摘要
利用DNA限制性内切酶图谱分析将一个带有脆壁克鲁维酵母 (Kluyveromycesfragilis) 蛋白二硫化物异构酶基因(KfPDI) 的10 kb 初始克隆缩短为4 kb 的亚克隆,并测定了该基因的DNA全序列。经分析发现: (1)该基因编码产物由520个氨基酸残基组成。(2) 它与乳酸克鲁维酵母(K. lactis) 蛋白二硫化物异构酶在氨基酸序列上的同源性为78。(3) 它与其他物种的PDI基因在核苷酸和蛋白质水平上的同源性较弱,
A 10 kb of primary DNA clone containing the Kluyveromyces fragilis protein disulfide isomerase gene (KfPDI) was mapped and shortened into a 4 kb of subclone, followed by the complete gene DNA sequencing and analyzing. The results show that: (1) the KfPDI protein is consisted of 520 amino acid residues; (2) the homologous identity between KfPDI and the KlPDI from K. lactis is 78% at amino acid level; (3) Although the homology between KfPDI and other known PDI genes is not perfect but two highly conserved activity domains of protein disulfide isomerase can be found among all of them.
出处
《高技术通讯》
EI
CAS
CSCD
1999年第8期39-43,共5页
Chinese High Technology Letters
基金
863计划资助项目
关键词
脆壁克鲁维酵母
PDI
KfPDI
序列分析
Kluyveromyces fragilis, Protein disulfide isomerase gene (PDI), Sequence analysis