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Title: The calmodulin stimulated ATPase of Zea mays L.
Author: Briars, Sally-Anne
ISNI:       0000 0001 3479 3115
Awarding Body: University of Oxford
Current Institution: University of Oxford
Date of Award: 1989
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Maize coleoptile microsomal vesicles showing calmodulin-stimulated ATPase activity were isolated from 4.5 day old dark grown seedlings. Calmodulin-stiirmlated ATPase activity was maximal (8 nmoles min-1 (mg protein)-1) at 0.35 μM, inhibited by orthovanadate (Iso=20 μM), and specific for ATP. Calmodulin affinity chromatography was used to purify this ATPase after solubilisation with Triton X-100. Calmodulin-stimulated ATPase activity was present in the purified fraction, maximal stimulation (340 nmoles min-1 (mg protein)-1) occurring at 0.3 μM calmodulin. After reconstitution into asolectin liposomes, maximal calmodulinstimulated ATPase activity (500 nmoles min-1 (mg protein)-1) occurred at 0.025 μM. Affinity chromatography using buffers containing asolectin produced true basal activities; maximal calmodulin stimulation was at 0.01 μM (100 nmoles min-1 (mg protein)-1). These results suggest that a calmodulin-stimulated ATPase was purified from the microsomal fraction. Inclusion of protease inhibitors (PMSF, chymostatin) during purification and electrophoresis yielded a polypeptide of 140,000 Mr, similar to the Mr of erythrocyte calmodulin-stimulated, calcium-pumping ATPase (CSCPA). Polypeptides of Mr 91,000, 77-69,000, 51,000, and 40,000 were also present. A monospecific polyclonal antibody raised against erythrocyte CSCPA recognised the 140,000 Mr polypeptide from maize, giving strong evidence that maize cells may contain a polypeptide similar to erythrocyte CSCPA. The reaction mechanism of the proposed maize CSCPA was investigated. After purification in the presence of PMSF phosphorylation was present at 140,000 Mr; this turned over rapidly, was sensitive to hydroxylamine, dependent on calcium, inhibited by lanthanum and stimulated by calmodulin. This was consistent with formation of an acyl-phosphate intermediate, indicating that maize CSCPA is a P-type ATPase, having a reaction mechanism similar to that of the erythrocyte CSCPA. A monoclonal antibody (EA6) was raised to maize CSCPA purified without PMSF; this antibody recognised intact maize CSCPA and inhibited calmodulin-stimulated ATPase activity in microsomal fractions. This antibody also bound to other polypeptides present in microsomal and purified fractions, permitting tentative identification of proteolysis products.
Supervisor: Dewey, F. M. Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID:  DOI: Not available
Keywords: Botanical chemistry