Ercan Onur, Wels Michiel, Smid Eddy J, Kleerebezem Michiel
Kluyver Centre for Genomics of Industrial Fermentation, Delft, The Netherlands Top Institute Food and Nutrition, Wageningen, The Netherlands Laboratory of Microbiology, Wageningen University, Wageningen, The Netherlands NIZO food research, Ede, The Netherlands.
Top Institute Food and Nutrition, Wageningen, The Netherlands NIZO food research, Ede, The Netherlands.
Appl Environ Microbiol. 2015 Apr;81(7):2554-61. doi: 10.1128/AEM.03748-14. Epub 2015 Jan 30.
This paper describes the transcriptional adaptations of nongrowing, retentostat cultures of Lactococcus lactis to starvation. Near-zero-growth cultures (μ = 0.0001 h(-1)) obtained by extended retentostat cultivation were exposed to starvation by termination of the medium supply for 24 h, followed by a recovery period of another 24 h by reinitiating the medium supply to the retentostat culture. During starvation, the viability of the culture was largely retained, and the expression of genes involved in transcription and translational machineries, cell division, and cell membrane energy metabolism was strongly repressed. Expression of these genes was largely recovered following the reinitiation of the medium supply. Starvation triggered the elevated expression of genes associated with synthesis of branched-chain amino acids, histidine, purine, and riboflavin. The expression of these biosynthesis genes was found to remain at an elevated level after reinitiation of the medium supply. In addition, starvation induced the complete gene set predicted to be involved in natural competence in L. lactis KF147, and the elevated expression of these genes was sustained during the subsequent recovery period, but our attempts to experimentally demonstrate natural transformation in these cells failed. Mining the starvation response gene set identified a conserved cis-acting element that resembles the lactococcal CodY motif in the upstream regions of genes associated with transcription and translational machineries, purine biosynthesis, and natural transformation in L. lactis, suggesting a role for CodY in the observed transcriptome adaptations to starvation in nongrowing cells.
本文描述了乳酸乳球菌非生长状态的恒化器培养物对饥饿的转录适应性。通过延长恒化器培养获得的近零生长培养物(μ = 0.0001 h⁻¹)在培养基供应终止24小时后暴露于饥饿状态,随后通过重新向恒化器培养物供应培养基进行另外24小时的恢复期。在饥饿期间,培养物的活力基本得以保留,参与转录和翻译机制、细胞分裂以及细胞膜能量代谢的基因表达受到强烈抑制。培养基供应重新开始后,这些基因的表达基本恢复。饥饿引发了与支链氨基酸、组氨酸、嘌呤和核黄素合成相关的基因表达升高。发现这些生物合成基因的表达在培养基供应重新开始后仍保持在升高水平。此外,饥饿诱导了乳酸乳球菌KF147中预测参与自然感受态的完整基因集,并且这些基因的表达升高在随后的恢复期持续存在,但我们通过实验证明这些细胞中自然转化的尝试失败了。挖掘饥饿反应基因集在与乳酸乳球菌转录和翻译机制、嘌呤生物合成以及自然转化相关的基因上游区域鉴定出一个保守的顺式作用元件,其类似于乳酸乳球菌的CodY基序,这表明CodY在观察到的非生长细胞对饥饿的转录组适应性中发挥作用。