Ka. Hudak et Je. Thompson, SUBCELLULAR-LOCALIZATION OF SECONDARY LIPID METABOLITES INCLUDING FRAGRANCE VOLATILES IN CARNATION PETALS, Plant physiology, 114(2), 1997, pp. 705-713
Pulse-chase labeling of carnation (Dianthus caryophyllus L. cv Improve
d White Sim) petals with [C-74]acetate has provided evidence for a hyd
rophobic subcompartment of lipid-protein particles within the cytosol
that resemble oil bodies, are formed by blebbing from membranes, and a
re enriched in lipid metabolites (including fragrance volatiles) deriv
ed from membrane fatty acids. Fractionation of the petals during pulse
-chase labeling revealed that radio-labeled fatty acids appear first i
n microsomal membranes and subsequently in cytosolic lipid-protein par
ticles, indicating that the particles originate from membranes. This i
nterpretation is supported by the finding that the cytosolic lipid-pro
tein particles contain phospholipid as well as the same fatty acids fo
und in microsomal membranes. Radiolabeled polar lipid metabolites (met
hanol/ water-soluble) were detectable in bath in situ lipid-protein pa
rticles isolated from the cytosol and those generated in vitro from is
olated radiolabeled microsomal membranes. The lipid-protein particles
were also enriched in hexanal, trans-2-hexenal, 1-hexanol, 3-hexen-1-o
l, and 2-hexanol, volatiles of carnation flower fragrance that are der
ived from membrane fatty acids through the lipoxygenase pathway. There
fore, secondary lipid metabolites, including components of fragrance,
appear to be formed within membranes of petal tissue and are subsequen
tly released from the membrane bilayers into the cytosol by blebbing o
f lipid-protein particles.