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. 2012 Nov;194(22):6074–6087. doi: 10.1128/JB.01119-12

Table 2.

Oligonucleotides for cloning of genes in L. biflexa

Oligonucleotide Sequence (5′–3′)a Geneb
flaB1p(Kp)-1F CTCGCTGGTACCGATCGAACCTAAGATTAGCTCA PromflaB1
flaB1p(Xh)-2R GTCCTCGAGTTCCATATGTTTCCTCCTTGAAACTGATC PromflaB1
Z1_11612fF ACGTCATATGTTTCAAAACGTTTTCAA mfn1
Z1_11612SR AGTACTCGAGTTATTCCAATTCCCAGG mfn1
Z3_13198fF ATGTCATATGAAAACAAAACGAAATC mfn3
Z3_13198SR GTAAAACTCGAGCTAACGATAAATTAGATC mfn3
Z4_12631F AGAGACATATGATAAACAAAATAACAAAACC mfn4
Z4_12631SR AGGACTCGAGTTAGCGATAAATAAGAT mfn4
Z7_11436SR ATAAACTCGAGTTATTCCACATAAATT mfn7
Z9_10537fF GAAAACATATGCATACCCTGCT mfn9
Z9_10537SR ATAAACTCGAGTTATTTACTTTTTTTCAAAA mfn9
Z12_11028s4F GCTCATATGTATCGCTCTTTTTTAA mfn12
Z12_11028s4R TTATCCTCGAGCTATTCTTCTAATATAATACT mfn12
pRAT575_MPForv CTAAATCGGAACCCTAAAGG pRAT575 inserts
pRAT575_MPRev CCACAATCAGACAATGACC pRAT575 inserts
a

Restriction sites (GGTACC for KpnI, CATATG for NdeI, and CTCGAG for XhoI) are underlined.

b

The forward primer Z7_11436F (Table 1) was used for cloning in both E. coli and L. biflexa.