大肠杆菌 LGE 36 重组氨基乙酰化酶的一些选定特性

IF 1.3 Q4 FOOD SCIENCE & TECHNOLOGY Functional Foods in Health and Disease Pub Date : 2024-05-01 DOI:10.31989/ffhd.v14i5.1332
Hasmik Yepremyan
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引用次数: 0

摘要

背景:在合成 L- 氨基酸的过程中,氨基酰化酶得到了广泛应用。L- 氨基酸被广泛应用于食品、医药和保健领域。研究了金属离子和抑制剂对重组大肠杆菌 LGE 36 细胞内氨基酰化酶酶活性的影响。以乙酰基-D,L-蛋氨酸和甘氨酰-L-蛋氨酸二肽为底物。研究表明,加入 Co2+ 离子后,重组酶对 N-乙酰基-D,L-蛋氨酸的酰化酶活性提高了 3 倍。就甘氨酰-L-蛋氨酸而言,大肠杆菌 LGE 36 重组氨基酰化酶的肽酶活性增加了 40 多倍。所研究的其他一些金属离子并不能刺激酶的水解活性,其中一些甚至会抑制酶的水解活性。PCMB 可使重组氨基酰化酶完全失活,EDTA 可使酶活性降低 85%:本研究旨在探讨金属离子和抑制剂如何影响重组大肠杆菌 LGE 36 细胞内氨基酰化酶的酶活性:本研究采用大肠埃希菌 LGE 36 重组菌株生产的氨基酰化酶。大肠杆菌细胞在 37°C 的 M9 最低限度培养基中培养。为了评估氨酰化酶的活性,在 37°C 下使用 0.2 ml 终体积的反应混合物进行测定,该混合物包括 pH 值为 7.0 的 100 mM Na、K-磷酸缓冲液、0.2 mM CoCI2、40 mM N-乙酰基-D、L-蛋氨酸和适当浓度的酶。酰化酶活性的量化是指在 37°C 和 pH 7.0 条件下,1 分钟内催化形成 1µmol L-蛋氨酸的酶量:测定了大肠杆菌 LGE 36 重组细胞内氨基酰化酶的一些特征。 为研究金属离子和抑制剂的影响,以乙酰蛋氨酸和甘氨酰蛋氨酸为底物:本研究以及功能性食品正确策略的选择可以优化利用重组酶生产光学活性氨基酸的过程,从而获得食品和饲料添加剂。 关键词:离子、金属、抑制剂、乙酰蛋氨酸、甘甲硫氨酸、大肠杆菌重组氨基酰化酶、酶。
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Some selected properties of the recombinant aminoacylase from   Escherichia coli LGE 36
Background: Aminoacylase has seen extensive use in the synthesis of L-amino acids. L-amino acids are widely used in the food and medical industries, as well as in healthcare. The effect of metal ions and inhibitors on the enzyme activity of recombinant intracellular aminoacylase of Escherichia coli LGE 36 was studied. Acetyl-D,L-methionine and glycyl-L-methionine dipeptide were used as substrates. It has been shown that with the addition of Co2+ ions, the acylase activity of the recombinant enzyme towards N-acetyl-D,L-methionine increases 3 times. In the case of glycyl-L-methionine, the peptidase activity of the recombinant aminoacylase of Escherichia coli LGE 36 increases more than 40 times. A number of other metal ions studied do not stimulate the hydrolytic activity of the enzyme, moreover some of them even inhibit it. PCMB completely inactivates the recombinant aminoacylase, EDTA reduces enzyme activity by 85%. Objective: This study aims to investigate how metal ions and inhibitors affect the enzyme activity of recombinant intracellular aminoacylase Escherichia coli LGE 36. Methods: In this study, a recombinant strain-producer of aminoacylase derived from Escherichia coli LGE 36 was employed. Escherichia coli cells were cultured in M9 minimal medium supplemented at 37°C. To assess aminoacylase activity, assays were conducted at 37°C using a reaction mixture of 0.2 ml final volume comprising 100 mM Na, K-phosphate buffer at pH 7.0, 0.2 mM CoCI2, 40 mM N-acetyl-D, L-methionine, and the enzyme in the appropriate concentration. Acylase activity was quantified as the amount of enzyme catalyzing the formation of 1µmol of L-methionine within 1 minute at 37°C and pH 7.0. Results: Some characteristics of the recombinant intracellular aminoacylase from E. coli LGE 36 were determined.  For investigating the impact of metallic ions and inhibitors, acetylmethionine and glycylmethionine were employed as the substrates. Conclusion: The present study and the choice of right strategies for functional food products allows optimizing the process for production of optically active amino acids using the recombinant enzyme to obtain food and feed additives. Keywords:  ion, metals, inhibitors, acetylmethionine, glycylmethionine, recombinant aminoacylase from Escherichia coli, enzyme.
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来源期刊
Functional Foods in Health and Disease
Functional Foods in Health and Disease FOOD SCIENCE & TECHNOLOGY-
CiteScore
2.20
自引率
20.00%
发文量
47
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