首页> 外文期刊>British Microbiology Research Journal >Utilization of Terminalia superba Sawdust asSubstrate for Laccase Production by Trametes sp.Isolate B7 under Solid State Fermentation
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Utilization of Terminalia superba Sawdust asSubstrate for Laccase Production by Trametes sp.Isolate B7 under Solid State Fermentation

机译:利用榄仁木屑作为底物在固态发酵条件下由曲霉菌分离物B7生产漆酶

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Laccases catalyze a broad range of substrates due to their low substrate specificity and strong oxidative potentials. It can be produce from different sources which include plants, prokaryotes, arthropods and fungi especially Trametes sp. In this study laccases were produced by Trametes sp. isolate B7 utilizing sawdust as substrate in solid state fermentation. A fraction of the crude enzyme solution was partially purified and characterized. The highest total soluble protein (3.6 mg/mL) and laccase activity (2356 U/mL) were obtained on day 14 and 18 respectively at pH 5.0. The laccase was 2.3 and 9.0 times purified with 1487 U/mL and 5380 U/mL specific activity for pellets and dialysate respectively. The purified laccase was active in acidic pH (3.0 - 6.0) and temperature at 20 - 80°C while, stability was highest at pH 6.0 (89% for 24 hr) and 70°C (100% for 1 hr). Manganese, Lead, Mercury, Copper and Magnesium ions significantly increased laccase activity whereas Aluminium, Potassium, Iron and Zinc ions decrease activity of the purified enzyme (P = .05). EDTA activated laccase activity at 2 mM (117%) while L-cysteine inhibited enzyme activity at 1 mM - 5mM concentrations. Kinetic studies of the purified laccase showed KM 33 μM and Vmax 1.91 μMol./min/mL with molecular weight of ~36 kDa using N-PAGE. The purified laccase remained active in acidic conditions with high thermostability and resistance to inhibition of most of the metallic ions and EDTA tested. Thus, the enzyme was a versatile tool for biotechnological, industrial and bioremediation processes including polycyclic aromatic hydrocarbons, pesticides and dye wastewaters among other xenobiotics.
机译:漆酶由于低的底物特异性和强的氧化电位而催化多种底物。它可以从不同的来源生产,包括植物,原核生物,节肢动物和真菌,特别是Trametes sp。在这项研究中,漆酶由Trametes sp。生产。在固态发酵中利用木屑作为底物分离出B7。一部分粗酶溶液被部分纯化和表征。在pH 5.0的第14天和第18天分别获得最高的总可溶性蛋白(3.6 mg / mL)和漆酶活性(2356 U / mL)。漆酶分别以沉淀物和透析液的1487 U / mL和5380 U / mL的比活性纯化2.3和9.0倍。纯化的漆酶在酸性pH(3.0-6.0)和20-80°C的温度下具有活性,而稳定性在pH 6.0(89%持续24小时)和70°C(100%持续1小时)时最高。锰,铅,汞,铜和镁离子显着提高了漆酶活性,而铝,钾,铁和锌离子则降低了纯化酶的活性(P = 0.05)。 EDTA在2 mM(117%)下激活漆酶活性,而L-半胱氨酸在1 mM-5mM浓度下抑制酶活性。纯化的漆酶的动力学研究表明,使用N-PAGE测得的KM为33μM,Vmax为1.91μMol。/ min / mL,分子量约为36 kDa。纯化的漆酶在酸性条件下保持活性,并具有很高的热稳定性,并且对大多数金属离子和EDTA的抑制都有抵抗力。因此,该酶是生物技术,工业和生物修复过程的多功能工具,包括多环芳烃,农药和染料废水以及其他异生物。

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