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. 1998 Jan;180(2):435–439. doi: 10.1128/jb.180.2.435-439.1998

TABLE 1.

Transfer of Tn4555 oriT derivatives

Expt Plasmid(s)a Selective mediumb Transfer frequencyc
1 pFD576 Ap + Sm 1.2 × 10−1 ± 1.2
2 pFD601 Cm + Sm <10−7
3 pFD576 + pFD601 Ap + Sm 2.3 × 10−2 ± 1
4 pFD576 + pFD601 Cm + Sm 3.3 × 10−3 ± 2.4
5 pFD576 + pFD601 Ap + Cm + Sm 2.9 × 10−3 ± 1.7
6 pFD576 + pSG335 Cm + Sm <10−7 to 4.7 × 10−6d
7 pFD576ΔoriT1 Ap + Sm 5.1 × 10−4 ± 1
8 pFD576ΔoriT2 Ap + Sm 1.9 × 10−4 ± 1.5
9 pFD648 Ap + Sm <10−7
a

All matings were triparental matings with a strain containing the plasmids indicated, HB101 (1) as the recipient, and the RK231 conjugation helper strain (5). Matings were performed aerobically as described previously except that incubations were for only 4 h prior to plating on selective medium (28). 

b

Selective medium was L-agar (18) supplemented with the following antibiotics where indicated: streptomycin (Sm), 25 μg/ml; ampicillin (Ap), 50 μg/ml; and chloramphenicol (Cm) 25 μg/ml. 

c

Transfer frequency is the number of transconjugants per input donor cell ± the standard deviation. 

d

Results were variable with this set of plasmids ranging from undetectable to a transfer frequency near the lower end of detectable.