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Table 5 Primers used in this study

From: Optimization of ethylene glycol production from (d)-xylose via a synthetic pathway implemented in Escherichia coli

Primer

Sequence

Cloning of gldA

 gldA_rbs_f

CCTCTAGAGTCGACCTGCAGAGGAGGATTCATATGGACCGCATTA

 gldA_rbs_r

GCCAAAACAGAAGCTTTTATTCCCACTCTTGCAGG

Cloning of fucO

 fucO_rbs_f

TTGGATCCAGGAGGATTCATATGGCTAACAGAATGATTCT

 fucO_rbs_r

TTAAGCTTTTACCAGGCGGTATGGTAA

Cloning of yqhD

 yqhD_rbs_f

CCTCTAGAGTCGACCTGCAGAGGAGGATTCATATGAACAACTTTA

 yqhD_rbs_r

GCCAAAACAGAAGCTTTTAGCGGGCGGCTTCGT

Verification primers for gene knock-outs

 xylB_loc_f

GTTATCGGTAGCGATACCGGGCATTTT

 xylB_loc_r

GGATCCTGAATTATCCCCCACCCGGTCAGGCA

 yqhD_loc_f

CGCCATACAACAAACGCACA

 yqhD_loc_r

CCAGATGCCAGCGGATAACA

 gldA_loc_f

CGGTTCAGGAGCTGCAAACGCTG

 gldA_loc_r

TAAGAGTCACAGATTCGACCTTC

 fucO_loc_f

ACAACATCATGGGCTTATCG

 KANseq_rev

ATGCGATGTTTCGCTTGGTG

 aldA_loc_f

TCATCCATGCATGGCAAACG

 aldA_loc_r

ACTGCCGAAGAGGTGAATAA

  1. Restriction sites are italicized and the start codons are shown in bolditalics.