Literature DB >> 2514624

Phosphanilic acid inhibits dihydropteroate synthase.

R G Eagon1, A T McManus.   

Abstract

Intact cells of Pseudomonas aeruginosa were more susceptible to phosphanilic acid (PA) than cells of Escherichia coli. In cell extracts, the dihydropteroate synthases of P. aeruginosa and E. coli were about equally susceptible to inhibition by PA. These results suggest that cells of P. aeruginosa are more permeable to PA than cells of E. coli. Although a weak inhibitor, PA acted on dihydropteroate synthase in the same manner as the sulfonamides with which PA is structurally related. Inhibition of E. coli by PA in a basal salts-glucose medium was prevented by p-aminobenzoic acid (pABA). However, pABA did not protect P. aeruginosa from PA under these conditions, possibly because pABA itself exhibited an inhibitory effect. PA also appeared to have a second mode of action. The mechanism was not elucidated.

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Year:  1989        PMID: 2514624      PMCID: PMC172791          DOI: 10.1128/AAC.33.11.1936

Source DB:  PubMed          Journal:  Antimicrob Agents Chemother        ISSN: 0066-4804            Impact factor:   5.191


  4 in total

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2.  Silver phosphanilamidopyrimidine. A new silver sulfadiazine analogue effective against Pseudomonas infection in burned mice.

Authors:  M S Wysor; R E Zollinhofer
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3.  Kinetics of transport of glucose, fructose, and mannitol by Pseudomonas aeruginosa.

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4.  Antibacterial activity of phosphanilic acid, alone and in combination with trimethoprim.

Authors:  M Misiek; R E Buck; T A Pursiano; D R Chisholm; Y H Tsai; K E Price; F Leitner
Journal:  Antimicrob Agents Chemother       Date:  1985-12       Impact factor: 5.191

  4 in total
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3.  Inhibition of Pneumocystis carinii dihydropteroate synthetase by para-acetamidobenzoic acid: possible mechanism of action of isoprinosine in human immunodeficiency virus infection.

Authors:  J A Kovacs; F Powell; D Voeller; C J Allegra
Journal:  Antimicrob Agents Chemother       Date:  1993-06       Impact factor: 5.191

4.  Identification of a class of sulfonamides highly active against dihydropteroate synthase form Toxoplasma gondii, Pneumocystis carinii, and Mycobacterium avium.

Authors:  L C Chio; L A Bolyard; M Nasr; S F Queener
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  4 in total

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