Leishmania donovani promastigotes were collected, washed, resuspended
in buffer, and assayed for sucrase activity. No activity was observed
in the intact washed cells, but activity was measurable when the cells
were permeabilized with Triton X-100. Intracellular sucrase activity
was highest in promastigotes grown at pH 7.4, somewhat lower in promas
tigotes grown at pH 5.5, and significantly lower in ''amastigotes'' gr
own at pH 5.5. No trehalase, lactase, or maltase activities were obser
ved. Assay of the medium in which the cells had grown showed that most
the sucrase activity was extracellular, i.e. was secreted into the me
dium during growth.