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Purification and characterisation of an intracellular carbonic anhydrase from the unicellular green alga Coccomyxa.
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1995 (English)In: Planta, ISSN 0032-0935, E-ISSN 1432-2048, Vol. 195, no 3, 345-51 p.Article in journal (Refereed) Published
Abstract [en]

An intracellular carbonic anhydrase (CA; EC 4.2.1.1) was purified and characterised from the unicellular green alga Coccomyxa sp. Initial studies showed that cultured Coccomyxa cells contain an intracellular CA activity around 100 times higher than that measured in high-CO2-grown cells of Chlamydomonas reinhardtii CW 92. Purification of a protein extract containing the CA activity was carried out using ammonium-sulphate precipitation followed by anion-exchange chromatography. Proteins were then separated by native (non-dissociating) polyacrylamide gel electrophoresis, with each individual protein band excised and assayed for CA activity. Measurements revealed CA activity associated with two discrete protein bands with similar molecular masses of 80 +/- 5 kDa. Dissociation by denaturing polyacrylamide gel electrophoresis showed that both proteins contained a single polypeptide of 26 kDa, suggesting that each 80-kDa native protein was a homogeneous trimer. Isoelectric focusing of the 80-kDa proteins also produced a single protein band at a pH of 6.5. Inhibition studies on the purified CA extract showed that 50% inhibition of CA activity was obtained using 1 microM azetazolamide. Polyclonal antibodies against the 26-kDa CA were produced and shown to have a high specific binding to a single polypeptide in soluble protein extracts from Coccomyxa cells. The same antiserum, however, failed to cross-react with soluble proteins isolated from two different species of green algae, Chlamydomonas reinhardtii and Chlorella vulgaris. Correspondingly, antisera directed against pea chloroplastic CA, extracellular CA from C. reinhardtii and human CAII, showed no cross-hybridisation to the 26-kDa polypeptide in Coccomyxa.(ABSTRACT TRUNCATED AT 250 WORDS)

Place, publisher, year, edition, pages
1995. Vol. 195, no 3, 345-51 p.
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URN: urn:nbn:se:umu:diva-34524PubMedID: 7766041OAI: oai:DiVA.org:umu-34524DiVA: diva2:322709
Available from: 2010-06-08 Created: 2010-06-08 Last updated: 2017-12-12

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