Watson Michael R, Lin Yu-Fei, Hollwey Elizabeth, Dodds Rachel E, Meyer Peter, McDowall Kenneth J
Centre for Plant Sciences and School of Biology, Faculty of Biological Sciences, University of Leeds, LS2 9JT, United Kingdom.
Astbury Centre for Structural Molecular Biology, University of Leeds, LS2 9JT, United Kingdom School of Molecular and Cellular Biology, Faculty of Biological Sciences, University of Leeds, LS2 9JT, United Kingdom
G3 (Bethesda). 2016 Jul 7;6(7):2195-201. doi: 10.1534/g3.116.029405.
The plasmid vector pGreenII is widely used to produce plant transformants via a process that involves propagation in Escherichia coli However, we show here that pGreenII-based constructs can be unstable in E. coli as a consequence of them hampering cell division and promoting cell death. In addition, we describe a new version of pGreenII that does not cause these effects, thereby removing the selective pressure for mutation, and a new strain of E. coli that better tolerates existing pGreenII-based constructs without reducing plasmid yield. The adoption of the new derivative of pGreenII and the E. coli strain, which we have named pViridis and MW906, respectively, should help to ensure the integrity of genes destined for study in plants while they are propagated and manipulated in E. coli The mechanism by which pGreenII perturbs E. coli growth appears to be dysregulation within the ColE1 origin of replication.
质粒载体pGreenII广泛用于通过在大肠杆菌中繁殖的过程来产生植物转化体。然而,我们在此表明,基于pGreenII的构建体在大肠杆菌中可能不稳定,因为它们会阻碍细胞分裂并促进细胞死亡。此外,我们描述了一种不会引起这些效应的新型pGreenII,从而消除了突变的选择压力,以及一种能更好地耐受现有基于pGreenII的构建体而不降低质粒产量的新型大肠杆菌菌株。采用我们分别命名为pViridis和MW906的新型pGreenII衍生物和大肠杆菌菌株,应有助于确保在大肠杆菌中繁殖和操作时用于植物研究的基因的完整性。pGreenII干扰大肠杆菌生长的机制似乎是ColE1复制起点内的失调。