dc.creatorLeone, Francisco Assis
dc.creatorMasui, Douglas Chodi
dc.creatorSouza Bezerra, Thais Milena de
dc.creatorGarcon, Daniela Pereira
dc.creatorValenti, Wagner Cotroni
dc.creatorAugusto, Alessandra Silva
dc.creatorMcNamara, John Campbell
dc.date.accessioned2013-09-25T14:38:29Z
dc.date.accessioned2018-07-04T15:57:32Z
dc.date.available2013-09-25T14:38:29Z
dc.date.available2018-07-04T15:57:32Z
dc.date.created2013-09-25T14:38:29Z
dc.date.issued2012
dc.identifierJOURNAL OF MEMBRANE BIOLOGY, NEW YORK, v. 245, n. 4, pp. 201-215, APR, 2012
dc.identifier0022-2631
dc.identifierhttp://www.producao.usp.br/handle/BDPI/33709
dc.identifier10.1007/s00232-012-9431-9
dc.identifierhttp://dx.doi.org/10.1007/s00232-012-9431-9
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1629717
dc.description.abstractWe investigated modulation by ATP, Mg2+, Na+, K+ and NH4 (+) and inhibition by ouabain of (Na+,K+)-ATPase activity in microsomal homogenates of whole zoeae I and decapodid III (formerly zoea IX) and whole-body and gill homogenates of juvenile and adult Amazon River shrimps, . (Na+,K+)-ATPase-specific activity was increased twofold in decapodid III compared to zoea I, juveniles and adults, suggesting an important role in this ontogenetic stage. The apparent affinity for ATP ( (M) = 0.09 +/- A 0.01 mmol L-1) of the decapodid III (Na+,K+)-ATPase, about twofold greater than the other stages, further highlights this relevance. Modulation of (Na+,K+)-ATPase activity by K+ also revealed a threefold greater affinity for K+ ( (0.5) = 0.91 +/- A 0.04 mmol L-1) in decapodid III than in other stages; NH4 (+) had no modulatory effect. The affinity for Na+ ( (0.5) = 13.2 +/- A 0.6 mmol L-1) of zoea I (Na+,K+)-ATPase was fourfold less than other stages. Modulation by Na+, Mg2+ and NH4 (+) obeyed cooperative kinetics, while K+ modulation exhibited Michaelis-Menten behavior. Rates of maximal Mg2+ stimulation of ouabain-insensitive ATPase activity differed in each ontogenetic stage, suggesting that Mg2+-stimulated ATPases other than (Na+,K+)-ATPase are present. Ouabain inhibition suggests that, among the various ATPase activities present in the different stages, Na+-ATPase may be involved in the ontogeny of osmoregulation in larval The NH4 (+)-stimulated, ouabain-insensitive ATPase activity seen in zoea I and decapodid III may reflect a stage-specific means of ammonia excretion since functional gills are absent in the early larval stages.
dc.languageeng
dc.publisherSPRINGER
dc.publisherNEW YORK
dc.relationJOURNAL OF MEMBRANE BIOLOGY
dc.rightsCopyright SPRINGER
dc.rightsclosedAccess
dc.subject(NA+,K+)-ATPASE ACTIVITY
dc.subjectGILL MICROSOME
dc.subjectCATION-BINDING SITE
dc.subjectMACROBRACHIUM AMAZONICUM
dc.subjectONTOGENETIC STAGE
dc.subjectENVIRONMENTAL SALINITY
dc.titleKinetic Analysis of Gill (Na+,K+)-ATPase Activity in Selected Ontogenetic Stages of the Amazon River Shrimp, (Decapoda, Palaemonidae): Interactions at ATP- and Cation-Binding Sites
dc.typeArtículos de revistas


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