Leung P S, Preiss J
J Bacteriol. 1987 Sep;169(9):4355-60. doi: 10.1128/jb.169.9.4355-4360.1987.
The nucleotide sequence of a 1.4-kilobase-pair fragment containing the Salmonella typhimurium LT2 glgC gene coding for ADPglucose synthetase was determined. The glgC structural gene contains 1,293 base pairs, having a coding capacity of 431 amino acids. The amino acid sequence deduced from the nucleotide sequence shows that the molecular weight of ADPglucose synthetase is 45,580. Previous results of the total amino acid composition analysis and amino acid sequencing (M. Lehmann and J. Preiss, J. Bacteriol. 143:120-127, 1980) of the first 27 amino acids from the N terminus agree with that deduced from nucleotide sequencing data. Comparison of the Escherichia coli K-12 and S. typhimurium LT2 ADPglucose synthetase shows that there is 80% homology in their nucleotide sequence and 90% homology in their deduced amino acid sequence. Moreover, the amino acid residues of the putative allosteric sites for the physiological activator fructose bisphosphate (amino acid residue 39) and inhibitor AMP (amino acid residue 114) are identical between the two enzymes. There is also extensive homology in the putative ADPglucose binding site. In both E. coli K-12 and S. typhimurium LT2, the first base of the translational start ATG of glgA overlaps with the third base TAA stop codon of the glgC gene.
测定了一个1.4千碱基对片段的核苷酸序列,该片段包含编码ADP葡萄糖合成酶的鼠伤寒沙门氏菌LT2 glgC基因。glgC结构基因含有1293个碱基对,编码能力为431个氨基酸。从核苷酸序列推导的氨基酸序列表明,ADP葡萄糖合成酶的分子量为45580。先前对N端前27个氨基酸进行的总氨基酸组成分析和氨基酸测序结果(M. Lehmann和J. Preiss,《细菌学杂志》143:120 - 127,1980)与从核苷酸测序数据推导的结果一致。大肠杆菌K - 12和鼠伤寒沙门氏菌LT2的ADP葡萄糖合成酶的比较表明,它们的核苷酸序列有80%的同源性,推导的氨基酸序列有90%的同源性。此外,两种酶中生理激活剂果糖二磷酸(氨基酸残基39)和抑制剂AMP(氨基酸残基114)的假定变构位点的氨基酸残基是相同的。在假定的ADP葡萄糖结合位点也有广泛的同源性。在大肠杆菌K - 12和鼠伤寒沙门氏菌LT2中,glgA翻译起始ATG的第一个碱基与glgC基因的第三个碱基TAA终止密码子重叠。