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Study of analysis methods to monitor sporulation during fermentation of Bacillus subtilis to produce endospores

机译:监测枯草芽孢杆菌发酵产生孢子过程中孢子形成分析方法的研究

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摘要

Bacterial endospores, mainly of Bacillus subtilis, B. atrophaeus or Geobacillus stearothermophilus, are used as biological indicator for the validation of sterilization processes in various industrial processes and applications. Commonly used spores for sterilization studies are spores of B. subtilis, due to their high degree of resistance to chemical and physical treatments, reproducible inactivation response, and ease of use. To prevent falsified results in the validation of sterilization processes, theses spores must have high and comparable D-values as well as a homogeneous distribution of the resistance within every charge. The main influence on the resistance properties is the fermentation process, which lead to the necessity of well-defined methods and analytics of the spore formation for the production process. udTo produce suspensions containing homogeneously equipped spores, a reproducible fed batch fermentation strategy with optimized concentrations of media components has been developed (VLB; data not yet published). To increase spore resistance, different influence factors such as fermentation time, temperature and composition of sporulation media were investigated. udA systematic screening of fermentation capabilities towards optimal spore formation, production and efficiency was performed. A collection of commonly used sterilization-recommended B. subtilis strains was evaluated by applying a set of different molecular biological techniques and classical microbiological assays. Quantitative real time PCR was used to study transcriptomic changes during the sporulation; here major sporulation events (e.g., sigma factors; from Stuelke, Joerg, SubtiWiki) were studied. MALDI-TOF-TOF analyses were conducted to follow changes in the protein spectra (Momo et al, 2013) from during initiation of sporulation until maturation of the dormant spore. The EloTrace® System (Junne et al, 2010) allowed us to characterize the morphological and physiological of the transition of the sporulating cultures using an electro-optical approach. Established and reproducible methods for measuring spore resistance were used to determine batch-specific resistance properties to selected sterilization methods (hydrogen peroxide or UV-C radiation treatments; Raguse et al, 2016).
机译:细菌内生菌,主要是枯草芽孢杆菌,萎缩芽孢杆菌或嗜热脂肪地芽孢杆菌,被用作生物指示剂,用于验证各种工业过程和应用中的灭菌过程。灭菌研究中常用的孢子是枯草芽孢杆菌的孢子,因为它们对化学和物理处理具有高度的抵抗力,可再现的灭活反应,并且易于使用。为了防止在验证灭菌过程中出现伪造的结果,这些孢子必须具有较高且可比的D值,并且每次装料中电阻的均质分布。对抗性特性的主要影响是发酵过程,这导致必须采用明确定义的方法并对生产过程中的孢子形成进行分析。为了生产包含均一装备的孢子的悬浮液,已经开发了具有最佳培养基成分浓度的可重现的补料分批发酵策略(VLB;数据尚未公布)。为了提高孢子抵抗力,研究了不同的影响因素,例如发酵时间,温度和孢子形成培养基的组成。 ud对发酵能力进行了系统的筛选,以优化孢子的形成,产量和效率。通过应用一组不同的分子生物学技术和经典的微生物分析方法,评估了常用的灭菌推荐枯草芽孢杆菌菌株的集合。实时定量PCR用于研究孢子形成过程中的转录组变化。在这里研究了主要的孢子形成事件(例如sigma因子;来自Stuelke,Joerg,SubtiWiki)。进行MALDI-TOF-TOF分析以追踪从孢子形成开始到休眠孢子成熟期间蛋白质光谱的变化(Momo等,2013)。 EloTrace®系统(Junne等人,2010)使我们能够使用电光方法表征孢子培养的过渡形态和生理特性。已建立的可再现的测量孢子抗性的方法用于确定对选定灭菌方法(过氧化氢或UV-C辐射处理; Raguse等人,2016)的批次特异性抗性。

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