Pathways of CO2 Fixation in the CAM Plant Kalanchoe daigremontiana. II* Effects of O2 and CO2 Concentration on Light and Dark CO2 Fixation

1975 ◽  
Vol 2 (2) ◽  
pp. 155
Author(s):  
C.B Osmond ◽  
O Bjorkman

Steady-state fixation of CO*2 by leaves of K. daigremontiana was examined at O*2 concentrations of 4, 20 and 36%. Oxygen concentration had no effect on the rate of dark CO*2 fixation, whereas CO*2 fixation in the light was substantially inhibited by 20 and 36% O*2. Dark CO*2 fixation showed a high affinity for CO*2 (half-saturated at about 3 �M at 16�C) whereas CO*2 fixation in the light showed a much lower affinity for CO*2 (half-saturated at about 9 �M at 16�C and 37 �M at 29�C). The inhibition by O*2 of CO*2 fixation in the light was observed at intercellular CO*2 pressures up to 850 �bar. It was associated with a positive CO*2 compensation point which was abolished in 4% O*2, and a post- illumination burst of CO*2 evolution which was not modified by low O*2. The response of dark and light CO*2 fixation in K. daigremontiana to O*2 concentration is discussed in comparison with photosynthetic CO*2 fixation in C*3 and C*4 plants.

1975 ◽  
Vol 53 (11) ◽  
pp. 1132-1138 ◽  
Author(s):  
E. Nalborczyk ◽  
L. J. Lacroix ◽  
R. D. Hill

The influence of day length, light quality, temperature, drought, and oxygen concentration on gas exchange of Kalanchoe daigremontiana was investigated. The ratio of photosynthesis to dark CO2 fixation with plants under a long-day and short-warm-night regime was 2.0 and under a short-day and long-cool-night regime, 0.2. With drought conditions this value may be less than 0.02. Under low oxygen concentrations high photosynthetic rates of about 20 mg CO2 dm−2 h−1 were observed with a compensation point of about 20 ppm. Restricting CO2 supply to dark periods produced plants with a δ13C value of −10.6‰. Restricting CO2 supply to light periods gave a δ13C value of −25.9‰, whereas no control of CO2 gave δ13C values of −15‰. The data obtained suggest that variations in δ13C values in Kalanchoe result from changes in the proportion of light and dark CO2 fixation.Far-red light and oxygen promoted the release of CO2 from Kalanchoe after the plants had undergone a period of dark CO2 fixation. Maximum release occurred within about 1 h. The effect could be reversed by removal of either far-red light or oxygen. Decreases in the acidity of the plants accompanied CO2 release, which indicated that decarboxylation of a C4 acid was the source of the CO2.


1981 ◽  
Vol 8 (6) ◽  
pp. 641
Author(s):  
E Medina ◽  
CB Osmond

Kalanchoe daigremontiana was grown at 25/15 and 34/24°C and net CO2 fixation and acid synthesis were measured at 8, 15 and 24°. The ratio of net dark CO2 fixation to acid accumulation was nearly 1 at all temperatures tested. Although the increased contribution of respiratory CO2 to total acid synthesis at high temperatures was demonstrated by incubating leaf discs in CO2-free air, it was not enough to account for the reduction of dark CO2 fixation. Plants grown at 25/15° temperature regime showed maximal rates of nocturnal acid accumulation at 15°, the rates decreasing markedly at 24°. Plants grown at 24/34° showed similar rates at 15 and 24°, but acid accumulation was significantly lower at 8°. Measurements of dark acid accumulation in CO2-free air indicated that 34/24° plants have reduced respiration rates in comparison with 25/15° plants. These observations are discussed in relation to hypotheses seeking to account for effects of temperature on crassulacean acid metabolism.


Molecules ◽  
2021 ◽  
Vol 26 (9) ◽  
pp. 2751
Author(s):  
Damian Jagleniec ◽  
Marcin Wilczek ◽  
Jan Romański

Combining three features—the high affinity of squaramides toward anions, cooperation in ion pair binding and preorganization of the binding domains in the tripodal platform—led to the effective receptor 2. The lack of at least one of these key elements in the structures of reference receptors 3 and 4 caused a lower affinity towards ion pairs. Receptor 2 was found to form an intramolecular network in wet chloroform, which changed into inorganic–organic associates after contact with ions and allowed salts to be extracted from an aqueous to an organic phase. The disparity in the binding mode of 2 with sulfates and with other monovalent anions led to the selective extraction of extremely hydrated sulfate anions in the presence of more lipophilic salts, thus overcoming the Hofmeister series.


1977 ◽  
Vol 55 (7) ◽  
pp. 706-713 ◽  
Author(s):  
Lars Chr. Petersen ◽  
Hans Degn ◽  
Peter Nicholls

1. Coupled, cytochrome-c-depleted ('stripped') rat liver mitochondria reducing oxygen in the presence of exogenous cytochrome c, with succinate or ascorbate as substrates, show marked declines in the steady-state reduction of cytochrome c in excess oxygen on addition of uncouplers. Calculated ratios of maximal turnover in the uncoupled state and in the energized state for the cytochrome c oxidase (EC 1.9.3.1) reaction lie between 3 and 6, as obtained with reconstituted oxidase-containing vesicles. The succinate-cytochrome c reductase activity in such mitochondria shows a smaller response to uncoupler than that of the oxidase.2. The respiration rates of uncoupled mitochondria oxidizing ascorbate in the presence of added cytochrome c follow a Michaelis–Menten relationship with respect to oxygen concentration, in accordance with the pattern found previously with the solubilized oxidase. But succinate oxidation tends to give nonlinear concave-upward double-reciprocal plots of respiration rate against oxygen concentration, in accordance with the pattern found previously with intact uncoupled mitochondria.3. From simultaneous measurements of cytochrome c steady-state reduction, respiration rate, and oxygen concentration during succinate oxidation under uncoupled conditions it is found that at full reduction of cytochrome c, apparent Km for oxygen is 0.9 μM and the maximal oxidase (aa3) turnover is 400 s−1 (pH 7.4, 30 °C).4. The redox state of cytochrome c in uncoupled systems reflects a simple steady state; the redox state of cytochrome c in energized systems tends towards an equilibrium condition with the terminal cytochrome a3, whose apparent potential under these conditions is more negative than that of cytochrome c.


1997 ◽  
Vol 17 (6) ◽  
pp. 2994-3004 ◽  
Author(s):  
M Kaouass ◽  
M Audette ◽  
D Ramotar ◽  
S Verma ◽  
D De Montigny ◽  
...  

Eukaryotic polyamine transport systems have not yet been characterized at the molecular level. We have used transposon mutagenesis to identify genes controlling polyamine transport in Saccharomyces cerevisiae. A haploid yeast strain was transformed with a genomic minitransposon- and lacZ-tagged library, and positive clones were selected for growth resistance to methylglyoxal bis(guanylhydrazone) (MGBG), a toxic polyamine analog. A 747-bp DNA fragment adjacent to the lacZ fusion gene rescued from one MGBG-resistant clone mapped to chromosome X within the coding region of a putative Ser/Thr protein kinase gene of previously unknown function (YJR059w, or STK2). A 304-amino-acid stretch comprising 11 of the 12 catalytic subdomains of Stk2p is approximately 83% homologous to the putative Pot1p/Kkt8p (Stk1p) protein kinase, a recently described activator of low-affinity spermine uptake in yeast. Saturable spermidine transport in stk2::lacZ mutants had an approximately fivefold-lower affinity and twofold-lower Vmax than in the parental strain. Transformation of stk2::lacZ cells with the STK2 gene cloned into a single-copy expression vector restored spermidine transport to wild-type levels. Single mutants lacking the catalytic kinase subdomains of STK1 exhibited normal parameters for the initial rate of spermidine transport but showed a time-dependent decrease in total polyamine accumulation and a low-level resistance to toxic polyamine analogs. Spermidine transport was repressed by prior incubation with exogenous spermidine. Exogenous polyamine deprivation also derepressed residual spermidine transport in stk2::lacZ mutants, but simultaneous disruption of STK1 and STK2 virtually abolished high-affinity spermidine transport under both repressed and derepressed conditions. On the other hand, putrescine uptake was also deficient in stk2::lacZ mutants but was not repressed by exogenous spermidine. Interestingly, stk2::lacZ mutants showed increased growth resistance to Li+ and Na+, suggesting a regulatory relationship between polyamine and monovalent inorganic cation transport. These results indicate that the putative STK2 Ser/Thr kinase gene is an essential determinant of high-affinity polyamine transport in yeast whereas its close homolog STK1 mostly affects a lower-affinity, low-capacity polyamine transport activity.


2003 ◽  
Vol 185 (16) ◽  
pp. 4748-4754 ◽  
Author(s):  
Daniel H. Broder ◽  
Charles G. Miller

ABSTRACT Extracts of a multiply peptidase-deficient (pepNABDPQTE iadA iaaA) Salmonella enterica serovar Typhimurium strain contain an aspartyl dipeptidase activity that is dependent on Mn2+. Purification of this activity followed by N-terminal sequencing of the protein suggested that the Mn2+-dependent peptidase is DapE (N-succinyl-l,l-diaminopimelate desuccinylase). A dapE chromosomal disruption was constructed and transduced into a multiply peptidase-deficient (MPD) strain. Crude extracts of this strain showed no aspartyl peptidase activity, and the strain failed to utilize Asp-Leu as a leucine source. The dapE gene was cloned into expression vectors in order to overproduce either the native protein (DapE) or a hexahistidine fusion protein (DapE-His6). Extracts of a strain carrying the plasmid overexpresssing native DapE in the MPD dapE background showed a 3,200-fold elevation of Mn2+-dependent aspartyl peptidase activity relative to the MPD dapE+ strain. In addition, purified DapE-His6 exhibited Mn2+-dependent peptidase activity toward aspartyl dipeptides. Growth of the MPD strain carrying a single genomic copy of dapE on Asp-Leu as a Leu source was slow but detectable. Overproduction of DapE in the MPD dapE strain allowed growth on Asp-Leu at a much faster rate. DapE was found to be specific for N-terminal aspartyl dipeptides: no N-terminal Glu, Met, or Leu peptides were hydrolyzed, nor were any peptides containing more than two amino acids. DapE is known to bind two divalent cations: one with high affinity and the other with lower affinity. Our data indicate that the form of DapE active as a peptidase contains Zn2+ in the high-affinity site and Mn2+ in the low-affinity site.


1966 ◽  
Vol 41 (5) ◽  
pp. 755-759 ◽  
Author(s):  
Walter E. Splittstoesser

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