Formation of alpha-dicarbonyl compounds in beer during storage of Pilsner

J Agric Food Chem. 2008 Jun 11;56(11):4134-44. doi: 10.1021/jf703696p. Epub 2008 May 8.

Abstract

With the aim of determining the formation of alpha-dicarbonyl intermediates during beer aging on the shelf, alpha-dicarbonyls were identified and quantified after derivatization with 1,2-diaminobenze to generate quinoxalines. The sensory effects of alpha-dicarbonyls were evaluated by the quantification of key Strecker aldehydes and by GC-olfactometry (GCO)analysis of beer headspace using solid phase microextraction. Four alpha-dicarbonyls, reported here for the first time, were detected in fresh and aged beers, three were derived from the 2,3-enolization pathway of mono- and disaccharides, and the fourth was derived from the epimerization of 3-deoxy-2-hexosulose. Ten alpha-dicarbonyls were quantified during beer processing and during different periods of beer aging at 28 degrees C. The aging periods were from 15 to 105 days. During beer aging, 1-deoxydiuloses were produced and degraded, while 1,4-dideoxydiuloses were produced at the highest rates. The GCO analysis indicated that forced beer aging increased the amounts of furaneol, trans-2-nonenal, and phenylacetaldehyde. The blockage of alpha-dicarbonyls inhibited the accumulation of sensory-active aldehydes in the beer headspace.

MeSH terms

  • Acetaldehyde / analogs & derivatives
  • Acetaldehyde / analysis
  • Aldehydes / analysis
  • Beer / analysis*
  • Chromatography, Gas
  • Deoxyglucose / analogs & derivatives
  • Deoxyglucose / analysis
  • Food Handling
  • Food Preservation*
  • Furans / analysis
  • Humans
  • Smell
  • Time Factors

Substances

  • Aldehydes
  • Furans
  • 2-nonenal
  • furaneol
  • Deoxyglucose
  • 3-deoxyglucosone
  • Acetaldehyde
  • phenylacetaldehyde