Muñoz C, Guillén F, Martínez A T, Martínez M J
Centro de Investigaciones Biológicas, Consejo Superior de Investigaciones Cientificus, Madrid, Spain.
Appl Environ Microbiol. 1997 Jun;63(6):2166-74. doi: 10.1128/aem.63.6.2166-2174.1997.
Two laccase isoenzymes produced by Pleurotus eryngii were purified to electrophoretic homogeneity (42- and 43-fold) with an overall yield of 56.3%. Laccases I and II from this fungus are monomeric glycoproteins with 7 and 1% carbohydrate content, molecular masses (by sodium dodecyl sulfate-polyacrylamide gel electrophoresis) of 65 and 61 kDa, and pIs of 4.1 and 4.2, respectively. The highest rate of 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonate) oxidation for laccase I was reached at 65 degrees C and pH 4, and that for laccase II was reached at 55 degrees C and pH 3.5. Both isoenzymes are stable at high pH, retaining 60 to 70% activity after 24 h from pH 8 to 12. Their amino acid compositions and N-terminal sequences were determined, the latter strongly differing from those of laccases of other basidiomycetes. Antibodies against laccase I reacted with laccase II, as well as with laccases from Pleurotus ostreatus, Pleurotus pulmonarius, and Pleurotus floridanus. Different hydroxy- and methoxy-substituted phenols and aromatic amines were oxidized by the two laccase isoenzymes from P. eryngii, and the influence of the nature, number, and disposition of aromatic-ring substituents on kinetic constants is discussed. Although both isoenzymes presented similar substrate affinities, the maximum rates of reactions catalyzed by laccase I were higher than those of laccase II. In reactions with hydroquinones, semiquinones produced by laccase isoenzymes were in part converted into quinones via autoxidation. The superoxide anion radical produced in the latter reaction dismutated, producing hydrogen peroxide. In the presence of manganous ion, the superoxide union was reduced to hydrogen peroxide with the concomitant production of manganic ion. These results confirmed that laccase in the presence of hydroquinones can participate in the production of both reduced oxygen species and manganic ions.
杏鲍菇产生的两种漆酶同工酶被纯化至电泳纯(纯化倍数分别为42倍和43倍),总产率为56.3%。该真菌的漆酶I和漆酶II是单体糖蛋白,碳水化合物含量分别为7%和1%,(通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳测得)分子量分别为65 kDa和61 kDa,pI分别为4.1和4.2。漆酶I氧化2,2'-联氮-双(3-乙基苯并噻唑啉-6-磺酸)的最高速率出现在65℃和pH 4时,漆酶II的则出现在55℃和pH 3.5时。两种同工酶在高pH下都很稳定,在pH 8至12下24小时后仍保留60%至70%的活性。测定了它们的氨基酸组成和N端序列,后者与其他担子菌漆酶的有很大不同。抗漆酶I的抗体与漆酶II以及平菇、肺形侧耳和佛罗里达侧耳的漆酶发生反应。杏鲍菇的两种漆酶同工酶氧化了不同的羟基和甲氧基取代酚及芳香胺,并讨论了芳香环取代基的性质、数量和位置对动力学常数的影响。虽然两种同工酶表现出相似的底物亲和力,但漆酶I催化反应的最大速率高于漆酶II。在与对苯二酚的反应中,漆酶同工酶产生的半醌部分通过自氧化转化为醌。后一反应中产生的超氧阴离子自由基发生歧化反应,生成过氧化氢。在锰离子存在下,超氧阴离子被还原为过氧化氢,同时产生锰离子。这些结果证实,对苯二酚存在时漆酶可参与活性氧和锰离子的产生。