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Antimicrobial Agents and Chemotherapy, November 1999, p. 2766-2772, Vol. 43, No. 11
Istituto di Genetica Biochimica ed
Evoluzionistica, CNR, Pavia 27100, Italy,1 and
Departments of Microbiology,2
Chemistry,3 and
Biochemistry,4 La Trobe University,
Bundoora, Victoria 3083, Australia
Received 6 May 1999/Returned for modification 10 August
1999/Accepted 4 September 1999
All known DNA ligases catalyze the formation of a phosphodiester
linkage between adjacent termini in double-stranded DNA via very
similar mechanisms. The ligase family can, however, be divided into two
classes: eubacterial ligases, which require NAD+ as a
cofactor, and other ligases, from viruses, archaea, and eukaryotes,
which use ATP. Drugs that discriminate between DNA ligases from
different sources may have antieubacterial activity. We now report that
a group of arylamino compounds, including some commonly used
antimalarial and anti-inflammatory drugs and a novel series of
bisquinoline compounds, are specific inhibitors of eubacterial DNA
ligases. Members of this group of inhibitors have different heterocyclic ring systems with a common amino side chain in which the
two nitrogens are separated by four carbon atoms. The potency, but not
the specificity of action, is influenced by the DNA-binding characteristics of the inhibitor, and the inhibition is noncompetitive with respect to NAD+. The arylamino compounds appear to
target eubacterial DNA ligase in vivo, since a Salmonella
Lig
0066-4804/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Specific Inhibition of the Eubacterial DNA Ligase
by Arylamino Compounds
strain that has been rescued with the ATP-dependent
T4 DNA ligase is less sensitive than the parental
Salmonella strain.
*
Corresponding author. Present address: Department of
Biochemistry, La Trobe University, Bundoora, Victoria 3083, Australia. Phone: 61 3 9479 3044. Fax: 61 3 9479 2467. E-mail:
gcia{at}bioserve.latrobe.edu.au.
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