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枯草芽孢杆菌葡萄糖脱氢酶基因的克隆及其序列分析 被引量:4

Cloning and sequencing of glucose dehydrogenase from B.subtilis
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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
关键词 葡萄糖脱氢酶基因 PCR扩增 DNA序列分析 枯草芽孢杆菌 克隆 D-核糖 Bacillus subtilis glucose dehydrogenase PCR DNA sequencing
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  • 2梁志超,刘敏,王毓三.血清葡萄糖的葡萄糖脱氢酶测定法[J].临床检验杂志,1996,14(1):20-21. 被引量:8
  • 3李艳,李静.葡萄糖氧化酶及其应用[J].食品工程,2006(3):9-11. 被引量:33
  • 4赵晓芳,张宏福.葡萄糖氧化酶的功能及在畜牧业中的应用[J].广东饲料,2007,16(1):34-35. 被引量:49
  • 5Ken Inose,Masako Fujikawa, Tomohiko Yamazaki.Clonging and expression of the gene encoding catalytic subunit of thermostable glucose dehydrogenase from Burkholderia cepacia in Escherichia coli[J].Biochimica et Biophysica Acta,2003, 1645:133-138.
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