IDENTIFICATION AND SUBCELLULAR-LOCALIZATION OF 2 ISOENZYMES OF APYRASE FROM SOLANUM-TUBEROSUM

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IDENTIFICATION AND SUBCELLULAR-LOCALIZATION OF 2 ISOENZYMES OF APYRASE FROM SOLANUM-TUBEROSUM

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IDENTIFICATION AND SUBCELLULAR-LOCALIZATION OF 2 ISOENZYMES OF APYRASE FROM SOLANUM-TUBEROSUM

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Título: IDENTIFICATION AND SUBCELLULAR-LOCALIZATION OF 2 ISOENZYMES OF APYRASE FROM SOLANUM-TUBEROSUM
Autor: Kettlun, Ana María; Leyton, Mario; Valenzuela, M. A.; Mancilla, Marta; Traverso Cori, A.
Resumen: Two forms of ATP-diphosphohydrolase were identified in Solanum tuberosum tuber var. Ultimus. Their hydrolytic activity ratios (ATPase/ADPase) were over 10 for form A and 1 for form B. In the potato tuber homogenate the hydrolytic activity ratio is 3.0, as a result of contributions of the two forms of apyrase. These two apyrases (A and B) were partially separated and the possibility that they are produced as an artifact by partial proteolysis or subunit aggregation was excluded. The subcellular localization of the Ultimus isoapyrases was studied by differential centrifugation. These enzymes are localized in distinct compartments. The high ratio enzyme (A) lies mainly in the soluble fraction, while the low ratio apyrase (B) is principally bound to membranes. The two isoapyrases differ greatly in their kinetic properties and pI, but only slightly in M(r). Both enzymes immunocross-react with antiapyrase Desiree, which is important for isoenzyme detection by the immunowestern blot. This is the first example of two isoenzymes of apyrase in the same variety of S. tuberosum.
Descripción: Artículo de publicación ISI
URI: http://www.captura.uchile.cl/handle/2250/13878
Fecha: 1992-06
Cita del item: PHYTOCHEMISTRY 31 (6): 1889-1894


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