Lipids of Pavlova lutheri: Cellular site and metabolic role of DGCC

Pavlova lutheri contains triacylglycerols (TAG), monogalactosyldiacylglycerols (MGDG), galactosyldiacylglycerols (DGDG), sulfoquivonosyldiacylglycerols (SQDG), diacylglyceryl hydroxymethyl-N,N,N-trimethyl-β-alanine (DGTA), diacylglyceryl carboxyhydroxymethylcholine (DGCC) and diacylglyceryl glucuronide (DGGA) as major lipid components. Prominent fatty acids are 14:0, 16:0, 16:1, 18:4, 20:5, 22:5 and 22:6. In MGDG and DGDG, 18:4 and 20:5 predominate, while SQDG contains high proportions of 14:0 and 16:0. DGCC is enriched in 16:0 and 20:5, DGGA in 18:1, 22:5 and 22:6, and DGTA in 22:6. Analysis of subcellular membrane fractions demonstrated an accumulation of DGCC, DGTA and DGGA in non-plastid membranes. On incubation of cells with [1-14C] oleic acid, after 60 min of pulse, 30% of the incorporated label was found in TAG and 70% in polar lipids. DGCC (52%) and DGTA (12%) were the most strongly labelled polar lipids. Within 72 h of chase, in DGCC and in TAG the label rapidly decreased to 11 % and 17%, respectively, but in MGDG it increased in the same time up to 35% of the total. Only minor changes were observed in DGTA and no significant label was recorded in DAG during the chase-period. The shift of label from 18:1 to 18:4, 20:5 and 22:6 reflected further elongation and/or desaturation of the substrate. Very similar results obtained using [2-14C] acetate as precursor suggested that DGCC acts as a primary acceptor of de novo-formed or exogenous fatty acids which subsequently undergo processing and redistribution. It is suggested that C18 and C20 fatty acids are transferred individually from the cytoplasm to the chloroplast allowing the synthesis of eukaryotic MGDG without the import of DAG. © 1997 Elsevier Science Ltd. All rights reserved

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