Not all cyanobacterial strains produce toxins. However, the toxin-producing strains cannot be distinguished from the nontoxin-producing strains by traditional light microscopy, commonly used to monitor water bodies. An alternative for the differentiation of potentially toxic strains from nontoxic strains is to use molecular methods to detect the presence of toxin biosynthetic genes. Such methods are already available and could be used for the detection and identification of potential microcystin and nodularin producers present in environmental samples (Attogene catalog number NA2024).
Screening for the toxin itself, can be very costly. In turn, real time PCR for the detection of the anaC gene in cyanobacterial strains and environmental samples can be a key indicator for the prescense of cyanobacteria capable of expressing the Anatoxin toxin. Attogen has thus, designed primer pairs targeting a the conserved anaC gene region in order to enable the amplification and detection of several producer genera using real time PCR. Screening for the toxin genes can save significant costs and act as a triage for samples needing to be analyzed for the toxin itself.
- *150ul AnaC region specific primer (1039) 10uM mixture (150 reactions)
1039F 5′- GCY AAC ACT GAA GTT TTT GTC TT -3′
1039R 5′- AAA TCC CAA TAR CCT GTC ATC AA -3′
Target Length: 110
- *150ul AnaC region specific primer (441) 10uM mixture 2 (150 reactions)
Target Lenth: 93
441F 5′- GTC AGA GGT TTT ACA AGC TCC TTG -3′
441R 5′- GTY GAR CCA GAT GTA TAA AGA ATA TAA GC -3′
- **150ul 16S cyanobacteria specific region-specific primer mixture 10uM (150 reactions) –
Target length: 73bp
16SF 5’- AGC CAC ACT GGG ACT GAG ACA-3′
16SR 5’- TCG CCC ATT GCG GAA A-3′
- 5ml PCR clean water