Okuyama M, Okuno A, Shimizu N, Mori H, Kimura A, Chiba S
Division of Applied Bioscience, Graduate School of Agriculture, Hokkaido University, Sapporo, Japan.
Eur J Biochem. 2001 Apr;268(8):2270-80. doi: 10.1046/j.1432-1327.2001.02104.x.
cDNA encoding Schizosaccharomyces pombe alpha-glucosidase was cloned from a library constructed from mRNA of the fission yeast, and expressed in Saccharomyces cerevisiae. The cDNA, 4176 bp in length, included a single ORF composed of 2910 bp encoding a polypeptide of 969 amino-acid residues with M(r) 106 138. The deduced amino-acid sequence showed a high homology to those of alpha-glucosidases from molds, plants and mammals. Therefore, the enzyme was categorized into the alpha-glucosidase family II. By site-directed mutagenesis, Asp481, Glu484 and Asp647 residues were confirmed to be essential in the catalytic reaction. The carboxyl group (-COOH) of the Asp647 residue was for the first time shown to be the most likely proton donor acting as the acid catalyst in the alpha-glucosidase of family II. Studies with the chemical modifier conduritol B epoxide suggested that the carboxylate group (-COO-) of the Asp481 residue was the catalytic nucleophile, although the role of the Glu484 residue remains obscure.
从粟酒裂殖酵母的mRNA构建的文库中克隆出编码粟酒裂殖酵母α-葡萄糖苷酶的cDNA,并在酿酒酵母中表达。该cDNA长度为4176 bp,包含一个由2910 bp组成的单一开放阅读框,编码一个969个氨基酸残基的多肽,分子量为106138。推导的氨基酸序列与来自霉菌、植物和哺乳动物的α-葡萄糖苷酶具有高度同源性。因此,该酶被归类为α-葡萄糖苷酶家族II。通过定点诱变,证实Asp481、Glu484和Asp647残基在催化反应中是必需的。首次表明Asp647残基的羧基(-COOH)最有可能是作为II型α-葡萄糖苷酶中酸催化剂的质子供体。用化学修饰剂环氧化物处理的研究表明,Asp481残基的羧酸盐基团(-COO-)是催化亲核试剂,尽管Glu484残基的作用仍不清楚。