A gene encoding endochitinase activity was isolated by PCR from Saccharomyc
es cerevisiae NCYC686 and placed under the control of fungal transcriptiona
l elements regulating glucoamylase expression. Following transformation of
Aspergillus awamori with this expression construct, heterologous endochitin
ase was induced in positive transformants by the addition of starch to the
growth medium. A series of optimisation and process development studies wer
e then undertaken, the result of which was the production of heterologous e
ndochitinase activity at 343 U g(-1) of total protein. It was found also th
at the yield of enzyme decreased upon scale-up from shake flask to 3 l pilo
t scale.