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热球菌HJ21高温α-淀粉酶基因克隆、表达及性质研究

王淑军 吕明生 秦松 陆兆新 房耀维 邓祥元 林谦 刘红飞

王淑军, 吕明生, 秦松, 陆兆新, 房耀维, 邓祥元, 林谦, 刘红飞. 热球菌HJ21高温α-淀粉酶基因克隆、表达及性质研究[J]. 海洋学报, 2011, 33(3): 158-164.
引用本文: 王淑军, 吕明生, 秦松, 陆兆新, 房耀维, 邓祥元, 林谦, 刘红飞. 热球菌HJ21高温α-淀粉酶基因克隆、表达及性质研究[J]. 海洋学报, 2011, 33(3): 158-164.
WANG Shu-jun, LU Ming-sheng, QIN Song, LU Zhao-xin, FANG Yao-wei, DENG Xiang-yuan, LIN Qian, LIU Hong-fei. Cloning, expression, purification and characterization of thermostable and acid-stable α-amylase from Thermococuus HJ21[J]. Haiyang Xuebao, 2011, 33(3): 158-164.
Citation: WANG Shu-jun, LU Ming-sheng, QIN Song, LU Zhao-xin, FANG Yao-wei, DENG Xiang-yuan, LIN Qian, LIU Hong-fei. Cloning, expression, purification and characterization of thermostable and acid-stable α-amylase from Thermococuus HJ21[J]. Haiyang Xuebao, 2011, 33(3): 158-164.

热球菌HJ21高温α-淀粉酶基因克隆、表达及性质研究

基金项目: 国家自然科学基金项目(40746030);江苏省科技支撑计划(BE2008340);江苏省高校自然科学研究重大项目(09KJA170001)。

Cloning, expression, purification and characterization of thermostable and acid-stable α-amylase from Thermococuus HJ21

  • 摘要: 通过简并引物扩增热球菌(Thermococcus siculi) HJ21高温α-淀粉酶保守区域之间的序列,再利用Site-finding技术获得两端未知序列。构建了在N端添加了His6标签的表达载体pEt-28a-His6-THJA后转化E. coli,在 IPTG诱导下表达。进一步纯化后SDS-PAGE电泳检测达到电泳纯,重组酶分子量为50 KDa。重组酶最适作用温度和pH值分别为90 ℃,pH 5.0。重组酶在pH为5.5时最稳定;K,Sr2+,Mg2+, Na对α-淀粉酶活力的促进作用不显著,Cu2+,Pb2+,Hg2+,Zn2+,N-溴代丁酰亚胺和三氯乙酸对该酶有显著抑制作用。
  • PRAKASH B, VIDYASAGAR M, MADHUKUMAR M S, et al. Production, purification, and characterization of two extremely halotolerant, thermostable, and alkali-stable a-amylases from Chromohalobacter sp. TVSP 101[J]. Process Biochemistry, 2009, 44:210-215.
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  • 收稿日期:  2010-08-09

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