Sequential Statistical Optimization of Media Components for the Production of Glucoamylase by Thermophilic Fungus Humicola grisea MTCC 352.

Q2 Biochemistry, Genetics and Molecular Biology Enzyme Research Pub Date : 2014-01-01 Epub Date: 2014-07-09 DOI:10.1155/2014/317940
Vinayagam Ramesh, Vytla Ramachandra Murty
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引用次数: 11

Abstract

Glucoamylase is an industrially important enzyme which converts soluble starch into glucose. The media components for the production of glucoamylase from thermophilic fungus Humicola grisea MTCC 352 have been optimized. Eight media components, namely, soluble starch, yeast extract, KH2PO4, K2HPO4, NaCl, CaCl2, MgSO4 ·7H2O, and Vogel's trace elements solution, were first screened for their effect on the production of glucoamylase and only four components (soluble starch, yeast extract, K2HPO4, and MgSO4 ·7H2O) were identified as statistically significant using Plackett-Burman design. It was fitted into a first-order model (R (2) = 0.9859). Steepest ascent method was performed to identify the location of optimum. Central composite design was employed to determine the optimum values (soluble starch: 28.41 g/L, yeast extract: 9.61 g/L, K2HPO4: 2.42 g/L, and MgSO4 ·7H2O: 1.91 g/L). The experimental activity of 12.27 U/mL obtained was close to the predicted activity of 12.15. High R (2) value (0.9397), low PRESS value (9.47), and AARD values (2.07%) indicate the accuracy of the proposed model. The glucoamylase production was found to increase from 4.57 U/mL to 12.27 U/mL, a 2.68-fold enhancement, as compared to the unoptimized medium.

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嗜热真菌腐霉MTCC 352产糖淀粉酶培养基组分的序列统计优化。
葡萄糖淀粉酶是一种重要的工业酶,可将可溶性淀粉转化为葡萄糖。对嗜热真菌腐霉MTCC 352生产葡萄糖淀粉酶的培养基组成进行了优化。首先筛选了可溶性淀粉、酵母提取物、KH2PO4、K2HPO4、NaCl、CaCl2、MgSO4·7H2O和Vogel微量元素溶液等8种培养基组分对葡萄糖淀粉酶生成的影响,采用Plackett-Burman设计筛选出4种培养基组分(可溶性淀粉、酵母提取物、K2HPO4和MgSO4·7H2O)具有统计学显著性。拟合为一阶模型(R(2) = 0.9859)。采用最陡上升法确定最优位置。采用中心组合设计确定了最佳配比(可溶性淀粉28.41 g/L、酵母膏9.61 g/L、K2HPO4 2.42 g/L、MgSO4·7H2O 1.91 g/L)。实验得到的活性为12.27 U/mL,与预测的12.15 U/mL接近。较高的R(2)值(0.9397),较低的PRESS值(9.47)和AARD值(2.07%)表明所提模型的准确性。葡萄糖淀粉酶产量从4.57 U/mL增加到12.27 U/mL,比未优化的培养基提高了2.68倍。
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Enzyme Research
Enzyme Research Biochemistry, Genetics and Molecular Biology-Biochemistry
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