Skip to Content
Merck
  • Chilling-related cell damage of apple (Malus × domestica Borkh.) fruit cortical tissue impacts antioxidant, lipid and phenolic metabolism.

Chilling-related cell damage of apple (Malus × domestica Borkh.) fruit cortical tissue impacts antioxidant, lipid and phenolic metabolism.

Physiologia plantarum (2014-06-20)
Rachel S Leisso, David A Buchanan, Jinwook Lee, James P Mattheis, Chris Sater, Ines Hanrahan, Christopher B Watkins, Nigel Gapper, Jason W Johnston, Robert J Schaffer, Maarten L A T M Hertog, Bart M Nicolaï, David R Rudell
ABSTRACT

'Soggy breakdown' (SB) is an internal flesh disorder of 'Honeycrisp' apple (Malus × domestica Borkh.) fruit that occurs during low temperature storage. The disorder is a chilling injury (CI) in which visible symptoms typically appear after several weeks of storage, but information about the underlying metabolism associated with its induction and development is lacking. The metabolic profile of flesh tissue from wholly healthy fruit and brown and healthy tissues from fruit with SB was characterized using gas chromatography-mass spectrometry (GC-MS) and liquid chromatograph-mass spectrometry (LC-MS). Partial least squares discriminant analysis (PLS-DA) and correlation networks revealed correlation among ester volatile compounds by composition and differences in phytosterol, phenolic and putative triacylglycerides (TAGs) metabolism among the tissues. anova-simultaneous component analysis (ASCA) was used to test the significance of metabolic changes linked with tissue health status. ASCA-significant components included antioxidant compounds, TAGs, and phytosterol conjugates. Relative to entirely healthy tissues, elevated metabolite levels in symptomatic tissue included γ-amino butyric acid, glycerol, sitosteryl (6'-O-palmitoyl) β-d-glucoside and sitosteryl (6'-O-stearate) β-d-glucoside, and TAGs containing combinations of 16:0, 18:3, 18:2 and 18:1 fatty acids. Reduced metabolite levels in SB tissue included 5-caffeoyl quinate, β-carotene, catechin, epicatechin, α-tocopherol, violaxanthin and sitosteryl β-d glucoside. Pathway analysis indicated aspects of primary metabolism differed according to tissue condition, although differences in metabolites involved were more subtle than those of some secondary metabolites. The results implicate oxidative stress and membrane disruption processes in SB development and constitute a diagnostic metabolic profile for the disorder.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
Methanol, NMR reference standard
Supelco
2-Butanol, analytical standard
Supelco
2-Methyl-1-propanol, analytical standard
Supelco
Acetone, Pharmaceutical Secondary Standard; Certified Reference Material
Sigma-Aldrich
2-Methyl-1-propanol, BioUltra, for molecular biology, ≥99.5% (GC)
Supelco
Methanol, analytical standard
Sigma-Aldrich
1-Propanol, ≥99%, FG
Sigma-Aldrich
1-Butanol, anhydrous, 99.8%
Sigma-Aldrich
Heptanal, ≥95%, FCC, FG
Sigma-Aldrich
Acetone, natural, ≥97%
Sigma-Aldrich
Acetone, ≥99%, meets FCC analytical specifications
Sigma-Aldrich
2-Methyl-1-butanol, ≥99%, FG
Sigma-Aldrich
Methyl 2-methylbutyrate, ≥98%, FCC, FG
Sigma-Aldrich
2-Methyl-1-butanol, natural, 99%, FG
Sigma-Aldrich
Methyl 2-methylbutyrate, natural, ≥98%, FCC, FG
Sigma-Aldrich
2-Methyl-1-propanol, anhydrous, 99.5%
Sigma-Aldrich
Ethyl propionate, natural, ≥97%, FCC, FG
Sigma-Aldrich
Acetone, suitable for HPLC, ≥99.9%
Sigma-Aldrich
Methanol, anhydrous, 99.8%
Sigma-Aldrich
Ethyl propionate, ≥97%, FCC, FG
Sigma-Aldrich
Hexyl butyrate, ≥98%, FG
Sigma-Aldrich
Hexyl propionate, ≥97%, FG
Sigma-Aldrich
Heptaldehyde, 95%
Sigma-Aldrich
1-Propanol, natural, ≥98%, FG
Supelco
Acetone, analytical standard
Supelco
1-Propanol, analytical standard
Sigma-Aldrich
1-Aminocyclopropanecarboxylic acid, ≥98% (TLC), powder
Sigma-Aldrich
myo-Inositol, ≥99% (GC), BioReagent
Sigma-Aldrich
myo-Inositol, ≥99%
Supelco
1-Butanol, Pharmaceutical Secondary Standard; Certified Reference Material