A putrescine biosensor has been developed. Putrescine oxidase, peroxid
ase, and bovine serum albumin were cross-linked directly on the surfac
e of a graphite electrode by glutaraldehyde. The sensor was used to de
termine putrescine at 0 mV (vs. Ag/AgCl reference electrode) in a pota
ssium phosphate buffer (pH 7.4) solution containing 4 mM dopamine (3-h
ydroxytyramine). The response of putrescine was linear up to 600 mu M
with a standard deviation of 2.8%. The detection limit was 5 mu M. The
response time was around 30 s. The lifetime was-over 30 days when the
electrode was used every day. The interferences of cadaverine and spe
rmidine could be eliminated by added dopamine which, apparently, inhib
its the enzymatic conversion of these substrates more strongly than th
at of putrescine.