Calderini Elia, Celebioglu Hasan Ufuk, Villarroel Julia, Jacobsen Susanne, Svensson Birte, Pessione Enrica
Department of Life Sciences and Systems Biology, Università di Torino, Torino, Italy.
Enzyme and Protein Chemistry Group, Department of Biotechnology and Biomedicine, Technical University of Denmark, Lyngby, Denmark.
Proteomics. 2017 Mar;17(5). doi: 10.1002/pmic.201600178.
Probiotic cultures encounter oxidative conditions during manufacturing, yet protein abundance changes induced by such stress have not been characterized for some of the most common probiotics and starters. This comparative proteomics investigation focuses on the response by Lactobacillus acidophilus NCFM to H O simulating an oxidative environment. Bacterial growth was monitored by BioScreen and batch cultures were harvested at exponential phase for protein profiling of stress responses by 2D gel based comparative proteomics. Proteins identified in 19 of 21 spots changing in abundance due to H O were typically related to carbohydrate and energy metabolism, cysteine biosynthesis, and stress. In particular, increased cysteine synthase activity may accumulate a cysteine pool relevant for protein stability, enzyme catalysis, and the disulfide-reducing pathway. The stress response further included elevated abundance of biomolecules reducing damage such as enzymes from DNA repair pathways and metabolic enzymes with active site cysteine residues. By contrast, a protein-refolding chaperone showed reduced abundance, possibly reflecting severe oxidative protein destruction that was not overcome by refolding. The proteome analysis provides novel insight into resistance mechanisms in lactic acid bacteria against reactive oxygen species and constitutes a valuable starting point for improving industrial processes, food design, or strain engineering preserving microorganism viability.
益生菌培养物在制造过程中会遇到氧化条件,然而,对于一些最常见的益生菌和发酵剂,这种应激诱导的蛋白质丰度变化尚未得到表征。这项比较蛋白质组学研究聚焦嗜酸乳杆菌NCFM对模拟氧化环境的H₂O₂的反应。通过BioScreen监测细菌生长,并在指数期收获分批培养物,用于基于二维凝胶的比较蛋白质组学分析应激反应的蛋白质谱。在因H₂O₂而丰度发生变化的21个斑点中的19个中鉴定出的蛋白质通常与碳水化合物和能量代谢、半胱氨酸生物合成及应激有关。特别地,半胱氨酸合酶活性增加可能会积累一个与蛋白质稳定性、酶催化及二硫键还原途径相关的半胱氨酸库。应激反应还包括减少损伤的生物分子丰度升高,如来自DNA修复途径的酶和具有活性位点半胱氨酸残基的代谢酶。相比之下,一种蛋白质重折叠伴侣蛋白丰度降低,这可能反映了严重的氧化蛋白质破坏,无法通过重折叠克服。蛋白质组分析为乳酸菌抵抗活性氧的机制提供了新的见解,并为改进工业过程、食品设计或保持微生物活力的菌株工程构成了有价值的起点。