Green Brian D, Keller Martin
Diversa Corporation, San Diego, CA 92121, USA.
Curr Opin Biotechnol. 2006 Jun;17(3):236-40. doi: 10.1016/j.copbio.2006.05.004. Epub 2006 May 15.
The metagenomic analysis of environmental microbial communities continues to be a rapidly developing area of study. DNA isolation, the first step in capturing the uncultivated majority, has seen many advances in recent years. Protocols have been developed to distinguish DNA from live versus dead cells and to separate extracellular from intracellular DNA. Looking to increase our understanding of the role that members of a microbial community play in ecological processes, several techniques have been developed that are enabling greater in-depth analysis of environmental metagenomes. These include the development of environmental gene tags and the serial analysis of 16S rRNA gene sequence tags. In addition, new screening methods have been designed to select for specific functional genes within metagenomic libraries. Finally, new cultivation methods continue to be developed to improve our ability to capture a greater diversity of microorganisms within the environment.
环境微生物群落的宏基因组分析仍是一个快速发展的研究领域。DNA分离作为捕获绝大多数未培养微生物的第一步,近年来取得了许多进展。已开发出一些方案来区分活细胞与死细胞中的DNA,并将细胞外DNA与细胞内DNA分离。为了增进我们对微生物群落成员在生态过程中所起作用的理解,已开发出几种技术,能够对环境宏基因组进行更深入的分析。这些技术包括环境基因标签的开发以及16S rRNA基因序列标签的序列分析。此外,还设计了新的筛选方法,以在宏基因组文库中选择特定的功能基因。最后,新的培养方法也在不断开发,以提高我们捕获环境中更多样化微生物的能力。