Purification and characterization of the constitutive form of laccase from the basidiomycete Coriolus hirsutus and effect of inducers on laccase synthesis

An isolate of Coriolus hirsutus constitutively expresses substantial amounts of extracellular laccase on a defined growth medium. The most efficient inducer of extracellular laccase synthesis was syringaldazine, which increased the enzyme yield by 1000% at a concentration of 0·11 μM. The constitutive form of the enzyme was purified 312‐fold. Laccase from C. hirsutus , with an estimated molecular mass of 55 kDa and pI of 4·0, is a monomeric glycoprotein containing 12% carbohydrate consisting of mannose and N ‐acetylglucosamine. The laccase was found to contain 3·9–4·1 copper atoms per molecule. The absorption spectrum shows a maximum at 610 nm and a shoulder at 330 nm, which is typical of laccase possessing type 1 and type 3 copper atoms. The parameters of the first type of copper were determined by EPR as g ⊥ =2·046 and g ∥ =2·200, A ∥ =8·103×10 −3  cm −1 . Laccase was found to be a pH‐stable and thermostable enzyme. With organic substrates it exhibits a pH optimum of 4·5, but with the inorganic substrate K 4 [Fe(CN) 6 ] this decreased to 3·5. The highest efficiency of catalysis was observed with sinapinic acid as the substrate. The kinetic constants k cat and K m of this reaction were 578 s −1 and 24 μM respectively. It was established that the kinetics of the assayed reaction shows a Ping Pong mechanism.