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基于分子生物学的混合培养物中细菌定量方法:前景与局限

Molecular biology-based methods for quantification of bacteria in mixed culture: perspectives and limitations.

作者信息

Nagarajan Karthiga, Loh Kai-Chee

机构信息

Department of Chemical and Biomolecular Engineering, National University of Singapore, 4 Engineering Drive 4, Singapore, 117576, Singapore.

出版信息

Appl Microbiol Biotechnol. 2014 Aug;98(16):6907-19. doi: 10.1007/s00253-014-5870-9. Epub 2014 Jun 15.

Abstract

Species-specific enumeration of mixed community is invaluable as it facilitates a better understanding of the significance of the individual strains, their interactions, and the underlying mechanisms of community dynamics. Mixed microbial community has been characterized by microbiological, biochemical, or molecular biology-based methods. While microbiological and biochemical techniques do not provide adequate quantitative information of the members of the consortia and require additional techniques for a more comprehensive analysis, molecular biology-based methods analyze the microbial consortium based on specific DNA sequences and do not require isolation and culturing of bacteria for quantitative analysis. These methods outshine conventional culture-based techniques in terms of better sensitivity, reproducibility, and reliability. Quantitative molecular biology methods have been classified as PCR-based and probe hybridization methods. The PCR-based methods includes quantitative real-time PCR and terminal restriction fragment length polymorphism, while fluorescent in situ hybridization and DNA microarrays fall under probe hybridization methods. The workflow, the quantification methods, and their potential applications are discussed in this review by highlighting their advantages and possible limitations.

摘要

对混合群落进行物种特异性计数非常重要,因为它有助于更好地理解各个菌株的重要性、它们之间的相互作用以及群落动态的潜在机制。混合微生物群落已通过基于微生物学、生物化学或分子生物学的方法进行了表征。虽然微生物学和生物化学技术无法提供共生体成员足够的定量信息,并且需要额外的技术进行更全面的分析,但基于分子生物学的方法基于特定的DNA序列分析微生物群落,并且不需要分离和培养细菌进行定量分析。这些方法在灵敏度、可重复性和可靠性方面优于传统的基于培养的技术。定量分子生物学方法已被分类为基于PCR的方法和探针杂交方法。基于PCR的方法包括定量实时PCR和末端限制性片段长度多态性,而荧光原位杂交和DNA微阵列则属于探针杂交方法。本综述通过强调其优点和可能的局限性,讨论了这些方法的工作流程、定量方法及其潜在应用。

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