Colonna-Romano S, Riccio A, Guida M, Defez R, Lamberti A, Iaccarino M, Arnold W, Priefer U, Pühler A
Nucleic Acids Res. 1987 Mar 11;15(5):1951-64. doi: 10.1093/nar/15.5.1951.
Rhizobium leguminosarum, biovar viceae, strain RCC1001 contains two glutamine synthetase activities, GSI and GSII. We report here the identification of glnA, the structural gene for GSI. A 2 kb fragment of DNA was shown to complement the Gln- phenotype of Klebsiella pneumoniae glnA mutant strains. DNA sequence analysis revealed an open reading frame (ORF) of 469 codons specifying a polypeptide of 52,040 daltons. Its deduced amino acid sequence was found to be highly homologous to other glutamine synthetase sequences. This ORF was expressed in Escherichia coli minicells and the corresponding polypeptide reacted with an antiserum raised against GSI. Upstream of glnA we found an ORF of 111 codons (ORF111) preceded by the consensus sequence for an ntrA-dependent promoter. Minicells experiments showed a protein band, with a molecular weight in good agreement with that (10,469) deduced from the nucleotide sequence. On the basis of homology studies we discuss the possibility that the product of ORF111 is equivalent to the PII protein of E. coli and plays a similar role in regulation of nitrogen metabolism.
豌豆根瘤菌生物变种菜豆致病变种RCC1001菌株含有两种谷氨酰胺合成酶活性,即GSI和GSII。我们在此报告GSI的结构基因glnA的鉴定。一段2 kb的DNA片段被证明可弥补肺炎克雷伯菌glnA突变菌株的Gln-表型。DNA序列分析揭示了一个由469个密码子组成的开放阅读框(ORF),其编码一个52,040道尔顿的多肽。发现其推导的氨基酸序列与其他谷氨酰胺合成酶序列高度同源。该ORF在大肠杆菌小细胞中表达,相应的多肽与针对GSI产生的抗血清发生反应。在glnA上游,我们发现了一个由111个密码子组成的ORF(ORF111),其前面是一个依赖ntrA的启动子的共有序列。小细胞实验显示出一条蛋白带,其分子量与从核苷酸序列推导的分子量(10,469)高度吻合。基于同源性研究,我们讨论了ORF111的产物等同于大肠杆菌的PII蛋白并在氮代谢调节中发挥类似作用的可能性。