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J Biol Chem ; 269(16): 12074-9, 1994 Apr 22.
Artículo en Inglés | MEDLINE | ID: mdl-8163511

RESUMEN

The H(+)-ATPase from Schizosaccharomyces pombe belongs to the group of transport ATPases which displays two main conformational states, E1 and E2 (P-type ATPase). In this report, we show that, as in the case of other P-type ATPase, the purified enzyme exhibits a p-nitrophenylphosphatase activity which can be completely inhibited by vanadate. In aqueous medium, p-nitrophenyl phosphate hydrolysis proceeds at only 0.5% of the rate of ATP hydrolysis, and both activities can be stimulated 3- to 4-fold by decreasing the pH from 7.5 to 6.5. Addition of the organic solvent dimethyl sulfoxide (10-40%), which has been shown to favor the E2 conformation, stimulates the p-nitrophenylphosphatase activity but inhibits the ATPase activity. At pH 7.5, the Km for p-nitrophenyl phosphate decreases when dimethyl sulfoxide is present. In the presence of 30% (v/v) dimethyl sulfoxide, the phosphatase activity can be inhibited by ATP (K(i) 300 microM) or by P(i) (K(i) 1 mM). The H(+)-ATPase incorporated into liposomes retains pNPPase activity, but it does not support H+ transport. Gel electrophoresis reveals that the pattern of H(+)-ATPase cleavage by trypsin changes when vanadate, Me2SO, or both compounds are present in the medium, regardless of the pH used during trypsinization. We propose that p-nitrophenyl phosphate is hydrolyzed by a H(+)-ATPase conformation distinct from that which hydrolyzes ATP, most probably an E2-like form. We also suggest that, in addition to the E1-E2 transition, the enzyme activity can be regulated by protons at another step of the catalytic cycle.


Asunto(s)
4-Nitrofenilfosfatasa/metabolismo , Membrana Celular/enzimología , ATPasas de Translocación de Protón/metabolismo , Schizosaccharomyces/enzimología , 4-Nitrofenilfosfatasa/antagonistas & inhibidores , 4-Nitrofenilfosfatasa/aislamiento & purificación , Dimetilsulfóxido/farmacología , Electroforesis en Gel de Poliacrilamida , Activación Enzimática , Cinética , Liposomas , Peso Molecular , Fragmentos de Péptidos/aislamiento & purificación , Fosfatos/farmacología , ATPasas de Translocación de Protón/aislamiento & purificación , Tripsina , Vanadatos/farmacología
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