Wartmann Thomas, Stoltenburg Regina, Böer Erik, Sieber Heike, Bartelsen Oliver, Gellissen Gerd, Kunze Gotthard
Institut für Pflanzengenetik und Kulturpflanzenforschung, Corrensstr. 3, 06466 Gatersleben, Germany.
FEMS Yeast Res. 2003 Apr;3(2):223-32. doi: 10.1016/S1567-1356(02)00190-3.
The ALEU2 gene, encoding beta-isopropylmalate dehydrogenase, was isolated from the non-conventional yeast Arxula adeninivorans. The isolated gene harbours an open reading frame of 1086 bp, encoding a putative protein of 362 amino acids. The derived protein sequence shares a high degree of homology with other fungal beta-isopropylmalate dehydrogenases thus confirming the identity of the gene. The isolated ALEU2 gene was tested for its suitability to complement the auxotrophy of an A. adeninivorans aleu2 host. For this purpose the plasmid pAL-ALEU2m which contains the ALEU2 gene as a selection marker and the 25S rDNA for targeting was employed in transformation experiments. Transformants harboured a single copy of the heterologous DNA and were found to be mitotically stable. For assessment of heterologous gene expression, two model genes were incorporated into the vector: the GFP gene, encoding intracellular green fluorescent protein, and the HSA gene, encoding the secreted human serum albumin. For expression control, both gene sequences were fused to the constitutive A. adeninivorans-derived TEF1 promoter and the Saccharomyces cerevisiae-derived PHO5 terminator. In the respective recombinant strains the GFP was localised in the cytoplasm, whereas more than 95% of the HSA accumulated in the culture medium. In initial fermentation trials using a 200-ml shake flask, maximal HSA product levels were observed after 96 h of cultivation.
从非常规酵母嗜腺嘌呤阿苏菌中分离出了编码β-异丙基苹果酸脱氢酶的ALEU2基因。分离出的基因含有一个1086 bp的开放阅读框,编码一个由362个氨基酸组成的推定蛋白。推导的蛋白序列与其他真菌β-异丙基苹果酸脱氢酶具有高度同源性,从而证实了该基因的身份。对分离出的ALEU2基因进行了测试,以确定其是否适合补充嗜腺嘌呤阿苏菌aleu2宿主的营养缺陷型。为此,在转化实验中使用了质粒pAL-ALEU2m,该质粒含有作为选择标记的ALEU2基因和用于靶向的25S rDNA。转化体含有单拷贝的异源DNA,并且发现其在有丝分裂过程中是稳定的。为了评估异源基因的表达,将两个模型基因整合到载体中:编码细胞内绿色荧光蛋白的GFP基因和编码分泌型人血清白蛋白的HSA基因。为了进行表达控制,将两个基因序列都与组成型的嗜腺嘌呤阿苏菌来源的TEF1启动子和酿酒酵母来源的PHO5终止子融合。在各自的重组菌株中,GFP定位于细胞质中,而超过95%的HSA积累在培养基中。在使用200 ml摇瓶进行的初始发酵试验中,培养96 h后观察到了最高的HSA产物水平。