The Bactericidal Action Of {beta}-Lactam Antibiotics on an Autolysin-deficient Strain of Bacillus subtilis

Division of Microbiology, National Institute for Medical Research, The Ridgeway, Mill Hill, London NW7 1AA, U.K. ABSTRACT SUMMARY: An autolysin-deficient mutant of Bacillus subtilis was completely tolerant to 5 h incubation with 50-100 µg cycloserine ml -1 whereas the wild-type was rapidly lysed and...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of general microbiology 1983-02, Vol.129 (2), p.465-478
Hauptverfasser: Rogers, Howard J, Thurman, Paul F, Burdett, Ian D. J
Format: Artikel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:Division of Microbiology, National Institute for Medical Research, The Ridgeway, Mill Hill, London NW7 1AA, U.K. ABSTRACT SUMMARY: An autolysin-deficient mutant of Bacillus subtilis was completely tolerant to 5 h incubation with 50-100 µg cycloserine ml -1 whereas the wild-type was rapidly lysed and killed by 12 µg ml -1 . Lysis also did not occur when low concentrations of β-lactams were added to exponentially growing cultures of the mutant, but over 90% of the bacteria were killed within 90-120 min. Protein, lipid and peptidoglycan synthesis as well as growth were inhibited after about 60 min. At this time, but not earlier, small amounts of these three cell components appeared in culture supernatants. Earlier, at about 20-30 min, the intracellular pools of amino acids started to decline rapidly and there was a temporary apparent increase in the rate of lipid synthesis. Neither of the latter phenomena occurred with cycloserine, with which protein and lipid synthesis declined only slowly and the rate of peptidoglycan synthesis was 80% inhibited within 30 min. Only occasional cells with damaged walls were seen 30-90 min after addition of either β-lactams or cycloserine to the cultures. It thus seems unlikely that wall hydrolysis or penetration by residual autolysins in the mutant are responsible for mass cell death caused by the β-lactams.
ISSN:0022-1287
1350-0872
1465-2080
DOI:10.1099/00221287-129-2-465