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1.
J Appl Microbiol ; 97(3): 640-6, 2004.
Article in English | MEDLINE | ID: mdl-15281946

ABSTRACT

AIMS: To discover novel laccases potential for industrial applications. METHODS AND RESULTS: Fungi were cultivated on solid media containing indicator compounds that enabled the detection of laccases as specific colour reactions. The indicators used were Remazol Brilliant Blue R (RBBR), Poly R-478, guaiacol and tannic acid. The screening work resulted in isolation of 26 positive fungal strains. Liquid cultivations of positive strains confirmed that four efficient laccase producers were found in the screening. Biochemical characteristics of the four novel laccases were typical for fungal laccases in terms of molecular weight, pH optima and pI. The laccases showed good thermal stability at 60 degrees C. CONCLUSIONS: Plate-test screening based on polymeric dye compounds, guaiacol and tannic acid is an efficient way to discover novel laccase producers. The results indicated that screening for laccase activity can be performed with guaiacol and RBBR or Poly R-478. SIGNIFICANCE AND IMPACT OF THE STUDY: Laccases have many potential industrial applications including textile dye decolourization, delignification of pulp and effluent detoxification. It is essential to find novel, efficient enzymes to further develop these applications. This study showed that relatively simple plate test screening method can be used for discovery of novel laccases.


Subject(s)
Fungi/isolation & purification , Industrial Microbiology , Laccase/biosynthesis , Anthraquinones , Coloring Agents , Culture Media , Fungi/enzymology , Guaiacol , Hydrogen-Ion Concentration , Indicators and Reagents , Molecular Weight , Polymers , Tannins , Temperature
2.
Appl Microbiol Biotechnol ; 59(2-3): 198-204, 2002 Jul.
Article in English | MEDLINE | ID: mdl-12111146

ABSTRACT

A novel laccase from the ascomycete Melanocarpus albomyces was purified and characterised. The enzyme was purified using anion exchange chromatography, hydrophobic interaction chromatography and gel filtration, and the purified laccase was biochemically characterised. It had activity towards typical substrates of laccases including 2,2'-azinobis-(3-ethylbenzthiazoline-6-sulphonate), dimethoxyphenol, guaiacol, and syringaldazine. The laccase showed good thermostability and it had a pH optimum at neutral pH, both unusual properties for most known fungal laccases. The activity of the laccase from M. albomyces was highest at 60-70 degrees C. With guaiacol and syringaldazine the pH optima were rather broad: 5-7.5 and 6-7, respectively. It retained 50% of its activity after 5 h incubation at 60 degrees C. The molecular weight of the laccase was about 80 kDa and the isoelectric point 4.0. The ultraviolet-visible absorption and electron paramagnetic resonance spectra of the purified laccase indicated that the typical three types of copper were present.


Subject(s)
Ascomycota/enzymology , Oxidoreductases/isolation & purification , Amino Acid Sequence , Enzyme Stability , Hydrogen-Ion Concentration , Laccase , Molecular Sequence Data , Oxidoreductases/chemistry , Oxidoreductases/metabolism , Temperature
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