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      Crassulacean acid metabolism: plastic, fantastic

      , , , ,
      Journal of Experimental Botany
      Oxford University Press (OUP)

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          Abstract

          The occurrence, activity and plasticity of the CAM pathway is described from an introductory viewpoint, framed by the use of the four "Phases" of CAM as comparative indicators of the interplay between environmental constraints and internal molecular and biochemical regulation. Having described a number of "rules" which seem to govern the CAM cycle and apply uniformly to most species, a number of key regulatory points can then be identified. These include temporal separation of carboxylases, based on the circadian expression of key genes and their control by metabolites. The role of a circadian oscillator and interplay between tonoplast and nuclear control are central to maintaining the CAM cycle. Control of reserve carbohydrates is often neglected, but the importance of daily partitioning (for growth and the subsequent night-time CAM activity) and use at night is shown to drive the CAM cycle. Finally, it is shown that the genotypic and phenotypic plasticity in patterns of CAM expression is mediated partly by environmental conditions and molecular signalling, but also by diffusive constraints in succulent tissues. A transformation system is now required to allow these key areas of control to be elucidated.

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          Most cited references75

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          Crassulacean Acid Metabolism: A Curiosity in Context

          C B Osmond (1978)
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            Mechanism of light regulation of Rubisco: a specific role for the larger Rubisco activase isoform involving reductive activation by thioredoxin-f.

            Rubisco activase is a nuclear-encoded chloroplast protein that is required for the light activation of ribulose 1,5-bisphosphate carboxylase/oxygenase (Rubisco) in vivo. In most plants examined to date, there are two isoforms of Rubisco activase arising from alternative splicing that differ only at the carboxyl terminus. Here we demonstrate with recombinant proteins that in Arabidopsis the larger isoform has a unique role in the regulation of Rubisco activity. At physiological ratios of ADP/ATP, the 46-kDa isoform has minimal ATP hydrolysis and Rubisco activation activity in comparison with the 43-kDa isoform. Analysis of a series of carboxyl-terminal deletion and Ala substitution mutants of the 46-kDa isoform revealed that the presence of Cys residues at positions 411 and 392 were essential to preserve a low ATP hydrolysis and Rubisco activation activity in the presence of ADP. Consequently, incubation of the 46-kDa isoform with DTT and thioredoxin-f increased both activities, whereas incubations with DTT alone or with thioredoxin-m were ineffective. Thioredoxin-f and DTT had no effect on the 43-kDa isoform. However, premixing both isoforms before conducting a reduction and oxidation cycle demonstrated that the activity of both isoforms could be regulated. Reduction and oxidation also modulated the activity of native activase proteins isolated from either Arabidopsis or spinach, but not tobacco, which only has the smaller isoform. These findings suggest that in plants containing both isoforms, Rubisco activase regulates the activity of Rubisco in response to light-induced changes in both the ADP/ATP ratio and the redox potential via thioredoxin-f.
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              Crassulacean acid metabolism in australian vascular epiphytes and some related species.

              The occurrence of crassulacean acid metabolism (CAM) among epiphytes and related plant species from tropical and subtropical rainforests in Eastern Australia was investigated. As judged from δ(13)C value and the absence of Kranz anatomy, indications of CAM were found in 66 species belonging to the families, Polypodiaceae (3), Orchidaceae (55), Asclepiadaceae (6) and Rubiaceae (2).Two thirds of orchidaceous plants examined appeared to use CAM. Those species with thicker leaves generally had less negative δ(13)C values, as did those species growing on more exposed sites; leaves thicker than about 1 mm in most species yielded δ(13)C values indicative of pronounced CAM. Two leafless species, Chiloschista phyllorhiza and Taeniophyllum malianum, which depend on chloroplast-containing, stomata-less roots for photosynthesis also showed δ(13)C values typical of CAM. Pseudobulbs and swollen stems, a characteristic of many orchids, were usually somewhat enriched in (13)C compared to corresponding leaves.In Polypodiaceae CAM was found in the genus Pyrrosia. While δ(13)C values were generally less negative with increasing frond thickness, the leaf morphology was extremely variable within species. Pyrrosia confluens plants from shaded habitats had long, relatively thin and darkgreen fronds whereas specimens from sun-exposed sites were characterized by short, thick, bleached fronds. Both types showed the capacity for nocturnal accumulation of titratable acidity and exhibited continuous net CO2 fixation during 12 h light/12 h dark cycles under laboratory conditions. Shade-fronds showed this capacity even when irradiance was lower than 2% of full sunlight during the 12 h light period.In Asclepiadaceae CAM was found in species of two genera which usually have fleshy leaves, Hoya and Dischidia. In Rubiaceae CAM was recorded in two genera of epiphytic ant plants, Hydnophytum and Myrmecodia.It is concluded that CAM is widespread in Australian epiphytes. It is most prevalent in species found in exposed microhabitats where the growing conditions are characterised by relatively high light intensities and short but frequent periods of water stress.
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                Author and article information

                Journal
                Journal of Experimental Botany
                Oxford University Press (OUP)
                1460-2431
                0022-0957
                April 1 2002
                April 01 2002
                April 1 2002
                April 1 2002
                April 01 2002
                April 1 2002
                : 53
                : 369
                : 569-580
                Article
                10.1093/jexbot/53.369.569
                a75bb54e-0caa-416c-a57e-12589090911c
                © 2002
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