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首页> 外文期刊>Biotechnology & Biotechnological Equipment >Characterization of Enzyme Endoxylanase Produced by Mutants Strains of Aspergillus Awamori K-1
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Characterization of Enzyme Endoxylanase Produced by Mutants Strains of Aspergillus Awamori K-1

机译:泡盛曲霉K-1突变株产生的酶内切木聚糖酶的表征

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Xylanolytic enzymes of microbial origin have received great attention due to their biotechnological utility and potential applications in a range of industrial processes but the observed effects vary depending on xylanase specificities. The goal of this investigation was to determine the endoxylanase enzyme production ability and molecular characteristics of fungal strains Aspergillus awamori K-1 and its mutant strains A59, A50, A45 and A60. The strains were cultivated in liquid culture with 1% wheat bran and 2% ground corn-cobs as inducer. Maximum enzyme production of parent strain Aspergillus awamori K-1 of 42,35 IU/ml and of mutant strains A59 - 96,91 IU/ml, A50 - 71,67 IU/ml, A45 - 74,04 IU/ml and A60 - 62,59 IU/ml was determined after 72?¢????96 h of cultivation. Extracellular endoxylanase was partially purified from the culture filtrates of five strains, using molecular sieve chromatography with two type of Sephadex?¢????G 50 and G100. The purification conditions were optimized and the main endoxylanase activity was determined in second fraction in case of Sephadex G100. The partial purified enzyme fractions showed the same band for all strains on SDS polyacrylamide gel electrophoresis (SDS-PAGE) with an apparent molecular weight of 32 kDa.
机译:微生物来源的木聚糖分解酶由于其生物技术用途和在一系列工业过程中的潜在应用而受到了极大的关注,但是观察到的效果取决于木聚糖酶的特异性。该研究的目的是确定真菌菌株泡盛曲霉K-1及其突变菌株A59,A50,A45和A60的内切木聚糖酶生产能力和分子特性。菌株在液体培养中以1%麦麸和2%磨碎的玉米芯作为诱导物进行培养。亲本菌株泡盛曲霉K-1的最大酶产量为42,35 IU / ml,突变菌株A59-96,91 IU / ml,A50-71,67 IU / ml,A45-74,04 IU / ml和A60培养72小时后测定62.59IU / ml。使用分子筛层析法,用两种类型的Sephadex TM 50 G100和G100,从五个菌株的培养滤液中部分纯化细胞外内切木聚糖酶。对于Sephadex G100,优化了纯化条件,并确定了第二部分的主要内切木聚糖酶活性。对于SDS聚丙烯酰胺凝胶电泳(SDS-PAGE)上的所有菌株,部分纯化的酶馏分均显示相同的条带,表观分子量为32 kDa。

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