Millard Pierre, Pérochon Julien, Létisse Fabien
TBI, Université de Toulouse, INSA, INRAE, CNRS, Toulouse, France.
Université Toulouse III-Paul Sabatier, Toulouse, France.
Appl Environ Microbiol. 2021 Jul 27;87(16):e0071921. doi: 10.1128/AEM.00719-21.
l-Rhamnose and l-fucose are the two main 6-deoxyhexoses Escherichia coli can use as carbon and energy sources. Deoxyhexose metabolism leads to the formation of lactaldehyde, whose fate depends on oxygen availability. Under anaerobic conditions, lactaldehyde is reduced to 1,2-propanediol, whereas under aerobic conditions, it should be oxidized into lactate and then channeled into the central metabolism. However, although this all-or-nothing view is accepted in the literature, it seems overly simplistic since propanediol is also reported to be present in the culture medium during aerobic growth on l-fucose. To clarify the functioning of 6-deoxyhexose sugar metabolism, a quantitative metabolic analysis was performed to determine extra- and intracellular fluxes in E. coli K-12 MG1655 (a laboratory strain) and in E. coli Nissle 1917 (a human commensal strain) during anaerobic and aerobic growth on l-rhamnose and l-fucose. As expected, lactaldehyde is fully reduced to 1,2-propanediol under anoxic conditions, allowing complete reoxidation of the NADH produced by glyceraldehyde-3-phosphate-dehydrogenase. We also found that net ATP synthesis is ensured by acetate production. More surprisingly, lactaldehyde is also primarily reduced into 1,2-propanediol under aerobic conditions. For growth on l-fucose, C-metabolic flux analysis revealed a large excess of available energy, highlighting the need to better characterize ATP utilization processes. The probiotic E. coli Nissle 1917 strain exhibits similar metabolic traits, indicating that they are not the result of the K-12 strain's prolonged laboratory use. E. coli's ability to survive in, grow in, and colonize the gastrointestinal tract stems from its use of partially digested food and hydrolyzed glycosylated proteins (mucins) from the intestinal mucus layer as substrates. These include l-fucose and l-rhamnose, two 6-deoxyhexose sugars, whose catabolic pathways have been established by genetic and biochemical studies. However, the functioning of these pathways has only partially been elucidated. Our quantitative metabolic analysis provides a comprehensive picture of 6-deoxyhexose sugar metabolism in E. coli under anaerobic and aerobic conditions. We found that 1,2-propanediol is a major by-product under both conditions, revealing the key role of fermentative pathways in 6-deoxyhexose sugar metabolism. This metabolic trait is shared by both E. coli strains studied here, a laboratory strain and a probiotic strain. Our findings add to our understanding of E. coli's metabolism and of its functioning in the bacterium's natural environment.
L-鼠李糖和L-岩藻糖是大肠杆菌可作为碳源和能源利用的两种主要的6-脱氧己糖。脱氧己糖代谢会导致乳醛的形成,其去向取决于氧气的可利用性。在厌氧条件下,乳醛被还原为1,2-丙二醇,而在有氧条件下,它应被氧化为乳酸,然后进入中心代谢途径。然而,尽管这种非此即彼的观点在文献中被认可,但它似乎过于简单化了,因为据报道在以L-岩藻糖为碳源的有氧生长过程中,丙二醇也存在于培养基中。为了阐明6-脱氧己糖代谢的功能,我们进行了定量代谢分析,以确定大肠杆菌K-12 MG1655(一种实验室菌株)和大肠杆菌Nissle 1917(一种人体共生菌株)在以L-鼠李糖和L-岩藻糖为碳源进行厌氧和好氧生长期间的胞外和胞内通量。正如预期的那样,在缺氧条件下,乳醛完全被还原为1,2-丙二醇,从而使甘油醛-3-磷酸脱氢酶产生的NADH得以完全再氧化。我们还发现,通过乙酸盐的产生确保了净ATP的合成。更令人惊讶的是,在有氧条件下,乳醛也主要被还原为1,2-丙二醇。对于以L-岩藻糖为碳源的生长,碳代谢通量分析显示有大量过剩的可用能量,这突出了更好地表征ATP利用过程的必要性。益生菌大肠杆菌Nissle 1917菌株表现出相似的代谢特征,表明这些特征并非K-12菌株长期实验室培养的结果。大肠杆菌在胃肠道中生存、生长和定殖的能力源于它利用肠道黏液层中部分消化的食物和水解的糖基化蛋白(黏蛋白)作为底物。这些底物包括L-岩藻糖和L-鼠李糖这两种6-脱氧己糖,其分解代谢途径已通过遗传学和生物化学研究得以确定。然而,这些途径的功能仅得到了部分阐明。我们的定量代谢分析提供了大肠杆菌在厌氧和好氧条件下6-脱氧己糖代谢的全面图景。我们发现,在两种条件下1,2-丙二醇都是主要的副产物,这揭示了发酵途径在6-脱氧己糖代谢中的关键作用。这里研究的两种大肠杆菌菌株,即一种实验室菌株和一种益生菌菌株,都具有这种代谢特征。我们的研究结果增进了我们对大肠杆菌代谢及其在细菌自然环境中功能的理解。