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Optimization of phytase production by Penicillium purpurogenum GE1 under solid state fermentation by using Box-Behnken design

机译:利用Box-Behnken设计优化固态发酵中产紫青霉GE1产生的植酸酶

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Phytase production by Penicillium purpurogenum GE1 isolated from soil around bean root nodules was investigated by solid state fermentation (SSF) using mixed substrates consisted of corn cob and corn bran. The SSF conditions were optimized by using one-variable-at-a-time strategy. The optimum conditions for phytase production were at 27^oC, pH 8 and 66% moisture content. The study of different carbon and nitrogen sources revealed that glucose and peptone registered the highest enzyme productivity (92+/-5.6U/g ds, 125+/-4.9U/g ds). Among different surfactants, maximum phytase productivity was observed with Tween 80 at 0.001 concentrations (170+/-4.2U/gds). A Box-Behnken design was employed to investigate the optimization of the most significant variables affecting the enzyme production. Maximal phytase production was detected after the addition of (g/5gds): 0.75 glucose, 0.375 peptone and 0, 01 tween 80. This result represented an improvement in phytase production of 2.6 folds when compared to that previously obtained using the basal medium under the same cultivation conditions. The generated model was found to be very adequate for phytase production (90% accuracy) as the experimental value was 444+/-3.5U/gds compared to 401U/gds for the predicted value. In brief, the production of phytase using corn cob and corn bran is a novel and cheap way for the production of this important enzyme and opens a new way for researchers to discover and explore this arena.
机译:通过固态发酵(SSF),使用由玉米芯和玉米糠组成的混合底物,研究了从豆根结节周围土壤中分离到的青霉青霉GE1产生的植酸酶。通过使用一次可变策略优化了SSF条件。植酸酶生产的最佳条件是27°C,pH 8和66%水分含量。对不同碳源和氮源的研究表明,葡萄糖和蛋白one的酶生产率最高(92 +/- 5.6U / g ds,125 +/- 4.9U / g ds)。在不同的表面活性剂中,吐温80在0.001浓度(170 +/- 4.2U / gds)下观察到最大的植酸酶生产率。采用Box-Behnken设计来研究影响酶产生的最重要变量的优化。加入(g / 5gds):0.75葡萄糖,0.375蛋白ept和0,01吐温80后,检测到最大植酸酶产量。与以前使用基础培养基在90℃下获得的植酸酶产量相比,该结果表明植酸酶产量提高了2.6倍。相同的栽培条件。发现生成的模型非常适合植酸酶的产生(90%的准确度),因为实验值为444 +/- 3.5U / gds,而预测值为401U / gds。简而言之,使用玉米芯和玉米糠生产植酸酶是一种生产这种重要酶的新颖而廉价的方法,为研究人员发现和探索这一领域开辟了一条新途径。

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