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Advantages of label free method in comparison with 2DE proteomic analysis of Butyrivibrio fibrisolvens 3071 grown on different carbon sources

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    SYSNO ASEP0563989
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleAdvantages of label free method in comparison with 2DE proteomic analysis of Butyrivibrio fibrisolvens 3071 grown on different carbon sources
    Author(s) Sechovcová, Hana (UZFG-Y) ORCID
    Rudl Kulhavá, Lucie (FGU-C) ORCID, RID
    Fliegerová, Kateřina (UZFG-Y) RID, ORCID
    Killer, Jiří (UZFG-Y) RID, ORCID
    Kopečný, Jan (UZFG-Y) RID, ORCID
    Source TitleItalian Journal of Animal Science - ISSN 1594-4077
    Roč. 21, č. 1 (2022), s. 1508-1519
    Number of pages12 s.
    Publication formOnline - E
    Languageeng - English
    CountryIT - Italy
    Keywordsbutyrivibrio fibrisolvens ; label-free ; 2DE ; proteomics ; rumen
    Subject RIVEE - Microbiology, Virology
    OECD categoryMicrobiology
    R&D ProjectsEF15_003/0000460 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    Method of publishingOpen access
    Institutional supportUZFG-Y - RVO:67985904 ; FGU-C - RVO:67985823
    UT WOS000868161000001
    EID SCOPUS85148463551
    DOI10.1080/1828051X.2022.2129477
    AnnotationThe aim of this study was the comparison of label-free method with 2DE to other analytical method of bacterium Butyrivibrio fibrisolvens extracellular protein samples. Label-free quantification (LF) method performed in this work was compared with previously obtained results of proteomic analysis using two-dimensional electrophoresis (2DE) and nano-liquid chromatography coupled with mass spectroscopy (nLC/MS). B. fibrisolvens as an important plant fibre degrader was cultivated on four different carbon sources (including xylan, xylose, glucose, and a mixture of xylan with glucose). The impact of growth substrate on protein profile was assessed by six pair-wise comparisons evaluating the significantly differently abundant extracellular proteins. Gel-free and gel-based methods resulted in substantially dissimilar results. The LC-MS/MS approach detected substrate-dependent differences in transport and binding membrane proteins (TBP) and nucleotidase, while the 2DE approach detected substrate effect on proteins included in protein synthesis and butyrate synthesis. On the other hand, both methods observed differentially regulated proteins involved in the glycolytic pathway, however, the only shared enzyme (protein detected both by 2DE and LC-MS/MS approach) was fructose-bisphosphate aldolase. The LC-MS/MS approach detected a high abundance of separated peptides. However, it cannot be easily considered as supreme to 2DE analysis. Both methods differ in sample preparation, their advantages and limitations. The study findings indicate these methods can complement each other and together they elucidate better the metabolic functions of B. fibrisolvens.
    WorkplaceInstitute of Animal Physiology and Genetics
    ContactJana Zásmětová, knihovna@iapg.cas.cz, Tel.: 315 639 554
    Year of Publishing2023
    Electronic addresshttps://www.tandfonline.com/doi/full/10.1080/1828051X.2022.2129477
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