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. 2003 Oct;47(10):3053–3060. doi: 10.1128/AAC.47.10.3053-3060.2003

TABLE 1.

Primers used in the PCR and RT-PCR analysis of M. smegmatis

Primer Sequence (5′→3′) Target
MSX-1 ACGAGCTCGGCCAGAACTTCCTGT erm
MSX-2 CGTCTTCGCGAGGTCCTGACACAA folD
MSX-3 GGTGAGCGGGGCAGTGGGTAG erm
MSX-4 CGGCGGATCTGCGTCAGACACT erm
MSX-5 GGTCACCGCGGACATGGTCAAG folD-Rv3355
MSX-6 ACCGACAGCCGCGATGATGATG folD
MS23-1 CGAATGGCGTAACGACTTCTCA 23S rRNA
MS23-2 GCGACACCCCTTCCACTCAG 23S rRNA
MSX-4acca ACCTCCGGACGGCGGATCTGCGTCAGACACT erm
MSX-5bspa CGATCGATGGTCACCGCGGACATGGTCAAG erm
MSpgaE-1 CGGTCGGGGATGCTGACAT pgaE
KN10_U2 CGCAGCACCACCGAGAA pYUB854
KN10_L1 AGGCAACTATGGATGAACGAAAT pYUB854
SACUP-2nota AAGGCGGCCGCTTGCAATCCAAACGAGAGTCTA pK19mobsacb
SACDN AATAGGATATCGGCATTTTCTTTTG pK19mobsacb
a

Underlined bases indicate restriction sites (acc, AccIII; bsp, Bsp106I; not, NotI) used to clone the amplimers into the expression vector pMV261.