Morris C J, Reeve J N
Department of Microbiology, Ohio State University, Columbus 43210.
J Bacteriol. 1988 Jul;170(7):3125-30. doi: 10.1128/jb.170.7.3125-3130.1988.
The DNA sequences of the argG genes of Methanosarcina barkeri MS and Methanococcus vannielii were determined. The polypeptide products of these methanogen genes have amino acid sequences which are 50% identical to each other and 38% identical to the amino acid sequence encoded by the exons of the human argininosuccinate synthetase gene. Introns in the human chromosomal gene separate regions which encode amino acids conserved in both the archaebacterial and human gene products. An open reading frame immediately upstream of argG in Methanosarcina barkeri MS codes for an amino acid sequence which is 45 and 31% identical to the sequences of the large subunits of carbamyl phosphate synthetase in Escherichia coli and Saccharomyces cerevisiae, respectively. If this gene encodes carbamyl phosphate synthetase in Methanosarcina barkeri, this is the first example, in an archaebacterium, of physical linkage of genes that encode enzymes which catalyze reactions in the same amino acid biosynthetic pathway.
测定了巴氏甲烷八叠球菌MS和万氏甲烷球菌的精氨酸琥珀酸合成酶基因(argG)的DNA序列。这些产甲烷菌基因的多肽产物具有彼此50%相同且与人精氨琥珀酸合成酶基因外显子编码的氨基酸序列38%相同的氨基酸序列。人类染色体基因中的内含子分隔了在古细菌和人类基因产物中均保守的编码氨基酸的区域。巴氏甲烷八叠球菌MS中argG上游紧邻的一个开放阅读框编码的氨基酸序列分别与大肠杆菌和酿酒酵母中氨甲酰磷酸合成酶大亚基的序列有45%和31%的相同性。如果该基因在巴氏甲烷八叠球菌中编码氨甲酰磷酸合成酶,那么这是古细菌中编码催化同一氨基酸生物合成途径中反应的酶的基因发生物理连锁的首个实例。