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. 2015 Oct 9;290(50):29920–29930. doi: 10.1074/jbc.M115.661249

TABLE 2.

Primers used in this study

F, forward; R, reverse. The underlined nucleotides designate respective restriction sites.

Primer name Sequence (5′–3′) Purpose
SDP13 F ATCTTTCAGGATTAAAAAAT hcaE knock-out
SDP14 R CTCTAGTGAAACTTGCGCAC
SDP15 F GAACCGAGTCGTGAGGTACT mhpA knock-out
SDP16 R AGTGAAGATAAGCGTGCATA
SDP17 F ATTTTGTTGTTAAAAACATGTAA mhpR knock-out
SDP18 R CCACCAGAATAGCCTGCGAT
SDP19 F GCTATCGAGCCACAGGACTG paaA knock-out
SDP20 R ATTACTCATTTTGAATCTCC
SDP21 F AACATCTGACGAGGTTAATA maoA knock-out
SDP22 R CGTTTTTTTGTCTGAAACAA
SDP31 F AGTCGAACGGTAACAGGAAGA 16S rRNA qPCR
SDP32 R GCAATATTCCCCACTGCTG
SDP33 F GAAAGAGCACGATCGCGTGG aceB qPCR
SDP34 R TTGCTCGGAATAAACGCCGC
SDP35 F GAAAGAGCACGATCGCGTGG aceK qPCR
SDP36 R GCAAGCTGGCGAATAGCGTT
SDP37 F TAAGGACACGTTGCAGGCCA acnA qPCR
SDP38 R GGCGGTAGGCAATTTCACGG
SDP39 F TGGTTCCCGTGAAGCTCTGG eno qPCR
SDP40 R TGCAGCAGCTTTGGCGTTAG
SDP41 F CAATTCGCGGGGTTGTTCGT pfkA qPCR
SDP42 R GGTTTTCGATAGCCACGGCG
SDP43 F GCAGAAATGCTGGCGCGTAT fadA qPCR
SDP44 R ATGTGCCCGCCGTTACCATA
SDP45 F ACCGCTAATGAAGTGGCCGA fadR qPCR
SDP46 R CTGCACAACGCCGACAGTTT
SDP47 F TGCTCGGTATGGCACCGAAT glcB qPCR
SDP48 R GGCTTTGATCCAAGGCGTCG
SDP49 F TACTGAAGGTCGGTCAGCCG glcC qPCR
SDP50 R CCTCCAGTAATGCGCGAACG
SDP51 F CGAAGGCGGCACCGAAATTG hcaE qPCR
SDP52 R CGGGCGGTTTGTCCATCACC
SDP53 F CAGACAGCCAGACACCTTGA hcaR qPCR
SDP54 R CGGATCGGTACTGACGAAA
SDP55 F CCCGGTTGGGCTGATGATGG mhpA qPCR
SDP56 R CGGCGTAGTGTGCGGCAGAA
SDP57 F GCGGTACGGCGATAGAGGCG mhpR qPCR
SDP58 R ACCTGGCTGGCCTTTTGCCC
SDP59 F CCACCGACGAATTACGCAGC prpB qPCR
SDP60 R TTCACCTGGCTACGGGCAAA
SDP61 F TATTTTGCCCGCCACGATGC prpR qPCR
SDP62 R GCGGCATTTCGCCAATCTCA
Orf306F2 GGCTGCCATCATCCCATGGGAACACCCGCTA Amplification of orf306 as NcoI-BamHI fragment to be cloned in pET15b
Orf306R3 CGCGGATCCCTATTCCCCGTCAAGATAC
Orf306F5 GGCTGCCATCATCGGATCCGAACACCCGCTA Amplification of orf306 as BamHI fragment using
Orf306R3 as reverse primer to be cloned in pGEX4T1
HcaRFP1 AGGAATTCAAGCTCCAGTTGGTAA Amplification of hcaR promoter to be cloned in pMP220
HcaRRP1 ACCTGCAGACGGGTAAAGTTCAGT
HcapET23bFP1 ATACGCATATGACCACACCCTCAGATTTGAA Amplification of hca operon as NdeI-SalI fragment to be cloned in pET23b
HcapET23bRP1 ACTACGTCGACCAGTGATTTAAGCGCGATGTT
MhpRF CCGAGCTGCAGATTAATTGACATTTCTATA Amplification of mhpR promoter to be cloned in pMP220
MhpRR CCGGAGAATTCTTCAGTACCTCACGAC