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Molecular approaches to the assessment of biodiversity in aquatic microbial communities

机译:评估水生微生物群落生物多样性的分子方法

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For the past 20 years, the increased development and routine application of molecular-based techniques has made it possible to carry out detailed evaluations of the biodiversity of aquatic microbial communities. It also offers great opportunities for finding out how this parameter responds to various environmental stresses. Most of these approaches involve an initial PCR amplification of a target, which is generally located within the ribosomal operon. The amplification is achieved by means of primers that are specific to the organisms of interest. The second step involves detecting sequence variations in the PCR fragments either by a cloning/sequencing analysis, which provides a complete characterization of the fragments, or by an electrophoretic analysis, which provides a visual separation of the mixture of fragments according to sequence polymorphism (denaturing or temperature gradient gel electrophoresis, single strand conformation polymorphism) or length polymorphism (terminal-restriction fragment length polymorphism, automated ribosomal intergenic spacer analysis). Other non-PCR-based methods are also commonly used, such as fluorescence in-situ hybridization and DNA re-association analysis. Depending on the technique used, the information gained can be quite different. Moreover, some of these analyses may be rather onerous in terms of time and money, and so not always suitable for screening large numbers of samples. The most widely used techniques are discussed in this paper to illustrate the principles, advantages and shortcomings of each of them. Finally, we will conclude by evaluating the techniques and discussing some emerging molecular techniques, such as real-time PCR and the microarray technique.
机译:在过去的20年中,基于分子的技术的不断发展和常规应用使得对水生微生物群落的生物多样性进行详细评估成为可能。它还为发现此参数如何响应各种环境压力提供了很大的机会。这些方法大多数涉及靶标的初始PCR扩增,该靶标通常位于核糖体操纵子内。扩增是通过对目的生物特异的引物实现的。第二步涉及通过克隆/测序分析(可提供片段的完整表征)或电泳分析(可根据序列多态性对片段混合物进行可视分离)检测PCR片段中的序列变异。或温度梯度凝胶电泳,单链构象多态性或长度多态性(末端限制性片段长度多态性,自动核糖体基因间间隔子分析)。还通常使用其他非基于PCR的方法,例如荧光原位杂交和DNA重新关联分析。根据所使用的技术,获得的信息可能会完全不同。而且,这些分析中的一些分析可能在时间和金钱上都相当繁重,因此并不总是适合于筛选大量样品。本文讨论了使用最广泛的技术,以说明每种技术的原理,优点和缺点。最后,我们将通过评估这些技术并讨论一些新兴的分子技术(例如实时PCR和微阵列技术)来得出结论。

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