C. Sarmiento et al., OLEATE DESATURATION AND ACYL TURNOVER IN SUNFLOWER (HELIANTHUS-ANNUUSL.) SEED LIPIDS DURING RAPID TEMPERATURE ADAPTATION, Planta, 205(4), 1998, pp. 595-600
In-vivo experiments with developing sunflower (Helianthus annuus L.) s
eeds demonstrated that oleate desaturase activity was stimulated by lo
w temperature (10 degrees C), repressed by high temperature (30 degree
s C) and rapidly restored by returning the seeds to low temperature. W
ithin time periods of 2-4 h, in which the denovo fatty acid synthesis
was negligible, the percentages of oleate (18:1) and linoleate (18:2)
were modified in the seed lipids as a consequence of temperature adapt
ation. When the seeds were transferred to low temperature, the 18:2 co
ntent increased in all lipids from both microsomal membranes and oil b
odies. After shifting to high temperature, the overall 18:2 content re
mained constant, but the 18:2 content decreased in diacylglycerols, ph
osphatidylcholine (PC) and other polar lipids of the two fractions and
also in triacylglycerols (TAGs) of the microsomes but increased in TA
Gs of the oil bodies. The results indicate that the mechanism for the
rapid adaptation of sunflower seeds to temperature changes involves (i
) the synthesis or activation of oleate desaturase at low temperature
and the reversible inhibition of this enzyme at high temperature and (
ii) the exchange of 18:1 and 18:2 between TAGs and PC. Under both low
and high temperature, 18:1 is transferred from reserve TAGs to PC and
18:2 is transferred from PC to reserve TAGs. At low temperature, 18:1
is desaturated to 18:2 thus allowing the enrichment of membrane lipids
with 18:2, the excess being stored in reserve TAGs. At high temperatu
re, however, and provided that oleate desaturase is repressed, the mem
brane lipids become enriched in 18:1 and the oil-body TAGs become enri
ched in 18:2.