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The constitutive AHSB4 promoter - a novel component of the Arxula adeninivorans-based expression platform

机译:组成型AHSB4启动子-基于Arxula adeninivorans的表达平台的新组成部分

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An Arxula adeninivorans-AHSB4 gene, encoding histone H4, was isolated and characterized. The gene includes a coding sequence of 363 bp disrupted by a 51-bp intron, similar to the situation in other fungal H4 genes. The identity of the gene was confirmed by the high degree of homology of the derived amino acid sequence with that of other H4 histones. The gene is strongly and constitutively expressed, maintaining this expression profile under salt-stress conditions. The AHSB4 promoter was tested for suitability in heterologous gene expression using genes encoding the intracellular green fluorescent protein and the secreted human serum albumin (HSA) for assessment. Plasmids incorporating respective expression cassettes were used to transform the host strain A. adeninivorans LS3, which forms budding cells at 30 degreesC, and strain 135, which forms mycelia under these conditions. Transformants of both types were found to harbor a single copy of the heterologous DNA. Strong constitutive expression was observed during culture in salt-containing and salt-free media, as expected from the expression profile of AHSB4. In 200-ml shake-flask cultures, maximal HSA levels of 20 mg l(-1) culture medium were achieved. This productivity could be increased to 50 mg l(-1) in strains harboring two copies of the expression cassette. The AHSB4 promoter thus provides an attractive component for constitutive heterologous gene expression under salt-free and salt-stress conditions. [References: 46]
机译:分离并鉴定了编码组蛋白H4的Arxula adeninivorans-AHSB4基因。该基因包括一个被51 bp内含子打断的363 bp编码序列,类似于其他真菌H4基因的情况。通过衍生的氨基酸序列与其他H4组蛋白的高度同源性证实了该基因的身份。该基因被强烈且组成性表达,在盐胁迫条件下保持该表达谱。使用编码细胞内绿色荧光蛋白的基因和分泌的人血清白蛋白(HSA)进行评估,测试了AHSB4启动子在异源基因表达中的适用性。在这些条件下,使用结合了各个表达盒的质粒来转化宿主菌株A. adeninivorans LS3和菌株135,该菌株在30℃下形成芽细胞,而菌株135在其上形成菌丝。发现两种类型的转化体均具有异源DNA的单个拷贝。如从AHSB4的表达谱所预期的,在含盐和无盐培养基中培养期间观察到强的组成型表达。在200 ml摇瓶培养物中,可达到20 mg l(-1)培养基的最大HSA水平。在具有两个表达盒拷贝的菌株中,这种生产率可以提高到50 mg l(-1)。 AHSB4启动子因此为无盐和盐胁迫条件下组成型异源基因表达提供了一个有吸引力的组件。 [参考:46]

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