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. 2003 Sep;69(9):5170–5177. doi: 10.1128/AEM.69.9.5170-5177.2003

TABLE 2.

Oligonucleotide primers used for PCR amplification of bacterial genes.

Target gene Primer Position (length [nt]) Consensus sequencea Reference organism PCR fragment size (bp) Target bacteria (target enzyme)
alkB Forward 495-521 (27) 5′-CIG IIC ACG AII TIG GIC ACA AGA AGG-3′ Rhodococcus sp. strain Q15 549 Hexadecane degraders (alkane hydroxylase)
Reverse 1018-1044 (27) 5′-IGC ITG ITG ATC III GTG ICG CTG IAG-3′
nirK Forward 560-589 (30) 5′-GGG CAT GAA CGG CGC GCT CAT GGT GCT GCC-3′ P. aureofaciens ATCC 13985 376 Nitrite oxidizers (Cu-nitrite reductase)
Reverse 906-935 (30) 5′-CGG GTT GGC GAA CTT GCC GGT GGT CCA GAC-3′
a

I, inosine.