Sanchez-Rivas C
Instituto de Investigaciones en Ingeniería Genética y Biología Molecular (INGEBI-CONICET), Buenos Aires.
Ann Inst Pasteur Microbiol. 1988 Jul-Aug;139(4):403-9. doi: 10.1016/0769-2609(88)90103-2.
Expression of plasmid-encoded resistances in regenerating protoplasts of Bacillus subtilis occurs only after wall synthesis has been resumed. This is observed for protoplasts obtained from cells already containing plasmids (pC194, pT127, pK545) or for plasmid-bearing cells coming from a PEG-mediated transformation. Recovery of expression needs a 2-h incubation of protoplasts, previously washed to get rid of their lysozyme content, in rich hypertonic medium (SMMP). A longer incubation (24-h) results in the obtention of regenerants; however, most of them have lost their resistant phenotype in contrast to those obtained from the usual solid regeneration plates. This finding suggests either a high curing effect or some kind of gene inactivation phenomenon. Discussion is focused on the critical points that have to be considered when polyethylenglycol-mediated transformation of protoplasts is applied to recombinant DNA technology.
枯草芽孢杆菌原生质体再生过程中,质粒编码抗性的表达仅在细胞壁合成恢复后才会出现。从已含有质粒(pC194、pT127、pK545)的细胞中获得的原生质体,或来自聚乙二醇介导转化的含质粒细胞,均观察到这种现象。表达的恢复需要将先前洗涤以去除溶菌酶含量的原生质体在丰富的高渗培养基(SMMP)中孵育2小时。较长时间的孵育(24小时)会得到再生体;然而,与从常规固体再生平板获得的再生体相比,大多数再生体已失去其抗性表型。这一发现表明存在高消除效应或某种基因失活现象。讨论集中在将聚乙二醇介导的原生质体转化应用于重组DNA技术时必须考虑的关键点上。