Arias M Enriqueta, Arenas María, Rodríguez Juana, Soliveri Juan, Ball Andrew S, Hernández Manuel
Departamento de Microbiología y Parasitología, Universidad de Alcalá, 28871 Alcalá de Henares, Madrid, Spain.
Appl Environ Microbiol. 2003 Apr;69(4):1953-8. doi: 10.1128/AEM.69.4.1953-1958.2003.
A new laccase (EC 1.10.3.2) produced by Streptomyces cyaneus CECT 3335 in liquid media containing soya flour (20 g per liter) was purified to homogeneity. The physicochemical, catalytic, and spectral characteristics of this enzyme, as well as its suitability for biobleaching of eucalyptus kraft pulps, were assessed. The purified laccase had a molecular mass of 75 kDa and an isoelectric point of 5.6, and its optimal pH and temperature were 4.5 and 70 degrees C, respectively. The activity was strongly enhanced in the presence of Cu(2+), Mn(2+), and Mg(2+) and was completely inhibited by EDTA and sodium azide. The purified laccase exhibited high levels of activity against 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonate) (ABTS) and 2,6-dimethoxyphenol and no activity against tyrosine. The UV-visible spectrum of the purified laccase was the typical spectrum of the blue laccases, with an absorption peak at 600 nm and a shoulder around 330 to 340 nm. The ability of the purified laccase to oxidize a nonphenolic compound, such as veratryl alcohol, in the presence of ABTS opens up new possibilities for the use of bacterial laccases in the pulp and paper industry. We demonstrated that application of the laccase from S. cyaneus in the presence of ABTS to biobleaching of eucalyptus kraft pulps resulted in a significant decrease in the kappa number (2.3 U) and an important increase in the brightness (2.2%, as determined by the International Standard Organization test) of pulps, showing the suitability of laccases produced by streptomycetes for industrial purposes.
由蓝链霉菌CECT 3335在含有大豆粉(每升20克)的液体培养基中产生的一种新型漆酶(EC 1.10.3.2)被纯化至同质。评估了该酶的物理化学、催化和光谱特性,以及其对桉木硫酸盐浆生物漂白的适用性。纯化后的漆酶分子量为75 kDa,等电点为5.6,其最佳pH值和温度分别为4.5和70℃。在Cu(2+)、Mn(2+)和Mg(2+)存在下,活性显著增强,而被EDTA和叠氮化钠完全抑制。纯化后的漆酶对2,2'-联氮-双(3-乙基苯并噻唑啉-6-磺酸)(ABTS)和2,6-二甲氧基苯酚表现出高活性,对酪氨酸无活性。纯化后的漆酶的紫外可见光谱是典型的蓝色漆酶光谱,在600 nm处有一个吸收峰,在330至340 nm左右有一个肩峰。纯化后的漆酶在ABTS存在下氧化非酚类化合物(如藜芦醇)的能力为细菌漆酶在制浆造纸工业中的应用开辟了新的可能性。我们证明,在ABTS存在下将蓝链霉菌的漆酶应用于桉木硫酸盐浆的生物漂白,导致卡伯值显著降低(2.3个单位),纸浆亮度显著提高(根据国际标准组织测试确定为2.2%),表明链霉菌产生的漆酶适用于工业用途。