Tyrosinase, laccase and coconut tissue were compared as active biocomponent
s in enzymatic detection of phenols. The obtained selectivity of biocatalyt
ic activity of tyrosinase was found to be dependent on the way of enzyme im
mobilisation. The measurements were carried out in flow-injection systems w
ith flow-through reactors and carbon paste based integrated biosensors. For
the use as a detector in a HPLC system the tyrosinase carbon paste bio sen
sor was found to be the most convenient. The obtained detection limits were
0.072, 0.037 and 0.032 mg l(-1) for hydroquinone, phenol and catechol, res
pectively.