Possot O, Sibold L, Aubert J P
Département des Biotechnologies, Institut Pasteur, Paris.
Res Microbiol. 1989 Jul-Aug;140(6):355-71. doi: 10.1016/0923-2508(89)90012-0.
The sequence of a 2,746-bp DNA fragment of Methanococcus voltae carrying the glnA gene for glutamine synthetase (GS), was established. A 1,338-bp open reading frame (ORF), encoding a 446-amino-acid polypeptide of 50,142 Da, was defined as glnA on the basis of its similarity to other glnA genes and on the ability of a DNA fragment carrying this ORF to complement an Escherichia coli Gln- mutant. No sequence homology was found between sequences flanking the M. volae glnA gene and other eubacterial glnA genes. In M. voltae, the gene was transcribed as a monocistronic unit and GS synthesis was partially repressed at high ammonia concentrations. At the amino acid sequence level, the highest similarity was found with GS of Bacillus subtilis and Clostridium acetobutylicum.
测定了沃氏甲烷球菌中一段携带谷氨酰胺合成酶(GS)的glnA基因的2746bp DNA片段的序列。一个1338bp的开放阅读框(ORF),编码一个50142Da的446个氨基酸的多肽,基于其与其他glnA基因的相似性以及携带该ORF的DNA片段对大肠杆菌Gln-突变体的互补能力,被定义为glnA。在沃氏甲烷球菌glnA基因侧翼序列与其他真细菌glnA基因之间未发现序列同源性。在沃氏甲烷球菌中,该基因作为一个单顺反子单元转录,并且在高氨浓度下GS合成受到部分抑制。在氨基酸序列水平上,与枯草芽孢杆菌和丙酮丁醇梭菌的GS具有最高的相似性。