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Table 1 Oligonucleotides used in this study for cloning of the genes cur_1714 and cur_1715. The sequences of the primers were derived from the prospective genes cur_1714 and cur_1715 and their flanking regions taken from the genome of C. urealyticum DSM 7109 [13]

From: Identification and characterization of smallest pore-forming protein in the cell wall of pathogenic Corynebacterium urealyticum DSM 7109

Oligonucleotides

Sequence 5’➝ 3’

Fwd_1714_XbaI

GTGTCTAGAGACCTACACTCTAGGAGTTTC

RP pX cur_1714 KpnI

CTGGTACCTTAGAAGCCGAATGCCTG

RP-cur1714-KpnI pXHis

GCTTAAAGGTACCGAAGCCGAATG

RevpXMJ19

CAGACCGCTTCTGCGTTCTG

Fwd Gst 1714 BamHI

CTGAGGATCCGGTAACGCAAC

Rev Gst 1714 EcoRI

GACGAATTCTTAGAAGCCGAATGC

Fwd Gst 1715BamHI

CAGTGGATCCAACGTCGACATG

Rev Gst 1715 EcoRI

CTAGAATTCCTACTTGTTCTCGG

Fwd GST Seq

CACTCCCGTTCTGGATAATG

Rev GST Seq

CACTCCGCTATCGCTACGTGAC

T7 Promotor

TAATACGACTCACTATAGGG

M13 reverse

CAGGAAACAGCTATGAC

  1. Recognition sites for the restriction enzymes are underlined