%0 Journal Article
%T 重组嗜热乳糖酶在毕赤酵母中的表达、纯化与活性分析
%A 李洪波
%A 罗海燕
%A 张树琴
%A 吴东海
%J 食品与生物技术学报
%D 2018
%R 10.3969/j.issn.1673-1689.2018.08.005
%X 为获得耐高温的重组乳糖酶，PCR扩增激烈热球菌（Pyrococcus furious）乳糖酶基因、构建毕赤酵母分泌型表达载体pPICZαA/Lac并转化毕赤酵母X-33菌株。重组酵母转化子经甲醇诱导，重组嗜热乳糖酶实现了分泌表达并经蛋白印迹验证。纯化前上清液中乳糖酶总活力高达125 U/mL，经镍亲合纯化得重组酶，SDS-PAGE显示其纯度在95%以上，比活力1 800 U/mg，该酶最适温度在105 ℃左右且热稳定性好，具有很强的水解乳糖能力。</br>In order to obtain the recombinant thermostable lactase，a DNA fragment containing the mature lactase gene was amplified from Pyrococcus furious by PCR and cloned into pPICZaA，generating a fusion protein with the alpha factor from baker's yeast and integrated into the genome of Pichia pastoris strain X-33. Recombinant yeast transformants with high-level recombinant lactase production was identified by Western blotting，secreting as much as 125 U/mL induction by methanol. The recombinant thermostability lactase was purified by Ni+-NTA affinity chromatography and SDS-PAGE results shown that the purity was over 95%. The specific activity was about 1 800 U/mg and the optimal temperature was about 105 ℃. It was also showed that the purified lactase from P. pastoris has a highly thermostability and strong ability to hydrolysis lactose
%K 嗜热乳糖酶 激烈热球菌 毕赤酵母 分泌表达 纯化&lt
%K /br&gt
%K thermophile lactase
%K Pyrococcus furious
%K Pichia pastoris
%K secretory expression
%K purification
%U http://spyswjs.cnjournals.com/spyswjs/ch/reader/view_abstract.aspx?file_no=201808005&flag=1