摘要
根据Lampel报道的葡萄糖脱氢酶基因序列设计合成两条引物[1] ,以野生型枯草芽孢杆菌染色体DNA为模板 ,PCR扩增得到含有葡萄糖脱氢酶基因的大约 780bp的DNA片段 ,将其克隆到 pUC -T载体中。序列分析表明 ,克隆得到的葡萄糖脱氢酶基因含有 783bp ,编码 2 6 1个氨基酸的蛋白质。得到的基因序列与文献报道的进行比较 ,其核苷酸同源率为 75 .5 % ,编码氨基酸序列的同源率为 83.9%
Chromosomal DNA as template, gene of glucose dehydrogenase from Bacillus subtilis was cloned in plasmid pUC T by PCR. Followed by sequening, the sequence of the fragment from Bacillus subtilis had a little difference from the sequence of glucose dehydrogenase in other paper. Gene of glucose dehydrogenase was composed of 783 base pairs coded for glucose dehydrogenase of 261 amino acids.
出处
《工业微生物》
CAS
CSCD
北大核心
2001年第3期23-24,28,共3页
Industrial Microbiology