Gamma-glutamyl transfer reactions by glutaminase from Pseudomonas nitroreducens IFO 12694 and their application for the syntheses of theanine and gamma-glutamylmethylamide

In a mixture containing gamma-glutamyl donor (donor) and gamma glutamyl acceptor (acceptor), the glutaminase of Pseudomonas nitroreducens IFO 12694 simultaneously catalyzed a gamma-glutamyl transfer reaction and hydrolysis of the donor. The variation of the activities responding to the concentration...

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Veröffentlicht in:Bioscience, biotechnology, and biochemistry biotechnology, and biochemistry, 1998, Vol.62 (7), p.1279-1283
Hauptverfasser: Tachiki, T. (Ritsumeikan Univ., Kyoto (Japan). Faculty of Science and Engineering), Yamada, T, Mizuno, K, Ueda, M, Shiode, J, Fukami, H
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container_end_page 1283
container_issue 7
container_start_page 1279
container_title Bioscience, biotechnology, and biochemistry
container_volume 62
creator Tachiki, T. (Ritsumeikan Univ., Kyoto (Japan). Faculty of Science and Engineering)
Yamada, T
Mizuno, K
Ueda, M
Shiode, J
Fukami, H
description In a mixture containing gamma-glutamyl donor (donor) and gamma glutamyl acceptor (acceptor), the glutaminase of Pseudomonas nitroreducens IFO 12694 simultaneously catalyzed a gamma-glutamyl transfer reaction and hydrolysis of the donor. The variation of the activities responding to the concentration of glutathione and glycylglycine indicated that the enzyme might be classified in a group of glutaminases that shows hydrolysis prior to transfer reaction. On the other hand, the results with glutamine and ethylamine or methylamine indicated that the enzyme was active in the transfer reaction with suppressed hydrolysis of glutamine, and suggested the possibility of using the reaction for producing gamma-glutamylethylamide (theanine) or gamma-glutamylethylamide (gamma-GMA). In fact, in a mixture containing high concentrations of substrates (0.7 M glutamine, 1.5 M ethylamine or methylamine) and 0.5 unit/ml glutaminase (borate buffer pH 11), 270 mM (47 g/L theanine or 250 mM (38 g/L) gamma-GMA was formed in 7 h of incubation at 30 degrees C
doi_str_mv 10.1271/bbb.62.1279
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Psychology</topic><topic>glutaminase</topic><topic>HIDROLASAS</topic><topic>HYDROLASE</topic><topic>HYDROLASES</topic><topic>Mission oriented research</topic><topic>Physiology and metabolism</topic><topic>PSEUDOMONAS</topic><topic>Pseudomonas nitroreducens</topic><topic>theanine</topic><topic>γ-glutamyl transfer reaction</topic><topic>γ-glutamylmethylamide</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tachiki, T. (Ritsumeikan Univ., Kyoto (Japan). Faculty of Science and Engineering)</creatorcontrib><creatorcontrib>Yamada, T</creatorcontrib><creatorcontrib>Mizuno, K</creatorcontrib><creatorcontrib>Ueda, M</creatorcontrib><creatorcontrib>Shiode, J</creatorcontrib><creatorcontrib>Fukami, H</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Bioscience, biotechnology, and biochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tachiki, T. (Ritsumeikan Univ., Kyoto (Japan). 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source Oxford University Press Journals All Titles (1996-Current); J-STAGE (Japan Science & Technology Information Aggregator, Electronic) Freely Available Titles - Japanese; Open Access Titles of Japan; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Free Full-Text Journals in Chemistry
subjects AMIDAS
AMIDE
AMIDES
Biological and medical sciences
Biology of microorganisms of confirmed or potential industrial interest
BIOSINTESIS
BIOSYNTHESE
BIOSYNTHESIS
Biotechnology
Fundamental and applied biological sciences. Psychology
glutaminase
HIDROLASAS
HYDROLASE
HYDROLASES
Mission oriented research
Physiology and metabolism
PSEUDOMONAS
Pseudomonas nitroreducens
theanine
γ-glutamyl transfer reaction
γ-glutamylmethylamide
title Gamma-glutamyl transfer reactions by glutaminase from Pseudomonas nitroreducens IFO 12694 and their application for the syntheses of theanine and gamma-glutamylmethylamide
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