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. 2017 Mar 8;8:327. doi: 10.3389/fmicb.2017.00327

Table 1.

List of primers utilized in quantification of gene expression by semi-quantitative RT-PCR.

Gene Protein Primer Sequence
glcH Glucose transporter Forward GCTTTTATGGCAGGTTCTTT
Reverse CAAATAGCCGCAAGACTCAG
prk Phosphoribulokinase Forward ATGGTGGTGTTGTTGGAGAT
Reverse CCTTTCAGCA TTGTCACGAT
fbaA Fructose 1-6 biphosphate aldolase Forward ATAGGTGAAGAGGTTGGGAG
Reverse ATCAGAAGCAGCCAATACAG
glpA Glucose-1P-adenylyltransferase Forward TTGCGTTTTAGGCGTTAGAA
Reverse TCGTTCCCTGACCTACTCCA
tal Transaldolase Forward TATTTGGCTTTTCTCAGGC
Reverse GTCCTTCCCTGTTTCTGCT
gap3 Glyceraldehyde-3-phosphate dehydrogenase Forward GGTAACGCAAGAAGAAGTCA
Reverse TGAGTTTTGTTGACCACCAT
prk Pyruvate kinase Forward TTCAATTGGTATGGGGTGTA
Reverse GGGTTCCTGCTGTTTCTACT
rbcS Ribulose-1,5-bisphosphate carboxylase/oxygenase small subunit Forward CCTGGAGACA TTTGGCTT
Reverse GTCTGCA TGGAGCCACTT
rbcL Ribulose-1,5-bisphosphate carboxylase/oxygenase large subunit Forward TCGCCCTCTTGTTGGTTG
Reverse CCTGGCCTGTCTGTTGCT
rnpB RNase subunit B Forward TCCCAAAAGACCAGACTTGCT
Reverse GTATGTTTCTGTGGCACTCTCCT
rnpB RNase subunit B (used in natural samples; Holtzendorff et al., 2002) Forward GGCAAGGGTGCAAAGGTG
Reverse GCCGGGGTTTACCTAGCC