Regulation of malic-acid metabolism in Crassulacean-acid-metabolism plants in the dark and light: In-vivo evidence from 13C-labeling patterns after 13CO2 fixation

Planta ◽  
1988 ◽  
Vol 175 (2) ◽  
pp. 184-192 ◽  
Author(s):  
C. B. Osmond ◽  
J. A. M. Holtum ◽  
M. H. O'Leary ◽  
C. Roeske ◽  
O. C. Wong ◽  
...  
2002 ◽  
Vol 29 (6) ◽  
pp. 749 ◽  
Author(s):  
Richard Haslam ◽  
Anne Borland ◽  
Howard Griffiths

This paper originates from a presentation at the IIIrd International Congress on Crassulacean Acid Metabolism, Cape Tribulation, Queensland, Australia, August 2001. The regulation and flexibility of the crassulacean acid metabolism (CAM) pathway has been investigated in the 'extreme epiphyte' Tillandsia usneoides (L.). Submerging strands of T. usneoides under water, thereby inhibiting the supply of atmospheric CO2, allowed non-invasive in vivo manipulation of the supply of CO2 during the nocturnal Phase I of CAM. Once the plants were removed from submersion, T. usneoides maintained open stomata, and net CO2 uptake occurred throughout most of the photoperiod. Variability in the expression of CAM allowed T. usneoides to compensate for restricted CO2 availability through Phase I of CAM by adjusting gas exchange rates through the photoperiod and subsequent dark period to maintain a constant internal supply of CO2 in the light. Furthermore, T. usneoides demonstrated a gradual, rather than rapid, change in phosphoenolpyruvate carboxylase (PEPC) activation across the day-night cycle, such that PEPC and Rubisco appear to work in tandem in order to maintain carbon balance for this extreme atmospheric bromeliad.


1982 ◽  
Vol 69 (2) ◽  
pp. 456-459 ◽  
Author(s):  
Christa Buser-Suter ◽  
Andres Wiemken ◽  
Philippe Matile

1996 ◽  
Vol 317 (3) ◽  
pp. 653-658 ◽  
Author(s):  
Robert P. WALKER ◽  
Richard C. LEEGOOD

We have previously shown that phosphoenolpyruvate carboxykinase (PEPCK) is phosphorylated in vivo in the cotyledons of darkened cucumber seedlings and that phosphorylation is reversed by light [Walker and Leegood (1995) FEBS Lett. 362, 70–74]. In this study the molecular mass of PEPCK was estimated in a range of gluconeogenic seedlings and in leaves of C4 plants and plants with Crassulacean acid metabolism (CAM). Phosphorylation of PEPCK was studied in these plants by feeding tissues with [32P]Pi and assessing phosphorylation by SDS/PAGE and autoradiography of either total proteins or of immunoprecipitated protein. In gluconeogenic seedlings and most CAM plants PEPCK had a molecular mass of 74 kDa, whereas in C4 grasses the molecular mass of PEPCK was always smaller and varied from 67–71 kDa. In all gluconeogenic seedlings and leaves of CAM plants PEPCK was phosphorylated, but it was not phosphorylated in all species of C4 grasses studied. In CAM plants, phosphorylation of PEPCK occurred at night and dephosphorylation occurred during the day. In C4 grasses phosphorylation occurred when leaves were darkened and the enzyme was dephosphorylated following illumination, but it was only phosphorylated in those plants with larger (71 kDa) molecular mass forms of PEPCK.


1975 ◽  
Vol 2 (3) ◽  
pp. 389 ◽  
Author(s):  
BG Sutton

Enzymes involved in the movement of carbon from glucan to malic acid in the crassulacean acid metabolism (CAM) plant, Kalanchoe daigremontiana were assayed. The kinetic characteristics determined for the enzymes from this plant were similar to those already known for the same enzymes from non-CAM tissue. °-Amylase activity could not be demonstrated in the CAM leaf and glucokinase activity was low. These results, together with a high level of phosphorylase, suggested that the latter enzyme was involved in trasfer of glucan breakdown products to glycolysis. The activity of pyruvate kinase was only 1.7% of the activity of phosphoenolpyruvate (PEP) carboxylase, suggesting that pyruvate production from PEP at night posed little drain on PEP supply for malic acid synthesis. Starch losses and glycolytic enzyme activities of non-CAM plants were sufficient to allow dark acidification comparable to that of CAM plants.


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