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Probe/primer details

PAO846 Tested for in situ hybridization.
Full name
(Alm et al. 1996)
S-S-Rhodo-0846-a-A-18
Accession no. pB-623
Taxonomy Candidatus Accumulibacter phosphatis; Candidatus Accumulibacter; unclassified Betaproteobacteria; Betaproteobacteria; Proteobacteria; Bacteria
Specificity Candidatus Accumulibacter phosphatis
Category bacteria of relevance in wastewater treatment
Target rRNA 16S rRNA
Modified version(s) ACCBA846
Position 846-866
Sequence 5'- GTT AGC TAC GGC ACT AAA AGG -3'
G+C content [%] 48
Length [nt] 21
Check specificity/coverage
Formamide [%] 35
Hybridization efficiency
References

Identification of polyphosphate-accumulating organisms and design of 16S rRNA-directed probes for their detection and quantitation. Crocetti GR, Hugenholtz P, Bond PL, Schuler A, Keller J, Jenkins D, Blackall LL. Applied and environmental microbiology. 2000. Pubmed

In situ identification of polyphosphate- and polyhydroxyalkanoate-accumulating traits for microbial populations in a biological phosphorus removal process. Liu WT, Nielsen AT, Wu JH, Tsai CS, Matsuo Y, Molin S. Environmental microbiology. 2001. Pubmed

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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).
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.
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
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.