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首页> 外文期刊>Beneficial Microbe >Transcriptome analysis and physiology of Bifidobacterium longum NCC2705 cells under continuous culture conditions.
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Transcriptome analysis and physiology of Bifidobacterium longum NCC2705 cells under continuous culture conditions.

机译:连续培养条件下长双歧杆菌NCC2705细胞的转录组分析和生理学。

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A central issue in the use of probiotics in food and food supplements is their sensitivity to many environmental stress factors. The resistance of probiotic cells to lethal stress can be improved by application of homologous or heterologous sub-lethal stress during culture. This screening procedure is generally performed using batch cultures. Continuous cultures could be a suitable and more efficient method to test different stress factors on one culture instead of repeating several batch cultures. However, before testing stresses using continuous cultures, the physiological stability of continuously produced cells over a considered time period must be first evaluated. A continuous culture of Bifidobacterium longum NCC2705 was maintained for 211 h at a dilution rate of 0.1 per h, mimicking a deceleration growth phase culture. Stable viable cell counts were measured over the culture period, decreasing only moderately from 8.8 to 8.6 log10 cfu/ml. A slight shift in metabolite production, characterized by increased lactate and decreased acetate, formate and ethanol concentrations was observed. Susceptibilities to antibiotics and stress conditions were stable (cefotaxim, ampicillin, ceftazidime) or moderately affected (simulated gastric juices, heat, bile salts, tetracycline, chloramphenicol, penicillin, vancomycin and neomycin) over culturing time. Comparison of gene transcription profiles between samples collected after 31 h of continuous culture and samples collected after 134 and 211 h revealed only limited changes in expression of 1.0 and 3.8% of total genes, respectively. Based on these results, we propose that continuous culture can be used to produce bacterial cells with stable physiological properties suitable for fast and efficient screening of sub-lethal stress conditions.
机译:在食品和食品补充剂中使用益生菌的主要问题是它们对许多环境压力因素的敏感性。益生菌细胞对致死应激的抗性可以通过在培养过程中施加同源或异源亚致死应激来提高。该筛选程序通常使用分批培养进行。连续培养可能是一种合适且更有效的方法,可以在一种培养上测试不同的压力因素,而不是重复多次分批培养。但是,在使用连续培养物测试压力之前,必须首先评估在考虑的时间段内连续产生的细胞的生理稳定性。长双歧杆菌NCC2705的连续培养以每小时0.1的稀释速率保持211 h,与减速生长相培养相似。在整个培养过程中测得稳定的活细胞计数,仅从8.8 log 10 cfu / ml适度降低。观察到代谢产物的轻微变化,其特征在于乳酸增加,乙酸盐,甲酸和乙醇浓度降低。在培养时间内,对抗生素的敏感性和应激条件稳定(头孢噻肟,氨苄青霉素,头孢他啶)或受到中等程度的影响(模拟胃液,热量,胆盐,四环素,氯霉素,青霉素,万古霉素和新霉素)。连续培养31小时后收集的样品与134和211小时后收集的样品之间的基因转录谱比较表明,分别只有1.0和3.8%的总基因表达发生了有限的变化。根据这些结果,我们建议连续培养可用于生产具有稳定生理特性的细菌细胞,适合快速有效地筛选亚致死性应激条件。

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