Carbonic Anhydrase: Mechanism, Structure and Importance in Higher Plants
Carbonic Anhydrase: Mechanism, Structure and Importance in Higher Plants
Carbonic Anhydrase: Mechanism, Structure and Importance in Higher Plants
INTRODUCTION
Carbonic anhydrase is a ubiquitous zinc-metalloenzyme important for photosynthesis
because of its property to convert CO2 to HCO3- reversibly. The occurrence of carbonic
anhydrase in plants was confirmed by Bradfield in 1947. The rate of photosynthesis and
CO2 fixation gets directly affected due to any change in the activity of carbonic anhydrase.
It is the only carbon metabolism enzyme which shows fluctuations in the activity among
different species with varying CO2 concentration in the environment. Carbonic anhydrase
is one of the fastest enzymes known for hydrating 106 molecules of CO2 per second. The
rate of reaction of this enzyme is typically limited by the rate of diffusion of its substrates.
In leaves of C3 plants the enzyme represents 1% to 2% concentration of the total soluble
protein, second only to RuBisCO in concentration. About 86% to 95% of the total carbonic
anhydrase is found in chloroplasts, while the rest is completely restricted to the cytosol of
mesophyll cells. A correlation was found by Khan between carbonic anhydrase activity
and photosynthetic rate suggesting that the enzyme serves as a biochemical marker for
productivity as this helps in carbon sequestration. The activity of Carbonic anhydrase is
mainly keeping up by light, Zn and CO2 concentration. This enzyme provides the supply
of CO2 to the phosphoenolpyruvate carboxylase in C4 and Crassulacean Acid Metabolism
(CAM) plants and RuBisCO in Calvin-Benson cycle (C3 plants) (Figure 1). Carbonic
anhydrase is concerned in a mixture of physiological processes. The present review,
however, lays emphasis on recent aspects of carbonic anhydrase in higher plants.
Structure
Carbonic Anhydrase structures are unique and are evolutionary characterized into
dissimilar classes, such as alpha anhydrases (α), beta anhydrases (β), gamma anhydrases
(γ) and delta anhydrases (δ). These are found majorly, whereas, there also exist two more
class of anhydrases called epsilon anhydrases (ε) and zeta anhydrases (ζ), which are limited
to the bacterial kingdom and protists, respectively. The α-class is found throughout the
animal kingdom, in the periplasm. The ɑ-carbonic anhydrases were widely identified in
vertebrates, algae and in eubacteria as reported by Chirica et al. The β-carbonic ahydrases
are mostly found in higher plants; micro-algae; Eubacteria; Archaebacteria; Cyanobacteria
2
and Fungi. The γ-carbonic anhydrases are discovered in the algae. δ-carbonic anhydrases
have only been described in some diatoms. The δ-carbonic anhydrase families appears to
be a case of convergent evolution with almost no sequence similarity with the ɑ-, β- or γ-
carbonic anhydrase types. ε-carbonic anhydrase is part of the carboxysome shell and has
additional domains that serve the function in bacteria. ζ-carbonic anhydrase is limited to
maline protists and resembles the β-carbonic anhydrase family, with other metals such as
Cd or Co substitute for Zn.
Figure 1: A generic model for the operation of a CCM showing the potential roles of CA
in the process
Isozymes
Isozymes or isoenzymes are basically enzymes that only differ in the sequences of amino
acid but catalyze the same chemical reaction. Carbonic anhydrase has various isozymes
that play a great role in various physiological processes of higher plants.
For the activation of catalytic site, water bounds to Zn, which can be ionized to form a
hydroxide bridge (carbonic anhydrase), polarized by a base to generate nucleophilic
catalysis or displaced by the substrate (Figure 2).
Higher plants show similarity between cytoplasmic and chloroplastic carbonic anhydrases
in kinetic properties, affinity for CO2 and sensitivity to inhibitors. It has been shown that
from the purification of the Solanum cytosolic isoform that it is structurally and
biochemically similar to the chloroplastic form, although its monomeric mass is larger. The
difference of expression between cytoplasm and chloroplast carbonic anhydrase because
difference of promoter region between the two kinds of carbonic anhydrases. The
bicarbonate (HCO3–) pools are maintained by cytoplastic carbonic anhydrases, and
compensate leakage of free CO2 from the cytoplasm. Chloroplast carbonic anhydrases
appear to be associated with other enzymes of the Calvin cycle in a large multienzyme
complex. Chloroplast fraction in C3 is associate with the carbonic anhydrase activity, there
are at least 10 to 15% of the total activity is cytoplastic.
gas and ion exchange, the provision of bicarbonate for anaplerotic reactions, and
fatty acid biosynthesis.
The increased amount of two carbonic anhydrases identified with MALDI-TOF MS
could be involved in freezing tolerance during cold acclimation in the purified
plasma membrane fraction from Arabidopsis leaves.
There is evidence that during the immune response of plants to pathogens, carbonic
anhydrase plays a very important role, acting as a salicylic acid binding protein3
(SABP3). Experimentally, this dual activity of chloroplastic carbonic anhydrases
has been observed in tobacco. Finally, the carbonic anhydrase function in plant
immunity has been defined enigmatically as oxidative stress protection.
CONCLUSION
Carbonic anhydrase plays critical role in all photosynthetic CO2 concentrating
mechanisms. Carbon dioxide being main culprit behind the global warming is cause of
concern for present generation as well as for the future generations. Therefore, need of hour
is to think of the present and sustaining of the future. This review attempts to present a
picture of the physiological role of carbonic anhydrase in plants, in the fixation of
greenhouse gas like CO2 from the atmosphere and its role as biochemical marker for carbon
sequestration.
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