Skip to main content

Table 2 Oligonucleotides used in this study

From: Corynebacterium glutamicum as platform for the production of hydroxybenzoic acids

Oligonucleotide

Sequence (5′–3′)

Restriction site

del_cg3349-54-up-s

ACCAAGCTTCATTTTCTAGTTGAGATTCATTATCATAACGCTTGACAGTACAACTATGTC

HindIII

del_cg3349-54-up-as

GCTTCCGGGGTGAATGACGGAGCCGCTGCGGAGGTTCCAGAGCCACCGCGCTG

–

del_cg3349-54-down-s

CGCAGCGGCTCCGTCATTCACCCCGGAAGCTGGCGCTACGCCCTCCTCGAAC

–

del_cg3349-54-down-as

ACCTCTAGATTTCTGTCTTGAGGGTTCGTGGGGGCTG

XbaI

check-cg3349-54-s

AAAGGCTCCATGAATTCCTCACGGAGGATCTC

–

check-cg3349-54-as

ACATCACAAGTAGAAACCCGCATTTTCTGTAGTTTTTAC

–

(A)-aroF*-s

TTCGCTCTTCAAAGCTGCTTAAGGAGGCTATCTATGACCGATGAACAGGTGCTGATGACCCCAG

SapI

(A)-aroF*-as

TACGCTCTTCTGATTTATGCCACGCGTGCGGTCAGCTG

SapI

(A)-aroH-s

TTCGCTCTTCAAAGTATACCATGGTAAGGAGGTTCAGCATGAACAGAACTGACGAACTCCGTACTGCGCGTATTG

SapI

(A)-aroH-as

TACGCTCTTCTGATTTAGAAGCGGGTATCTACCGCAGAGGCGAGTTTTTC

SapI

(B)-qsuB-s

TTCGCTCTTCAATCTCTATCAAGGAGGATCGGCATGCGTACATCCATTGCCACTGTTTGTTTGTC

SapI

(B)-qsuB-as

TACGCTCTTCTTCGTTAGTTTGGGATTCCCCGCTCGAGGTC

SapI

(B)-irp9-s

TTCGCTCTTCAATCTCTATCAAGGAGGATCGGCATGAAGATCTCCGAGTTCCTCCACCTGGCAC

SapI

(B)-irp9-as

TACGCTCTTCTTCGTTACACCATCAGGTATGGTGCAATGGAGGCCAGCTTTTCGCGAGTTTCG

SapI

(B)-hyg5-s

TTCGCTCTTCAATCTCTATCAAGGAGGATCGGCATGAACCCATCCTCCTTGGTGCTGAAC

SapI

(B)-hyg5-as

TACGCTCTTCTTCGTTACATGACCACGCCTTCGATTTCCACGAG

SapI

(B)-ubiC-s

TTCGCTCTTCAATCTCTATCAAGGAGGATCGGCATGTCACACCCCGCGTTAACGCAACTG

SapI

(B)-ubiC-as

TACGCTCTTCTTCGTTAGTACAACGGTGACGCCGGTAAAAACAGTTCTGTTAG

SapI

tkt’-s

CATGGATCCAAGGAGGTTCAGCATGACCACCTTGACGCTGTCACCTGAACTTCAG

BamHI

tkt’-as

AGAGCTCTTCAGCCCATAGCGTGCTCACGGATACCGAAGTG

SapI

‘tkt-s

TTTGCTCTTCTGGCTCCATCCTCAACGGCATTTCCCTCC

SapI

‘tkt-as

TCTGAATTCTTAACCGTTAATGGAGTCCTTGGCCGCTGCCAC

EcoRI

pMKEx2_own-s

CCCTCAAGACCCGTTTAGAGGC

–

pMKEx2_own-as

TTAATACGACTCACTATAGGGGAATTGTGAGC

–

pEKEx3-s

GCAAATATTCTGAAATGAGCTGTTGACAATTAATCATC

–

pEKEx3-as

CGTTCTGATTTAATCTGTATCAGGCTGAAAATCTTCTC

–

  1. Restriction sites are underlined; SapI cuts outside of its recognition site, the obtained 5′-overhangs after SapI cleavage used for Electra Cloning are shown in bold. In case of native tkt two separate PCR fragments were assembled using Electra Cloning to eliminate an internal SapI restriction site