Peroxidation of membrane lipids in minimally processed cucumbers packaged under modified atmospheres

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Karakas B., Yıldız F.

FOOD CHEMISTRY, vol.100, no.3, pp.1011-1018, 2007 (SCI-Expanded, Scopus)

  • Publication Type: Article / Article
  • Volume: 100 Issue: 3
  • Publication Date: 2007
  • Doi Number: 10.1016/j.foodchem.2005.10.055
  • Journal Name: FOOD CHEMISTRY
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Page Numbers: pp.1011-1018
  • Keywords: lipid peroxidation, minimal processing, cucumber, modified atmospheres, CHILLING TEMPERATURES, XYLENOL ORANGE, FRESH FRUITS, PLANT-TISSUE, VEGETABLES, CALCIUM, HYDROPEROXIDES, PHYSIOLOGY, DISORDERS, OXIDATION
  • Open Archive Collection: AVESIS Open Access Collection
  • Akdeniz University Affiliated: Yes

Abstract

The effect of storage conditions and physical tissue damage on membrane peroxidation in minimally processed cucumber tissue was investigated. Lipid peroxidation in samples stored under modified atmospheric packaging (MAP) and in covered Petri dishes (non-MAP) were determined by the FOX2 and TBARS assays. The initial level of lipid hydroperoxides and TBARS were found as 1.44–2.00 and 0.11–0.20 nmol/g, respectively. The levels of lipid hydroperoxides increased by five- to sixfold in chilled non-MAP tissues over 10 days. MAP with higher levels of oxygen was generally more effective in reducing the generation of lipid hydroperoxides and TBARS. The effect of dipping treatments using solutions containing CaCl2 and/or ascorbic acid on peroxidation were also investigated. Tissue hardness of MAP sealed samples increased for the first 3 days for all tissues but chilled tissues started to soften on the sixth day.

The effect of storage conditions and physical tissue damage on membrane peroxidation in minimally processed cucumber tissue was investigated. Lipid peroxidation in samples stored under modified atmospheric packaging (MAP) and in covered Petri dishes (non-MAP) were determined by the FOX2 and TBARS assays. The initial level of lipid hydroperoxides and TBARS were found as 1.44-2.00 and 0.11-0.20 nmol/g, respectively. The levels of lipid hydroperoxides increased by five- to sixfold in chilled non-MAP tissues over 10 days. MAP with higher levels of oxygen was generally more effective in reducing the generation of lipid hydroperoxides and TBARS. The effect of dipping treatments using solutions containing CaCl2 and/or ascorbic acid on peroxidation were also investigated. Tissue hardness of MAP sealed samples increased for the first 3 days for all tissues but chilled tissues started to soften on the sixth day. (c) 2005 Elsevier Ltd. All rights reserved.