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. 2001 Oct;67(10):4671–4677. doi: 10.1128/AEM.67.10.4671-4677.2001

TABLE 1.

PCR primers used for amplifying the LmPH fragments

Primera Nucleotide sequenceb Positionsc Specificity
phe1f GA(G/A)GGCATCAA(A/G)AT(C/T) 121–134 Universal
phe2f CC(C/T/G)TTCATGTC(C/G)GG(T/A/C)GC 628–644 Universal
phe3r CAG(C/G)CG(A/G)T(A/T)ACC(G/T)CGCCAGAACC 797–819 Universal
phe4r AT(C/T)TG(G/A)TGCAC(C/A)GGCA(G/A)CC 1355–1373 Universal
pheUf CCAGG(C/G)(C/G/T)GA(G/A)AA(A/G)GAGA(A/G)GAA(G/A)CT 195–218 Universal
pheUr CGG(A/T)A(G/A)CCGCGCCAGAACCA 796–815 Universal
pheLr GG(A/G/C)A(G/T/C)(A/G)TTG(C/T)CCGGGTC 757–774 Group I
pheMHr GAT(T/C/G)GGCAC(A/G)TTGTCTTC 760–777 Groups II and III
pheHr GTGGCCATGTCGCCATTGA 660–668 Group III
a

f, forward primer; r, reverse primer. 

b

Degenerate nucleotides are indicated in parentheses. 

c

Corresponding to the dmpN sequence of Pseudomonas sp. strain CF600.