Magalhães P O, Ferraz A, Milagres A F M
Departamento de Biotecnologia, Faculdade de Engenharia Química de Lorena, Lorena, SP, Brazil.
J Appl Microbiol. 2006 Aug;101(2):480-6. doi: 10.1111/j.1365-2672.2006.02946.x.
Ceriporiopsis subvermispora produces endoglucanase and beta-glucosidase when cultivated on cellulose or wood, but biodegradation of cellulose during biopulping by C. subvermispora is low even after long periods. To resolve this discrepancy, we grew C. subvermispora on Pinus taeda wood chips and purified the major beta-glucosidases it produced. Kinetic parameters were determined to clear if this fungus produces enzymes capable of yielding assimilable glucose from wood.
Ceriporiopsis subvermispora was grown on P. taeda wood chips under solid-state fermentation. After 30 days, the crude extract obtained from enzyme extraction with sodium acetate buffer 50 mmol l(-1), pH 5.4, was filtrated in membranes with a molecular mass exclusion limit of 100 kDa. Enzyme purification was carried out using successively Sephacryl S-300 gel filtration. The retained fraction attained 76% of beta-glucosidase activity with 3.7-fold purification. Two beta-glucosidases were detected with molecular mass of 110 and 53 kDa. We have performed a characterization of the enzymatic properties of the beta-glucosidase of 110 kDa. The optimum pH and temperature were 3.5 and 60 degrees C, respectively. The K(m) and V(max) values were respectively 3.29 mmol l(-1) and 0.113 micromol min(-1) for the hydrolysis of p-nitrophenyl-beta-glucopyranoside (pNPG) and 2.63 mmol l(-1) and 0.103 micromol min(-1), towards cellobiose. beta-Glucosidase activity was strongly increased by Mn(2+) and Fe(3+), while Cu(2+) severely inhibited it.
Ceriporiopsis subvermispora produces small amounts of beta-glucosidase when grown on wood. The gel filtration and polyacrylamide gel electrophoresis data revealed the existence of two beta-glucosidases with 110 and 53 kDa. The 110 kDa beta-glucosidase from C. subvermispora can be efficiently purified in a single step by gel filtration chromatography. The enzyme has an acid pH optimum with similar activity on pNPG and cellobiose and is thus typical beta-glucosidase.
Ceriporiopsis subvermispora produces beta-glucosidase with limited action during wood decay making able its use for the production of biomechanical and biochemical pulps. The results presented in this paper show the importance of studying the behaviour of beta-glucosidases during biopulping.
黄孢原毛平革菌在纤维素或木材上培养时会产生内切葡聚糖酶和β - 葡萄糖苷酶,但即使经过长时间培养,其在生物制浆过程中对纤维素的生物降解率仍很低。为解决这一差异,我们将黄孢原毛平革菌接种在火炬松木屑上,并纯化其产生的主要β - 葡萄糖苷酶。通过测定动力学参数来确定这种真菌是否能产生可从木材中产生可同化葡萄糖的酶。
将黄孢原毛平革菌在固态发酵条件下接种于火炬松木屑上。30天后,用50 mmol l(-1)、pH 5.4的醋酸钠缓冲液提取酶,所得粗提物经截留分子量为100 kDa的膜过滤。依次使用Sephacryl S - 300凝胶过滤进行酶纯化。截留级分的β - 葡萄糖苷酶活性回收率达76%,纯化倍数为3.7倍。检测到两种分子量分别为110 kDa和53 kDa的β - 葡萄糖苷酶。我们对110 kDa的β - 葡萄糖苷酶的酶学性质进行了表征。其最适pH和温度分别为3.5和60℃。对硝基苯基 - β - 吡喃葡萄糖苷(pNPG)水解的K(m)和V(max)值分别为3.29 mmol l(-1)和0.113 μmol min(-1),对纤维二糖的K(m)和V(max)值分别为2.63 mmol l(-1)和0.103 μmol min(-1)。Mn(2+)和Fe(3+)能显著提高β - 葡萄糖苷酶活性,而Cu(2+)则严重抑制该酶活性。
黄孢原毛平革菌在木材上生长时产生少量β - 葡萄糖苷酶。凝胶过滤和聚丙烯酰胺凝胶电泳数据显示存在分子量为110 kDa和53 kDa的两种β - 葡萄糖苷酶。通过凝胶过滤色谱可一步高效纯化黄孢原毛平革菌的110 kDaβ - 葡萄糖苷酶。该酶最适pH呈酸性,对pNPG和纤维二糖具有相似活性,是典型的β - 葡萄糖苷酶。
黄孢原毛平革菌在木材腐朽过程中产生的β - 葡萄糖苷酶作用有限,使其可用于生物机械浆和生物化学浆的生产。本文结果表明了研究生物制浆过程中β - 葡萄糖苷酶行为的重要性。