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首页> 外文期刊>RSC Advances >Enhanced production of extracellular proteolytic enzyme excreted by a newly isolated Bacillus subtilis FBL-1 through combined utilization of statistical designs and response surface methodology
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Enhanced production of extracellular proteolytic enzyme excreted by a newly isolated Bacillus subtilis FBL-1 through combined utilization of statistical designs and response surface methodology

机译:通过组合利用统计设计和响应面方法,增强了通过新分离的芽孢杆菌FBL-1排出的细胞外蛋白水解酶的生产

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摘要

An extracellular protease producing strain FBL-1 was newly isolated from soil, and it was identified as Bacillus subtilis through 16S rDNA sequence analysis. B. subtilis FBL-1 was used for extracellular protease production, and culture conditions were optimized by statistical methods. Three statistical approaches such as Plackett-Burman design, steepest ascent path analysis, and Box-Behnken design were successfully combined to optimize protease production, which resulted in significant enhancement of production. Through Plackett-Burman experimental design, fructose and yeast extract were screened as the significant components for the production of extracellular protease. The center points of each parameter were predetermined by the steepest ascent method. Based on the results obtained by Box-Behnken experimental design, the optimized level of significant parameters for protease production was determined by multiple regression analysis. The optimized levels of parameters were fructose 32.42 g L-1, yeast extract 15.02 g L-1, and incubation time 35.78 h. Protease activity predicted by the quadratic model developed in this work was 578.55 U mL(-1), which was only 2.67% different from the experimental protease activity obtained by verification studies. The protease activity was significantly enhanced by 7.0-fold compared with the activity obtained from basal medium.
机译:产生菌株FBL-1的细胞外蛋白酶从土壤中新分离,并通过16S RDNA序列分析鉴定为枯草芽孢杆菌。 B.枯草芽孢杆菌FBL-1用于细胞外蛋白酶生产,通过统计方法优化培养条件。三种统计方法如Phackett-Burman设计,最陡峭的上升路径分析和Box-Behnken设计,以优化蛋白酶生产,导致生产的显着增强。通过Plackett-Burman实验设计,将果糖和酵母提取物作为用于生产细胞外蛋白酶的重要组成部分。每个参数的中心点被最陡峭的上升方法预定。基于Box-Behnken实验设计获得的结果,通过多元回归分析确定了蛋白酶生产的显着参数的优化水平。优化的参数水平是果糖32.42g L-1,酵母提取物15.02g L-1,并孵育时间35.78小时。在本作品中开发的二次模型预测的蛋白酶活性为578.55u ml(-1),其与通过验证研究获得的实验蛋白酶活性不同的2.67%。与从基础培养基获得的活性相比,蛋白酶活性显着提高7.0倍。

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  • 来源
    《RSC Advances 》 |2016年第56期| 共9页
  • 作者单位

    Yeungnam Univ Dept Food Sci &

    Technol 280 Daehak Ro Gyongsan 38541 South Korea;

    Yeungnam Univ Dept Food Sci &

    Technol 280 Daehak Ro Gyongsan 38541 South Korea;

    Yogi Vemana Univ Dept Microbiol Kadapa 516003 AP India;

    Yeungnam Univ Dept Food Sci &

    Technol 280 Daehak Ro Gyongsan 38541 South Korea;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学 ;
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