Pesquisa Agropecuária Brasileira · 1990 · 15 citations · 0 references
Life SciencesMicrobiologyBacteriologyMicrobial PathogenesisMycologyAntibacterial AgentsBacterial GrowthBacterial PathogenesisBacterial Plant PathogensBacterial SporesFungal PhysiologyAntagonistic MicroorganismsBacillus SubtilisBacterial InhibitionBactericidal AgentsBacteriostatic ActivityMycelial GrowthPathogen Growth InhibitionPathogen Inhibition
Urethane is potentially carcinogenic and teratogenic to human and has been reported to be a contaminant of various kinds of alcoholic beverages. Enzymatic removal of urethane is one possible approach to remove this cancer-causing chemical from alcoholic beverages. Among Bacillus licheniformis strains, IFO 12107 showed the highest urethane hydrolyzing activity when cultivated in a urethane-containing white medium. The enzyme was purified about 300-fold by means of several chromatographic steps to homogeneity. The enzyme activity was strongly inhibited by batho- and o-phenanthroline. The complete loss of enzyme activity following treatment with bathophenanthroline was fully restored by the addition of Fe3+ at a ratio of 4 iron atoms to 1 mol apoenzyme. This result was obtained by the incorporation of 59Fe3+ into apourethanase. ESR spectroscopy showed that the enzyme contained a typical high-spin Fe3+. The urethanase hydrolyzed carbamyl ester derivatives more rapidly than amide derivatives. The molecular weight of the native enzyme was about 160 kDa (gel-filtration), and that of the subunit was 42 kDa (sodium dodecyl sulfate-polyacrylamide gel electrophoresis, SDS-PAGE). This shows the enzyme to be a homotetramer. The pI and Km values were 5.5 and 0.17 mM, respectively. The enzyme was considerably resistant to high concentrations of ethanol, which is a great advantage for the industrial removal of urethane from alcoholic beverages.