A Clark type, amperometric multienzyme electrode employing glucose oxi
dase and mutarotase, was used to determine the enzymatic activity of a
model enzyme, invertase, in soluble and immobilized forms. A calibrat
ion curve with linear range up to 70 IU of invertase activity correspo
nding to the 6.0 nA/s of electrode response was sketched. It is shown
that, multienzyme electrodes can be utilized as a very rapid, reliable
and sensitive tool for the determination of enzymatic activity either
in a free or immobilized form. (C) 1997 Elsevier Science Limited. All
rights reserved.