Ben Younes S, Mechichi T, Sayadi S
Laboratoire des Bioprocédés, Centre de Biotechnologie de Sfax, Sfax, Tunisia.
J Appl Microbiol. 2007 Apr;102(4):1033-42. doi: 10.1111/j.1365-2672.2006.03152.x.
To characterize the white rot fungus Perenniporia tephropora with respect to its laccase and to test its ability to decolourize synthetic dyes.
Under the culture conditions utilized, P. tephropora produced one laccase isozyme, which was purified to electrophoretic homogeneity by ammonium sulfate precipitation, size-exclusion chromatography and anion-exchange chromatography. The protein was monomeric with a molecular mass of 63 kDa (SDS-PAGE) and had an isoelectric point of 3.3. The N-terminal amino acid sequence was SIGPVADLTVTNANI and the highest similarity value was found to the laccase from Lentinus tigrinus (86.6%). The optimum pH of the enzyme varied and was substrate dependent. It was 4.0 and 5.0 for 2,6-dimethoxyphenol (DMP) and 2,2'-azino-di(3-ethyl-benzthiazoline-6-sulfonate) (ABTS), respectively. Under standard assay conditions, K(m) values of the enzyme were 7.3 and 0.4 mmol l(-1) towards DMP and ABTS, respectively. The laccase was inhibited by NaN(3), EDTA and p-coumarate but not by SDS and NaBr. Laccase was stable in the presence of some metal ions such as Cu(2+), Co(2+), Ca(2+), Cd(2+), Mg(2+), Mn(2+), Mo(2+), Ni(2+), Li(+) and Al(3+). The crude enzyme as well as the purified laccase was able to decolourize dyes from the textile industries, including remazol brilliant blue R, neolane blue and neolane pink. However, several other dyes were partially or not decolourized. In the presence of 1-hydroxybenzotriazole as mediator, only the decolourization of neolane yellow was achieved, while the decolourization of most of the dyes was just slightly improved.
This study is the first report on the purification and the characterization of the laccase from the white rot fungus P. tephropora. The high levels of laccase secreted by this fungal strain as well as its stability suggest that it could be a useful tool for environmental applications.
对白腐菌黄白卧孔菌的漆酶进行特性鉴定,并测试其对合成染料的脱色能力。
在所采用的培养条件下,黄白卧孔菌产生了一种漆酶同工酶,通过硫酸铵沉淀、尺寸排阻色谱和阴离子交换色谱将其纯化至电泳纯。该蛋白为单体,分子量为63 kDa(SDS-PAGE),等电点为3.3。其N端氨基酸序列为SIGPVADLTVTNANI,与虎皮香菇漆酶的相似度最高(86.6%)。该酶的最适pH值因底物而异。对2,6-二甲氧基苯酚(DMP)和2,2'-联氮-双(3-乙基苯并噻唑啉-6-磺酸)(ABTS)的最适pH值分别为4.0和5.0。在标准测定条件下,该酶对DMP和ABTS的Km值分别为7.3和0.4 mmol l(-1)。NaN(3)、EDTA和对香豆酸盐可抑制该漆酶,而SDS和NaBr则不能。漆酶在一些金属离子如Cu(2+)、Co(2+)、Ca(+)、Cd(2+)、Mg(2+)、Mn(2+)、Mo(2+)、Ni(2+)、Li(+)和Al(3+)存在时稳定。粗酶以及纯化后的漆酶能够使纺织工业中的染料脱色,包括活性艳蓝R、新蓝和新粉。然而,其他几种染料只能部分脱色或不能脱色。在1-羟基苯并三唑作为介质存在的情况下,仅实现了新黄的脱色,而大多数染料的脱色仅略有改善。
本研究首次报道了对白腐菌黄白卧孔菌漆酶的纯化和特性鉴定。该真菌菌株分泌的高水平漆酶及其稳定性表明它可能是环境应用中的一种有用工具。