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The crystal structure of XdpB, the bacterial old yellow enzyme, in an FMN-free form

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    SYSNO ASEP0489548
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleThe crystal structure of XdpB, the bacterial old yellow enzyme, in an FMN-free form
    Author(s) Zahradník, Jiří (MBU-M) ORCID
    Kolenko, P. (CZ)
    Palyzová, Andrea (MBU-M) RID, ORCID
    Černý, J. (CZ)
    Kolářová, L. (CZ)
    Kyslíková, Eva (MBU-M)
    Marešová, Helena (MBU-M) RID, ORCID
    Grulich, Michal (MBU-M) RID
    Nunvář, J. (CZ)
    Šulc, M. (CZ)
    Kyslík, Pavel (MBU-M) RID, ORCID
    Schneider, B. (CZ)
    Article numbere0195299
    Source TitlePLoS ONE. - : Public Library of Science - ISSN 1932-6203
    Roč. 13, č. 4 (2018)
    Number of pages18 s.
    Languageeng - English
    CountryUS - United States
    KeywordsGLYCEROL TRINITRATE REDUCTASE ; N-ETHYLMALEIMIDE REDUCTASE ; OXIDATIVE STRESS-RESPONSE
    Subject RIVEE - Microbiology, Virology
    OECD categoryMicrobiology
    Institutional supportMBU-M - RVO:61388971
    UT WOS000429505000037
    EID SCOPUS85045154045
    DOI10.1371/journal.pone.0195299
    AnnotationOld Yellow Enzymes (OYES) are NAD(P)H dehydrogenases of not fully resolved physiological roles that are widespread among bacteria, plants, and fungi and have a great potential for biotechnological applications. We determined the apo form crystal structure of a member of the OYE class, glycerol trinitrate reductase XdpB, from Agrobacterium bohemicum R89-1 at 2.1 A resolution. In agreement with the structures of the related bacterial OYEs, the structure revealed the TIM barrel fold with an N-terminal beta-hairpin lid, but surprisingly, the structure did not contain its cofactor FMN. Its putative binding site was occupied by a pentapeptide TTSDN from the C-terminus of a symmetry related molecule. Biochemical experiments confirmed a specific concentration-dependent oligomerization and a low FMN content. The blocking of the FMN binding site can exist in vivo and regulates enzyme activity. Our bioinformatic analysis indicated that a similar self-inhibition could be expected in more OYEs which we designated as subgroup OYE C1. This subgroup is widespread among G-bacteria and can be recognized by the conserved sequence GxxDYP in proximity of the C termini. In proteobacteria, the C1 subgroup OYEs are typically coded in one operon with short-chain dehydrogenase. This operon is controlled by the tetR-like transcriptional regulator. OYEs coded in these operons are unlikely to be involved in the oxidative stress response as the other known members of the OYE family because no upregulation of XdpB was observed after exposing A. bohemicum R89-1 to oxidative stress.
    WorkplaceInstitute of Microbiology
    ContactEliška Spurná, eliska.spurna@biomed.cas.cz, Tel.: 241 062 231
    Year of Publishing2019
Number of the records: 1  

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