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首页> 外文期刊>FEMS Microbiology Letters >Evaluation of the catalase promoter for expressing the alkaline xylanase gene (alx) in Aspergillus niger
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Evaluation of the catalase promoter for expressing the alkaline xylanase gene (alx) in Aspergillus niger

机译:评价过氧化氢酶启动子在黑曲霉中表达碱性木聚糖酶基因(alx)

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摘要

Aspergillus niger represents a promising host for the expression of recombinant proteins, but only a few expression systems are available for this organism. In this study, the inducible catalase promoter (PcatR) from A. niger was characterized. For this, constructs were developed and checked for the expression of the alkaline xylanase gene transcriptionally fused under the cat R promoter. Two versions of the catalase (catR) promoter sequence from A. niger (P _(cat300), P _(cat924)) were isolated and tested for their ability to drive expression of the alkaline xylanase (alx) gene. P _(cat924) showed better efficiency (more than 10-fold increase in AlX activity compared to P _(cat300)) under the optimized culture conditions. Induction of the catR promoter with 0.20% H _2O _2 and 1.5% CaCO _3 in the culture medium, further increased expression of AlX 2.61- and 2.20-fold, respectively, clarifying its inducible nature. Specific induction or repression of the catR promoter provides the possibility for utilization of this promoter in heterologous protein production.
机译:黑曲霉代表了重组蛋白表达的有希望的宿主,但是该生物仅有少数表达系统可用。在这项研究中,表征了来自黑曲霉的诱导型过氧化氢酶启动子(PcatR)。为此,开发了构建体并检查了在cat R启动子下转录融合的碱性木聚糖酶基因的表达。分离了来自黑曲霉的两个版本的过氧化氢酶(catR)启动子序列(P_(cat300),P_(cat924)),并测试了它们驱动碱性木聚糖酶(alx)基因表达的能力。在优化的培养条件下,P_(cat924)显示出更好的效率(与P_(cat300)相比,AlX活性提高了10倍以上)。在培养基中用0.20%H _2O _2和1.5%CaCO _3诱导catR启动子后,AlX的表达分别增加了2.61倍和2.20倍,从而阐明了其诱导性。 catR启动子的特异性诱导或抑制为在异源蛋白质生产中利用该启动子提供了可能性。

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