Dai MingHua, Ziesman Sara, Ratcliffe Thomas, Gill Ryan T, Copley Shelley D
Department of Molecular, Cellular, and Developmental Biology and Cooperative Institute for Research in Environmental Sciences, University of Colorado at Boulder, CO 80309, USA.
Metab Eng. 2005 Jan;7(1):45-52. doi: 10.1016/j.ymben.2004.09.002.
Protoplast fusion has been used to combine genes from different organisms to create strains with desired properties. A recently developed variant on this approach, genome shuffling, involves generation of a genetically heterogeneous population of a single organism, followed by recursive protoplast fusion to allow recombination of mutations within the fused protoplasts. These are powerful techniques for engineering of microbial strains for desirable industrial properties. However, there is a prevailing opinion that it will be difficult to use these methods for engineering of Gram-negative bacteria because the outer membrane makes protoplast fusion more difficult. Here we describe the successful use of protoplast fusion in Escherichia coli. Using two auxotrophic strains of E. coli, we obtained prototrophic strains by recombination in fused protoplasts at frequencies of 0.05-0.7% based on the number of protoplasts subjected to fusion. This frequency is three-four orders of magnitude better than those previously reported for recombination in fused protoplasts of Gram-negative bacteria such as E. coli and Providencia alcalifaciens.
原生质体融合已被用于组合来自不同生物体的基因,以创造具有所需特性的菌株。这种方法最近开发的一个变体,即基因组重排,涉及生成单个生物体的遗传异质群体,然后进行递归原生质体融合,以允许融合原生质体内的突变重组。这些都是用于改造具有理想工业特性的微生物菌株的强大技术。然而,有一种普遍的观点认为,将这些方法用于革兰氏阴性菌的工程改造将很困难,因为外膜使原生质体融合更加困难。在这里,我们描述了原生质体融合在大肠杆菌中的成功应用。使用两株营养缺陷型大肠杆菌菌株,基于融合的原生质体数量,我们通过融合原生质体中的重组获得了原养型菌株,频率为0.05 - 0.7%。这个频率比之前报道的革兰氏阴性菌(如大肠杆菌和产碱普罗威登斯菌)融合原生质体中的重组频率高三个到四个数量级。