Van Hofwegen Dustin J, Hovde Carolyn J, Minnich Scott A
Department of Biological Sciences University of Idaho, Moscow, Idaho, USA.
Bi-State School of Food Science, University of Idaho, Moscow, Idaho, USA.
J Bacteriol. 2016 Feb 1;198(7):1022-34. doi: 10.1128/JB.00831-15.
The isolation of aerobic citrate-utilizing Escherichia coli (Cit(+)) in long-term evolution experiments (LTEE) has been termed a rare, innovative, presumptive speciation event. We hypothesized that direct selection would rapidly yield the same class of E. coli Cit(+) mutants and follow the same genetic trajectory: potentiation, actualization, and refinement. This hypothesis was tested with wild-type E. coli strain B and with K-12 and three K-12 derivatives: an E. coli ΔrpoS::kan mutant (impaired for stationary-phase survival), an E. coli ΔcitT::kan mutant (deleted for the anaerobic citrate/succinate antiporter), and an E. coli ΔdctA::kan mutant (deleted for the aerobic succinate transporter). E. coli underwent adaptation to aerobic citrate metabolism that was readily and repeatedly achieved using minimal medium supplemented with citrate (M9C), M9C with 0.005% glycerol, or M9C with 0.0025% glucose. Forty-six independent E. coli Cit(+) mutants were isolated from all E. coli derivatives except the E. coli ΔcitT::kan mutant. Potentiation/actualization mutations occurred within as few as 12 generations, and refinement mutations occurred within 100 generations. Citrate utilization was confirmed using Simmons, Christensen, and LeMaster Richards citrate media and quantified by mass spectrometry. E. coli Cit(+) mutants grew in clumps and in long incompletely divided chains, a phenotype that was reversible in rich media. Genomic DNA sequencing of four E. coli Cit(+) mutants revealed the required sequence of mutational events leading to a refined Cit(+) mutant. These events showed amplified citT and dctA loci followed by DNA rearrangements consistent with promoter capture events for citT. These mutations were equivalent to the amplification and promoter capture CitT-activating mutations identified in the LTEE.IMPORTANCE E. coli cannot use citrate aerobically. Long-term evolution experiments (LTEE) performed by Blount et al. (Z. D. Blount, J. E. Barrick, C. J. Davidson, and R. E. Lenski, Nature 489:513-518, 2012, http://dx.doi.org/10.1038/nature11514 ) found a single aerobic, citrate-utilizing E. coli strain after 33,000 generations (15 years). This was interpreted as a speciation event. Here we show why it probably was not a speciation event. Using similar media, 46 independent citrate-utilizing mutants were isolated in as few as 12 to 100 generations. Genomic DNA sequencing revealed an amplification of the citT and dctA loci and DNA rearrangements to capture a promoter to express CitT, aerobically. These are members of the same class of mutations identified by the LTEE. We conclude that the rarity of the LTEE mutant was an artifact of the experimental conditions and not a unique evolutionary event. No new genetic information (novel gene function) evolved.
在长期进化实验(LTEE)中分离出的能利用需氧柠檬酸盐的大肠杆菌(Cit(+))被认为是一种罕见的、创新性的、推测性的物种形成事件。我们假设直接选择会迅速产生同一类大肠杆菌Cit(+)突变体,并遵循相同的遗传轨迹:增强、实现和优化。我们用野生型大肠杆菌B菌株、K-12以及三种K-12衍生物对这一假设进行了验证:一种大肠杆菌ΔrpoS::kan突变体(在稳定期存活方面受损)、一种大肠杆菌ΔcitT::kan突变体(缺失厌氧柠檬酸盐/琥珀酸盐反向转运蛋白)以及一种大肠杆菌ΔdctA::kan突变体(缺失需氧琥珀酸盐转运蛋白)。大肠杆菌通过在添加柠檬酸盐的基本培养基(M9C)、添加0.005%甘油的M9C或添加0.0025%葡萄糖的M9C中培养,很容易且能反复实现对需氧柠檬酸盐代谢的适应。从除大肠杆菌ΔcitT::kan突变体之外的所有大肠杆菌衍生物中分离出了46个独立的大肠杆菌Cit(+)突变体。增强/实现突变在短短12代内就出现了,而优化突变在100代内出现。使用西蒙斯、克里斯蒂安森和勒马斯特·理查兹柠檬酸盐培养基确认了柠檬酸盐利用情况,并通过质谱法进行了定量分析。大肠杆菌Cit(+)突变体以团块和长的未完全分裂的链状生长,这种表型在丰富培养基中是可逆的。对四个大肠杆菌Cit(+)突变体进行的基因组DNA测序揭示了导致一个优化的Cit(+)突变体所需的突变事件序列。这些事件显示citT和dctA基因座扩增,随后是与citT启动子捕获事件一致的DNA重排。这些突变等同于在LTEE中鉴定出的扩增和启动子捕获CitT激活突变。
大肠杆菌不能需氧利用柠檬酸盐。布朗特等人(Z. D. 布朗特、J. E. 巴里克、C. J. 戴维森和R. E. 伦斯基,《自然》489:513 - 518,2012,http://dx.doi.org/10.1038/nature11514)进行的长期进化实验发现,经过33000代(15年)后出现了一株能需氧利用柠檬酸盐的单一大肠杆菌菌株。这被解释为一次物种形成事件。在此我们表明为什么这可能不是一次物种形成事件。使用类似的培养基,在短短12至100代内就分离出了46个独立的能利用柠檬酸盐的突变体。基因组DNA测序揭示了citT和dctA基因座的扩增以及DNA重排,以捕获一个启动子来需氧表达CitT。这些是LTEE鉴定出的同一类突变的成员。我们得出结论,LTEE突变体的罕见性是实验条件造成的假象,而不是一个独特的进化事件。没有新的遗传信息(新的基因功能)进化出来。