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Table 1 Primers used in the detection of cyanotoxin producing genes in St. George Lake samples and amplification parameters of PCR

From: Occurrence of a single-species cyanobacterial bloom in a lake in Cyprus: monitoring and treatment with hydrogen peroxide-releasing granules

Targeting gene

Primer name

Sequence 5′–3’

Amplicon size (bp)

Annealing temperature (°C)

Reference or source of sequence for primers design

cyrJ

cyrJ_F

AGTAATCCCGCCTGTCATAGA

109

60

This study; KY550407.1

cyrJ_R

ACTGAGCATTGTCTCGGTAAAC

cyrB

cyrB_F

GCCTGAGTACCTATCTGCTTAAC

95

60

This study; EU140798.1

cyrB_R

AGCCTGAAACTGCTCCATATC

sxtA

sxtA_F

GCGTACATCCAAGCTGGACTCG

683

55

[41]

sxtA_R

GTAGTCCAGCTAAGGCACTTGC

anaC

anaC_F

TCTGGTATTCAGTCCCCTCTAT

366

58

[42]

anaC_R

CCCAATAGCCTGTCATCAA

mcyB

mcyB_F

CCTCAGACAATCAACGGTTAGT

119

60

This study; CP020771.1

mcyB_R

AAAGGCAGAAGGCACCATATAA

mcyE

mcyE_F

CTGGTGGGAAAGGACTGATTTA

95

60

This study; CP020771.1

mcyE_R

CGCCCTCAAGTCAAGAAAGA

  1. The primers were designed using deposited sequences or taken from references. Cyr, sxt, ana and mcy genes are involved in cylindrospermopsin, saxitoxin, anatoxin and microcystin synthesis, respectively