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作 者:白晓阳[1] 季朝能[1] 姜涛[1] 盛小禹[1] 毛裕民[1]
机构地区:[1]复旦大学生命科学学院,遗传学研究所上海200433
出 处:《中国生物化学与分子生物学报》2001年第4期506-509,共4页Chinese Journal of Biochemistry and Molecular Biology
基 金:国家自然科学基金资助项目 (No .39870 40 2 )&&
摘 要:为研究体外磷酸根离子对嗜热菌 (Thermussp .30 4 1)碱性磷酸酶TAPND2 7耐热性的影响 ,通过克隆于高表达质粒上编码TAPND2 7的基因在E .coli中的诱导表达和蛋白产物的纯化 ,获得了电泳纯的TAPND2 7.耐热性实验表明磷酸根离子能显著提高该酶的热稳定性 ,在 10mmol L磷酸根离子存在下 ,TAPND2 7的Tm 值从 91℃上升到了 97℃ ;酶的动力学实验证实无机磷酸盐 (Pi)对TAP ND2 7的酶活性有可逆竞争性抑制作用 ,Ki 值为 0 99× 10 -4 mol L .上述结果说明 ,TAPND2 7耐热性的提高是由于磷酸根离子对TAPND2 7活性位点的竞争性结合 ,这种结合 ,推测为Pi 与氨基酸残基间的非共价相互作用 ,减小了TAPND2 7的自由能 。To understand how inorganic phosphate (P\-i) influences the thermostability of alkaline phosphatase (TAPND27) from \%Thermus\% p.3041 in vitro , The gene coding for TAPND27 in high expression plasmid was induced and expressed in \%E.coli,\% and purified TAPND27 was obtained. Thermostability measurement suggested that P i could greatly improve the thermostability of TAPND27. In the presence of 10 mmol/L phosphate, The T m value of TAPND27 increased from 91℃ to 97℃. Enzymatic kinetic experiment verified that P i is a reversible competitive inhibitor, with a K i value 0\^99×10 -4 mol/L. Those results proved that the improved thermostability of TAPND27 is due to reversible interaction between P\-i and the enzyme, which was assumed to be weak noncovalent bond. This interaction decreases the free energy of TAPND27, thus results in improvement of thermostabililty.
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