赭曲霉固态培养生产α淀粉酶和纤维素酶的可行性分析

Fungal Territory Pub Date : 1900-01-01 DOI:10.36547/ft.321
S. Khan, A. Mathur
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引用次数: 1

摘要

随着工业上重要酶的需求和应用的不断增长,有必要探索具有不同特异性和活性的酶的新来源。酶是化学合成的安全替代品,因为副作用最小,易于制造。固体发酵(SSF)是一种具有成本效益的替代农业残留物或废物的深层发酵,经常被用作培养多种生物生产代谢物的底物。本研究以小麦麸皮为底物,在相对湿度为90%、温度为30℃条件下培养7天,对α淀粉酶和纤维素酶的生产能力进行了研究,是目前少有的研究报告之一。结果表明,赭曲霉(Aspergillus ochraceus, MTCC 1877)可能是这两种酶的潜在来源。结果表明,赭曲霉(Aspergillus ochraceus) SSF提取物(MTCC 1877) α -淀粉酶活性明显高于长尾木霉(ITCC 7839)。相反,长achiatum木霉(ITCC 7839)的SSF提取物具有较高的纤维素酶活性。结果表明,赭曲霉(Aspergillus ochraceus, MTCC 1877)可能是这两种酶的来源。酶活性的变化可能归因于实验培养条件,可以进一步优化以提高酶产量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
PRODUCTION OF ALPHA AMYLASE AND CELLULASE FROM SOLID STATE CULTURE OF ASPERGILLUS OCHRACEUS: A FEASIBILITY ANALYSIS
The growing demand and application of industrially important enzyme necessitate the need to explore new sources with diverse enzymes ranging in their specificity and activities. Enzymes are safe alternatives to chemical synthesis due to minimum side effect and ease of manufacturing. Solid state fermentation (SSF) is a cost-effective alternative to submerged fermentation with agro-residues or waste, often being used as substrate for growing diverse organisms for production of metabolites. Current study is one of the scarce report on exploring alpha amylase and cellulase production ability Aspergillus ochraceus (MTCC 1877) using wheat bran as substrate at relative humidity of 90% and at 30 ºC, for 7 days. Result showed the potential of Aspergillus ochraceus (MTCC 1877), as potential source of the two enzymes. Results revealed comparatively higher alpha amylase activity in the SSF extract of Aspergillus ochraceus (MTCC 1877) in comparison to Trichoderma longibrachiatum (ITCC 7839). On the contrary, comparatively higher cellulase activity was observed in the SSF extract of Trichoderma longibrachiatum (ITCC 7839). The results showed the potential of Aspergillus ochraceus (MTCC 1877) as a source of the two enzymes. Variation in enzymes activity may be attributed to the experimental culture conditions and may be further optimized to enhance the enzymes yield.
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