Metaproteomics and ultrastructure characterization of <i>Komagataeibacter</i> spp. involved in high-acid spirit vinegar production
Author(s)
Andrés-Barrao, Cristina
Saad, Maged M
Cabello Ferrete, Elena
Chappuis, Marie-Luise
Ortega Pérez, Ruben
Perret, Xavier
Barja, François
Date issued
2016
In
Food Microbiology, Elsevier
Vol
55
From page
112
To page
122
Subjects
<i>Komagataeibacter</i> 2D-DIGE TCA cycle BCAA Electron microscopy Membrane polysaccharides
Abstract
Acetic acid bacteria (AAB) are widespread microorganisms in nature, extensively used in food industry to transform alcohols and sugar alcohols into their corresponding organic acids. Specialized strains are used in the production of vinegar through the oxidative transformation of ethanol into acetic acid. The main AAB involved in the production of high-acid vinegars using the submerged fermentation method belong to the genus <i>Komagataeibacter</i>, characterized by their higher ADH stability and activity, and higher acetic acid resistance (15-20%), compared to other AAB.<br> In this work, the bacteria involved in the production of high-acid spirit vinegar through a spontaneous acetic acid fermentation process was studied. The analysis using a culture-independent approach revealed a homogeneous bacterial population involved in the process, identified as <i>Komagataeibacter</i> spp. Differentially expressed proteins during acetic acid fermentation were investigated by using 2DDIGE and mass spectrometry. Most of these proteins were functionally related to stress response, the TCA cycle and different metabolic processes. In addition, scanning and transmission electron microscopy and specific staining of polysaccharide SDS-PAGE gels confirmed that <i>Komagataeibacter</i> spp. lacked the characteristic polysaccharide layer surrounding the outer membrane that has been previously reported to have an important role in acetic acid resistance in the genus <i>Acetobacter</i>.
Publication type
journal article
File(s)![Thumbnail Image]()
Loading...
Name
Andres-Barrao_C._Metaproteomics_20190325.pdf
Type
Main Article
Size
1.5 MB
Format
Adobe PDF
