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Characterization of a proteolytic enzyme derived from a Bacillus strain that effectively degrades prion protein
Author(s) -
Yoshioka M.,
Miwa T.,
Horii H.,
Takata M.,
Yokoyama T.,
Nishizawa K.,
Watanabe M.,
Shinagawa M.,
Murayama Y.
Publication year - 2007
Publication title -
journal of applied microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.889
H-Index - 156
eISSN - 1365-2672
pISSN - 1364-5072
DOI - 10.1111/j.1365-2672.2006.03080.x
Subject(s) - proteases , protease , subtilisin , proteinase k , serine protease , microbiology and biotechnology , biology , proteolytic enzymes , enzyme , biochemistry
Aims: The purpose of this paper was to screen candidate bacterial strains for the production of proteases suitable for application to the degradation of pathogenic forms of prion protein (PrP Sc ). This paper describes the biochemical characteristics and proteolytic activity of the isolated protease. Methods and Results: After screening more than 200 bacterial proteases for keratinolytic activity, we identified a Bacillus stain that produced a protease exhibiting high‐degradation activity against a scrapie PrP Sc . Sequence analysis indicated that this serine‐protease belonged to the Subtilisin family and had optimum pH and temperature ranges of 9–10 and 60–70°C. Western blotting analysis revealed that the protease was also capable of decomposing bovine spongiform encephalopathy‐infected brain homogenate. In addition, the protease was demonstrated to degrade dried PrP Sc that had become firmly attached to a plastic surface considerably more effectively than proteinase K or PWD‐1, a previously reported keratinase. Conclusions: These results indicate that the isolated protease exhibited higher activity for PrP Sc degradation compared with other proteases examined. Significance and Impact of the Study: This protease could be used under moderate conditions for the decontamination of precision instruments that are susceptible to PrP Sc contamination.