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作 者:王明道[1] 邢岩[1] 邱爽 王红阳[1] 孙利鹏 邱立友[1] WANG Mingdao;XING Yan;QIU Shuang;WANG Hongyang;SUN Lipeng;QIU Liyou(Key Laboratory of Enzyme Engineering of Agricultural Microbiology,Ministry of Agriculture,Henan Agricultural University,Zhengzhou 450002,China;Henan Yangshao Bio-products Co.LTD,Mianchi 472400,China)
机构地区:[1]河南农业大学农业部农业微生物酶工程重点实验室,河南郑州450002 [2]河南仰韶生化工程有限公司,河南渑池472400
出 处:《信阳师范学院学报(自然科学版)》2018年第2期197-202,共6页Journal of Xinyang Normal University(Natural Science Edition)
基 金:科技部"十二五"农村领域科技计划项目(2013AA102101-2);河南省重点科技攻关计划项目(142102110086)
摘 要:选择来源于极端嗜热菌Thermosipho melanesiensis(DSM12029)的普鲁兰酶基因,以购自德国菌种保藏中心的基因组为模板,扩增出普鲁兰酶基因TM-pulA;利用酶切酶连构建了重组质粒pET21a-TM-pulA;转入大肠杆菌Rosetta(DE3)菌株中诱导表达并经纯化后,进行了水解产物分析和酶学性质测定.结果显示:TM-pulA为Ⅰ型普鲁兰酶,最适pH为5.8;最适温度是80℃;70℃下半衰期为4.75 h;Mn^(2+)、Co^(2+)、AL^(3+)、Fe^(3+)、SDS及EDTA对其酶活有不同程度的抑制作用;该酶的K_m、V_(max)、K_(cat)及K_(cat)/Km值分别为4.68 g·L^(-1)、0.0085 mmol·L^(-1)·s^(-1)、71.18 s^(-1)、15.21 L·g^(-1)·s^(-1).The pullulanase gene TM-pulA was choosed from the extreme thermophilic bacterium Thermosipho melanesiensis(DSM12029)and cloned by using the genome purchased from the Leibniz Institute DSMZ-German Collection of Microorganisms and Cell Cultures as the template.The plasmid pET21a containing TM-pulA was constructed by restriction enzyme digestion and linking method.The recombinant plasmid was transferred into strain Escherichia coli Rosetta(DE3).After purification,the hydrolysis products were analyzed and the enzymatic properties were determined.The results are as follows:TM-pulA is a typeⅠpullulanase;the optimum pH is 5.8;the optimum temperature is 80℃;The half-life is 4.75 h;Mn 2+,Co 2+,Al 3+,Fe 3+,SDS and EDTA inhibit the activity of enzymes in different degrees;the value of K m,V max,K cat and K cat/K m are 4.68 g·L-1,0.0085 mmol·L-1·s-1,71.18 s-1 and 15.21 L·g-1·s-1,respectively.
关 键 词:普鲁兰酶 Thermosipho melanesiensis 异源表达 酶学性质
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