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. 2000 May;74(10):4541–4548. doi: 10.1128/jvi.74.10.4541-4548.2000

TABLE 1.

Oligonucleotides used for the construction of MpB GroEL deletion mutants

Oligonucleotide Sequence (5′→3′)a Corresponding positionsb
F1 ccggatccATGGCCGCTAAAGATGTA 1–6
F2 ggatccatgAAAGCTGTTATTAGTGCTG 122–127
F6 ggtgaagcttAACTATGGTTATAATGCAGC 475–480
F7 ccggatccGGTAATGAAGCCCGAATT 9–14
F8 ccggatccGGAGTTAATGTATTAGCAG 19–24
F9 gaggatccGTAACTTTAGGTCCAAAAG 29–34
F10 ttccaagcttTTATCTGTACCATGTTCAG 134–139
R1 acggatccTTACATCATTCCaCCC 545–548
R2 gaattcttaACCTTTTCCATCTTTTACG 470–474
R3 caataagcttTTCAACAGCTGCACCAGT 404–408
R4 gaattcttaTTCAACAGCTGCACGAG 404–408
R7 caataagcttGATTTCACGAGCTACTGA 53–57
R8 gaattcttaATTGGAAACAATTTGACGTAA 452–457
R9 gaattcttaAGATGTTTTTCCAGCCACTC 422–427
a

Uppercase letters indicate Buchnera groEL sequences, and lowercase letters indicate sequences which are not part of the gene. Restriction sites (EcoRI, BamHI, and HindIII) are boldfaced, start codons are double underlined, and termination codons are single underlined. 

b

Numbering refers to the corresponding positions of the amino acid residues of MpB GroEL.