Mellon F M, Casselton L A
School of Biological Sciences, Queen Mary College, London, UK.
Curr Genet. 1988 Nov;14(5):451-6. doi: 10.1007/BF00521268.
Seven transformants having varying numbers of non-homologously integrated copies of the isocitrate lyase gene, acu-7, were analysed for enzyme activity. Maximum levels of activity, 3.8 times that of the wild type, were observed in a transformant with only two gene copies whereas eight gene copies in another transformant led to only 25% wild type activity. Acu+ transformants were not selected directly for expression of acu-7 but as cotransformants. Analysis of 14 transformants not expressing acu-7 showed that four contained transforming DNA sequences and significantly, two had evidence of non-homologously integrated tandem duplications of the entire acu-7 plasmid DNA. The site of integration of the gene was thus important in determining whether or not it was expressed and to what level it was expressed. A comparison of induced and uninduced levels of enzyme activity confirmed that the enzyme was still tightly regulated.
对七个含有不同数量异柠檬酸裂解酶基因acu - 7非同源整合拷贝的转化体进行了酶活性分析。在一个仅含有两个基因拷贝的转化体中观察到了最高活性水平,是野生型的3.8倍,而在另一个含有八个基因拷贝的转化体中,活性仅为野生型的25%。Acu +转化体不是直接选择用于acu - 7的表达,而是作为共转化体。对14个不表达acu - 7的转化体进行分析表明,其中四个含有转化DNA序列,重要的是,有两个有证据表明整个acu - 7质粒DNA存在非同源整合串联重复。因此,基因的整合位点对于确定其是否表达以及表达水平至关重要。对诱导和未诱导的酶活性水平进行比较证实,该酶仍然受到严格调控。