Unlabeled Helper Oligonucleotides Increase the In Situ Accessibility to 16S rRNA of Fluorescently Labeled Oligonucleotide Probes
- 1 August 2000
- journal article
- research article
- Published by American Society for Microbiology in Applied and Environmental Microbiology
- Vol. 66 (8) , 3603-3607
- https://doi.org/10.1128/aem.66.8.3603-3607.2000
Abstract
Target site inaccessibility represents a significant problem for fluorescence in situ hybridization (FISH) of 16S rRNA with oligonucleotide probes. Here, unlabeled oligonucleotides (helpers) that bind adjacent to the probe target site were evaluated for their potential to increase weak probe hybridization signals in Escherichia coli DSM 30083 T . The use of helpers enhanced the fluorescence signal of all six probes examined at least fourfold. In one case, the signal of probe Eco474 was increased 25-fold with the use of a single helper probe, H440-2. In another case, four unlabeled helpers raised the FISH signal of a formerly weak probe, Eco585, to the level of the brightest monolabeled oligonucleotide probes available for E. coli . The temperature of dissociation and the mismatch discrimination of probes were not significantly influenced by the addition of helpers. Therefore, using helpers should not cause labeling of additional nontarget organisms at a defined stringency of hybridization. However, the helper action is based on sequence-specific binding, and there is thus a potential for narrowing the target group which must be considered when designing helpers. We conclude that helpers can open inaccessible rRNA regions for FISH with oligonucleotide probes and will thereby further improve the applicability of this technique for in situ identification of microorganisms.Keywords
This publication has 28 references indexed in Scilit:
- Gene organization and primary structure of a ribosomal RNA operon from Escherichia coliPublished by Elsevier ,2004
- Structure of a bacterial 30S ribosomal subunit at 5.5 Å resolutionNature, 1999
- Placement of protein and RNA structures into a 5 Å-resolution map of the 50S ribosomal subunitNature, 1999
- Covalent DNA-Streptavidin Conjugates as Building Blocks for Novel Biometallic NanostructuresAngewandte Chemie International Edition in English, 1998
- Capture of Single-Stranded DNA Assisted by Oligonucleotide ModulesAnalytical Biochemistry, 1998
- Phylogenetic identification and in situ detection of individual microbial cells without cultivation.1995
- Identification of Whole Fixed Bacterial Cells with Nonradioactive 23S rRNA-Targeted Polynucleotide Probes.1994
- A Quantitative Model of the Escherichia coli 16 S RNA in the 30 S Ribosomal SubunitJournal of Molecular Biology, 1994
- Collection of small subunit (16S- and 16S-like) ribosomal RNA structures: 1994Nucleic Acids Research, 1994
- Optimizing fluorescent in situ hybridization with rRNA‐targeted oligonucleotide probes for flow cytometric identification of microorganismsCytometry, 1993