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. 2009 Mar 20;191(10):3375–3383. doi: 10.1128/JB.01608-08

TABLE 5.

Expression of TrbJ and TrbK in recipients of multicopy plasmidsa

pBBRMCS5 derivative (description or genotype) pPZP200 derivative (description or genotype) Conjugation efficiencyb (SD) Exclusion coefficientc
pHC012 (vector) pUP200 (vector) 0.69 (0.2) 1
pJZ381 (traR)d pPZP200 (vector) 0.002 (0.001) 345
pUP402 (Ptac-trbJ) pUP200 (vector) 0.08 (0.009) 8.6
pHC012 (vector) pUP403 (Ptac-trbJ) 0.18 (0.03) 3.8
pHC368 (Ptac-trbK) pUP200 (vector) 0.10 (0.04) 6.9
pHC012 (vector) pUP404 (Ptac-trbK) 0.21 (0.04) 3.3
pUP402 (Ptac-trbJ) pUP404 (Ptac-trbK) 0.007 (0.002) 98.6
pHC368 (Ptac-trbK) pUP403 (Ptac-trbJ) 0.022 (0.004) 31.4
pHC361 (Ptac-trbJK) pPZP200 (vector) 0.002 (0.0008) 345
a

The donor strain in each experiment was WCF5(pCF218), which overexpresses TraR and has an octopine-type Ti plasmid marked with a Kmr determinant. Transconjugants were selected using the Kmr gene of the Ti plasmid, the Spr gene of pUP200 or its derivatives, and the Gmr gene of pHC012 or its derivatives.

b

Number of transconjugants per donor.

c

The exclusion coefficient is the number of transconjugants per donor for the no-exclusion control (top line) divided by the number of transconjugants of the tested recipient strain per donor.

d

The overexpression of TraR by pJZ381 induces the expression of all tra and trb genes (6).