Skip to main content
. 2000 Jan;68(1):415–419. doi: 10.1128/iai.68.1.415-419.2000

TABLE 2.

Enumeration of the transposition events after transfer of pYT645 into TM4000a

Mutagen Mating Tetr coloniesb
Clnr coloniesc
Total no. of colonies tested Clns Clnr Tets Tetr
pYT645A 1 24 19 5 3 0
2 20 2 0
3 24 2 0
4 30 28 2 2 0
5 36 4 0
pYT645B 6 103 88 15 31 4
7 19 3 0
8 50 9 0
9 45 41 4 9 0
10 23 4 3
a

Each mating filter was resuspended in 3 ml of MPBS buffer. Aliquots of 0.2 ml were added to BHIS-gentamicin-rifampin-tetracycline or BHIS-gentamicin-rifampin-clindamycin plates. 

b

Colonies on one tetracycline plate from each mating were counted, and the numbers are shown. Four plates, from matings 1, 4, 6, and 9, were replica plated onto BHIS-clindamycin plates to count Clns and Clnr colonies among the Tetr colonies. 

c

The number of colonies on one clindamycin plate from each mating is shown. Clnr colonies were transferred to tetracycline plates individually with sterile toothpicks. There is a discrepancy between the numbers of Tetr Clnr colonies obtained in this way and the numbers obtained after an initial tetracycline selection. This may suggest that the structures of the cointegrates allow the loss of the tetQ gene by homologous recombination.