首页> 美国卫生研究院文献>Journal of Bacteriology >Biosynthesis of bacterial glycogen: primary structure of Salmonella typhimurium ADPglucose synthetase as deduced from the nucleotide sequence of the glgC gene.
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Biosynthesis of bacterial glycogen: primary structure of Salmonella typhimurium ADPglucose synthetase as deduced from the nucleotide sequence of the glgC gene.

机译:细菌糖原的生物合成:鼠伤寒沙门氏菌ADP葡萄糖合成酶的一级结构由glgC基因的核苷酸序列推导。

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摘要

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.
机译:确定了含有鼠伤寒沙门氏菌LT2 glgC基因的1.4碱基对片段的核苷酸序列,该基因编码ADP葡萄糖合成酶。 glgC结构基因包含1,293个碱基对,编码能力为431个氨基酸。由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45,580。 N末端前27个氨基酸的总氨基酸组成分析和氨基酸测序的先前结果(M.Lehmann和J.Preiss,J.Bacteriol.143:120-127,1980)与核苷酸推导的结果一致。排序数据。大肠杆菌K-12和鼠伤寒沙门氏菌LT2 ADP葡萄糖合成酶的比较表明,它们的核苷酸序列具有80%的同源性,并且其推导的氨基酸序列具有90%的同源性。此外,生理活化剂果糖双磷酸酯(氨基酸残基39)和抑制剂AMP(氨基酸残基114)的推定变构位点的氨基酸残基在两种酶之间是相同的。推定的ADP葡萄糖结合位点也具有广泛的同源性。在大肠杆菌K-12和鼠伤寒沙门氏菌LT2中,glgA的翻译起始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。

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