6533b7d8fe1ef96bd126ad9f

RESEARCH PRODUCT

Comparative morphological characteristics of three Brettanomyces bruxellensis wine strains in the presence/absence of sulfur dioxide

Benoit DivolMaret Du ToitMarlie LouwHervé Alexandre

subject

0301 basic medicine[ SDV.AEN ] Life Sciences [q-bio]/Food and Nutrition030106 microbiologyFood spoilageBrettanomycesBrettanomyces bruxellensisWineSaccharomyces cerevisiaeMicrobiologyMicrobiologyCell membrane03 medical and health scienceschemistry.chemical_compoundMicroscopy Electron TransmissionmedicineFluorescence microscopeSulfur DioxidePresence absenceSulfur dioxideWineDekkerabiologyGeneral Medicinebiology.organism_classificationYeastmedicine.anatomical_structureMicroscopy FluorescencechemistryBiochemistryFood MicrobiologyMicroscopy Electron ScanningFood Science

description

International audience; The red wine spoilage yeast Brettanomyces bruxellensis has been the subject of numerous investigations. Some of these studies focused on spoilage mechanisms, sulfur dioxide tolerance and nutrient requirements. Pseudomycelium formation, although a striking feature of this species, has however been poorly investigated. Furthermore, literature regarding the induction mechanism of pseudomycelium formation in this yeast is limited and lacks clarity, as results published are contradictory. This study elucidates this phenomenon among strains from geographically different areas. Potential environmental cues were investigated, to attain a better understanding of this mechanism and its role as a survival strategy. SO2 was previously reported to induce this morphological change however results obtained in this study did not support this. Nevertheless, the results obtained using scanning and transmission electron microscopy illustrate, for the first time in this yeast, deformity to the cell membrane and alterations to the fibrillar layers in SO2 treated cells. In addition, the SO2 exposed cultures displayed cell size variations, with cells displaying a decrease in length as well as delayed growth, with a prolonged lag phase. Fluorescence microscopy demonstrated a decrease in metabolic activity and the appearance of inclusion body-like structures in the cells following exposure to SO2.

https://doi.org/10.1016/j.ijfoodmicro.2016.08.040