首页> 外文期刊>International Journal of Molecular Sciences >Optimization of Xylanase Production from Penicillium sp.WX-Z1 by a Two-Step Statistical Strategy: Plackett-Burman and Box-Behnken Experimental Design
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Optimization of Xylanase Production from Penicillium sp.WX-Z1 by a Two-Step Statistical Strategy: Plackett-Burman and Box-Behnken Experimental Design

机译:通过两步统计策略优化从青霉菌WX-Z1产生的木聚糖酶的生产:Plackett-Burman和Box-Behnken实验设计

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The objective of the study was to optimize the nutrition sources in a culture medium for the production of xylanase from Penicillium sp.WX-Z1 using Plackett-Burman design and Box-Behnken design. The Plackett-Burman multifactorial design was first employed to screen the important nutrient sources in the medium for xylanase production by Penicillium sp.WX-Z1 and subsequent use of the response surface methodology (RSM) was further optimized for xylanase production by Box-Behnken design. The important nutrient sources in the culture medium, identified by the initial screening method of Placket-Burman, were wheat bran, yeast extract, NaNO3, MgSO4, and CaCl2. The optimal amounts (in g/L) for maximum production of xylanase were: wheat bran, 32.8; yeast extract, 1.02; NaNO3, 12.71; MgSO4, 0.96; and CaCl2, 1.04. Using this statistical experimental design, the xylanase production under optimal condition reached 46.50 U/mL and an increase in xylanase activity of 1.34-fold was obtained compared with the original medium for fermentation carried out in a 30-L bioreactor.
机译:这项研究的目的是使用Plackett-Burman设计和Box-Behnken设计优化培养基中的营养来源,以从青霉菌WX-Z1生产木聚糖酶。首先采用Plackett-Burman多因素设计来筛选培养基中重要的营养源,以生产青霉菌WX-Z1产生的木聚糖酶,随后通过Box-Behnken设计进一步优化响应面方法(RSM)的生产木聚糖酶的使用。 。通过Placket-Burman初步筛选方法确定的培养基中重要的营养来源是麦麸,酵母提取物,NaNO 3 ,MgSO 4 和CaCl < sub> 2 。最大木聚糖酶产量的最佳量(克/升)为:麦麸32.8;酵母提取物1.02; NaNO 3 ,12.71; MgSO 4 ,0.96;和CaCl 2 ,1.04。使用这种统计实验设计,与在30 L生物反应器中进行发酵的原始培养基相比,在最佳条件下木聚糖酶的产量达到46.50 U / mL,木聚糖酶活性提高了1.34倍。

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