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解淀粉杆菌DC-12产纤溶酶发酵条件的优化
引用本文:柴海云,崔堂兵.解淀粉杆菌DC-12产纤溶酶发酵条件的优化[J].现代食品科技,2012,28(10):1350-1355.
作者姓名:柴海云  崔堂兵
作者单位:华南理工大学生物科学与工程学院
基金项目:国家自然科学基金项目(31171732);中央高校基本业务费项目(2011ZM0136)
摘    要:用响应面法对产纤溶酶的解淀粉芽孢杆菌D-12的发酵条件进行了优化。首先通过单因素实验考察了各因素对产酶的影响,后在此基础上采用Plackett-Burman设计得出发酵时间、糊精浓度、细菌学蛋白胨浓度三个最重要的影响因素,接着通过最陡爬坡实验逼近酶活的最高区域,然后通过中心组合设计实验对显著因素进行优化,最后响应面法进行分析,得到的最佳发酵条件为:细菌学蛋白胨浓度2.25%,糊精浓度2.65%,发酵时间45 h。在此条件下,酶活为96.340 IU/mL。验证实验所得酶活为98.947 IU/mL,因此本优化工艺结果比较可靠。

关 键 词:解淀粉芽孢杆菌  纤溶酶  Plackett-Burman(PB)设计  中心组合设计  响应面
收稿时间:2012/6/11 0:00:00

Optimization of the Fermentation Conditions for Fibrinolytic Enzyme Produced by Bacillus Amyloliquefaciens by Response Surface
CAI Hai-yun and CUI Tang-bing.Optimization of the Fermentation Conditions for Fibrinolytic Enzyme Produced by Bacillus Amyloliquefaciens by Response Surface[J].Modern Food Science & Technology,2012,28(10):1350-1355.
Authors:CAI Hai-yun and CUI Tang-bing
Affiliation:(School of Bioscience and Bioengineering,South China University of Technology,Guangzhou 510006,China)
Abstract:The fermentation conditions for fibrinolytic enzyme produced by Bacillus amyloliquefaciens was optimized by response surface methodology.Firstly,the impact of single factor on fibrinolytic enzyme production was studied and three factors with the most significant effect on fibrinolytic enzyme production were obtained by Plackett-Burman design.The way to reach the highest fibrinolytic activity area was investigated through the steepest climbing experiments.Different levels of the most three significant factors were optimized using central composite designs and response surface analysis.As a result,the optimal fermentation conditions for fibrinolytic enzyme were the concentration of bacteria peptone 2.25%,concentration dextrin 2.65% and fermentation time 45 h.Under these conditions,the enzyme activity was 96.340 IU/mL.Validation experiment showed the activity of fibrinolytic enzyme was 98.947 IU/mL.
Keywords:Bacillus amyloliquefaciens  fibrinolytic enzyme  Plackett-Burman(PB) design  central composite design  response surface analysis
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