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Characterisation of Aspergillus niger prolyl aminopeptidase

Authors :
Albert J. J. van Ooyen
Antoine P. H. A. Moers
Peter J. Schaap
Daniƫlle E. J. W. Basten
Source :
Molecular Genetics and Genomics 272 (2005) 6, Molecular Genetics and Genomics, 272(6), 673-679
Publication Year :
2005

Abstract

We have cloned a gene (papA) that encodes a prolyl aminopeptidase from Aspergillus niger. Homologous genes are present in the genomes of the Eurotiales A. nidulans, A. fumigatus and Talaromyces emersonii, but the gene is not present in the genome of the yeast Saccharomyces cerevisiae. Cell extracts of strains overexpressing the gene under the control of its own promoter showed a fourfold to sixfold increase in prolyl aminopeptidase activity, but no change in phenylalanine or leucine aminopeptidase activity. The overexpressed enzyme was subsequently purified and characterised. The enzyme specifically removes N-terminal proline and hydroxyproline residues from peptides. It is the first enzyme of its kind from a eukaryotic organism that has been characterised.

Details

Language :
English
ISSN :
16174615
Volume :
272
Issue :
6
Database :
OpenAIRE
Journal :
Molecular Genetics and Genomics
Accession number :
edsair.doi.dedup.....3eda5f4af7ff06b9210fb1f3f259bd48