Wartmann T, Bellebna C, Böer E, Bartelsen O, Gellissen G, Kunze G
Institut für Pflanzengenetik und Kulturpflanzenforschung, Corrensstrasse 3, 06466 Gatersleben, Germany.
Appl Microbiol Biotechnol. 2003 Oct;62(5-6):528-35. doi: 10.1007/s00253-003-1323-6. Epub 2003 May 6.
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 degrees C, 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.
分离并鉴定了一个来自嗜腺嘌呤丛赤壳菌-AHSB4的编码组蛋白H4的基因。该基因包含一个363 bp的编码序列,被一个51 bp的内含子打断,这与其他真菌H4基因的情况类似。通过推导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。该基因强烈且组成型表达,在盐胁迫条件下保持这种表达模式。使用编码细胞内绿色荧光蛋白和分泌型人血清白蛋白(HSA)的基因来评估AHSB4启动子在异源基因表达中的适用性。将包含各自表达盒的质粒用于转化宿主菌株嗜腺嘌呤丛赤壳菌LS3(其在30℃下形成芽殖细胞)和菌株135(其在这些条件下形成菌丝体)。发现这两种类型的转化体都含有单拷贝的异源DNA。正如从AHSB4的表达模式所预期的那样,在含盐水和无盐培养基培养期间观察到了强烈的组成型表达。在200 ml摇瓶培养中,培养基中HSA的最大水平达到20 mg l(-1)。在含有两个拷贝表达盒的菌株中,该产量可提高到50 mg l(-1)。因此,AHSB4启动子为在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。