Lopandic K, Deana A D, Barbaric S, Pinna L A
Istituto di Chimica Biologica, Università di Padova, Italy.
Biochem Int. 1987 Apr;14(4):627-33.
In this paper evidences are presented strongly confirming that an extracellular 32P-phosphopeptide phosphatase activity of yeast is accounted for by acid phosphatase. Dephosphorylation of 32P phosphoseryl peptides was achieved with whole yeast cells, thus demonstrating extracellular location of protein phosphatase activity. The acid phosphatase and protein phosphatase activity copurified throughout purification procedure. Purified enzyme showed the same pH-profile and had the same Km value with phosphopeptide substrate as intact cells. Protein phosphatase activity is repressed by phosphate in the same manner as acid phosphatase activity, showing that not only repressible but also constitutive acid phosphatase displays protein phosphatase activity. Using mutant strains defective in acid phosphatase activity it was confirmed that acid phosphatase and protein phosphatase activities are the products of the same gene(s).
本文提供的证据有力地证实,酵母的一种细胞外32P - 磷酸肽磷酸酶活性是由酸性磷酸酶引起的。用完整的酵母细胞实现了32P磷酸丝氨酸肽的去磷酸化,从而证明了蛋白质磷酸酶活性的细胞外定位。在整个纯化过程中,酸性磷酸酶和蛋白质磷酸酶活性共同纯化。纯化后的酶与完整细胞具有相同的pH曲线,并且与磷酸肽底物具有相同的Km值。蛋白质磷酸酶活性与酸性磷酸酶活性一样受到磷酸盐的抑制,这表明不仅可抑制的而且组成型的酸性磷酸酶都具有蛋白质磷酸酶活性。使用酸性磷酸酶活性缺陷的突变菌株证实,酸性磷酸酶和蛋白质磷酸酶活性是同一基因的产物。