Water Conservation in Kalanchoe blossfeldiana in Relation to Carbon Dioxide Dark Fixation

The succulent Kalanchoe blossfeldiana v. Poel. var Tom Thumb was treated on long and short photoperiods for 6 weeks during which short day plants developed thicker leaves, flowered prolifically, and exhibited extensive net dark fixation of carbon dioxide. In contrast, long day plants remained vegetative and did not develop thicker leaves or exhibit net carbon dioxide dark fixation. When examined after the photoperiodic state described, long day plants showed approximately three times more water loss over a 10-day period than short day plants. Water loss is similar during light and dark periods for short day plants but long day plants exhibited two times more water loss during the day than at night. The latter plants also lost three and one-half times more water during the light period than short day plants. The water conservation by short day plants is correlated with conditions of high carbon dioxide dark fixation and effects of its related Crassulacean acid metabolism on stomatal behavior.     

Carbon Dioxide Fixation in Neuronal and Astroglial Cells in Culture

The concentration of potassium in the extracellular fluid has been found to stimulate the rate of CO2 fixation by astroglial cells grown in primary culture. Raising the concentration of extracellular potassium increased both the initial rate of formation of the 14C-labeled products of 14CO2 fixation and the final steady-state level of these products within the cells. In contrast, neither veratridine nor L-glutamate affected the rate of CO2 fixation in astroglial cells. The very low rate of CO2 fixation found in primarily neuronal cultures was unaffected by increased extracellular potassium as was CO2 fixation in fibroblasts. When cultured alone, astroglial cells release a large fraction of the 14C-labeled products of CO2 fixation into the surrounding medium. Mixed cultures of astroglia and neurons also fix CO2 but, in contrast to astroglia cultured alone, release only a small fraction of the 14C-labeled products into the culture medium.     

Studies on Dark Fixation of Carbon Dioxide in Kalanchoe: I. Effect of Water Stress and Growth Retardants

Rooted cuttings of Kalanchoë blossfeldiana cv. Feuer Bluteand K. crenatum failed to show a net dark CO₂ fixation whenraised in dilute nutrient solution. Dark CO₂ fixation (CAM)in these plants was initiated either by increasing the soluteconcentration or lowering the water potential of the nutrientsolution by addition of mannitol (0.11 M and 0.25 M) and carbowax4000 (0.16 M and 0.3 M). Initiation was also brought about byspraying the leaves with B-9 (N,dimethylamino-succinamicacid,300mg1^–1) or by addition of CCC (2 chloroethyl trimethylammonium chloride, 300 or 750 mg1^–1) to the nutrient medium.Failure of CAM in dilute solution was suggested to be due tolack of accumulation of photosynthates in the leaves. Waterstress and growth retardants brought about reduction of monilizationand/or translocation thereby leading to accumulation of assimilatesin the leaves and to initiation of dark CO₂ fixation.     

Resolution of Net Dark Fixation of Carbon Dioxide into Its Respiration and Gross Fixation Components in Bryophyllum daigremontianum

Dark respiration rate increased with temperature between 10and 24°C (Q₁₀ =2.3–2.7). The rate of gross dark CO₂fixation (GDF) was affected by temperature, but irregularly.Cumulative GDF was not affected by temperature in this range.Cumulative respiration increased from 17 per cent of cumulativeGDF at 10°C, to 72 per cent at 24°C and was thus responsiblefor the 65 per cent drop in net dark fixation between thesetwo temperatures. and respiration rates were functions of the light intensityin the preceding light period. The function for cumulativeGDFwas of the saturation form, maximum accumulation being obtainedat 12 mW cm^–2. It is concluded that both GDF and respirationrates depend on levels of substrates formed during the lightperiod. However, the rate of GDF did not appear to be directlyrelated to the rate of respiration.     

Dark Carbon Dioxide Fixation under Aerobic and Anaerobic Conditions in Maize Leaves after Preillumination in the Absence of Oxygen: Ribulose 1,5-Bisphosphate Can Serve as a Primary Acceptor of Carbon Dioxide

When dark ¹⁴CO₂ fixation in maize leaves was carried out under anaerobic conditions after preillumination in the absence of O₂, the ¹⁴C incorporation in aspartic acid was transient; its maximum level was very low compared with that of malic acid. The addition of 5% O₂ during the dark fixation period increased the total uptake of ¹⁴CO₂ and the ¹⁴C incorporation into aspartic acid.     

Enhanced Dark Carbon Dioxide Fixation in Maize: Effect of the Oxygen Concentration during Preillumination on CO(2) Uptake and the Intramolecular Labeling Pattern of Malate and Aspartate

The enhanced dark CO₂ uptake after a preillumination period under varying O₂ concentrations has been measured with maize, a C₄ plant. For comparison the same study has been conducted with tomato, a C₃ plant. Increasing the O₂ concentration during preillumination inhibits by 70% the subsequent dark CO₂ uptake in tomato but stimulates 2-fold this CO₂ uptake in maize. The O₂ enhancement of CO₂ uptake in maize is due to the enhancement of malate and aspartate synthesis. The percentages of radioactivity incorporated in the C-4 of malate and aspartate vary from 74 to 87% when O₂ concentration during preillumination is increased from 0 to 100%.     

Carbon Dioxide Fixation by Cells of Streptococcus faecalis var. liquefaciens

Fixation of NaH(14)CO(3) by a heavy cell suspension of Streptococcus faecalis var. liquefaciens was studied. Several nutrients, pyridoxal, riboflavine, adenine, uracil, and O(2) stimulated (14)CO(2) incorporation into cells only under conditions that were adequate for synthesis of cell macromolecules. Biotin increased CO(2) incorporation in the absence of extensive synthesis of macromolecules, whereas O(2) inhibited incorporation under these conditions. When (14)CO(2) fixation was occurring during synthesis of macromolecules, 71% of the (14)C was incorporated into cells and 29% occurred extracellularly. Ninety-three per cent of the cellular (14)C was in protein and 5.5% was in nucleic acid. Aspartic acid was the only amino acid in the protein fraction that was radioactive. Eighty-three per cent of the extracellular (14)C was resistant to precipitation by trichloroacetic acid. When (14)CO(2) fixation was occurring in cells that were not carrying on extensive synthesis of macromolecules, 38% of the (14)C was incorporated into cells and 59% occurred in the supernatant fluid. Sixty-nine per cent of the cellular (14)C was in protein, 21% was in low-molecular-weight compounds, and 9% was in nucleic acid. Addition of unlabeled aspartate to the medium inhibited incorporation of (14)CO(2). Based on studies of the rate of (14)CO(2) fixation, the cells fix CO(2) into a pool of intermediates which are either used for synthesis, primarily protein, or are excreted into the medium.     

Carbon Dioxide Fixation by Barley Roots

The non-volatile, 80 per cent.ethanol-soluble products of fixationhave been investigated in excised roots, using C^14O₂ and radiochromatography. The main radioactive compounds separated were malic, citric(or iso-citric), aspartic, and glutamic acids, asparagine andglutamine. Less activity was present in serine, tyrosine, -ketoglutaricacid, and alanine, and in a number of unidentified compounds. The uptake of C^14O₂ was inhibited by virtually anaerobic conditions. From the above observations it is considered likely that C¹⁴is transformed through the reactions of the tricarboxylic acidcycle. C¹⁴ in the soluble fraction was markedly increased by maintainingthe root material in water rather than in a nutrient solutionprior to exposure to C^14O₂ This increase was chiefly in malicacid.     

Studies on Dark Fixation of Carbon Dioxide in Kalanchoe: II. Effect of Interaction of Photoperiodic Induction with Water Stress and Growth Retardants

In Kalanchoë blossfeldiana von Poellnitz cv. Tom Thumband cv. Feuer Blute interaction of CO₂ fixation with photoperiodicinduction and water stress was examined. It was found that TomThumb raised in dilute culture solution and kept in photoinductivecycles (8 h light and 16 h dark) flowered but failed to showa net dark CO₂ fixation. A net dark fixation was observed whenthe concentration of the culture solution was increased or plantswere sprayed with 300 or 750 mg 1^–1 CCC or 300 or 2000mg 1^–1 B-9. In a non-inductive photoperiod no net darkfixation was observed with these treatments although there wasa tendency for dark fixation to increase. Feuer Blute did not flower in inductive photoperiods when keptin half strength solution. It is suggested that in Tom Thumbboth photoperiodic induction and water stress are required forinitiation of net CO₂ dark fixation. In Feuer Blute where CAMis occurring normally photo-induction is sufficient to induceflowering. In half strength solution CO2 dark fixation is disturbedand floral induction also does not occur.     

Effect of Different Carbon Sources on the Ammonium Induction of Different Forms of NADP-Specific Glutamate Dehydrogenase in Chlorella sorokiniana Cells Cultured in the Light and Dark

The ammonium induction of the chloroplast-localized NADP-specific glutamate dehydrogenase (NADP-GDH) was shown not to be a light-dependent process per se in Chlorella sorokiniana. In the dark without exogenous organic substrates, the cells synthesized low levels of fully active NADP-GDH, provided endogenous starch reserves had not been depleted. When cells were supplied with exogenous acetate, the rate of induction of NADP-GDH activity per milliliter of culture in the dark was equal to or slightly greater than the rate observed under photosynthetic conditions without an organic carbon source. Glucose supported only a low rate of induction of NADP-GDH activity in the dark. Both acetate and glucose inhibited induction of enzyme activity in the light. The NADP-GDH holoenzyme had at least 7 different electrophoretic forms. These forms differed in net charge and/or molecular weight. Their difference in molecular weight was due to the presence of 2 subunits with similar antigenic properties but different molecular weights (M_r = 55,500 and 53,000; α-and β-subunits, respectively). Depending upon the cultural conditions and length of the induction period, a wide variation was observed in the α:β subunit ratio and in the numbers and sizes of the NADP-GDH holoenzymes.     

Transport and Fixation of Inorganic Carbon in the Cells of Chlorella vulgaris 11h Grown under Ordinary Air

Intracellular accumulation of inorganic carbon (C_i) and itsfixation in photosynthesis were investigated using siliconeoil layer filtering centrifugation technique with the cellsof Chlorella vulgaris 11h grown under ordinary air. Both CO₂and HCO₃^– were transported into the cells from the reactionmedium and accumulated in the cells, but the rate of transportwas much faster for the former than the latter. ¹⁴C-fixationfrom the total transported C_i was much more efficient when CO₂was added in the external medium than when HCO₃^– was added.This indicates that CO₂ and HCO₃^– were not converted tothe common compound in the cells during the initial period ofphotosynthesis. Accumulation of Cⁱ into the cells was much lesssusceptible to low temperature than its fixation. Accumulationof Cⁱ was also observed in the dark. Ethoxyzolamide, an inhibitorof carbonic anhydrase (CA), inhibited the fixation of accumulatedCO₂ in the cells, suggesting that CA enhanced the supply ofCO₂ to the reaction site of ribulose bisphosphate carboxylasein the stroma. Mechanism for transport and fixation of Cⁱ duringphotosynthesis in low-CO₂ cells of C. vulgaris 1lh was proposedfrom these results. (Received March 19, 1986; Accepted June 26, 1986)     

Pre-illumination as a Factor in the Dark Fixation of Carbon Dioxide by Leaf Disks of Kalanchoe blossfeldiana var. Feuer Blute

Dark fixation of CO₂ by leaf disks or whole leaves taken fromplants of variety ‘Feuer Blute’ was measured using¹⁴CO₂. Results indicate that dark fixation by leaf disks isindependent of photoperiodic induction of the plant, but isquantitatively related to the amount of light, over a fairlywide range, to which the leaf is exposed in the single precedinglight period.     

Effect of Ammonia on Dark CO2 Fixation by Anabaena Cells Treated with Methionine Sulfoximine

Dark CO₂ fixation by Anabaena cylindrica was stimulated aboutthree-fold by the addition of NH₄Cl to the cells. The ¹⁴CO₂incorporation experiments showed that ¹⁴C is most rapidly incorporatedinto aspartate and then glutamine by adding NH4CI. Glutamineaccumulated predominantly after the addition of NH₄Cl showingthat NH₄ is incorporated into glutamine by glutamine synthetase.The stimulating effect of NH4Cl on CO₂ fixation and amino acidsynthesis was suppressed by methionine sulfoximine, an inhibitorof glutamine synthetase. It was suggested that dark CO₂ fixationwas stimulated by the action of glutamine synthesis which isenhanced by ammonia. (Received February 10, 1981; Accepted April 2, 1981)     

Nitrogen Fixation and Carbon Dioxide Assimilation in Rhizobium japonicum

In free-living Rhizobium japonicum cultures, the stimulatory effect of CO₂ on nitrogenase (acetylene reduction) activity was mediated through ribulose bisphosphate carboxylase activity. Two mutant strains (CJ5 and CJ6) of R. japonicum defective in CO₂ fixation were isolated by mitomycin C treatment. No ribulose bisphosphate carboxylase activity could be detected in strain CJ6, but a low level of enzyme activity was present in strain CJ5. Mutant strain CJ5 also exhibited pleiotropic effects on carbon metabolism. The mutant strains possessed reduced levels of hydrogen uptake, formate dehydrogenase, and phosphoribulokinase activities, which indicated a regulatory relationship between these enzymes. The CO₂-dependent stimulation of nitrogenase activity was not observed in the mutant strains. Both mutant strains nodulated soybean plants and fixed nitrogen at rates comparable to that of the wild-type strain.     

Dark Carbon Fixation: An Important Process in Lake Sediments

Close to redox boundaries, dark carbon fixation by chemoautotrophic bacteria may be a large contributor to overall carbon fixation. Still, little is known about the relative importance of this process in lake systems, in spite the potentially high chemoautotrophic potential of lake sediments. We compared rates of dark carbon fixation, bacterial production and oxygen consumption in sediments from four Swedish boreal and seven tropical Brazilian lakes. Rates were highly variable and dark carbon fixation amounted up to 80% of the total heterotrophic bacterial production. The results indicate that non-photosynthetic carbon fixation can represent a substantial contribution to bacterial biomass production, especially in sediments with low organic matter content.