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Bactericidal and virucidal activity of the alkalophilic P395D/L241V/T343A mutant of vanadium chloroperoxidase
Author(s) -
Renirie R.,
Dewilde A.,
Pierlot C.,
Wever R.,
Hober D.,
Aubry J.M.
Publication year - 2008
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.1365-2672.2008.03742.x
Subject(s) - humanities , art , technical university , art history , library science , computer science
Aims: Vanadium chloroperoxidase and its directed evolution mutant P395D/L241V/T343A were investigated for their antibacterial and antiviral potential at slightly alkaline pH and at a H 2 O 2 concentration that is low compared to current nonenzymatic formulations. Methods and Results: Two bacteria (the Gram‐negative Pseudomonas aeruginosa and the Gram‐positive Staphylococcus aureus ) and two viruses (the enveloped Herpes Simplex Virus and the nonenveloped Coxsackievirus B4) were incubated with the P395D/L241V/T343A mutant, 10 mmol l −1 H 2 O 2 and 100 mmol l −1 Br − at pH 8. Strong microbial reduction was observed and bactericidal and virucidal activities of the mutant were three to six orders of magnitude higher than for the wild‐type enzyme. Conclusions: The P395D/L241V/T343A mutant of vanadium chloroperoxidase has a broad antimicrobial activity at alkaline conditions. Significance and Impact of the Study: For many disinfection formulations, antimicrobial activity at slightly alkaline pH values is required. To date, only the wild‐type vanadium chloroperoxidase has been studied for its antibacterial activity, and only at acidic to neutral pH values. Its antiviral activity (e.g. useful for the cleaning of medical equipment) was not studied before. The observed activity for the alkalophilic P395D/L241V/T343A mutant is an important step forward in the application of this robust enzyme as a component in disinfection formulations.