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重组嗜热乳糖酶在毕赤酵母中的表达、纯化与活性分析 被引量:1
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作者 李洪波 罗海燕 +1 位作者 张树琴 吴东海 《食品与生物技术学报》 CAS CSCD 北大核心 2018年第8期812-816,共5页
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... 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。 展开更多
关键词 嗜热乳糖酶 激烈球菌 毕赤酵母 分泌表达 纯化
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Isolation and Production of Novel β-galactosidase from a Newly Isolated, Moderate Thermophile, Bacillus sp. Strain B1.1
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作者 Phimchanok Jaturapiree Suganya Phuengjayaeam +2 位作者 Pomtip Seangsawang Witsanu Srila Chirakam Muangnapoh 《Journal of Food Science and Engineering》 2012年第7期395-402,共8页
The enzyme β-galactosidase (lactase; EC 3.2.1.23) is a commercially important enzyme due to its various applications in dairy and food industries, which are based on the β-galactosidase-catalysed hydrolysis of lac... The enzyme β-galactosidase (lactase; EC 3.2.1.23) is a commercially important enzyme due to its various applications in dairy and food industries, which are based on the β-galactosidase-catalysed hydrolysis of lactose into glucose and galactose. The objectives of this work were to identify novel and attractive sources of this industrially relevant enzyme, and to study the effect of selected growth parameters (carbon source, lactose concentration, nitrogen source, peptone concentration, initial pH and temperature) on the formation of β-galactosidase. Based on a screening of isolates from Tha Pai hot spring, Mae Hong Son Province, Thailand, strain BI.1 was selected for further studies. Strain BI.1 is a Gram-positive, rod-shaped, catalase-positive bacterium that forms endospores. Based on the sequence of the 16S rDNA determined, this isolate is most closely related to Anoxybacillus sp. and Bacillus sp., and hence the strain is designated as Bacillus sp. B 1. I.β-Galactosidase was produced by this strain with lactose and peptone as carbon and nitrogen sources, respectively. Optimal enzyme production occurred at an initial culture pH of 8.5 and at 45 ℃. Under these optimum culture conditions, maximal volumetric and specific β-galactosidase activity of 0.478 U mL^-1 and 0.338 U mg^-1 protein, respectively, were obtained after 13 h of cultivation in a medium contain 2.5% lactose, 2.0% peptone, 0.3% K2HPO4, 0.1% KH2PO4 and 0.05% MgSOa·7H2O. 展开更多
关键词 Β-GALACTOSIDASE ISOLATION PRODUCTION THERMOPHILE prebiotic.
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