Hr. Singal et al., POD PHOTOSYNTHESIS AND SEED DARK CO2 FIXATION SUPPORT OIL SYNTHESIS IN DEVELOPING BRASSICA SEEDS, Journal of Biosciences, 20(1), 1995, pp. 49-58
Rate of photosynthesis and activities of photosynthetic carbon reducti
on cycle enzymes were determined in pods (siliqua), whereas rate of da
rk CO2 fixation, oil content and activities of enzymes involved in dar
k CO2 metabolism were measured in seeds of Brassica campestris L. cv.
Toria at different stages of pod/seed development. The period between
14 and 35 days after anthesis corresponded to active phase of seed dev
elopment during which period, seed dry weight and oil content increase
d sharply. Rate of pod photosynthesis and activities of photosynthetic
carbon reduction cycle enzymes were maximum in younger pods but suffi
ciently high levels were retained up to 40 days after anthesis. The ra
te of dark (CO2)-C-14 fixation in seeds increased up to 21 days after
anthesis and declined thereafter but maintaining sufficiently high rat
es till 35 days after anthesis. Similarly various enzymes viz., phosph
oenolpyruvate carboxylase, NAD(+)-malate dehydrogenase and NADP(+)-mal
ic enzyme, involved in dark CO2 metabolism retained sufficient activit
ies during the above period. These enzyme activities were more than ad
equate to maintain the desired supply of malate which mainly arises fr
om dark CO2 fixation in seeds and further translocated to leucoplasts
for onward synthesis of fatty acids. Enzyme localization experiments r
evealed phosphoenolpyruvate carboxylase and enzymes of sucrose metabol
ism to be present only in cytosol, whereas enzymes of glycolysis were
present both in cytosolic and leucoplastic fractions. These results in
dicated that oil synthesis in developing Brassica seeds is supported b
y pod photosynthesis and dark CO2 fixation in seeds as the former serv
es as the source of sucrose and the latter as a source of malate.