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Browsing by Author "Fitzgerald, Gerald F."

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    Identification and characterization of an oleate hydratase-encoding gene from Bifidobacterium breve
    (Landes Bioscience, 2013)
    O’Connell, Kerry Joan
    ;
    Motherway, Mary O’Connell
    ;
    Hennessey, Alan A.
    ;
    Brodhun, Florian  
    ;
    Ross, R. Paul
    ;
    Feussner, Ivo  
    ;
    Stanton, Catherine
    ;
    Fitzgerald, Gerald F.
    ;
    van Sinderen, Douwe
    Bifidobacteria are common commensals of the mammalian gastrointestinal tract. Previous studies have suggested that a bifidobacterial myosin cross reactive antigen (MCRA) protein plays a role in bacterial stress tolerance, while this protein has also been linked to the biosynthesis of conjugated linoleic acid (CLA) in bifidobacteria. In order to increase our understanding on the role of MCRA in bifidobacteria we created and analyzed an insertion mutant of the MCRA-encoding gene of B. breve NCFB 2258. Our results demonstrate that the MCRA protein of B. breve NCFB 2258 does not appear to play a role in CLA production, yet is an oleate hydratase, which contributes to bifidobacterial solvent stress protection.
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    Myosin-cross-reactive antigen (MCRA) protein from Bifidobacterium breve is a FAD-dependent fatty acid hydratase which has a function in stress protection
    (Biomed Central Ltd, 2011)
    Rosberg-Cody, Eva
    ;
    Liavonchanka, Alena
    ;
    Goebel, Cornelia
    ;
    Ross, R. Paul
    ;
    O’Sullivan, Orla
    ;
    Fitzgerald, Gerald F.
    ;
    Feussner, Ivo  
    ;
    Stanton, Catherine
    Background: The aim of this study was to determine the catalytic activity and physiological role of myosin-cross-reactive antigen (MCRA) from Bifidobacterium breve NCIMB 702258. MCRA from B. breve NCIMB 702258 was cloned, sequenced and expressed in heterologous hosts (Lactococcus and Corynebacterium) and the recombinant proteins assessed for enzymatic activity against fatty acid substrates. Results: MCRA catalysed the conversion of palmitoleic, oleic and linoleic acids to the corresponding 10-hydroxy fatty acids, but shorter chain fatty acids were not used as substrates, while the presence of trans-double bonds and double bonds beyond the position C12 abolished hydratase activity. The hydroxy fatty acids produced were not metabolised further. We also found that heterologous Lactococcus and Corynebacterium expressing MCRA accumulated increasing amounts of 10-HOA and 10-HOE in the culture medium. Furthermore, the heterologous cultures exhibited less sensitivity to heat and solvent stresses compared to corresponding controls. Conclusions: MCRA protein in B. breve can be classified as a FAD-containing double bond hydratase, within the carbon-oxygen lyase family, which may be catalysing the first step in conjugated linoleic acid (CLA) production, and this protein has an additional function in bacterial stress protection.

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