The present study was undertaken to develop a specific and sensitive method
which allows the detection of trace amounts of the potentially allergenic
bioindustrial enzymes Pectinex Ultra-SPL (pectinase) and Gamylo 200L (amyla
se) in apple juice. This was achieved by an immunoblotting procedure based
on sodium dodecyl sulfate (SDS) electrophoretic separation, followed by an
immunochemical detection step using polyclonal rabbit antisera directed aga
inst these enzymes and, secondly, alkaline phosphatase labelled antibodies
in combination with a highly sensitive enhanced chemiluminescent (ECL) dete
ction method. In a juice spiked with enzyme at various concentrations betwe
en 10,000 and 1 ppm (1.0-0.0001%), the detection limit was 10 ppm (=0.001%)
for Pectinex Ultra-SPL and I ppm (=0.0001%) for Gamylo 200L, respectively.
Since the enzyme preparations contain less than 5% of enzymes, the detecti
on limit for the pure enzymes is markedly lower, at least below 1 ppm.
Whereas in the samples withdrawn during the initial stages of the industria
l production process of apple juice. Pectinex Ultra-SPL and Gamylo 200L com
ponents were detectable in concentrations between 50 and 100 ppm, after cle
aring. ultrafiltration and pasteurization, neither pectinase nor amylase wa
s detectable in the final consumer's product. Under the conditions employed
, the bioindustrial enzymes Pectinex Ultra-SPL and Gamylo 200L, were virtua
lly removed during the course of production.
The risk of sensitizing consumers by intake of apple juice seems to be marg
inal. This view is supported by the results of an animal model (anaphylaxis
test), in which neither gastro-enteral reactions in guinea pigs and mice,
nor IgE or IgG production by orally feeding these animals with apple juice
concentrate, could be induced.