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. 2015 May 19;10(5):e0127634. doi: 10.1371/journal.pone.0127634

Table 1. Primers used for construction of plasmids.

Oligonucleotide Primer
WT-NdeI-N CGCGGCATATGTTTGATTTACTCCTGC
WT-XhoI-C TCGCACTCGAGAAAATCGAAGGCATGT
H59A-N GGCATCGACCCCGCTACCCACATGCAGTTGCCC
H59A-C CAACTGCATGTGGGTAGCGGGGTCGATGCCGCC
H61A-N GACCCCCATACCGCCATGCAGTTGCCCTTCATG
H61A-C GAAGGGCAACTGCATGGCGGTATGGGGGTCGAT
H183A-N GCGGTGCCGACGGTGGCCGCGGAGAACGGCGAA
H183A-C GCCGTTCTCCGCGGCCACCGTCGGCACCGCGCC
H239A-N CTGTACCTGGTAGCTATTTCCAGCCGCGAGGCG
H239A-C CTCGCGGCTGGAAATAGCTACCAGGTACAGCGG
K150A-N GTGAACAGCTTCGCGCACTTCATGGCCTACAAG
K150A-C GTAGGCCATGAAGTGCGCGAAGCTGTTCACCCC
D316A-N ACCACCGCCACCGCCCACTGCTGCTTCTGCGCC
D316A-C GCAGAAGCAGCAGTGGGCGGTGGCGGTGGTATG
Y155A-N CACTTCATGGCCGCCAAGAACGCCATCATGGCC
Y155A-C CATGATGGCGTTCTTGGCGGCCATGAAGTGCTT
S289A-N GGCTACGTGATGGCCCCGCCGTTCCGTCCCGTC
S289A-C GGGACGGAACGGCGGGGCCATCACGTAGCCGGC
N337A-N TTCAGCAAGATTCCCGCTGGCACGGCCGGCATC
N337A-C GCCGGCCGTGCCAGCGGGAATCTTGCTGAAGTC

These plasmids were verified by DNA sequencing. Underlined nucleotides indicate the designated site for mutation or the restriction site.