Drosophila melanogasterwas reared under LD 12:12. Fat body was isolated in form of cells and cell groups from dissected larvae or prepupae by treatment with collagenase and hyaluronidase and subsequent centrifugation. Tyrosine aminotransferase of the fat body showed an extremely sharp pH dependence, with two narrow, well separable maxima at pH 5.6 and 6.0, possibly caused by different isoenzymes. Enzyme activity at pH 5.6 exhibited biphasic circadian rhythms in both wild‐type 3rd instar larvae and early prepupae. At pH 6.0, the rhythmicity was much weaker, perhaps even absent. In larvae from an ebony strain, at either pH the basal tyrosine aminotransferase activity was enhanced, and the rhythmicity was altered.