화학공학소재연구정보센터
Applied Microbiology and Biotechnology, Vol.57, No.1-2, 98-102, 2001
Purification and characterization of laccase isozymes from the white-rot basidiomycete Ganoderma lucidum
Ganoderma lucidum, a medicinal white-rot basidiomycete, produces many laccase isozymes in liquid culture. Three laccase isozymes (GaLc 1, 2, 3) have been purified 32.4-fold from the crude enzyme protein through anion exchange chromatography, preparative get electrophoresis. and electroelution. Their estimated molecular weights are 65-68 kDa. and they contain 7-10% N-linked carbohydrates. The three isozymes have identical N-terminal amino acid sequences: G-I-G-P-T. The optimum pH and temperature both for each isozyme singly and the isozyme mixture are pH 3.5 and 20 degreesC, respectively. One isozyme (GaLc 3) is quite stable at pH 4.0-10.0, and shows good stability when incubated at temperatures lower than 40 degreesC. The K-m values of GaLc 3 for o-tolidine and 2.2'-azino-bis-(3-ethylthiazoline-6-sulfonate) (ABTS) are 401.6 muM and 3.7 muM respectively. and the V-max of Gal-c 3 for these substrates is 0.0198 OD min(-1)unit(-1) and 0.0142 OD min(-1)unit(-1), respectively.