Faculty of Human Life and Environment, Nara Women's University, Nara, Japan.
PLoS One. 2011 Jan 20;6(1):e16355. doi: 10.1371/journal.pone.0016355.
Escherichia coli is not assumed to be naturally transformable. However, several recent reports have shown that E. coli can express modest genetic competence in certain conditions that may arise in its environment. We have shown previously that spontaneous lateral transfer of non-conjugative plasmids occurs in a colony biofilm of mixed E. coli strains (a set of a donor strain harbouring a plasmid and a plasmid-free recipient strain). In this study, with high-frequency combinations of strains and a plasmid, we constructed the same lateral plasmid transfer system in liquid culture. Using this system, we demonstrated that this lateral plasmid transfer was DNase-sensitive, indicating that it is a kind of transformation in which DNase-accessible extracellular naked DNA is essential. However, this transformation did not occur with purified plasmid DNA and required a direct supply of plasmid from co-existing donor cells. Based on this feature, we have termed this transformation type as 'cell-to-cell transformation'. Analyses using medium conditioned with the high-frequency strain revealed that this strain released a certain factor(s) that promoted cell-to-cell transformation and arrested growth of the other strains. This factor is heat-labile and protease-sensitive, and its roughly estimated molecular mass was between ∼9 kDa and ∼30 kDa, indicating that it is a polypeptide factor. Interestingly, this factor was effective even when the conditioned medium was diluted 10(-5)-10(-6), suggesting that it acts like a pheromone with high bioactivity. Based on these results, we propose that cell-to-cell transformation is a novel natural transformation mechanism in E. coli that requires cell-derived DNA and is promoted by a peptide pheromone. This is the first evidence that suggests the existence of a peptide pheromone-regulated transformation mechanism in E. coli and in Gram-negative bacteria.
大肠杆菌被认为不能自然转化。然而,最近的几项研究表明,在某些环境条件下,大肠杆菌可以表达适度的遗传能力。我们之前已经表明,非接合质粒在混合大肠杆菌菌株的菌落生物膜中会自发发生侧向转移(一组携带质粒的供体菌株和无质粒的受体菌株)。在这项研究中,我们使用高频率的菌株组合和质粒构建了相同的液体培养中的侧向质粒转移系统。使用该系统,我们证明了这种侧向质粒转移对 DNase 敏感,表明它是一种转化形式,其中 DNase 可及的细胞外裸露 DNA 是必需的。然而,这种转化不能用纯化的质粒 DNA 发生,并且需要来自共存供体细胞的质粒的直接供应。基于此特征,我们将这种转化类型命名为“细胞间转化”。使用高频菌株处理的培养基进行的分析表明,该菌株释放了某种促进细胞间转化和其他菌株生长停滞的因子。该因子对热不稳定且对蛋白酶敏感,其大致估计的分子量在 9 kDa 到 30 kDa 之间,表明它是一种多肽因子。有趣的是,即使将条件培养基稀释 10(-5)-10(-6),该因子仍然有效,表明它像具有高生物活性的信息素一样发挥作用。基于这些结果,我们提出细胞间转化是大肠杆菌中一种新的自然转化机制,需要细胞衍生的 DNA,并受到肽信息素的促进。这是第一个表明在大肠杆菌和革兰氏阴性细菌中存在肽信息素调控转化机制的证据。