Comparison of fortimicins with other aminoglycosides and effects on bacterial ribosome and protein synthesis.

Abstract:

:Fortimicins are bicyclic aminoglycoside antibiotics that contain a fortamine moiety instead of the deoxystreptamine found in other aminoglysides. Fortimicin A had a bactericidal effect on Escherichia coli and Staphylococcus epidermidis and was found to inhibit protein synthesis in vivo. In vitro, fortimicin A inhibited polyuridylic acid-directed phenylalanine polymerization and induced misreading, as shown by leucine incorporation. In contrast, fortimicin B had no effect on either polymerization or misreading. In assays programmed with natural mRNA, only a weak polymerization inhibition effect was observed with fortimicin A, whereas a strong stimulation was seen in the presence of fortimicin B. Both fortimicins A and B inhibited dissociation of 70S ribosomes into their subunits and neither was able to displace [3H]dihydrostreptomycin, [3H]tobramycin, or [3H]gentamicin from their respective binding sites on the 70S particle.

authors

Moreau N,Jaxel C,Le Goffic F

doi

10.1128/aac.26.6.857

subject

Has Abstract

pub_date

1984-12-01 00:00:00

pages

857-62

issue

6

eissn

0066-4804

issn

1098-6596

journal_volume

26

pub_type

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