SCOPE: Chlorogenic acid (3-O-caffeoyl-quinic acid, C-QA), the caffeic ester of quinic acid, is one of the most abundant phenolic acids in Western diet. The majority of C-QA escapes absorption in the small intestine and reaches the colon, where the resident microbiota transforms it into several metabolites. C-QA conversion by the gut microbiota from nine subjects was compared to evaluate the variability of bacterial metabolism. It was investigated whether a potentially probiotic Bifidobacterium strain, capable of C-QA hydrolysis, could affect C-QA fate. METHODS AND RESULTS: Bioconversion experiments exploiting the microbiota from diverse subjects revealed that C-QA was metabolized through a succession of hydrogenation, dexydroxylation and ester hydrolysis, occurring in different order among the subjects. Transformation may proceed also through quinic acid residue breakdown, since caffeoyl-glycerol intermediates were identified (HPLC-MS/MS, Q-TOF). All the pathways converged on 3-(3-hydroxyphenyl)-propanoic acid, which was transformed to hydroxyphenyl-ethanol and/or phenylacetic acid in few subjects. A strain of Bifidobacterium animalis able to hydrolyze C-QA was added to microbiota cultures. It affected microbial composition but not to such an extent that C-QA metabolism was modified. CONCLUSION: A picture of the variability of microbiota C-QA transformations among subjects is provided. The transformation route through caffeoyl-glycerol intermediates is described for the first time.
SCOPE: Chlorogenic acid (3-O-caffeoyl-quinic acid, C-QA), the caffeic ester of quinic acid, is one of the most abundant phenolic acids in Western diet. The majority of C-QA escapes absorption in the small intestine and reaches the colon, where the resident microbiota transforms it into several metabolites. C-QA conversion by the gut microbiota from nine subjects was compared to evaluate the variability of bacterial metabolism. It was investigated whether a potentially probiotic Bifidobacterium strain, capable of C-QA hydrolysis, could affect C-QA fate. METHODS AND RESULTS: Bioconversion experiments exploiting the microbiota from diverse subjects revealed that C-QA was metabolized through a succession of hydrogenation, dexydroxylation and ester hydrolysis, occurring in different order among the subjects. Transformation may proceed also through quinic acid residue breakdown, since caffeoyl-glycerol intermediates were identified (HPLC-MS/MS, Q-TOF). All the pathways converged on 3-(3-hydroxyphenyl)-propanoic acid, which was transformed to hydroxyphenyl-ethanol and/or phenylacetic acid in few subjects. A strain of Bifidobacterium animalis able to hydrolyze C-QA was added to microbiota cultures. It affected microbial composition but not to such an extent that C-QA metabolism was modified. CONCLUSION: A picture of the variability of microbiota C-QA transformations among subjects is provided. The transformation route through caffeoyl-glycerol intermediates is described for the first time.
Authors: Pedro Mena; Iziar A Ludwig; Virginia B Tomatis; Animesh Acharjee; Luca Calani; Alice Rosi; Furio Brighenti; Sumantra Ray; Julian L Griffin; Les J Bluck; Daniele Del Rio Journal: Eur J Nutr Date: 2018-04-03 Impact factor: 5.614
Authors: Stefano Raimondi; Andrew Anighoro; Andrea Quartieri; Alberto Amaretti; Francisco A Tomás-Barberán; Giulio Rastelli; Maddalena Rossi Journal: Microbiologyopen Date: 2014-12-16 Impact factor: 3.139
Authors: Marta Simone; Caterina Gozzoli; Andrea Quartieri; Giuseppe Mazzola; Diana Di Gioia; Alberto Amaretti; Stefano Raimondi; Maddalena Rossi Journal: Biomed Res Int Date: 2014-08-28 Impact factor: 3.411
Authors: Sylvia H Duncan; Wendy R Russell; Andrea Quartieri; Maddalena Rossi; Julian Parkhill; Alan W Walker; Harry J Flint Journal: Environ Microbiol Date: 2016-01-21 Impact factor: 5.491