Characterization of prtA Delta mutants, generated by gene disruption, showe
d that the prfA gene is responsible for the majority of extracellular prote
ase activity secreted by Aspergillus nidulans at both neutral and acid pH,
The prtA Delta mutation was used to map the prtA gene to chromosome V, Thou
gh aspartic protease activity has never been reported in A, nidulans and th
e prtA Delta mutants appear to lack detectable acid protease activity, a ge
ne (prtB) encoding a putative aspartic protease was isolated from this spec
ies. Comparison of the deduced amino acid sequence of PrtB to the sequence
of other aspergillopepsins suggests that the putative prtB gene product con
tains an eight-amino-acid deletion prior to the second active site Asp resi
due of the protease, RT-PCR experiments showed that the prtB gene is expres
sed, albeit at a low level. (C) 2000 Academic Press.