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. 2017 Dec 5;8:2393. doi: 10.3389/fmicb.2017.02393

Table 2.

Oligonucleotides used in this work.

Primers Sequence (5′- 3′) Utilization Amplicon size (bp)
pts1F TGCGGAAGCGGTTAATCGGCT gutF DNA probea 618
pts1R CCACGACTCTTGCCTCCCGCA
ptsRF CGAACTGGAAGCAACCTGGGA gutR DNA probea 652
ptsRR CCGATGAATAATTGGCGCTGC
ptsBF GGAATGGAAGCTGTTGATGGC gutB DNA probea 643
ptsBR CAACGCCAATCAAGGTCCCGA
pgutBglIIF GAAGATCTACCATATGGCGATAATGAAAA Cloning of Pgut in pRCRa 186
pgutXmaIR TCGCTCCCGGGTCATTTCTTTTC
gutRXmaIF CGTGGTTAACCCGGGAATTTTAGTTG Cloning of gutR in pRCR16a 1952
gutRXbaIR GCTCTAGAAACGCACTGACTAGGATCA
gutMXmaIF TCCCCCCGGGTTAAATCAGTTGATGGA Cloning of gutM in pRCR16a 597
gutMXbaIR GCTCTAGAACAGCCCATAAAGCCC
gutRXmaIF CGTGGTTAACCCGGGAATTTTAGTTG Cloning of gutRM in pRCR16a 2472
gutMXbaIR GCTCTAGAACAGCCCATAAAGCCC
pPP1F CATAGTTCACTGGGCTACCA Sequencing of pPP1∗b
pPP1R TAGCGGTGCCTCCCTTTAAT

aPlasmidic DNA preparations of P. parvulus 2.6 was used as substrate for the PCR reactions. bPlasmidic DNA preparations of P. parvulus 2.6NR was used as substrate for the DNA sequencing.