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8JPW

Crystal Structure of Single-chain L-Glutamate Oxidase Mutant from Streptomyces sp. X-119-6

Summary for 8JPW
Entry DOI10.2210/pdb8jpw/pdb
DescriptorL-glutamate oxidase, FLAVIN-ADENINE DINUCLEOTIDE, 2-OXOGLUTARIC ACID, ... (5 entities in total)
Functional Keywordsamino acid oxidase, mutant, oxidoreductase
Biological sourceStreptomyces sp. X-119-6
Total number of polymer chains1
Total formula weight74369.08
Authors
Yamaguchi, H.,Takahashi, K.,Tatsumi, M.,Tagami, U.,Mizukoshi, T.,Miyano, H.,Sugiki, M. (deposition date: 2023-06-13, release date: 2023-08-09, Last modification date: 2024-05-08)
Primary citationYamaguchi, H.,Takahashi, K.,Tatsumi, M.,Tagami, U.,Mizukoshi, T.,Miyano, H.,Sugiki, M.
Development of a novel single-chain l-glutamate oxidase from Streptomyces sp. X-119-6 by inserting flexible linkers.
Enzyme.Microb.Technol., 170:110287-110287, 2023
Cited by
PubMed Abstract: L-glutamate oxidase (LGOX, EC: 1.4.3.11) is an oxidoreductase that catalyzes L-glutamate deamination. LGOX from Streptomyces sp. X-119-6 is used widely for L-glutamate quantification in research and industrial applications. This enzyme encoded as a single precursor chain that undergoes post-translational cleavage to four fragments by an endogenous protease to become highly active. Efficient preparation of active LGOX by heterologous expression without proteolysis process should be indispensable for wide application of this enzyme. Thus, developing an LGOX that requires no protease treatment should expand the potential applications of recombinant LGOX. In this report, we succeeded in obtaining an active single-chain LGOX by connecting the four fragments of the mature form with insertion of flexible linkers. The most active single-chain mutant showed the similar activity to that of the mature form from Streptomyces sp. X-119-6. The structure of this mutant was determined at 2.9 Å resolution by X-ray crystallography. It was revealed that this single-stranded mutant had the similar conformation to that of mature form. This single-chain LGOX can be produced efficiently and should expand LGOX applications.
PubMed: 37487431
DOI: 10.1016/j.enzmictec.2023.110287
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.66 Å)
Structure validation

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건을2024-10-30부터공개중

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