Neither phospholipase A1 (PLA A1) nor phospholipase A2 (PLA A2), nor their respective genes, have been identified in Giardia lamblia, even though they are essential for lipid metabolism in this parasite. A method to identify, isolate, and characterize these enzymes is needed. The activities of PLA A1 and PLA A2 were analyzed in a total extract (TE) and in vesicular (P30) and soluble (S30) subcellular fractions of G. lamblia trophozoites; the effects of several chemical and physicochemical factors on their activities were investigated. The assays were performed using substrate labeled with 14C, and the mass of the 14C-product was quantified. PLA A1 and PLA A2 activity was present in the TE and the P30 and S30 fractions, and it was dependent on pH and the concentrations of protein and Ca2+. In all trophozoite preparations, PLA A1 and PLA A2 activities were inhibited by ethylenediaminetetraacetic acid and Rosenthal's inhibitor. These results suggest that G. lamblia possesses several PLA A1 and PLA A2 isoforms that may be soluble or associated with membranes. In addition to participating in G. lamblia phospholipid metabolism, PLA A1 and PLA A2 could play important roles in the cytopathogenicity of this parasite.
ACTIVITY OF INTRACELLULAR PHOSPHOLIPASE A1 AND A2 IN GIARDIA LAMBLIA
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Javier Vargas-Villarreal, Brenda Leticia Escobedo-Guajardo, Benito David Mata-Cárdenas, Rebeca Palacios-Corona, Elva Cortes-Gutiérrez, Mario Morales-Vallarta, Adriana Sampayo-Reyes, Salvador Said-Fernández; ACTIVITY OF INTRACELLULAR PHOSPHOLIPASE A1 AND A2 IN GIARDIA LAMBLIA. J Parasitol 1 October 2007; 93 (5): 979–984. doi: https://doi.org/10.1645/GE-1038R3.1
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