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Biofouling ; 26(2): 141-53, 2010.
Article in English | MEDLINE | ID: mdl-19882418

ABSTRACT

The antifouling (AF) potential of hydrogen peroxide (H(2)O(2)) produced enzymatically in a coating containing starch, glucoamylase, and hexose oxidase was evaluated in a series of laboratory tests and in-sea field trials. Dissolved H(2)O(2) inhibited bacterial biofilm formation by eight of nine marine Proteobacteria, tested in microtiter plates. However, enzymatically produced H(2)O(2) released from a coating did not impede biofilm formation by bacteria in natural seawater tested in a biofilm reactor. A field trial revealed a noticeable effect of the enzyme system: after immersion in the North Sea for 97 days, the reference coating without enzymes had 35-40 barnacles, 10% area coverage by diatoms and 15% area coverage by tunicates. The enzyme containing coating had only 6-12 barnacles, 10% area coverage by diatoms and no tunicates. The enzyme system had a performance similar to a copper-based commercial coating and thus appears to have potential as a non-persistent AF agent.


Subject(s)
Biofilms/drug effects , Biofouling/prevention & control , Hydrogen Peroxide/pharmacology , Proteobacteria/drug effects , Alcohol Oxidoreductases/chemistry , Biofilms/growth & development , Bioreactors , Glucan 1,4-alpha-Glucosidase/chemistry , Hydrogen Peroxide/chemistry , Microbial Sensitivity Tests , Proteobacteria/physiology , Seawater/chemistry , Starch/chemistry
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