{"title":"Formation of γ-glutamylglycyglycine by extracellular glutaminase of Aspergillus oryzae","authors":"Kenji Tomita, Toshihiro Yano, Hidehiko Kumagai, Tatsurokuro Tochikura","doi":"10.1016/0385-6380(88)90108-2","DOIUrl":null,"url":null,"abstract":"<div><p>γ-Glutamylglycylglycine (γ-GluGlyGly) was formed through the γ-glutamyltranspeptidase (GGT) reaction catalyzed by glutaminase in a water extract of wheat bran <em>koji</em> obtained with <em>Aspergillus oryzae</em> MA-27-IM. The yield of γ-GluGlyGly was about 18% from <span>l</span>-glutamine in a reaction mixture containing 50 mM <span>l</span>-glutamine, 50 mM glycylglycine, and the extract (0.1 unit ml as GGT activity) in a 100 mM Tris-HCl buffer solution (pH 7.2), which was incubated for 7 h at 30°C. The γ-GluGlyGly formed was purified by ion exchange chromatographies, and the identified by chemical and enzymatic methods as well as by infrared and PMR spectroscopic analyses.</p></div>","PeriodicalId":15702,"journal":{"name":"Journal of Fermentation Technology","volume":"66 3","pages":"Pages 299-304"},"PeriodicalIF":0.0000,"publicationDate":"1988-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0385-6380(88)90108-2","citationCount":"18","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Fermentation Technology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/0385638088901082","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 18
Abstract
γ-Glutamylglycylglycine (γ-GluGlyGly) was formed through the γ-glutamyltranspeptidase (GGT) reaction catalyzed by glutaminase in a water extract of wheat bran koji obtained with Aspergillus oryzae MA-27-IM. The yield of γ-GluGlyGly was about 18% from l-glutamine in a reaction mixture containing 50 mM l-glutamine, 50 mM glycylglycine, and the extract (0.1 unit ml as GGT activity) in a 100 mM Tris-HCl buffer solution (pH 7.2), which was incubated for 7 h at 30°C. The γ-GluGlyGly formed was purified by ion exchange chromatographies, and the identified by chemical and enzymatic methods as well as by infrared and PMR spectroscopic analyses.
以米曲霉MA-27-IM制备的麦麸曲水提物为原料,经谷氨酰胺酶催化γ-谷氨酰转肽酶(GGT)反应生成γ-谷氨酰甘氨酸(γ-GluGlyGly)。在100 mM Tris-HCl缓冲液(pH 7.2)中,用50 mM l-谷氨酰胺、50 mM甘氨酸和提取物(0.1单位ml GGT活性)混合反应,在30℃下培养7 h, γ-GluGlyGly的产率约为18%。形成的γ-GluGlyGly通过离子交换色谱纯化,并通过化学和酶学方法以及红外和PMR光谱分析进行鉴定。