1. Intracellular β-Carbonic Anhydrase of the Unicellular Green Alga Coccomyxa1 : Cloning of the cDNA and Characterization of the Functional Enzyme Overexpressed in Escherichia coli
- Author
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Hiltonen, Thomas, Björkbacka, Harry, Forsman, Cecilia, Clarke, Adrian K., and Samuelsson, Göran
- Subjects
DNA, Complementary ,Sequence Homology, Amino Acid ,Molecular Sequence Data ,Cell Fractionation ,Protein Structure, Secondary ,Recombinant Proteins ,Kinetics ,Chlorophyta ,Escherichia coli ,Amino Acid Sequence ,Cloning, Molecular ,Oxidation-Reduction ,Research Article ,Carbonic Anhydrases - Abstract
Carbonic anhydrase (CA) (EC 4.2.1.1) enzymes catalyze the reversible hydration of CO2, a reaction that is important in many physiological processes. We have cloned and sequenced a full-length cDNA encoding an intracellular β-CA from the unicellular green alga Coccomyxa. Nucleotide sequence data show that the isolated cDNA contains an open reading frame encoding a polypeptide of 227 amino acids. The predicted polypeptide is similar to β-type CAs from Escherichia coli and higher plants, with an identity of 26% to 30%. The Coccomyxa cDNA was overexpressed in E. coli, and the enzyme was purified and biochemically characterized. The mature protein is a homotetramer with an estimated molecular mass of 100 kD. The CO2-hydration activity of the Coccomyxa enzyme is comparable with that of the pea homolog. However, the activity of Coccomyxa CA is largely insensitive to oxidative conditions, in contrast to similar enzymes from most higher plants. Fractionation studies further showed that Coccomyxa CA is extrachloroplastic.
- Published
- 1998