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Table 1 Primer sets used in this study

From: The facilitating role of phycospheric heterotrophic bacteria in cyanobacterial phosphonate availability and Microcystis bloom maintenance

Primer

Sequence (5′-3′)

Efficiencya

Function

27F

AGAGTTTGATCCTGGCTCAG

 

For bacterial 16S rDNA amplification, identification, and 16S rDNA standard plasmid construction

1492R

TACGGCTACCTTGTTACGACTT

515F

GTGNCAGCMGCCGCGGTAA

95.39%

For qPCR of total bacterial 16S rDNA

806R

GGACTACNSGGGTATCTAb

PsudmPJ-Fc

GAGCGCAAGGCGATGGGCAT

 

For Pseudomonas strains phnJ gene amplification and Pseudomonadales standard plasmid construction

PsudmPJ-Rc

ACTCGCCGACGATGCCCAGCAC

PsudmoPJ-622Fc

GACGAACAGACCAARCGCATGAT

90.30%

For qPCR of phnJ in Pseudomonadales

PsudmoPJ-910Rc

GGTGACGGGTCTGGATCAC

RhizoPJ-F3c

ATCATCCAGACGCGCCACCGCATT

 

For Rhizobium strains phnJ gene amplification and Rhizobiales standard plasmid construction

RhizoPJ-R3c

AGTCGGTGCGCATCAGGAA

RhizobPJ-153Fc

ATGCCSATGCCYTATGGSTGGGG

87.29%

For qPCR of phnJ in Rhizobiales

RhizobPJ-558Rc

CGACCTTSACCGGRTAGGC

Methyl-Fc

AGGACCAGGAATTCGTGCT

 

For Methylobacterium strains phnJ gene amplification and Rhodospirillales standard plasmid construction

Methyl-Rc

TGTCCGAGCAGACGAACAT

RhispiPJ-242Fc

CCCTATGGYTGGGGCAC

97.66%

For qPCR of phnJ in Rhodospirillales

RhispiPJ-494Rc

GGATCGGCACCTGRTAGAC

  1. aAmplification efficiency for each qPCR primer set
  2. bOne base was modified from G to N (shown in italics) to match the cyanobacterial 16S rDNA sequence
  3. cDesigned in this study