首页 | 本学科首页   官方微博 | 高级检索  
     

毕赤酵母产重组木聚糖酶发酵条件的优化及其酶学性质
引用本文:史红玲,汪俊卿,邬敏辰,高树娟. 毕赤酵母产重组木聚糖酶发酵条件的优化及其酶学性质[J]. 中国生物制品学杂志, 2012, 25(10): 1362-1365
作者姓名:史红玲  汪俊卿  邬敏辰  高树娟
作者单位:1. 江南大学医药学院,江苏无锡,214122
2. 江南大学工业生物技术教育部重点实验室,江苏无锡,214122
摘    要:目的优化毕赤酵母工程菌GS115/xyn11A产重组木聚糖酶的发酵条件,并检测其酶学性质。方法采用单因素试验和L(934)正交试验考察摇瓶发酵条件下培养基起始pH值、诱导剂甲醇添加量、诱导温度及诱导时间对产酶活性的影响;并分析重组木聚糖酶的酶学性质。结果影响重组毕赤酵母产酶的因素重要性依次为:培养基起始pH值>诱导时间>诱导温度>甲醇添加量,重组酵母产酶最佳条件为:起始pH值7.5,甲醇添加量1.5%,32℃诱导96 h,在此条件下进行诱导表达重组木聚糖酶的酶活性可达228.35 IU/ml;酶的最适反应温度为50℃,最适反应pH值为5.5,在低于40℃和pH 4.5~7.5的范围内较稳定。结论优化了毕赤酵母产重组木聚糖酶的发酵条件,为木聚糖酶的工业化生产及应用提供了依据。

关 键 词:木聚糖酶  毕赤酵母  发酵  优化  酶活力

Optimization of condition for fermentation of recombinant Pichia pastoris and enzymatic properties of xylanase produced
Abstract:Objective To optimize the condition for fermentation of recombinant Pichia pastoris GS115/xyn11A and determine the enzymatic properties of produced xylanase.Methods The effects of the initial pH value,methanol concentration as well as temperature and time for induction on expression of xylanase in recombinant P.pastoris GS115/xyn11A were investigated by single factor test and L9(34)orthogonal test,and the enzymatic properties of recombinant xylanase were analyzed.Results In the order of importance to expression of xylanase in recombinant P.pastoris,the influencing factors were initial pH value of medium,time for induction,temperature for induction and methanol concentration.The optimal initial pH value,methanol concentration as well as temperature and time for induction were 7.5,1.5%,32 ℃ and 96 h respectively.Under the optimal condition,the recombinant xylanase reached an activity of 228.35 IU/ml,of which the optimal working temperature and pH value were 50 ℃ and 5.5 respectively,and showed high stability at 40 ℃ or below and pH 4.5 ~ 7.5.Conclusion The condition for fermentation of recombinant P.pastoris GS115/xyn11A was optimized,which provided a basis for industrial production and application of xylanase.
Keywords:Xylanase  Pichia pastoris  Fermentation  Optimization  Enzymatic activity
本文献已被 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号