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. 2004 Jan;70(1):61–68. doi: 10.1128/AEM.70.1.61-68.2004

TABLE 3.

Analysis of LEE insertion site

Strain PCR analysis of the selC sitea
PCR analysis of the pheU site
PCR analysis of the pheV site
Gene present by PFGE analysisd
selC site LEE right side LEE left side CP4-int pheU site LEE right side LEE left sideb int-phe pheV site int-phec
NV100 I NR NR NR D + D + pheV
NV163 I NR NR NR D + D + pheV or pheU
NV169 I NR NR NR I NR NR D + (2.4 kb) pheV
NV220 I NR NR NR D D + (2.4 kb) pheV
NV258 I NR NR NR D + D + pheV
NV270 I NR NR NR I NR NR D + pheV
NV2 D + + I NR NR I NR selC
NV10 D + D + + (2.3 kb) + D + pheU
NV19 D I NR NR D + pheV
NV92 D + + D + D + selC
NV95 D + I NR NR D + selC
NV281 D + D + + (6.0 kb) + D + ND
a

PCRs were performed with the primers shown in Fig. 1. I, intact site; D, disrupted site; NR, not relevant due to an intact selC, pheU, or pheV site; ND, not determined; +, amplification; −, no amplification.

b

Amplicon sizes distinct from that obtained with the RDEC-I reference strain are indicated in parentheses.

c

Amplicon sizes distinct from that obtained with the 84110-1 reference strain are indicated in parentheses.

d

tRNA locus present in the DNA fragment containing the LEE.