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A method for purifying two isozymes of Candida rugosa lipase.

机译:一种纯化皱纹假丝酵母脂肪酶的两种同工酶的方法。

摘要

PROCEDURE FOR THE CLEANSING OF TWO ISOENZYMES Candida rugosa lipase. A method for purifying THESE TWO LIPASES EXTRACELLULAR lipase COMMERCIAL GROSS rugosa. The method comprising a single step CROMATOGRAFIA Hydrophobic IN agarose matrix. VERY DIFFERENT ELUTION CONDITIONS OF PERMIT FULL TWO SEPARATION AND PURIFICATION OF ACTIVITY Lipase enzymes (lipases AYB) PRESENT IN THE COMMERCIAL starting extract. IS USED THEREFOR BUFFER CONCENTRATE pH 6 to 8, with which elute from the column much of the contaminants present in the extract; Then with the same buffer solution more dilute CRAWLING THE LIPASE B. THEREAFTER WITH DI O POLIALCOHOL dissolved in buffer elutes THE DILUTED lipase, whose solution by concentration by ultrafiltration and gel permeation chromatography MOLECULAR dextran, REMOVED THE ALCOHOL. APPLIED industrially enzyme purification.
机译:清洁两种同工酶皱纹念珠菌脂肪酶的程序。一种提纯这两种脂肪酶的商业粗毛的胞外脂肪酶的方法。该方法包括一步CROMATOGRAFIA疏水性IN琼脂糖基质。两种完全分离和纯化活性的洗脱条件,商业起始提取物中存在脂肪酶(脂肪酶AYB)。用于pH 6至8的浓缩缓冲液,可将其从色谱柱中洗脱出萃取液中存在的许多污染物。然后用相同的缓冲溶液稀释。将DI O溶解在缓冲液中的处理剂洗脱稀释的脂肪酶,稀释的脂肪酶通过超滤和凝胶渗透色谱法通过分子右旋糖酐浓缩,除去了酒精。工业上应用酶纯化。

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