probeBase 2016
Published on probeBase 2016 (https://probebase.csb.univie.ac.at)

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Probe/primer details

DSS658 Tested for in situ hybridization.
Full name
(Alm et al. 1996)
S-*-Dsb-0658-a-A-18
Accession no. pB-84
Taxonomy Desulfobacteraceae [1]; Desulfobacterales [1]; Deltaproteobacteria [1]; delta/epsilon subdivisions [1]; Proteobacteria [1]; Bacteria [1]
Specificity Desulfobacteraceae and other Bacteria
Category sulfate-reducing microbes [1]
Target rRNA 16S rRNA
Position 658-675
Sequence 5'- TCC ACT TCC CTC TCC CAT -3'
G+C content [%] 56
Length [nt] 18
Check specificity/coverage [2]
Formamide [%] 60
Hybridization efficiency [2]
References

Diversity and vertical distribution of cultured and uncultured Deltaproteobacteria in an intertidal mud flat of the Wadden Sea. Mussmann M, Ishii K, Rabus R, Amann R. Environmental microbiology. 2005. Pubmed [2]

Manz W., Eisenbrecher M., Neu T. R. and Szewzyk U. (1998). Abundance and spatial organization of Gram-negative sulfate-reducing bacteria in activated sludge investigated by in situ probing with specific 16S rRNA targeted oligonucleotides. FEMS Microbiol. Ecol. 25: 43-61.

Remarks 80 % FA for CARD-FISH
Used in Microarray SRP-PhyloChip [1]
Freshwater Sediment-Microarray [1]

Print [1]

Glossary
Name (Alm et al., 1996). Probe designation according to Alm, E. W., Oerther, D. B., Larsen, N., Stahl, D. A., Raskin, L. (1996). The oligonucleotide probe database. Appl Environ Microbiol 62: 3557-9. Abstract (PUBMED) [2].
Position. Probe position according to the E. coli gene numbering.
Sequence. Sequence in IUPAC code: R=G/A, Y=T/C, M=A/C, K=G/T, S=G/C, W=A/T, H=A/C/T, B=G/T/C, V=G/C/A, D=G/A/T, N=G/A/T/C
Tm. Dissoziation temperature according to: Tm=64.9 + 41 x ((G + C - 16.4)/length).
Hybridization efficiency. Use this tool to assess in silico sensitivity (i.e. the hybridization efficiency of the oligonucleotide with its fully complementary target sequence, calculated with ProbeMelt [2].
Formamide. Percent formamide in the hybridization buffer for optimal hybridization conditions in FISH experiments.
Coverage. Coverage of the three domains calculated using the SILVA reference database 106 if no or a single mismatch is allowed. The detailed method is described in Klindworth et al., 2012. Nucleic Acids Res. 10.1093/nar/gks808 Full Text [2]
Check specificity/coverage. Use these options to reveal the in silico specificity (i.e. number of matching rRNA sequences outside the target taxon) and coverage (i.e. percentage of matching rRNA sequences within the target taxon) of an oligonucleotide against the most recent SSU and LSU rRNA sequence databases.

probeBase by Daniel Greuter, Alexander Loy, Matthias Horn, and Thomas Rattei, Department of Microbiology and Ecosystem Science, University of Vienna
Questions, comments, bug reports, and suggestions are welcome at probebase@microbial-ecology.net
Greuter et al. 2016. Nucleic Acids Res. 10.1093/nar/gkv1232

Imprint

Source URL:https://probebase.csb.univie.ac.at/pb_report/probe/84

Links
[1] https://probebase.csb.univie.ac.at/https [2] https://probebase.csb.univie.ac.at/http