Lipid metabolism during aging of high-α-linolenate-phenotype potato tubers

• Published in: Archives of biochemistry and biophysics 2002-06, Vol.402 (1), p.136-148
• Main Authors: Zabrouskov, Vladimir, Knowles, N.Richard
• Format: Article
• Language: English
• Subjects: Aging; alpha-Linolenic Acid - metabolism; Chromatography, High Pressure Liquid; Fatty acid desaturase; Fatty Acid Desaturases - metabolism; Flavin-Adenine Dinucleotide - metabolism; Lipid Metabolism; Lipid molecular species; Lipid Peroxidation; MALDI-TOF MS; Mitochondria; Phenotype; Phosphatidylcholines - metabolism; Phosphatidylethanolamines - metabolism; Solanum tuberosum - metabolism; Solanum tuberosum L; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization; Sterols; Up-Regulation
• ISSN: 0003-9861; 1096-0384
• DOI: 10.1016/S0003-9861(02)00069-3

Previous studies demonstrated that high levels of α-linolenate in cell membranes of potato tubers (achieved by overexpressing fatty acid desaturases) enhances lipid peroxidation, oxidative stress, and tuber metabolic rate, effectively accelerating the physiological age of tubers. This study details the changes in lipid molecular species of microsomal and mitochondrial membranes from wild-type (WT) and high-α-linolenate tubers during aging. The microsomal and mitochondrial polar lipids of high-α-linolenate tubers were dominated by 18:3/18:3 and 16:0/18:3 molecular species. Relative to WT tubers, high-α-linolenate tubers had a substantially higher 16:0/18:n to 18:n/18:n molecular species ratio in mitochondria and microsomes, potentially reflecting a compensatory response to maintain membrane biophysical properties in the face of increased unsaturation. Phosphatidylcholine (PC) and phosphatidylethanolamine (PE) accounted for 53 and 37% of polar lipids, respectively, in mitochondria from younger WT and high-α-linolenate tubers. The relative proportions of these phospholipids (PL) did not change during aging of WT tubers. In contrast, PE increased to dominate the PL pool of mitochondria during aging of high-α-linolenate tubers. While aging effected an increase in mitochondrial 18:3-bearing PCs and PEs in WT tubers, the concentration of 18:3-bearing PCs fell with a concomitant increase in 18:3-bearing PEs during aging of high-α-linolenate tubers. These age- and high-α-linolenate-induced changes had no effect on the respiration rate and functional integrity of isolated mitochondria. Differential increases in the respiration rates of WT and high-α-linolenate tubers during aging were therefore a consequence of unsaturation-dependent alterations in the microenvironments of cells. Microsomal 18:3-bearing PCs, PEs, digalactosyldiacylglycerols (DGDG), and monogalactosyldiacylglycerols all increased in WT tubers during aging. In contrast, a selective loss of 18:3-bearing PCs and DGDGs from microsomes of high-α-linolenate tubers likely reflects a greater susceptibility of membranes to peroxidative catabolism during aging. Aging resulted in an increase in sterol/PL ratio in microsomes from WT tubers, due primarily to a decline in PL. In high-α-linolenate tubers, the increase in sterol/PL ratio during aging was due to increases in Δ5-avenasterol and stigmasterol, indicating membrane rigidification and likely contributing to increased membrane permeability. Age-induced chan