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. 2005 Jun;187(12):4116–4126. doi: 10.1128/JB.187.12.4116-4126.2005

TABLE 1.

PCR primers used in this worka

Primer Sequenceb Source/positionc GenBank accession no.
Hindu AGGAAGCTTATATGTCAGATTTGC nifHa, (−)11-13 M10587
Bamhu GGATCCGACCCGAAAGCC nifHa, 115-132 M10587
Apalu GTGCACATGACGATGTCGACT nifHa, 344-364 M10587
NarI GCGCCCGTTACAGATCAG nifHa, 564-547 M10587
MluI TCCGACGCGTACTGGATCA nifHa, 701-683 M10587
BclI CTTGATCATGCCGAAGTCGAG nifHa, 831-811 M10587
XbaI TCCTCTAGACAGCGGCAGTTAT nifHa, 912-891 M10587
1 CTGAAACCCAACAAAAG nifHa, (−)135-(−)119 M10587
2 GCAAGGCGATTAAGTTG pIC20R, 385-369 L08913
3 AGTCGGCAAATAATGTC ΩTc, 2543-2559 U35135
4 AAAACGCTGTCATTCTC nifHa, 1033-1017 U80928
a

All the oligonucleotides are shown in the 5′ to 3′ direction.

b

Nucleotides that were modified to generate the corresponding restriction site (underlined) are shown in boldface.

c

Positions correspond to the start codon of the indicated sequence (nifHa) or to the initial nucleotide in the reported sequence (pIC20R and ΩTc).