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p3GnT8/β3GalT7催化活性的研究
引用本文:吴艳,郭毅,孙其昌,贾伟,沈力,鞠思敏,吴士良. p3GnT8/β3GalT7催化活性的研究[J]. 苏州大学学报(自然科学版), 2009, 29(5)
作者姓名:吴艳  郭毅  孙其昌  贾伟  沈力  鞠思敏  吴士良
作者单位:吴艳,郭毅,孙其昌,沈力,鞠思敏,WU Yan,GUO Yi,SUN Qi-chang,SHEN Li,JU Si-ming(苏州大学医学部生物化学与分子生物学系,江苏苏州,2151232;苏州大学生化上程研究所,江苏苏州,215123);贾伟,吴士良,JIA Wei,WU Shi-hang(苏州大学医学部生物化学与分子生物学系,江苏苏州,2151232;苏州大学生化上程研究所,江苏苏州,215123;苏州大学医学部生物化学与分子生物学系,江苏苏州,2151232.苏州大学生化上程研究所,江苏苏州,215123)
基金项目:国家自然科学基金,国防科工委资助项目
摘    要:目的 进一步验证β1,3半乳糖基转移酶(β3GalT7)的催化功能.方法 将重组表达载体pGEX-6p-1-β3GnT8/GalT7转化BL21大肠杆菌,经IPTG诱导表达后,得到GST-β3GnT8/GalT7融合蛋白,分别进行β3GAIT7和β3GnT8反应体系的酶促反应,利用高效液相色谱(HPLC)进行检测.结果 HPLC检测结果表明,β3GalIT7同时具有β3GalT7和β3GnT8的活性.结论 β3GalT7具有双重酶活性,拟初步重命名为β3GnT8/β3GalT7.
Abstract:
Objective To determine the catalytic activity of the (31, 3-N-acetylglucosyltransferase β3GnT8)/β1, 3-galactosyltransferases (β3GalT7). Methods The recombinant plasmid was transformed into E. Coli BL21. Then a fusion protein was expressed after the induction by IPTG. After testified by Western blot, we purified the expression products by affinity chromatography. After renaturation, its enzyme activity was assayed by HPLC. Results It suggested that β3GalT7 own the catalytic activities of β3GalT7 and β3GnT8. Conclusion It has both activities of GalTs and GnTs, so we renamed it as β3GnT8/β3GalT7.

关 键 词:β1,3半乳糖基转移酶  β1,3-N-乙酰氨基葡萄糖转移酶  催化活性  高效液相色谱

Research of the Catalytic Activity of p3GnT8/p3GalT7
WU Yan,GUO Yi,SUN Qi-chang,JIA Wei,SHEN Li,JU Si-ming,WU Shi-hang. Research of the Catalytic Activity of p3GnT8/p3GalT7[J]. Suzhou University Journal of Medical Science, 2009, 29(5)
Authors:WU Yan  GUO Yi  SUN Qi-chang  JIA Wei  SHEN Li  JU Si-ming  WU Shi-hang
Abstract:
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