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Optimization of glucoamylase production by Colletotrichum sp. KCP1 using statistical methodology

机译:炭疽菌的葡糖淀粉酶生产的优化。使用统计方法的KCP1

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摘要

Glucoamylase is a key enzyme used in the food processing as well as in commercial production of glucose from starch. A natural fungal strain identified as Colletotrichum sp. KCP1 using 18S rDNA partial genome sequencing has been studied for optimization of glucoamylase production. Media components were screened and optimized through the statistical approach for the synthesis of glucoamylase in solid state fermentation using wheat bran as the substrate. The medium components influencing the enzyme production were identified using Plackett-Burman design. Among various variables screened along with wheat bran as major growth substrate, starch, whey, and casein acid hydrolyasate were found to be most significant. The optimum concentrations of these significant parameters were determined employing the response surface central composite design, revealing starch concentration (1.5 g), whey (0.1 mL), and casein acid hydrolysate (0.1 g) per 5 g of wheat bran for highest enzyme production.
机译:葡糖淀粉酶是一种关键酶,用于食品加工以及从淀粉中商业生产葡萄糖。鉴定为Colletotrichum sp。的天然真菌菌株。已经对使用18S rDNA部分基因组测序的KCP1进行了葡糖淀粉酶生产的优化研究。通过统计方法筛选和优化培养基成分,以小麦麸为底物,在固态发酵中合成葡糖淀粉酶。使用Plackett-Burman设计鉴定了影响酶产生的培养基成分。在以麦麸为主要生长底物进行筛选的各种变量中,发现淀粉,乳清和酪蛋白酸水解产物最为重要。这些重要参数的最佳浓度是通过响应表面中央复合设计确定的,显示出每5克麦麸中的淀粉浓度(1.5 g),乳清(0.1 mL)和酪蛋白酸水解产物(0.1 g)可产生最高的酶。

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