1

Sequence of PCR primers designed to amplify specific gene fragments of the parathion hydrolase-encoding gene of FB or other parathion-degrading bacteria present in the mixed continuous cultures derived from surface watera

NameNucleotide sequenceSize of PCR product (bp)
with F196with F225with F450
F1965′-CGCGTCCTATCACAATCTC-3′XXX
F2255′-TTTCACACTGACTCACGAGG-3′XXX
F4505′-CGCCACTTTCGATGCGAT-3′XXX
R4685′-TCGCATCGAAAGTGGCGG-3′290262X
R6035′-ACACTAACTCCTGAAAGGGG-3′426b398153
R7575′-TCAGTATCATCGCTGTGACC-3′580552308
R8405′-CTTCTAGACCAATCGCACTG-3′663b635391
NameNucleotide sequenceSize of PCR product (bp)
with F196with F225with F450
F1965′-CGCGTCCTATCACAATCTC-3′XXX
F2255′-TTTCACACTGACTCACGAGG-3′XXX
F4505′-CGCCACTTTCGATGCGAT-3′XXX
R4685′-TCGCATCGAAAGTGGCGG-3′290262X
R6035′-ACACTAACTCCTGAAAGGGG-3′426b398153
R7575′-TCAGTATCATCGCTGTGACC-3′580552308
R8405′-CTTCTAGACCAATCGCACTG-3′663b635391
a

Names consist of the letter F (forward) or R (reverse) followed by the number of base pairs in the gene sequence between the first base of the initiation codon and the nucleotide to which the 5′ nucleotide of the primer is complementary. The right three columns list the expected fragment size of the reverse primers in combination with each of the three forward primers. The combination of F450 and R468 was not investigated since these two primers are complementary to the same region of the gene.

b

Fragments used to screen DNA for parathion hydrolase gene.

1

Sequence of PCR primers designed to amplify specific gene fragments of the parathion hydrolase-encoding gene of FB or other parathion-degrading bacteria present in the mixed continuous cultures derived from surface watera

NameNucleotide sequenceSize of PCR product (bp)
with F196with F225with F450
F1965′-CGCGTCCTATCACAATCTC-3′XXX
F2255′-TTTCACACTGACTCACGAGG-3′XXX
F4505′-CGCCACTTTCGATGCGAT-3′XXX
R4685′-TCGCATCGAAAGTGGCGG-3′290262X
R6035′-ACACTAACTCCTGAAAGGGG-3′426b398153
R7575′-TCAGTATCATCGCTGTGACC-3′580552308
R8405′-CTTCTAGACCAATCGCACTG-3′663b635391
NameNucleotide sequenceSize of PCR product (bp)
with F196with F225with F450
F1965′-CGCGTCCTATCACAATCTC-3′XXX
F2255′-TTTCACACTGACTCACGAGG-3′XXX
F4505′-CGCCACTTTCGATGCGAT-3′XXX
R4685′-TCGCATCGAAAGTGGCGG-3′290262X
R6035′-ACACTAACTCCTGAAAGGGG-3′426b398153
R7575′-TCAGTATCATCGCTGTGACC-3′580552308
R8405′-CTTCTAGACCAATCGCACTG-3′663b635391
a

Names consist of the letter F (forward) or R (reverse) followed by the number of base pairs in the gene sequence between the first base of the initiation codon and the nucleotide to which the 5′ nucleotide of the primer is complementary. The right three columns list the expected fragment size of the reverse primers in combination with each of the three forward primers. The combination of F450 and R468 was not investigated since these two primers are complementary to the same region of the gene.

b

Fragments used to screen DNA for parathion hydrolase gene.

Close
This Feature Is Available To Subscribers Only

Sign In or Create an Account

Close

This PDF is available to Subscribers Only

View Article Abstract & Purchase Options

For full access to this pdf, sign in to an existing account, or purchase an annual subscription.

Close