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Optimization of silk degumming protease production from Bacillus subtilis C4 using Plackett-Burman design and response surface methodology

机译:使用Plackett-Burman设计和响应面方法优化枯草芽孢杆菌C4的丝绸脱胶蛋白酶生产

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摘要

Bacillus subtilis C4 was isolated from waste water of a Thai-silk dyeing factory, and identified as a potent strain for producing silk-degumming protease. To optimize the protease production of this bacterial strain, seven fermentation variables were screened using a Plackett-Burman design, and were then further optimized via response surface methodology based on a central composite design. Three significant variables, i.e., soy flour, skimmed milk, and shaker speed, were selected. The optimal values were 2.0% soy flour, 0.1% skimmed milk, and a shaker speed of 280 rpm. The experimental result (1537 units/ml) in a medium optimized for protease production was in good agreement with the predicted value of a quadratic model (1576 units/ml), thus confirming its validity. In addition, the adequacy of the model was supported by a coefficient of determination (R~2) of 0.912. Protease production in the optimized medium (1537 units/ml) increased 2.2-fold over that of the non-optimized medium (729 units/ml) in the shaken flask culture. When the experiment was scaled up in a stirred tank reactor, 1891 units/ml protease activity was achieved at 27 h of cultivation, which was an overall 2.6-fold increase over the basal medium.
机译:枯草芽孢杆菌C4是从泰国丝绸染整厂的废水中分离出来的,并被确定为生产丝绸脱胶蛋白酶的有效菌株。为了优化该细菌菌株的蛋白酶生产,使用Plackett-Burman设计筛选了七个发酵变量,然后通过基于中央复合设计的响应面方法对它们进行了进一步优化。选择了三个重要变量,即大豆粉,脱脂牛奶和振动筛速度。最佳值为大豆粉2.0%,脱脂牛奶0.1%和振动筛速度280 rpm。在针对蛋白酶生产优化的培养基中的实验结果(1537单位/毫升)与二次模型的预测值(1576单位/毫升)非常吻合,从而证实了其有效性。此外,模型的确定性得到了0.912的确定系数(R〜2)的支持。在摇瓶培养中,优化培养基中的蛋白酶产量(1537单位/毫升)比未优化培养基中的蛋白酶产量(729单位/毫升)提高了2.2倍。当在搅拌釜反应器中扩大实验规模时,在培养27小时后达到了1891单位/ ml的蛋白酶活性,这比基础培养基总体提高了2.6倍。

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