Pyranoanthocyanin formation rates and yields as affected by cyanidin-3-substitutions and pyruvic or caffeic acids. (30th May 2021)
- Record Type:
- Journal Article
- Title:
- Pyranoanthocyanin formation rates and yields as affected by cyanidin-3-substitutions and pyruvic or caffeic acids. (30th May 2021)
- Main Title:
- Pyranoanthocyanin formation rates and yields as affected by cyanidin-3-substitutions and pyruvic or caffeic acids
- Authors:
- Zhu, Xiaoyi
Giusti, M. Monica - Abstract:
- Highlights: Pyranoanthocyanins (PACNs) were efficiently produced using different cyanidin-derivatives. PACN yield grew from 15 to 85% when cofactor changed from pyruvic to caffeic acid. Copigmentation may favor PACN formation by keeping reactants in close proximity. Glycosylation patterns affected PACN formation only with pyruvic acid (PA). Aromatic acylation hindered PACN formation. Abstract: Anthocyanin-derived pyranoanthocyanins (PACNs) offer potential as food colorants as they may exhibit higher stability than anthocyanins (ACNs). Our objective was to compare PACN formation rate and efficiency from different cyanidin-3-derivatives and cofactors, in order to facilitate PACN production. Four cyanidin-3-derivatives (cyanidin-3-glucoside, cyanidin-3-xylosylglucosylgalactoside, cyanidin-3-malonylglucoside and cyanidin-3-xylosyl(sinapoylglucosyl)galactoside) were incubated with pyruvic or caffeic acids (PA, CA) at 25 °C in the dark for two months. PACN formation was monitored by uHPLC-PDA-MS/MS over time. ACNs incubated with PA produced PACNs with yields increasing steadily over time, reaching 15% after 2 months. PACN formation with CA increased exponentially from the start, reaching 85% during storage. PACNs were efficiently produced from 3 of the 4 ACNs in the presence of CA, with minimal pigment loss. Copigmentation between CA and ACNs may facilitate PACN formation by keeping reactants in close proximity. Anthocyanin glycosylation and acylation affected PACN formation to aHighlights: Pyranoanthocyanins (PACNs) were efficiently produced using different cyanidin-derivatives. PACN yield grew from 15 to 85% when cofactor changed from pyruvic to caffeic acid. Copigmentation may favor PACN formation by keeping reactants in close proximity. Glycosylation patterns affected PACN formation only with pyruvic acid (PA). Aromatic acylation hindered PACN formation. Abstract: Anthocyanin-derived pyranoanthocyanins (PACNs) offer potential as food colorants as they may exhibit higher stability than anthocyanins (ACNs). Our objective was to compare PACN formation rate and efficiency from different cyanidin-3-derivatives and cofactors, in order to facilitate PACN production. Four cyanidin-3-derivatives (cyanidin-3-glucoside, cyanidin-3-xylosylglucosylgalactoside, cyanidin-3-malonylglucoside and cyanidin-3-xylosyl(sinapoylglucosyl)galactoside) were incubated with pyruvic or caffeic acids (PA, CA) at 25 °C in the dark for two months. PACN formation was monitored by uHPLC-PDA-MS/MS over time. ACNs incubated with PA produced PACNs with yields increasing steadily over time, reaching 15% after 2 months. PACN formation with CA increased exponentially from the start, reaching 85% during storage. PACNs were efficiently produced from 3 of the 4 ACNs in the presence of CA, with minimal pigment loss. Copigmentation between CA and ACNs may facilitate PACN formation by keeping reactants in close proximity. Anthocyanin glycosylation and acylation affected PACN formation to a lower degree than cofactors. … (more)
- Is Part Of:
- Food chemistry. Volume 345(2021)
- Journal:
- Food chemistry
- Issue:
- Volume 345(2021)
- Issue Display:
- Volume 345, Issue 2021 (2021)
- Year:
- 2021
- Volume:
- 345
- Issue:
- 2021
- Issue Sort Value:
- 2021-0345-2021-0000
- Page Start:
- Page End:
- Publication Date:
- 2021-05-30
- Subjects:
- Pyranoanthocyanin formation -- Cyanidin-3-derivatives -- Pyruvic acid -- Caffeic acid -- Copigmentation
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.2020.128776 ↗
- 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
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British Library HMNTS - ELD Digital store - Ingest File:
- 25530.xml