In this study, for the first time, the amount of 3-deoxy-d-erythro-hexos-2-ulose (3-DG) in fresh citrus andchestnut honeys was determined. 3-DG was measured as the corresponding quinoxalines after derivatization withorthophenylenediamine using reverse-phase high-performance liquid chromatography (RP-HPLC). Notwithstandingthe freshness of the samples, high levels of 3-DG were detected in both honeys. The comparison of 3-DG and 5-hydroxymethylfurfural (HMF) concentrations, which was also quantified by RP-HPLC, showed that citrus honeys hadthe lowest amount of 3-DG (107 mg/kg) and the highest of HMF (16.7 mg/kg), while chestnut honeys had the opposite(398 and 1.2 mg/kg, respectively). During thermal treatment, different 3-DG and HMF trends were highlighted between the citrus and chestnut honeys; at the end, 3-DG formation was more favored with respect to HMF formation. Moreover,in citrus honeys, a good correlation between 3-DG and HMF levels was observed, which was not found in chestnuthoneys, suggesting a role of the high pH values of these honeys on the degradation routes. The kinetic analysis showed thehighest k value for 3-DG and HMF formation in chestnut and citrus honeys, respectively. The lowest Ea values related to3-DG formation and the highest to HMF formation, indicating that the key intermediate 3-DG is easily formed at lowtemperatures, whilst the formation of HMF requires higher temperatures. For this reason, 3-DG seems to be an agingindex rather than a thermal index and its use, at least for honeys at high pH values, together with HMF, could improve their quality assessment.

Kinetics of 3-Deoxy-D-Erythro-Hexos-2-Ulose in Unifloral Honeys

ARENA, ELENA;FALLICO, Biagio
2011-01-01

Abstract

In this study, for the first time, the amount of 3-deoxy-d-erythro-hexos-2-ulose (3-DG) in fresh citrus andchestnut honeys was determined. 3-DG was measured as the corresponding quinoxalines after derivatization withorthophenylenediamine using reverse-phase high-performance liquid chromatography (RP-HPLC). Notwithstandingthe freshness of the samples, high levels of 3-DG were detected in both honeys. The comparison of 3-DG and 5-hydroxymethylfurfural (HMF) concentrations, which was also quantified by RP-HPLC, showed that citrus honeys hadthe lowest amount of 3-DG (107 mg/kg) and the highest of HMF (16.7 mg/kg), while chestnut honeys had the opposite(398 and 1.2 mg/kg, respectively). During thermal treatment, different 3-DG and HMF trends were highlighted between the citrus and chestnut honeys; at the end, 3-DG formation was more favored with respect to HMF formation. Moreover,in citrus honeys, a good correlation between 3-DG and HMF levels was observed, which was not found in chestnuthoneys, suggesting a role of the high pH values of these honeys on the degradation routes. The kinetic analysis showed thehighest k value for 3-DG and HMF formation in chestnut and citrus honeys, respectively. The lowest Ea values related to3-DG formation and the highest to HMF formation, indicating that the key intermediate 3-DG is easily formed at lowtemperatures, whilst the formation of HMF requires higher temperatures. For this reason, 3-DG seems to be an agingindex rather than a thermal index and its use, at least for honeys at high pH values, together with HMF, could improve their quality assessment.
2011
1,2-dicarbonyl compounds; 3-deoxyglucosulose synthesis; safety
File in questo prodotto:
File Dimensione Formato  
Arena et al 2011 Kinetics of 3-deoxy JFS.pdf

solo gestori archivio

Descrizione: Articolo
Tipologia: Versione Editoriale (PDF)
Licenza: Creative commons
Dimensione 151.05 kB
Formato Adobe PDF
151.05 kB Adobe PDF   Visualizza/Apri

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.11769/9619
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 8
  • ???jsp.display-item.citation.isi??? 7
social impact