nitrate results in heterocyst formation on nitrate-containing media. Northern (RNA) analysis detected a 1.5-kb moeA transcript in wild-type cells grown in the presence or absence of a combined nitrogen source.
在亚硝基胍诱变后,分离得到了鱼腥藻PCC 7120菌株的突变体,这些突变体在含硝酸盐的培养基上生长时会形成异形胞。分离出了6个独立的突变体,并对其中一个突变体AMC260菌株进行了表征,该菌株在硝酸盐存在的情况下会形成6%至8%的异形胞。对一个能互补AMC260突变体的1.8kb染色体片段进行了测序,鉴定出一个1.2kb的开放阅读框,命名为moeA。预测的鱼腥藻PCC 7120 MoeA多肽的推导氨基酸序列与大肠杆菌的MoeA具有37%的同一性,后者是钼蝶呤辅因子合成所必需的。各种钼酶,如硝酸还原酶,都需要钼蝶呤。鱼腥藻PCC 7120中moeA基因的中断产生了一个菌株AMC364,其表现出与AMC260相似的表型。我们发现AMC260和AMC364缺乏甲基紫精支持的硝酸还原酶活性。我们得出结论,moeA突变体无法代谢硝酸盐导致在含硝酸盐的培养基上形成异形胞。Northern(RNA)分析在有或没有联合氮源的情况下生长的野生型细胞中检测到一个1.5kb的moeA转录本。