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A Novel GH10 Xylanase Xynl3-3 from Alkaline Soil: Gene Cloning and Heterogenous Expression

机译:碱性土壤中的新型GH10木聚糖酶Xynl3-3:基因克隆和异源表达。

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Xylanase is the most critical xylan degrading glycoside hydrolases, xylan could be degraded into oligosaccharides, which could be further degraded to xylose by glucosidase and other side-chain Hydrolase. In this study, a novel GH family 10 Xyn13-3 from the genomic DNA of Alkaline Soil was cloned and successfully expressed in Pichia pastoris GS115. The deduced proteins showed low identities with known fungal xylanases which originated from Trichoderma gamsii (61%). The specific activity of purified Xyn13-3 measured by DNS method was 135.24 U/mg. This is a new xylanase that needs further investigation to characterize its use. In order to improve the activity of the recombinant xylanase, severals factors for the optimization of induced culture will be studied, including induction timing, induced time, inducer concentration and inducing temperature, as well as the following study on enzymatic properties which can provide worthful theory data for application.
机译:木聚糖酶是最关键的降解木聚糖的糖苷水解酶,木聚糖可以被降解为寡糖,其可以被葡糖苷酶和其他侧链水解酶进一步降解为木糖。在这项研究中,从碱性土壤基因组DNA克隆了一个新的GH家族10 Xyn13-3,并在毕赤酵母GS115中成功表达。推导的蛋白质与已知的源自木霉属木霉的真菌木聚糖酶(61%)显示出较低的同一性。通过DNS方法测得的纯化的Xyn13-3的比活性为135.24U / mg。这是一种新的木聚糖酶,需要进一步研究以表征其用途。为了提高重组木聚糖酶的活性,将研究诱导培养优化的几个因素,包括诱导时间,诱导时间,诱导剂浓度和诱导温度,以及以下有关酶学性质的研究,这些可以提供有价值的理论。申请数据。

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