Proteobacteria

Gluconobacter cerevisiae sp. nov., isolated from the brewery environment

  • 1Laboratory of Microbiology, Faculty of Sciences, Ghent University, K.L. Ledeganckstraat 35, B-9000 Ghent, Belgium
  • 2Laboratory of Biochemistry and Brewing, Faculty of Bioscience Engineering, Ghent University, Valentin Vaerwyckweg 1, B-9000 Ghent, Belgium
  • 3Research Group of Industrial Microbiology and Food Biotechnology (IMDO), Faculty of Sciences and Bioengineering Sciences, Vrije Universiteit Brussel, Pleinlaan 2, B-1050 Brussels, Belgium
  • 4BCCM/LMG Bacteria Collection, Faculty of Sciences, Ghent University, K. L. Ledeganckstraat 35, B-9000 Ghent, Belgium
  • Correspondence
    Peter Vandamme Peter.Vandamme{at}UGent.be
  • International Journal of Systematic and Evolutionary Microbiology 2014; 64(Pt 4):1134–1141 · https://doi.org/10.1099/ijs.0.059311-0

    View at publisher PubMed

    Abstract

    Three strains, LMG 27748T, LMG 27749 and LMG 27882 with identical MALDI-TOF mass spectra were isolated from samples taken from the brewery environment. Analysis of the 16S rRNA gene sequence of strain LMG 27748T revealed that the taxon it represents was closely related to type strains of the species Gluconobacter albidus (100 % sequence similarity), Gluconobacter kondonii (99.9 %), Gluconobacter sphaericus (99.9 %) and Gluconobacter kanchanaburiensis (99.5 %). DNA–DNA hybridization experiments on the type strains of these species revealed moderate DNA relatedness values (39–65 %). The three strains used d-fructose, d-sorbitol, meso-erythritol, glycerol, l-sorbose, ethanol (weakly), sucrose and raffinose as a sole carbon source for growth (weak growth on the latter two carbon sources was obtained for strains LMG 27748T and LMG 27882). The strains were unable to grow on glucose-yeast extract medium at 37 °C. They produced acid from meso-erythritol and sucrose, but not from raffinose. d-Gluconic acid, 2-keto-d-gluconic acid and 5-keto-d-gluconic acid were produced from d-glucose, but not 2,5-diketo-d-gluconic acid. These genotypic and phenotypic characteristics distinguish strains LMG 27748T, LMG 27749 and LMG 27882 from species of the genus Gluconobacter with validly published names and, therefore, we propose classifying them formally as representatives of a novel species, Gluconobacter cerevisiae sp. nov., with LMG 27748T ( = DSM 27644T) as the type strain.

    • These authors contributed equally to this work and are considered joint first authors.

    • The GenBank/EMBL/DDBJ accession numbers for the 16S rRNA gene sequences generated in this study are HG329624, HG329625, HG424633 and KF700364; for the 16S–23S ITS gene sequence, HG424630HG424632; for the dnaK gene sequences, HG329570–HG329587; for the groEL gene sequences, HG329588–HG329605 and for the rpoB gene sequences, HG329606–HG329623.

    • Four; Figs S1-S4 supplementary figures are available with the online version of this paper.

    Abbreviations:
    AAB
    acetic acid bacteria
    ITS
    internal transcribed spacer
    MALDI-TOF
    matrix-assisted laser desorption/ionization time-of-flight
    MLSA
    multilocus sequence analysis
    RAPD
    random amplified polymorphic DNA