{"title":"Purification of β-Glucosidase, One of the Flavor-enhancing Food Enzymes, from Peppermint (Mentha piperita L.) and Its Biochemical Characterization","authors":"H. Kara, Sabiha Tümay Akgün, S. Sinan, Y. Turan","doi":"10.9734/ajrb/2022/v10i430233","DOIUrl":null,"url":null,"abstract":"Aims: Determination of the biochemical properties of β-glucosidase in peppermint, which is rich in aromatic compounds. \nStudy Design: β-glucosidase was purified from mint, and biochemical characterization of the purified enzyme was performed. \nPlace and Duration of Study: This study was carried out in the Faculty of Arts and Sciences Biochemistry laboratory. \nMethodology: Enzyme purification was performed by hydrophobic interaction chromatography using a Sepharose 4B-L-tyrosine-1-naphthylamine gel. Optimum pH, temperature, and substrate specificity of the purified enzyme were determined. The effects of glucose, δ-gluconolactone and some heavy metals on the enzyme activity were investigated. \nResults: The enzyme was purified with 8-fold and 28% yield. The purified protein from mint was visualized at 65 kDa on SDS-PAGE. The substrate specificity of the purified β-glucosidase from mint was determined against para- and ortho-nitrophenyl β-D-glucopyranoside (p/o-NPG) substrates. The Km values were 0.4 and 0.9 mM, and the Vmax values were 102.2 EU and 96.6 EU, respectively. While the optimum pH for the purified enzyme was 6, the optimum temperature was 35°C. Effects of heavy metals Ag+2, Fe+3, Zn+2, Cu+2, and Pb+2 on the purified enzyme activity were investigated. Relative activities of heavy metals were introduced into the reaction medium as 0.75 mM samples without any known inhibitors in the environment. Fe+3 increased the enzyme activity, and Ag+2, Pb+2, Cu+2, and Zn+2 inhibited the enzyme, and their relative activities were 78, 76, 22, and 31%, respectively. Glucose and δ-gluconolactone competitively inhibited the enzyme activity when p-NPG was the substrate. Ki values of glucose and δ-gluconolactone were determined as 0.034±0.001 and 0.038±0.002 mM, respectively. \nConclusion: Determination of the biochemical properties of β-glucosidase from mint, which has commercial and pharmacological importance due to the phenolic substances it contains, will contribute to studies on improving food quality.","PeriodicalId":8535,"journal":{"name":"Asian Journal of Research in Biochemistry","volume":"33 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-09-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Asian Journal of Research in Biochemistry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.9734/ajrb/2022/v10i430233","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1
Abstract
Aims: Determination of the biochemical properties of β-glucosidase in peppermint, which is rich in aromatic compounds.
Study Design: β-glucosidase was purified from mint, and biochemical characterization of the purified enzyme was performed.
Place and Duration of Study: This study was carried out in the Faculty of Arts and Sciences Biochemistry laboratory.
Methodology: Enzyme purification was performed by hydrophobic interaction chromatography using a Sepharose 4B-L-tyrosine-1-naphthylamine gel. Optimum pH, temperature, and substrate specificity of the purified enzyme were determined. The effects of glucose, δ-gluconolactone and some heavy metals on the enzyme activity were investigated.
Results: The enzyme was purified with 8-fold and 28% yield. The purified protein from mint was visualized at 65 kDa on SDS-PAGE. The substrate specificity of the purified β-glucosidase from mint was determined against para- and ortho-nitrophenyl β-D-glucopyranoside (p/o-NPG) substrates. The Km values were 0.4 and 0.9 mM, and the Vmax values were 102.2 EU and 96.6 EU, respectively. While the optimum pH for the purified enzyme was 6, the optimum temperature was 35°C. Effects of heavy metals Ag+2, Fe+3, Zn+2, Cu+2, and Pb+2 on the purified enzyme activity were investigated. Relative activities of heavy metals were introduced into the reaction medium as 0.75 mM samples without any known inhibitors in the environment. Fe+3 increased the enzyme activity, and Ag+2, Pb+2, Cu+2, and Zn+2 inhibited the enzyme, and their relative activities were 78, 76, 22, and 31%, respectively. Glucose and δ-gluconolactone competitively inhibited the enzyme activity when p-NPG was the substrate. Ki values of glucose and δ-gluconolactone were determined as 0.034±0.001 and 0.038±0.002 mM, respectively.
Conclusion: Determination of the biochemical properties of β-glucosidase from mint, which has commercial and pharmacological importance due to the phenolic substances it contains, will contribute to studies on improving food quality.
目的:测定富含芳香化合物的薄荷中β-葡萄糖苷酶的生化特性。研究设计:从薄荷中纯化β-葡萄糖苷酶,并对纯化酶进行生化表征。研究地点和时间:本研究在文理学院生物化学实验室进行。方法:采用Sepharose 4b - l -酪氨酸-1-萘胺凝胶,采用疏水相互作用层析进行酶纯化。确定了纯化酶的最佳pH、温度和底物特异性。研究了葡萄糖、δ-葡萄糖内酯和一些重金属对酶活性的影响。结果:酶的纯度为8倍,产率为28%。纯化后的薄荷蛋白在SDS-PAGE上以65 kDa可见。测定了薄荷中纯化的β-葡萄糖苷酶对对硝基苯和邻硝基苯β- d -葡萄糖苷(p/o-NPG)底物的特异性。Km值分别为0.4和0.9 mM, Vmax值分别为102.2 EU和96.6 EU。纯化酶的最适pH为6,最适温度为35℃。研究了重金属Ag+2、Fe+3、Zn+2、Cu+2和Pb+2对纯化酶活性的影响。将重金属的相对活性作为0.75 mM的样品引入反应介质中,环境中没有任何已知的抑制剂。Fe+3提高了酶活性,Ag+2、Pb+2、Cu+2和Zn+2抑制酶活性,其相对活性分别为78%、76%、22%和31%。当p-NPG为底物时,葡萄糖和δ-葡萄糖内酯竞争性地抑制酶活性。葡萄糖和δ-葡萄糖内酯Ki值分别为0.034±0.001和0.038±0.002 mM。结论:测定薄荷β-葡萄糖苷酶的生化特性,有助于改善食品品质的研究。薄荷β-葡萄糖苷酶因其所含酚类物质而具有重要的商业和药理意义。