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[利用新型复合蛋白水解酶制剂改进获取具有益生菌特性成分的技术]

[Improving the technology for obtaining an ingredient with probiotic properties using a new complex proteolytic enzyme preparation].

作者信息

Kuksova E V, Kostyleva E V, Sereda A S, Toloknova A A, Fursova E A, Volkova G S

机构信息

All-Russian Scientific Research Institute of Food Biotechnology - a branch of the Federal Research Centre of Nutrition, Biotechnology and Food Safety, 111033, Moscow, Russian Federation.

出版信息

Vopr Pitan. 2024;93(5):142-152. doi: 10.33029/0042-8833-2024-93-5-142-152. Epub 2024 Sep 16.

DOI:10.33029/0042-8833-2024-93-5-142-152
PMID:39563157
Abstract

The development of technologies for producing bacterial concentrates and enzyme preparations using domestic microbial strains is an urgent task. The use of whey protein hydrolysates as components of nutrient media for probiotic bacteria consortia for the cultivation of lactic acid and bifidobacteria makes it possible to improve and develop innovative processes for obtaining bacterial concentrates with the required functional properties for the production of dietary supplements. A consortium of probiotic microorganisms (lactic acid and bifidobacteria) was created in the All-Russian Scientific Research Institute of Food Biotechnology as a starter culture for specialized dairy products. Using strain Aspergillus oryzae 21-154 LAP a new complex enzyme preparation with a laboratory name Protoorizin LAP has been obtained providing the extensive hydrolysis of protein substrates. of the research was to evaluate the possibility of using the new domestic proteolytic enzyme preparation Protoorizin LAP in preparing whey-based nutrient media for culturing a consortium of probiotic microorganisms to obtain bacterial concentrates. . The object of the research was a symbiotic consortium, including lactic acid bacteria strains (Lactobacillus delbrueckii ssp. bulgaricus Д-16, Lactobacillus plantarum 578/25, Lactobacillus helveticus 842(D)-2, Lactococcus lactis subsp. lactis М-12, Streptococcus thermophilus В-92) and bifidobacteria (Bifidobacterium longum Б-2). Unclarified curd whey and whey protein concentrate were taken as the nutrient medium basis. The media were treated with β-galactosidase to reduce the lactose content. In order to hydrolyze proteins, the control culture medium was treated with commercial preparations: serine protease - Alcalase® 2.4 L and leucine aminopeptidase - Flavourzyme® 1000 L. In the experimental medium, two imported preparations were replaced with a laboratory sample of the enzyme preparation Protoorizin LAP. In the prepared nutrient media, the content of amine nitrogen, free amino acids and soluble protein was determined, and electrophoretic analysis of proteins and peptides was carried out. The consortium growth was monitored by the content of dry substances and reducing sugars, by active and titratable acidity, as well as by microscopy. The number of viable cells of lactic acid bacteria and bifidobacteria at the end of fermentation and in the resulting bacterial concentrates were determined by sieving on the appropriate selective agar media using an automatic colony counter. . The effectiveness of Protoorizin LAP in the hydrolysis of whey proteins significantly exceeded the result of the combined action of Alcalase® 2.4 L and Flavourzyme® 1000 L both in terms of reducing the undigested protein content, including immunogenic fractions, and in terms of the yield of soluble protein, amine nitrogen and amino acids. The nutrient media obtained using proteases ensured good growth and development of the probiotic consortium. Due to the high content of free amino acids, the dynamics of carbohydrate consumption, titratable acidity, and the number of viable cells were higher in the medium obtained using Protoorizin LAP than when using commercial preparations. At the same time, a high titer of probiotic strains and good cultural and morphological characteristics were obtained on all media. The experimental preparation Protoorizin LAP provided the increase in viability of bacterial cells after lyophilization. . The technological method that include application of the new proteolytic preparation Protoorizin LAP in preparing nutrient media based on whey proteins was developed. The method can be used in the technology of producing bacterial concentrates at the stage of culturing of the created lactic acid and bifidobacteria consortium. The bacterial concentrate can be recommended as a recipe ingredient in the manufacture of dietary supplements or foods for special dietary uses containing probiotics.

摘要

利用国产微生物菌株生产细菌浓缩物和酶制剂的技术开发是一项紧迫任务。使用乳清蛋白水解物作为益生菌菌群营养培养基的成分来培养乳酸菌和双歧杆菌,有助于改进和开发创新工艺,以获得具有生产膳食补充剂所需功能特性的细菌浓缩物。全俄食品生物技术科学研究院创建了益生菌微生物(乳酸菌和双歧杆菌)联合体,作为特种乳制品的发酵剂。使用米曲霉21 - 154 LAP菌株获得了一种新的复合酶制剂,实验室名称为Protoorizin LAP,可对蛋白质底物进行广泛水解。本研究的目的是评估使用新型国产蛋白水解酶制剂Protoorizin LAP制备基于乳清的营养培养基来培养益生菌微生物联合体以获得细菌浓缩物的可能性。本研究的对象是一个共生联合体,包括乳酸菌菌株(德氏乳杆菌保加利亚亚种Д - 16、植物乳杆菌578/25、瑞士乳杆菌842(D) - 2、乳酸乳球菌乳酸亚种М - 12、嗜热链球菌В - 92)和双歧杆菌(长双歧杆菌Б - 2)。以未澄清的凝乳清和乳清蛋白浓缩物作为营养培养基基础。对培养基进行β - 半乳糖苷酶处理以降低乳糖含量。为了水解蛋白质,对照培养基用市售制剂处理:丝氨酸蛋白酶 - Alcalase® 2.4 L和亮氨酸氨肽酶 - Flavourzyme® 1000 L。在实验培养基中,两种进口制剂被酶制剂Protoorizin LAP的实验室样品替代。在制备的营养培养基中,测定胺氮、游离氨基酸和可溶性蛋白的含量,并对蛋白质和肽进行电泳分析。通过干物质和还原糖含量、活性酸度和可滴定酸度以及显微镜观察来监测联合体的生长情况。通过使用自动菌落计数器在适当的选择性琼脂培养基上筛分,测定发酵结束时以及所得细菌浓缩物中乳酸菌和双歧杆菌的活细胞数。Protoorizin LAP在水解乳清蛋白方面的有效性在降低未消化蛋白质含量(包括免疫原性部分)以及可溶性蛋白、胺氮和氨基酸产量方面均显著超过Alcalase® 2.4 L和Flavourzyme® 1000 L联合作用的结果。使用蛋白酶获得的营养培养基确保了益生菌联合体的良好生长和发育。由于游离氨基酸含量高,使用Protoorizin LAP获得的培养基中碳水化合物消耗、可滴定酸度和活细胞数的动态变化高于使用市售制剂时的情况。同时,在所有培养基上均获得了高滴度的益生菌菌株以及良好的培养和形态特征。实验制剂Protoorizin LAP提高了冻干后细菌细胞的活力。开发了包括在基于乳清蛋白的营养培养基制备中应用新型蛋白水解制剂Protoorizin LAP的工艺方法。该方法可用于在已创建的乳酸菌和双歧杆菌联合体培养阶段生产细菌浓缩物技术中。该细菌浓缩物可推荐作为制造含有益生菌的膳食补充剂或特殊膳食用途食品的配方成分。

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