The effect of source or sink temperature on photosynthesis and 14C-partitioning in and export from a source leaf of Alstroemeria

The influence of source and sink temperature on leaf net C exchange rate (NCER), export, and partitioning in the C₃ monocotyledon Alstroemeria sp. cv. Jacqueline were examined. Leaf (i.e. source) temperature was varied between 12 and 35°C while source leaves were exposed to photorespiratory and nonphotorespiratory conditions during a 2-h steady-state ¹⁴CO₂ labelling period. Between 12 and 20°C, at ambient CO₂ and O₂, leaf NCER and export were similar with maximum rates of 9.71 ± 0.51 and 3.06 ± 0.36 μmol C m^-2 s^-1, respectively. Both NCER and export decreased above 20°C. At 35°C NCER was 30% of the rate at 20°C, but export was totally inhibited. Between 12 and 35°C, at the end of the 2-h feeding period, ¹⁴C was partitioned in the leaf as ethanol insolubles (3–10%), H₂O solubles (88–92%), and chloroform solubles (2–8%). However, above 25°C, less ¹⁴C was recovered in the starch fraction and more in the sugar fractions. At all temperatures, 86 to 94% of the labelled sugars was ¹⁴C-sucrose. In nonphotorespiratory conditions (i.e. 1 800 μI I^-1 CO₂ and 2% O₂). NCER and export were higher than the rates obtained at ambient CO₂ and O₂ at each temperature. Carbon dioxide enrichment sustained high NCER and export rates even at 35°C, Although CO₂ enrichment increased partitioning of ¹⁴C into starch, starch synthesis at 35°C was markedly reduced. Cooling the root-zone mass (i.e. a dominant sink) to 10°C, which simulated the commercial practice used to induce flowering, had no significant effect on source leaf NCER and export rates either during a 2-h steady-state labelling period or subsequently during a 21-h light-dark chase period. Furthermore, partitioning of ¹⁴C among leaf products at the end of the feed-chase period was not affected. Additional pulse and chase experiments using ¹¹CO₂ fed to source leaves of control and root-cooled plants showed that there was no difference in the direction of movement of ¹¹C-assimilates towards the flower or the root zone as a consequence of root cooling. Together, the data indicate that changing source strength, by manipulating photosynthesis and photorespiration, by varying the leaf temperature had a more profound effect on leaf export than manipulating sink activity.     

Changes in wheat DNA methylation pattern after chronic seed gamma-irradiation

Alterations of DNA methylation patterns of wheat two varieties--Odessa' albatross and Donetsk 48 have been studied. Seeds were irradiated for 4 months with low dose rate (3 x 10(-7) Gy/s). Six restriction endonucleases were used in the experiments. Primary distinction in DNA methylation patterns of the studied varieties has been demonstrated. The chronic irradiation resulted in the increase of methylation level on the sites of recognition for Glul and Sou3Al and in the decline of this index for the sites of recognition of GlaI and HpaII. The meaningful increase of chromosome aberration levels was demonstrated at the same accumulated dose of chronic irradiation. The role of changes of DNA methylation patterns in development of radiation damage and organism protective reactions is discussed.     

Enhancement of Ethylene Release from Leaf Tissue during Glycolate Decarboxylation : A Possible Role for Photorespiration

When leaf discs of Xanthium strumarium L. and Salvia splendens L. are incubated in sealed flasks in the light, more C₂H₄ gas is released in the presence of added CO₂ (30-200 millimolar NaHCO₃) than without CO₂. In Salvia, the maximum rate of C₂H₄ release occurs when sufficient CO₂ (above 125 millimolar NaHCO₃) is added to saturate photosynthesis confirming previous studies. The maximum rate of C₂H₄ release from illuminated discs is similar to the rate in the dark with or without CO₂ in both species. Glycolate enhances a CO₂-dependent C₂H₄ evolution from illuminated leaf discs. However, the maximum rate of C₂H₄ release with glycolate is the same as that observed with saturating CO₂. When photosynthesis is inhibited by darkness or by 3-(3,4-dichlorophenyl)-1,1-dimethylurea, glycolate has no effect.

Studies with [2,3-¹⁴C]-1-aminocyclopropane-1-carboxylic acid (ACC) show that the pattern of C₂H₄ release and the specific activity of the ¹⁴C₂H₄ in the presence and absence of glycolate is similar to that described above, indicating that glycolate does not alter uptake of the exogenously supplied precursor (ACC) or stimulate C₂H₄ release from an endogenous source at appreciable rates. Glycolate oxidase in vitro generates H₂O₂ which stimulates a slow breakdown of ACC to C₂H₄, but since exogenous glycolate is oxidized to CO₂ in both the light and the dark it is argued that the glycolate-dependent increase in C₂H₄ release from illuminated leaf discs is not mediated directly by the action of enzymes of glycolate catabolism. The effects of glycolate and CO₂ are not easily explained by changes in stomatal resistance. The data support the view that glycolate decarboxylation at subsaturating levels of CO₂ in the light stimulates C₂H₄ release by raising the CO₂ level in the tissue.

     

Effect of Oxygen Concentration on C-Photoassimilate Transport from Leaves of Salvia splendens L

Partitioning and transport of recently fixed photosynthate was examined following ¹⁴CO₂ pulse-labeling of intact, attached leaves of Salvia splendens L. maintained in an atmosphere of 300 microliters per liter CO₂ and 20, 210, or 500 milliliters per liter O₂. Under conditions of increasing O₂ (210, 500 milliliters per liter), a smaller percentage of the recently fixed ¹⁴C in the leaf was allocated to starch, whereas a greater percentage of the fixed ¹⁴C appeared in amino acids, particularly serine. The increase in ¹⁴C in amino acids was reflected in material exported from source leaves. A higher percentage of ¹⁴C in serine, glycine, and glutamate was recovered in petiole extracts when source leaves were maintained under elevated O₂ levels. Although pool sizes of these amino acids were increased in both the leaves and petioles with increasing photorespiratory activity, no significant changes in either ¹⁴C distribution or concentration of transport sugars (i.e. stachyose, sucrose, verbascose) were observed. The data indicate that, in addition to being recycled intracellularly into Calvin cycle intermediates, amino acids produced during photorespiration may also serve as transport metabolites, allowing the mobilization of both carbon and nitrogen from the leaf under conditions of limited photosynthesis.     

Critical level of radiation damage of root apical meristem and mechanisms for its recovery in Pisum sativum L

The dose dependencies of growth and cytogenetical values have been built to determine the critical level of root apical meristem damage induced by cute irradiation in the range from 2 to 20 Gr. We have analyzed the frequencies of aberrant anaphases and the aberration distribution per cell, on the one hand, and the growth of biomass, the survival and regeneration of the root meristem, on the other hand. The critical level of damage to the stem apical meristem and root of seedlings was defined as 44-48% of aberrant anaphase. Exceeding of this level leads to the launch of suicidal program through induction of multiaberrant damages and interphase cell death. It appears that competition of clones of non-aberrant cells, the cells bearing 1 and 2 damages and multiaberrant cells plays the primary role in the mechanisms of recovery. The regeneration provides full or partial restoration of the main root apical meristem. However these local processes are insufficient to restore morphogenesis and survival of seedlings in excess of the critical level damage.