Chlorogenic acid–arabinose hybrid domains in coffee melanoidins: Evidences from a model system. (15th October 2015)
- Record Type:
- Journal Article
- Title:
- Chlorogenic acid–arabinose hybrid domains in coffee melanoidins: Evidences from a model system. (15th October 2015)
- Main Title:
- Chlorogenic acid–arabinose hybrid domains in coffee melanoidins: Evidences from a model system
- Authors:
- Moreira, Ana S.P.
Coimbra, Manuel A.
Nunes, Fernando M.
Passos, Cláudia P.
Santos, Sónia A.O.
Silvestre, Armando J.D.
Silva, André M.N.
Rangel, Maria
Domingues, M. Rosário M. - Abstract:
- Highlights: Melanoidins are formed during coffee roasting. Arabinose was hypothesized as a binding site for chlorogenic acids in melanoidins. Chlorogenic acid–arabinose hybrids were obtained by dry heating of a model mixture. Two of these hybrid structures were identified in coffee derived samples. These results open new perspectives for their identification in coffee melanoidins. Abstract: Arabinose from arabinogalactan side chains was hypothesized as a possible binding site for chlorogenic acids in coffee melanoidins. To investigate this hypothesis, a mixture of 5- O -caffeoylquinic acid (5-CQA), the most abundant chlorogenic acid in green coffee beans, and (α1 → 5)-l -arabinotriose, structurally related to arabinogalactan side chains, was submitted to dry thermal treatments. The compounds formed during thermal processing were identified by electrospray ionization mass spectrometry (ESI-MS) and characterized by tandem MS (ESI-MS n ). Compounds composed by one or two CQAs covalently linked with pentose (Pent) residues (1–12) were identified, along with compounds bearing a sugar moiety but composed exclusively by the quinic or caffeic acid moiety of CQAs. The presence of isomers was demonstrated by liquid chromatography online coupled to ESI-MS and ESI-MS n . Pent1–2 CQA were identified in coffee samples. These results give evidence for a diversity of chlorogenic acid–arabinose hybrids formed during roasting, opening new perspectives for their identification in melanoidinHighlights: Melanoidins are formed during coffee roasting. Arabinose was hypothesized as a binding site for chlorogenic acids in melanoidins. Chlorogenic acid–arabinose hybrids were obtained by dry heating of a model mixture. Two of these hybrid structures were identified in coffee derived samples. These results open new perspectives for their identification in coffee melanoidins. Abstract: Arabinose from arabinogalactan side chains was hypothesized as a possible binding site for chlorogenic acids in coffee melanoidins. To investigate this hypothesis, a mixture of 5- O -caffeoylquinic acid (5-CQA), the most abundant chlorogenic acid in green coffee beans, and (α1 → 5)-l -arabinotriose, structurally related to arabinogalactan side chains, was submitted to dry thermal treatments. The compounds formed during thermal processing were identified by electrospray ionization mass spectrometry (ESI-MS) and characterized by tandem MS (ESI-MS n ). Compounds composed by one or two CQAs covalently linked with pentose (Pent) residues (1–12) were identified, along with compounds bearing a sugar moiety but composed exclusively by the quinic or caffeic acid moiety of CQAs. The presence of isomers was demonstrated by liquid chromatography online coupled to ESI-MS and ESI-MS n . Pent1–2 CQA were identified in coffee samples. These results give evidence for a diversity of chlorogenic acid–arabinose hybrids formed during roasting, opening new perspectives for their identification in melanoidin structures. … (more)
- Is Part Of:
- Food chemistry. Volume 185(2015)
- Journal:
- Food chemistry
- Issue:
- Volume 185(2015)
- Issue Display:
- Volume 185, Issue 2015 (2015)
- Year:
- 2015
- Volume:
- 185
- Issue:
- 2015
- Issue Sort Value:
- 2015-0185-2015-0000
- Page Start:
- 135
- Page End:
- 144
- Publication Date:
- 2015-10-15
- Subjects:
- Roasting -- Polysaccharides -- Arabinogalactans -- Caffeoylquinic acid -- Transglycosylation -- Mass spectrometry
Food -- Analysis -- Periodicals
Food -- Composition -- Periodicals
664 - Journal URLs:
- http://www.sciencedirect.com/science/journal/03088146 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.foodchem.2015.03.086 ↗
- Languages:
- English
- ISSNs:
- 0308-8146
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3977.284000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 5663.xml