首页> 外文期刊>International Biodeterioration & Biodegradation >Enzymatic production of N-acetyl-D-glucosamine by solid state fermentation of chitinase by Penicillium ochrochloron MTCC 517 using agricultural residues
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Enzymatic production of N-acetyl-D-glucosamine by solid state fermentation of chitinase by Penicillium ochrochloron MTCC 517 using agricultural residues

机译:agricultural草青霉MTCC 517使用农业残留物通过固态发酵几丁质酶的酶法生产N-乙酰基-D-氨基葡萄糖

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摘要

The optimization studies for production of chitinase were carried out by response surface methodology (RSM) based on statistics experimental design using three substrates, which were wheat, rice and red gram bran. 2(4) full factorial central composite design was applied to evaluate optimal combinations of variables. These variables were chitin concentration, initial moisture content, inoculum level, and incubation time. The results of second order polynomial showed that all four variables had significant effect on chitinase production. Maximum chitinase activity was recorded for wheat bran (2443.23 U g(-1)) than rice (1216.65 U g(-1)) and red gram bran (961.32 U g(-1)). An overall 3-fold increase in chitinase activity was achieved using optimized strategies of RSM. Growth of the fungus on all bran particles have been visualized by scanning electron microscopy. These results indicated the potential of Penicillium ochrochloron for economical production of chitinase using agricultural residues. TLC and HPLC analysis of colloidal chitin hydrolysate with partially purified chitinases revealed that the major reaction product was monomeric GIcNAc indicating the potential of these enzymes for efficient production of GIcNAc. (C) 2014 Elsevier Ltd. All rights reserved
机译:基于响应实验方法(RSM),基于统计学实验设计,使用小麦,稻米和赤克麸皮三种底物,进行了几丁质酶生产的优化研究。 2(4)全因式中心组合设计用于评估变量的最佳组合。这些变量是几丁质浓度,初始水分含量,接种量和孵育时间。二阶多项式的结果表明,所有四个变量均对几丁质酶的产生有显着影响。麦麸(2443.23 U g(-1))的最大几丁质酶活性高于大米(1216.65 U g(-1))和红克糠(961.32 U g(-1))。使用RSM的优化策略,几丁质酶活性总体提高了3倍。通过扫描电子显微镜可以看到真菌在所有麸皮颗粒上的生长。这些结果表明,利用农业残留物,草青霉有潜力经济地生产几丁质酶。具有部分纯化的几丁质酶的胶体几丁质水解产物的TLC和HPLC分析表明,主要反应产物是单体GIcNAc,表明这些酶具有有效生产GIcNAc的潜力。 (C)2014 Elsevier Ltd.保留所有权利

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