Ganesan Balasubramanian, Stuart Mark R, Weimer Bart C
Center for Integrated BioSystems, Utah State University, Logan, UT 84322-4700, USA.
Appl Environ Microbiol. 2007 Apr;73(8):2498-512. doi: 10.1128/AEM.01832-06. Epub 2007 Feb 9.
This study characterized the ability of lactococci to become nonculturable under carbohydrate starvation while maintaining metabolic activity. We determined the changes in physiological parameters and extracellular substrate levels of multiple lactococcal strains under a number of environmental conditions along with whole-genome expression profiles. Three distinct phases were observed, logarithmic growth, sugar exhaustion, and nonculturability. Shortly after carbohydrate starvation, each lactococcal strain lost the ability to form colonies on solid media but maintained an intact cell membrane and metabolic activity for over 3.5 years. ML3, a strain that metabolized lactose rapidly, reached nonculturability within 1 week. Strains that metabolized lactose slowly (SK11) or not at all (IL1403) required 1 to 3 months to become nonculturable. In all cases, the cells contained at least 100 pM of intracellular ATP after 6 months of starvation and remained at that level for the remainder of the study. Aminopeptidase and lipase/esterase activities decreased below detection limits during the nonculturable phase. During sugar exhaustion and entry into nonculturability, serine and methionine were produced, while glutamine and arginine were depleted from the medium. The cells retained the ability to transport amino acids via proton motive force and peptides via ATP-driven translocation. The addition of branched-chain amino acids to the culture medium resulted in increased intracellular ATP levels and new metabolic products, indicating that branched-chain amino acid catabolism resulted in energy and metabolic products to support survival during starvation. Gene expression analysis showed that the genes responsible for sugar metabolism were repressed as the cells entered nonculturability. The genes responsible for cell division were repressed, while autolysis and cell wall metabolism genes were induced neither at starvation nor during nonculturability. Taken together, these observations verify that carbohydrate-starved lactococci attain a nonculturable state wherein sugar metabolism, cell division, and autolysis are repressed, allowing the cells to maintain transcription, metabolic activity, and energy production during a state that produces new metabolites not associated with logarithmic growth.
本研究描述了乳酸球菌在碳水化合物饥饿条件下进入不可培养状态但仍保持代谢活性的能力。我们测定了多种乳酸球菌菌株在多种环境条件下生理参数和细胞外底物水平的变化以及全基因组表达谱。观察到三个不同阶段,对数生长期、糖耗尽期和不可培养期。碳水化合物饥饿后不久,每种乳酸球菌菌株失去在固体培养基上形成菌落的能力,但细胞膜保持完整且代谢活性维持超过3.5年。ML3是一种能快速代谢乳糖的菌株,在1周内进入不可培养状态。代谢乳糖缓慢(SK11)或完全不代谢乳糖(IL1403)的菌株需要1至3个月才进入不可培养状态。在所有情况下,饥饿6个月后细胞内至少含有100 pM的ATP,并在研究剩余时间内维持在该水平。在不可培养阶段,氨肽酶和脂肪酶/酯酶活性降至检测限以下。在糖耗尽和进入不可培养状态期间,产生了丝氨酸和蛋氨酸,而谷氨酰胺和精氨酸从培养基中耗尽。细胞保留了通过质子动力运输氨基酸以及通过ATP驱动转运肽的能力。向培养基中添加支链氨基酸导致细胞内ATP水平升高和产生新的代谢产物,表明支链氨基酸分解代谢产生能量和代谢产物以支持饥饿期间的存活。基因表达分析表明,随着细胞进入不可培养状态,负责糖代谢的基因受到抑制。负责细胞分裂的基因受到抑制,而自溶和细胞壁代谢基因在饥饿期间和不可培养期间均未被诱导。综上所述,这些观察结果证实,碳水化合物饥饿的乳酸球菌进入一种不可培养状态,其中糖代谢、细胞分裂和自溶受到抑制,使细胞在产生与对数生长无关的新代谢产物的状态下维持转录、代谢活性和能量产生。