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A purF mutant of Mycobacterium smegmatis has impaired survival during oxygen-starved stationary phase

机译:分枝杆菌的纯菌突变体在氧饥饿的固定阶段期间存活损害

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In this study it was demonstrated that a range of transposon mutants of Mycobacterium smegmatis, previously described as having impaired survival in carbon-starved stationary phase, were not markedly affected in O2-starved stationary-phase survival. One exception was 329B, a purine auxotroph, which showed a precipitous reduction in viability from 108 to 103?c.f.u. ml?1 during the first 5–10?d in O2-starved stationary phase. This was followed by an equally rapid recovery in culturability to a level within 10–100-fold of wild-type levels by 10–20?d into stationary phase. Transduction of the mutation into a clean genetic background demonstrated that the phenotype was due to the transposon insertion, which was shown to be in the purF gene. purF encodes phosphoribosylpyrophosphate amidotransferase, which catalyses the first committed step in purine biosynthesis. The M. smegmatis purF gene, which encodes a protein with a very high degree of similarity to the PurF homologues of Mycobacterium tuberculosis and Mycobacterium leprae, was cloned and shown to substantially complement the O2-starvation phenotype. The recovery in culturabilty of the purF mutant in O2-starved stationary phase did not involve movement of the transposon. In addition, when cells that had recovered culturability were retested, their survival kinetics in stationary phase were identical to the original culture, indicating that their recovery was not explained by the accumulation of suppressor mutations. It is concluded that the survival curve in O2-starved stationary phase for the purF mutant represents its true phenotype and is not a result of subsequent genetic changes in the culture. It is argued that the purF cells lose culturability for a finite period of time in stationary phase. Whether this is due to a fraction of the population dying and then regrowing using a previously undiscovered fermentation pathway, or becoming transiently dormant, or entering an active nonculturable state and subsequently undergoing resuscitation cannot be distinguished at this stage.
机译:在本研究中,证明了分枝杆菌的分枝杆菌的转座子突变体,以前描述的碳饥饿的固定相中的存活受损,在O2-饥饿的固定相存活中没有显着影响。一个例外是329b,嘌呤滋巢营养症,其急性降低了108至103〜103的活力。在o2饥饿的阶段的前5-10℃下m mlα1。然后在野生型水平10-100倍的野生型水平以内的培养性恢复等级,进入固定相。将突变转导入干净的遗传背景中表明表型是由于转座型插入,其显示在pURF基因中。 PURF编码磷酰基偏磷酸磷酸磷酸酶,其催化嘌呤生物合成中的第一个提出的步骤。克隆并显示将具有非常高度相似性与分枝杆菌的紫外线分泌物的紫外线同源物相似性的M. smogmatis purf基因,并显示基本上补充O2-饥饿表型。在O2饥饿的固定阶段的PURF突变体的培养物中的恢复并未涉及转座子的运动。此外,当回收培养性的细胞被重新测试时,它们的存活率在固定相中与原始培养相同,表明它们的恢复未被抑制突变的积累解释。得出结论,PURF突变体的O2-饥饿的固定相中的存活曲线代表了其真正的表型,并且不是培养物的后续遗传变化的结果。有人认为,PURF细胞在固定阶段的有限时间内失去了培养性。无论这是由于人口的一小部分染色,然后使用先前未被发现的发酵途径重新感到重新生成,或者变得瞬时休眠,或进入活性的不培养状态,随后在该阶段不能区分复苏。

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