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Formation of 2,6-DMBQ in anthocyanin-rich foods.

Authors :
Detering, Thorben
Berger, Ralf G.
Source :
LWT - Food Science & Technology. Dec2020, Vol. 134, pN.PAG-N.PAG. 1p.
Publication Year :
2020

Abstract

The naturally occurring 2,6-dimethoxybenzoquinone (DMBQ) has anti-bacterial, anti-fungal and anti-cancer activities. As it is probably formed in plants via oxidative degradation of the anthocyanin malvidin and its glycosides, a targeted analysis of the DMBQ concentration of different wines and grape juices was performed. Whereas no DMBQ was detected in white wines, concentrations between 28 and 137 μg/l were measured in red wines. In vivo formation kinetics in crushed anthocyanin-rich fruits were monitored, and up to 2.84 mg/kg DMBQ were found showing that its formation was triggered by cell disruption and catalysed by intrinsic oxidases. Ethanolic extraction of grape pomace, a cheap and sustainable source of malvidin-3- O -glucoside, yielded around 1.3 g/l corresponding to 272 mg/100 g dry matter. Solid phase purification of malvidin on XAD7HP resulted in the separation of 229 mg malvidin/100 g dry matter. A basidiomycetous laccase converted the purified malvidin to DMBQ with a yield of 94% followed by adsorption on XAD16N separating 65 mg DMBQ/100 g dry grape pomace under full food-grade conditions. DMBQ may contribute to the shelf life of malvidin-rich foods and is a promising candidate as a natural alternative to other food preservatives. • 2,6-Dimethoxybenzoquinone is a natural substance found in various plants. • Its concentration correlated to malvidin-3- O -glucoside in grape wines. • Cell disruption triggered its formation in anthocyanin-rich fruits. • A fungal laccase produced 65 mg of the quinone from 100 g dry grape pomace. • With its antibacterial properties, the quinone may be used in future food applications. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00236438
Volume :
134
Database :
Academic Search Index
Journal :
LWT - Food Science & Technology
Publication Type :
Academic Journal
Accession number :
146635713
Full Text :
https://doi.org/10.1016/j.lwt.2020.110178