Measuring Conjugated Linoleic Acid (CLA) Production by Bifidobacteria.


Journal

Methods in molecular biology (Clifton, N.J.)
ISSN: 1940-6029
Titre abrégé: Methods Mol Biol
Pays: United States
ID NLM: 9214969

Informations de publication

Date de publication:
2021
Historique:
entrez: 2 3 2021
pubmed: 3 3 2021
medline: 10 4 2021
Statut: ppublish

Résumé

The biological significance of conjugated fatty acids (CFAs) has been linked to positive health effects based on biomedical, in vitro, and clinical studies. Of note, conjugated linoleic acids (CLAs) are the most widely characterized fatty acids as geometric isomers cis-9,trans-11 and trans-10,cis-12 CLA occur naturally in ruminant fats, dairy products, and hydrogenated oils. Concerning CLAs, it is known that bacterial biohydrogenation, a process whereby ruminal bacteria or starter cultures of lactic acid bacteria have the ability to synthesize CLA by altering the chemical structure of essential fatty acids via enzymatic mechanisms, produces a multitude of isomers with desirable properties. Bifidobacterium species are classed as food grade microorganisms and some of these strains harness molecular determinants that are responsible for the bioconversion of free fatty acids to CLAs. However, molecular mechanisms have yet to be fully elucidated. Reports pertaining to CLAs have been attributed to suppressing tumor growth, delaying the onset of diabetes mellitus and reducing body fat in obese individuals. Given the increased attention for their bioactive properties, we describe in this chapter the qualitative and quantitative methods used to identify and quantify CLA isomers produced by bifidobacterial strains in supplemented broth media. These approaches enable rapid detection of potential CLA producing strains and accurate measurement of fatty acids in biological matrices.

Identifiants

pubmed: 33649950
doi: 10.1007/978-1-0716-1274-3_8
doi:

Substances chimiques

Linoleic Acids, Conjugated 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

87-100

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Auteurs

Grace Ahern (G)

Teagasc Food Research Centre, Moorepark, Fermoy, Co. Cork, Ireland.
School of Microbiology, University College Cork, Cork, Ireland.
APC Microbiome Ireland, University College Cork, Cork, Ireland.

Douwe van Sinderen (D)

School of Microbiology & APC Microbiome Ireland, University College Cork, Cork, Ireland.

Bo Yang (B)

State Key Laboratory of Food Science and Technology, School of Food Science and Technology, Jiangnan University, Wuxi, Jiangsu, P. R. China.

R Paul Ross (RP)

APC Microbiome Ireland, University College Cork, Cork, Ireland.

Catherine Stanton (C)

Teagasc Food Research Centre, Moorepark, Fermoy, Co. Cork, Ireland. Catherine.stanton@teagasc.ie.
APC Microbiome Ireland, University College Cork, Cork, Ireland. Catherine.stanton@teagasc.ie.

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