Uhde C, Schmidt R, Jording D, Selbitschka W, Pühler A
Lehrstuhl für Genetik, Universität Bielefeld, Germany.
J Bacteriol. 1997 Oct;179(20):6432-40. doi: 10.1128/jb.179.20.6432-6440.1997.
A screening method was used to identify Sinorhizobium meliloti mutants which are affected in stationary-phase survival. Of 20,000 individual colonies mutagenized with transposon Tn5-B20, 10 mutant strains which showed poor or no survival in the stationary phase were identified. Analyses of expression patterns of the promoterless lacZ genes in the mutant strains revealed individual induction patterns. Most strains were induced in stationary phase as well as under carbon limitation and in pure H2O, but none of the mutants was induced under heat, alkali stress conditions, or low oxygen tension. Plant inoculation tests revealed that the symbiotic proficiency of the mutants was not affected. Two mutants, however, showed gene induction not only in the stationary phase under free-living conditions but also in the bacteroid state. A long-term starvation test was carried out to examine the ability of the 10 mutants to survive prolonged stationary-phase conditions. All mutants showed a clear decrease in the colony-forming ability under the chosen experimental conditions. Staining with green and red fluorescent nucleic acid stain showed that the mutants fell into two different classes. Seven mutants died during stationary phase; the three other mutants remained viable but did not resume growth after prolonged starvation. Five of the ten Tn5-B20 insertions were cloned from the genomes of the mutant strains. Nucleotide sequence analyses established that the transposon had inserted in five distinctive genes. Database searches revealed that four of the tagged loci corresponded to already characterized genes whose gene products are involved in important cellular processes such as amino acid metabolism or aerobic respiration.
采用一种筛选方法来鉴定在稳定期存活方面受到影响的苜蓿中华根瘤菌突变体。在用转座子Tn5-B20诱变的20000个单菌落中,鉴定出10个在稳定期存活不佳或无法存活的突变菌株。对突变菌株中无启动子的lacZ基因表达模式的分析揭示了各自的诱导模式。大多数菌株在稳定期、碳限制条件下以及纯水中均被诱导,但在热、碱胁迫条件或低氧张力下,没有一个突变体被诱导。植物接种试验表明,突变体的共生能力未受影响。然而,有两个突变体不仅在自由生活条件下的稳定期,而且在类菌体状态下均显示出基因诱导。进行了一项长期饥饿试验,以检测这10个突变体在延长的稳定期条件下的存活能力。在所选实验条件下,所有突变体的菌落形成能力均明显下降。用绿色和红色荧光核酸染料染色表明,突变体分为两类。7个突变体在稳定期死亡;另外3个突变体仍存活,但在长期饥饿后未恢复生长。从突变菌株的基因组中克隆了10个Tn5-B20插入片段中的5个。核苷酸序列分析确定转座子已插入5个不同的基因中。数据库搜索显示,4个被标记的位点对应于已鉴定的基因,其基因产物参与重要的细胞过程,如氨基酸代谢或有氧呼吸。