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紫色红曲霉FBKL3.0018产酯化酶的酶学性质研究
引用本文:胡 娜,吴鑫颖,李付丽,王 艳,邱树毅,吴 海. 紫色红曲霉FBKL3.0018产酯化酶的酶学性质研究[J]. 中国酿造, 2017, 36(5): 123. DOI: 10.11882/j.issn.0254-5071.2017.05.026
作者姓名:胡 娜  吴鑫颖  李付丽  王 艳  邱树毅  吴 海
作者单位:1.贵州大学贵州省发酵工程与生物制药重点实验室,贵州贵阳550025;2.贵州大学酿酒与食品工程学院,贵州贵阳550025;3.青酒集团有限公司,贵州黔东南556000
基金项目:贵州省科技合作计划项目(黔科合LH字【2014】7675号);贵州省星火计划项目(黔科合成转字【2015】5337号)
摘    要:以从紫色红曲霉FBKL3.0018中固态发酵得到的粗酶制剂为研究对象,对该菌株的酯化酶酶学性质进行了较系统的研究。通过单因素实验确定该酶最适温度为40 ℃,在30 ℃条件下稳定性较好,最适pH值为6.5,在pH5.5~7.5条件下稳定性好。Fe2+、Na+、Mn2+、Mg2+、Li+、Zn2+对酯化酶酶活力有抑制作用,Ca2+在低浓度时有促进作用,高浓度时有抑制作用。K+对酯化酶酶活力有促进作用,并且随着K+浓度的升高,促进作用逐渐增强。吐温-80、十二烷基硫酸钠(SDS)、聚乙二醇6000、阿拉伯胶4种表面活性剂对酯化酶酶活力都有抑制作用。另外,甲醇和乙醇对该酯化酶酶活力有抑制作用,甲酸、乙酸、乳酸对酯化酶酶活力有促进作用。乙酸乙酯在低浓度时对酯化酶酶活力有抑制作用,含量为30%时反而有促进酶活力的作用。酯化酶最大反应速度Vmax为0.016 mol/(L·min),米氏常数Km为0.015 4 mol/L。

关 键 词:紫色红曲霉  固态发酵  酯化酶  酶学性质  

Enzymatic properties of esterifying enzyme from Monascus purpureus FBKL3.0018
HU Na,WU Xinying,LI Fuli,WANG Yan,QIU Shuyi,WU Hai. Enzymatic properties of esterifying enzyme from Monascus purpureus FBKL3.0018[J]. China Brewing, 2017, 36(5): 123. DOI: 10.11882/j.issn.0254-5071.2017.05.026
Authors:HU Na  WU Xinying  LI Fuli  WANG Yan  QIU Shuyi  WU Hai
Affiliation:1.Guizhou Key Lab of Fermentation Engineering and Biological Pharmacy, Guizhou University, Guiyang 550025, China; 2.School of
Liquor and Food Engineering, Guizhou University, Guiyang 550025, China; 3.Qingjiu Group Co., Ltd., Qiandongnan 556000, China
Abstract:Using the crude enzyme obtained from Monascus purpureus FBKL3.0018 by solid-state fermentation as research object, the enzymatic properties of the strain was studied systematically. By single factor experiments, the optimum temperature and pH of the enzyme was 40 ℃ and 6.5, respectively. The enzyme was stable at 30 ℃ and pH 5.5-7.5. Fe2+, Na+, Mn2+, Mg2+, Li+, and Zn2+ had inhibition effect on enzyme activity; Ca2+ showed promotion effect at low concentration, however, it showed inhibition effect at high concentration. K+ showed promotion effect on enzyme activity, and with the increase of K+ concentration, the promotion effect gradually enhanced. Tween-80, sodium dodecyl sulfate (SDS), polyethylene glycol-6000 and Arabic gum had inhibitory effect on enzyme activity. In addition, methanol and ethanol had inhibition effect on enzyme activity, formic acid, acetic acid and lactic acid had promotion function to enzyme activity. Ethyl acetate showed inhibition effect on esterifying enzyme activity at low concentration, but when the concentration was 30%, it showed promotion effect. The maximum reaction velocity (Vmax) of the esterifying enzyme was 0.016 mol/(L·min), Michaelis constant (Km) was 0.015 4 mol/L.
Keywords:Monascus purpureus  solid-state fermentation  esterifying enzyme  enzymatic properties  
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