Purification and characterization of a bacteriocin from an oenological strain of Leuconostoc mesenteroides subsp cremoris


Dundar H., SALİH B., Bozoglu F.

PREPARATIVE BIOCHEMISTRY & BIOTECHNOLOGY, vol.46, no.4, pp.354-359, 2016 (Journal Indexed in SCI) identifier identifier identifier

  • Publication Type: Article / Article
  • Volume: 46 Issue: 4
  • Publication Date: 2016
  • Doi Number: 10.1080/10826068.2015.1031395
  • Title of Journal : PREPARATIVE BIOCHEMISTRY & BIOTECHNOLOGY
  • Page Numbers: pp.354-359
  • Keywords: Bacteriocin, Leuconostoc mesenteroides, MALDI-TOF mass spectrometry, malolactic fermentation, reverse-phase chromatography, LACTIC-ACID BACTERIA, LISTERIA-MONOCYTOGENES, PTS PERMEASE, IDENTIFICATION, SENSITIVITY, PROTEINS, NISIN

Abstract

Malolactic fermentation (MLF), which improves organoleptic properties and biologic stability of some wines, may cause wine spoilage if uncontrolled. Bacteriocins were reported as efficient preservatives to control MLF through their bactericidal effect on malolactic bacteria. Leuconostoc mesenteroides subsp. cremoris W3 isolated from wine produces an inhibitory substance that is bactericidal against malolactic bacteria in model wine medium. Treatment of the culture supernatant of strain W3 with proteases eliminated the inhibitory activity, which proved that it is a true bacteriocin and we tentatively termed it mesentericin W3. The bacteriocin inhibited the growth of food-borne pathogenic bacteria such as Enterococcus faecalis, Listeria monocytogenes, and malolactic bacteria. It was active over a wide pH range and stable to organic solvents and heat. Mesentericin W3 was purified to homogeneity by a pH-mediated cell adsorption-desorption method, cation exchange, hydrophobic interaction, and reverse-phase chromatography. Matrix-assisted laser desorption/ionization time of flight (MALDI-TOF) mass spectroscopy (MS) and partial amino acid sequence analysis revealed that mesentericin W3 was identical to mesentericin Y105.