首页> 外文期刊>Bioresource Technology: Biomass, Bioenergy, Biowastes, Conversion Technologies, Biotransformations, Production Technologies >Cloning and expression of a novel, moderately thermostable xylanase-encoding gene (Cfl xyn11A) from Cellulomonas flavigena
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Cloning and expression of a novel, moderately thermostable xylanase-encoding gene (Cfl xyn11A) from Cellulomonas flavigena

机译:一种新的,适度热稳定的木薯纤维单胞菌编码基因(Cfl xyn11A)的克隆和表达

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摘要

The Cfl xyn11A gene, encoding the endo-1,4-beta-xylanase Cfl Xyn11A from Cellulomonas flavigena, was isolated from a genomic DNA library. The open reading frame of the Cfl xyn11A gene was 999 base pairs long and encoded a polypeptide (Cfl Xyn11A) of 332 amino acids with a calculated molecular mass of 35,110 Da. The Cfl xyn11A gene was expressed in Escherichia coil and the recombinant enzyme, with an estimated molecular weight of 31 kDa was purified and xylanase activity was measured. Cfl Xyn11A showed optimal activity at pH 6.5 and 55 degrees C. The enzyme demonstrated moderate thermal stability as Cfl Xyn11A maintained 50% of its activity when incubated at 55 degrees C for 1 h or at 45 degrees C for 6 h. This is the first report describing the cloning, expression and functional characterization of an endo-1,4-beta-xylanase-encoding gene from C. flavigena. Cfl Xyn11A may be suitable for industrial applications in the food and feed industries, or in the pre-treatment of lignocellulosic biomass required to improve the yields of fermentable sugars for bioethanol production.
机译:从基因组DNA文库中分离出Cfl ​​xyn11A基因,该基因编码来自黄褐肉胞菌的内切1,4-β-木聚糖酶Cfl Xyn11A。 Cfl xyn11A基因的开放阅读框长999个碱基对,并编码332个氨基酸的多肽(Cfl Xyn11A),计算分子量为35,110 Da。 Cfl xyn11A基因在大肠埃希菌中表达,并纯化了重组酶,估计分子量为31 kDa,并检测了木聚糖酶活性。 Cfl Xyn11A在pH 6.5和55摄氏度下显示最佳活性。当在55摄氏度下孵育1小时或在45摄氏度下孵育6小时时,Cfl Xyn11A保持50%的活性,因此该酶表现出中等的热稳定性。这是第一份描述黄褐线虫内源1,4-β-木聚糖酶编码基因的克隆,表达和功能表征的报告。 Cfl Xyn11A可能适用于食品和饲料工业中的工业应用,或用于提高生物乙醇生产用可发酵糖收率所需的木质纤维素生物质的预处理。

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