Protocols for 16S rDNA array analyses of microbial communities by sequence-specific labeling of DNA probes.

10Citations
Citations of this article
15Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

Analyses of complex microbial communities are becoming increasingly important. Bottlenecks in these analyses, however, are the tools to actually describe the biodiversity. Novel protocols for DNA array-based analyses of microbial communities are presented. In these protocols, the specificity obtained by sequence-specific labeling of DNA probes is combined with the possibility of detecting several different probes simultaneously by DNA array hybridization. The gene encoding 16S ribosomal RNA was chosen as the target in these analyses. This gene contains both universally conserved regions and regions with relatively high variability. The universally conserved regions are used for PCR amplification primers, while the variable regions are used for the specific probes. Protocols are presented for DNA purification, probe construction, probe labeling, and DNA array hybridizations.

Cite

CITATION STYLE

APA

Rudi, K., Treimo, J., Nissen, H., & Vegarud, G. (2003). Protocols for 16S rDNA array analyses of microbial communities by sequence-specific labeling of DNA probes. TheScientificWorldJournal, 3, 578–584. https://doi.org/10.1100/tsw.2003.44

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free