Expression and maintenance of plasmid resistance in regenerating protoplasts of Bacillus subtilis

C. Sanchez-Rivas
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Abstract

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.

枯草芽孢杆菌再生原生质体质粒抗性的表达与维持
质粒编码的抗性在枯草芽孢杆菌再生原生质体中只有在细胞壁合成恢复后才能表达。对于已经含有质粒(pC194, pT127, pK545)的细胞获得的原生质体或来自peg介导转化的质粒携带细胞,可以观察到这一点。恢复表达需要原生质体在富高渗培养基(SMMP)中孵育2小时,原生质体先前洗涤以去除其溶菌酶含量。较长的孵育时间(24小时)导致再生体的注意;然而,与通常的固体再生板相比,它们中的大多数已经失去了抗性表型。这一发现表明,要么是高固化效应,要么是某种基因失活现象。讨论了将原生质体的聚乙二醇介导转化应用于重组DNA技术时必须考虑的关键问题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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