通过酶处理黑曲霉生物质获得肽和氨基酸成分

E. M. Serba, P. Yu. Tadzhibova, L. V. Rimareva, M. B. Overchenko, N. I. Ignatova
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引用次数: 0

摘要

摘要 目前,人们特别关注利用曲霉菌的残余生物质作为生产食品和饲料原料的基质的研究。最有前途的方法是对菌丝生物质聚合物进行生物催化转化,从而增加具有生物价值的细胞成分的可用性。本研究的目的是开发酶法破坏真菌生物质细胞壁多糖和蛋白质物质的条件,以及酶法生产的次要原料,以获得肽氨基酸成分。已经确定,使用酶系统(包括细胞内蛋白酶和肽酶以及外源β-葡聚糖酶复合物)以及调节其暴露时间,可以生产出具有特定结构分数组成的发酵溶解物。对发酵溶解物真菌生物质中肽组分的分子量(MM)分布研究表明,水解 6 小时后,分子量超过 29.0 kDa 的肽的比例下降了 2.8 倍,12 小时后下降了 4.7 倍。分子量小于 1.6 kDa 的低分子量肽含量增加了 1.4 倍,占总量的 47.9%。对水解 6 小时和 12 小时后真菌生物质酶分离物中分子量小于 1000 Da 的肽的光谱进行了比较分析,结果表明其组成存在显著差异。随着水解时间的延长,MM 小于 500 Da 的肽和游离氨基酸的含量增加了 1.6 倍。研究结果证实,通过酶解处理真菌生物质,可以生产出富含肽氨基酸成分的功能性配料和膳食补充剂,其中游离氨基酸和短生物活性肽的含量占主导地位。
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Obtaining of Peptide and Amino Acid Ingredients by Enzymatic Treatment of Aspergillus oryzae Biomass

Abstract

Currently, special attention is being paid to research on the use of residual biomass of Aspergillus fungi as a substrate for the production of food and feed ingredients. The most promising method is biocatalytic conversion of mycelial biomass polymers, which increases the availability of biologically valuable cell components. The objective of the present study to develop conditions for the enzymatic destruction of cell wall polysaccharides and protein substances of fungal biomass and secondary raw materials of enzyme production, to obtain peptide-amino acid ingredients. It has been established that the use of the enzymatic system, including intracellular proteinases and peptidases and a complex of exogenous β-glucanases, as well as regulation of the duration of their exposure, provide for the production of fermentolysates with a given structural fractional composition. Molecular mass (MM) distribution studies of peptide fractions in the fungal biomass of fermentolysates showed that over 6 h of hydrolysis, the proportion of peptides with MM over 29.0 kDa decreased by 2.8 times, and over 12 h, by 4.7 times. The content of low molecular weight peptides with MM less than 1.6 kDa increased 1.4 times, which accounted for 47.9% of the total. Comparative analysis of the spectra of peptides with MM less than 1000 Da in enzyme isolates of fungal biomass after 6 and 12 h of hydrolysis showed significant differences in their compositions. The contents of peptides with MM less than 500 Da and of free amino acids increase with an increase in hydrolysis duration by 1.6 times. The results confirm the promise of creating functional ingredients and dietary supplements enriched in a peptide–amino acid component with a predominant content of free amino acids and short bioactive peptides resulting from enzymatic treatment of fungal biomass.

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