Neutral and acidic products derived from hydroxyl radical‐induced oxidation of arabinotriose assessed by electrospray ionisation mass spectrometry. (20th March 2014)
- Record Type:
- Journal Article
- Title:
- Neutral and acidic products derived from hydroxyl radical‐induced oxidation of arabinotriose assessed by electrospray ionisation mass spectrometry. (20th March 2014)
- Main Title:
- Neutral and acidic products derived from hydroxyl radical‐induced oxidation of arabinotriose assessed by electrospray ionisation mass spectrometry
- Authors:
- Moreira, Ana S. P.
da, Elisabete V.
Evtuguin, Dmitry V.
Coimbra, Manuel A.
Nunes, Fernando M.
Domingues, M. Rosário M. - Abstract:
- <abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <p>The oxidation of α‐(1 → 5)‐<sc>l</sc>‐arabinotriose (Ara<sub>3</sub>), an oligosaccharide structurally related to side chains of coffee arabinogalactans, was studied in reaction with hydroxyl radicals generated under conditions of Fenton reaction (Fe<sup>2+</sup>/H<sub>2</sub>O<sub>2</sub>). The acidic and neutral oxidation products were separated by ligand exchange/size‐exclusion chromatography, subsequently identified by electrospray ionisation mass spectrometry (ESI–MS) and structurally characterised by tandem MS (ESI–MS/MS). In acidic fraction were identified several oxidation products containing an acidic residue at the corresponding reducing end of Ara<sub>3</sub>, namely arabinonic acid, and erythronic, glyceric and glycolic acids formed by oxidative scission of the furanose ring. In neutral fractions were identified derivatives containing keto, hydroxy and hydroperoxy moieties, as well as derivatives resulting from the ring scission at the reducing end of Ara<sub>3</sub>. In both acidic and neutral fractions, beyond the trisaccharide derivatives, the corresponding di‐ and monosaccharide derivatives were identified indicating the occurrence of oxidative depolymerisation. The structural characterisation of these oxidation products by ESI–MS/MS allowed the differentiation of isobaric and isomeric species of acidic and neutral character. The species identified in this study may help<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <p>The oxidation of α‐(1 → 5)‐<sc>l</sc>‐arabinotriose (Ara<sub>3</sub>), an oligosaccharide structurally related to side chains of coffee arabinogalactans, was studied in reaction with hydroxyl radicals generated under conditions of Fenton reaction (Fe<sup>2+</sup>/H<sub>2</sub>O<sub>2</sub>). The acidic and neutral oxidation products were separated by ligand exchange/size‐exclusion chromatography, subsequently identified by electrospray ionisation mass spectrometry (ESI–MS) and structurally characterised by tandem MS (ESI–MS/MS). In acidic fraction were identified several oxidation products containing an acidic residue at the corresponding reducing end of Ara<sub>3</sub>, namely arabinonic acid, and erythronic, glyceric and glycolic acids formed by oxidative scission of the furanose ring. In neutral fractions were identified derivatives containing keto, hydroxy and hydroperoxy moieties, as well as derivatives resulting from the ring scission at the reducing end of Ara<sub>3</sub>. In both acidic and neutral fractions, beyond the trisaccharide derivatives, the corresponding di‐ and monosaccharide derivatives were identified indicating the occurrence of oxidative depolymerisation. The structural characterisation of these oxidation products by ESI–MS/MS allowed the differentiation of isobaric and isomeric species of acidic and neutral character. The species identified in this study may help in detection of roasting products associated with the free radical‐mediated oxidation of coffee arabinogalactans. Copyright © 2014 John Wiley &amp; Sons, Ltd.</p> </abstract> … (more)
- Is Part Of:
- Journal of mass spectrometry. Volume 49:Number 4(2014:Apr.)
- Journal:
- Journal of mass spectrometry
- Issue:
- Volume 49:Number 4(2014:Apr.)
- Issue Display:
- Volume 49, Issue 4 (2014)
- Year:
- 2014
- Volume:
- 49
- Issue:
- 4
- Issue Sort Value:
- 2014-0049-0004-0000
- Page Start:
- 280
- Page End:
- 290
- Publication Date:
- 2014-03-20
- Subjects:
- Mass spectrometry -- Periodicals
543.65 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1002/jms.3339 ↗
- Languages:
- English
- ISSNs:
- 1076-5174
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5012.179500
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3440.xml