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. 2007 Nov 2;190(1):240–250. doi: 10.1128/JB.01528-07

TABLE 2.

AS-48 production and resistance from E. faecalis JH2-2 harboring the plasmids used in this work

Plasmid AS-48 production zone of inhibition (mm)a Sensitivity to indicated amt (μg 5 μl−1) of AS-48b
0.5 1 3 6 9 18
pMB2 (positive control) 16 R R R R R R
pAM401 (negative control) ND S S S S S S
pAM401-81 16 R R R R R R
pAM401-81::Tn5PA ND R R R R S S
pAM401-81::Tn5B ND R R R R S S
pAM401-81::Tn5C 8 R R R R S S
pAM401-81X 11 R R R R R R
pAM401-52 11 R R R S S S
pAM401-58 ND R R S S S S
pAM401-81::Tn5PA/pMG36-Ac 7 R R R R S S
pAM401-58/pMG36-Ac ND R R S S S S
pAM401-81::Tn5B/pMG36-BCc 11 R R R R R R
a

AS-48 production was assayed in plates against the indicator strain E. faecalis JH2-2[pAM401] by using AS-48[pMB2] as a control (wild-type phenotype). ND, no detectable production.

b

To test AS-48 sensitivity, 5-μl spots containing different amounts of purified AS-48 were applied on lawns seeded with a standard inoculum of E. faecalis JH2-2 harboring different plasmids. The plates were examined for inhibition halos after 18 h of incubation at 37°C. R, resistant; S, sensitive.

c

Erythromycin was present during growth of the strains in liquid and solid media, and JH2-2[pAM401/pMG36e] was used as an indicator for AS-48 production.