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. 2017 Jul 12;8:1303. doi: 10.3389/fmicb.2017.01303

Table 2.

Primers used in this study.

Primer description Sequence 5′-3′ Tannaeling [°C] Product length [bp]
Quantitative reverse transcriptase PCR
cbbL_810F 5′ AGGTCTTGCGAACTACTGTC 51 306
cbbL_1115R CCAGAAGCAACTGGCATAAC
cbbM_647F TCTGCACGGTAGCACATTTC 51 330
cbbM_976R ATTTGACGGTCCTGCTGTTG
ChlR_821F TAAGCATTCTGCCGACATGG 51 284
ChlR_1104R CGATTTCCGGCAGTTTCTAC
rpoD_416F GATCAACGACATGGGCATTC 51 305
rpoD_720R CGTACTGTTCCAGCAGATAG
16S_280F GGTCGCTTCTCTTTGTATGC 51 285
16S_564R CCTTACCTGGTCTTGACATC
cbbO-m_700F ACCTCATCGCCATAATGCTC 51 223
cbbO-m_922R TTGCCGTCATGTTACTGGTC
cbbQ-m_2828F GTGGCGGCATACACCATTAG 51 147
cbbQ-m_2974R AGTCGAAGCGCACATCTTAC
cbbQ-1_9714F GGTAGGTCGCTTCCTAATCG 51 199
cbbQ-1_9912R GTGCGCTTCTACCAACTCAC
cbbO-1_12263F CGCATGCCATCAATGGTATC 51 263
cbbO-1_12525R GTCAATATCCGCTGGTTCAC
Protein expression
CbbLF_NheI GCTAGCACCATGGCTAAGACTTATAAC 501/602 1421
CbbLR_BamHI GGATCCGCCTTATGCTTAACATCTAGCTTAT
CbbMF_NheI GCTAGCATGGATCAGTCGAATCGTTATG 561/622 1386
CbbMR_BamHI GGATCCGCTTTGTGTACGCCCAACTTCTC
LysR1F_NheI GCTAGCATGCλCTTACATATAACCGCCCAGC 621/672 932
LysR1R_BamHI GGATCCGAGCGCGTGTCCGACATGG
LysR2F_NheI GCTAGCATGCCTGλAATTTCCATCC 511/612 950
LysR2R_BamHI GGATCCGAGCGAAATTGGTTAAACG
Preparation of Cy3-labeled DNA fragments
ncrQm-M_3427F AGCCGCTTCATAAAGTTC 56.3 371
ncrQm-M_3797R CAGATGCAGACACAATCTAC
ncrM-R2_4993F TGCAGCAACTTCTAAGTAACC 62.2 369
ncrM-R2_5361R ACAGGCGTTTAACCAATTTCG
ncrR2 L_7191F CTGGGCGGTTATATGTAAG 57.7 275
ncrR2-L_7465R TACACCGGCGTTATAAGTC
ncrS-Q1_9151F AACCACGTTCGTTTGATTG 57.5 331
ncrS-Q1_9531R TGGCTCGTCTTTAATAAGG

1For the first 5 cycles/2 for 25 additional cycles; Tannaeling, annealing temperature.