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Results
Significant differences were observed in the net photosynthetic
rates among the seven genotypes of triticale (Table
1). 6A-1093
consistently maintained highest photosynthetic rates (25.8 micromole
m-2s-l) at an irradiance of 1500 micro-moI
m-2s-1 followed by 801/1208 (23.2 micromole
m-2s-1).
The activity of RuBP carboxylase in leaf extracts was significantly
correlated with net photosynthetic rates. The leaves of 6A-1093
recorded highest enzyme activity (298.6 micromole mg-1 chl
hr-1) while the lowest activity was noticed in 6A-854
(Table
1). However there
was no significant difference in the leaf chlorophyll content among
seven triticale genotypes (Table
1). The kinetic
characteristics of RuBP carboxylase in leaf extracts were compared in
Table
2. The Km
(CO2) values of the enzyme were significantly low (8.36
microM) with corresponding high Vmax values (28.95
micromole
kg-1 prot s-1) in the leaves of 6A-1093. The
highest Km (CO2) and lowest Vmax values were obtained in
the leaves of 6A-854 (Table 2).
Discussion
The present findings provide a strong correlation between the net
CO2 assimilation rates and RuBP carboxylase activity
(Table 1). The results clearly show that
the differences in the CO2 assimilation rates were due to
the differences in the levels of RuBP carboxylase in leaves. The
rates of net photosynthesis and RuBP carboxylase activity were highly
correlated (r=0.93, P< 0.001) and the linear regression equation
of net photosynthesis on RuBP carboxylase activity was Y=9.05+8.45X.
The positive correlation between net photosynthetic rates and RuBP
carboxylase activity has been previously reported (Seeman and Berry
1982; Evans and Seeman 1984; Ramachandra Reddy and Das 1986). It is
suggested that the differences in the in vivo activity of RuBP
carboxylase in the leaves of triticale may also affect CO2
assimilation.
The superior photosynthetic rates in 6A-1093 among the genotypes used
in this study were presumed to be due to its efficient carboxylation
capacities as evidenced by lower Km (CO2) and high Vmax
values of RuBP corboxylase in leaf extracts. The Km (CO2)
values reported for triticale are comparable to those reported for
certain other C3 plants (Bird et al. 1982; Jordan and
Ogren 1983; Makino et al. 1985; Ramachandra Reddy and Das 1986; Paul
and Yeoh 1988). It is plausible that the genotypes with superior
photosynthetic performance would be highly useful in selecting
photosynthetically efficient triticale cultivars for obtaining
greater photosynthetic productivity. The in vitro kinetic
characteristics of RuBP carboxylase can be one of the useful targets
to obtain greater CO2 assimilation capacity in triticale.
The significant differences in the catalytic properties of RuBP
carboxylase also suggest that it might be possible to improve the
photosynthetic performance of certain triticale genotypes through
genetic manipulation of this enzyme.
Acknowledgements
Grateful thanks are due to Dr. J.P. Gustafson, University of
Missouri, Columbia, U.S.A. and Dr. T. Wolski, Triticale Breeding
Station, Warsaw, Poland for the supply of genetic stocks.
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