This Article Full Text Full Text (PDF) Services Similar articles in this journal Alert me to new issues of the journal Download to citation manager Citing Articles Citing Articles via Google Scholar Google Scholar Articles by Xiao, Y. Z. Articles by Wang, Y. P. Search for Related Content PubMed Articles by Xiao, Y. Z. Articles by Wang, Y. P. Agricola Articles by Xiao, Y. Z. Articles by Wang, Y. P.

Selective induction, purification and characterization of a laccase isozyme from the basidiomycete Trametes sp. AH28-2

     Laboratory of Structure Biology, School of Life Sciences, University of Science and Technology of China, Hefei, Anhui, 230026, P.R. of China

Y. Z. Xiao
J. Wu
Y. Z. Hong
Y. P. Wang

     Laboratory of Microorganism and Gene Technology, School of Life Sciences, Anhui University, Hefei, Anhui, 230039, P.R. of China

The white-rot fungus Trametes sp. AH28-2 can synthesize extracellular laccase by induction in cellobiose-based liquid culture medium. Both yields and composition of laccase isozymes, produced by Trametes sp. AH28-2, would be quite different with induction by different small-molecule aromatic compounds, o-toluidine, guaiacol and 3,5-dihydroxytoluene, which affected microbial growth and the synthesis of laccase isozymes differentially. Higher concentrations of the three inducers could considerably increase laccase isozymes yields but not change the laccase composition. Coculturing of Trametes sp. AH28-2 with either Aspergillus oryzae or Gloeophyllum trabeum showed a few effects on laccase production. Laccase isozyme, laccase B, was selectively induced by 3,5-dihydroxytoluene and purified to homogeneity by two-step chromatography. Purified laccase B appeared as blue, with a broad peak at about 600 nm and a shoulder peak at about 330 nm. The ratio of absorbance at 280 nm to that at 600 nm was 21. Every molecule of laccase B had approximately four copper atoms. Molecular mass of laccase B was estimated to be 74 kDa on SDS-PAGE, 72 kDa by FPLC and was determined to be 71 454 Da by mass spectrum. After being treated with N-glycosidase F, laccase B lost 25% of its molecular mass. The isoelectric point of laccase B was 4.0. Its optimal pH and temperature for oxidizing guaiacol were respectively 4.7 and 45 C. The half-life of the enzyme at 60 C was 14.0 min. The enzyme showed a good stability in a range of pH value of 3.5–7.5. The K_m values of the enzyme toward substrates syringaldazine, guaiacol, ABTS, and DMOP were respectively 28.0, 1249.0, 177.0 and 109.8 µM. The corresponding V_max are 504.0, 1910.0, 117.4 and 159.0 µM min^-1 mg^-1. In addition, activity of laccase B was inhibited strongly by sodium azide and cyanide, mildly by SDS and trifluoroacetic acid, but only weakly by dimethyl sulfoxide.

Key words: Aromatic compounds, 3,5-dihydroxytoluene, guaiacol, laccase isozyme, o-toluidine, Trametes sp. AH28-2