Effect of some inhibitors on kanamycin formation by Streptomyces kanamyceticus
Jazyk angličtina Země Spojené státy americké Médium print
Typ dokumentu časopisecké články
PubMed
1248783
DOI
10.1007/bf02879005
Knihovny.cz E-zdroje
- MeSH
- arsen farmakologie MeSH
- azidy farmakologie MeSH
- bacitracin farmakologie MeSH
- barbituráty farmakologie MeSH
- buněčná stěna MeSH
- chemická deprese MeSH
- chloramfenikol farmakologie MeSH
- cykloserin farmakologie MeSH
- dinitrofenoly farmakologie MeSH
- fluoridy farmakologie MeSH
- jodacetáty farmakologie MeSH
- kanamycin biosyntéza MeSH
- malonáty farmakologie MeSH
- rtuť farmakologie MeSH
- Streptomyces účinky léků metabolismus MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- arsen MeSH
- azidy MeSH
- bacitracin MeSH
- barbituráty MeSH
- chloramfenikol MeSH
- cykloserin MeSH
- dinitrofenoly MeSH
- fluoridy MeSH
- jodacetáty MeSH
- kanamycin MeSH
- malonáty MeSH
- rtuť MeSH
The formation of kanamycin is markedly inhibited by mercuric chloride, sodium iodoacetate, 2,4-dinitrophenol, sodium arsenite and sodium azide particularly when these are added at the start of fermentation. Less inhibition of kanamycin synthesis is observed in case of sodium 5,5-diethylbarbiturate, malonic acid, sodium arsenate and sodium fluoride. Inhibition of kanamycin synthesis is associated with growth inhibition in case of 2,4-dinitrophenol, sodium arsenite and sodium azide. Bacitracin and D-cycloserine have a stimulatory effect on kanamycin synthesis with slight inhibition of cellular growth. This stimulation might be due to accumulation of cell wallintermediates--aminosugar and sugar--which are shunted to the pathway of kanamycin synthesis. Penicillin lowers kanamycin synthesis by 65 percent as compared with 19 percent reduction of cellular growth. Chloramphenicol has a stimulatory effect at lower concentration (20 mug/ml), when it is added at 24 h of fermentation. At higher concentration (50 mug/ml) chloramphenicol shows marked inhibition of both cellular growth and antibiotic biosynthesis.
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Biochem Biophys Res Commun. 1962 Jul 3;8:186-90 PubMed
Acta Microbiol Acad Sci Hung. 1958;5(1):19-34 PubMed
Antimicrob Agents Chemother. 1973 Jul;4(1):6-10 PubMed
Appl Microbiol. 1956 Sep;4(5):232-6 PubMed
J Gen Microbiol. 1954 Jun;10(3):353-70 PubMed
Acta Microbiol Acad Sci Hung. 1958;5(1):11-7 PubMed
Appl Microbiol. 1957 Sep;5(5):339-43 PubMed
Biochem J. 1954 May;57(1):93-8 PubMed
Appl Microbiol. 1967 Jul;15(4):744-9 PubMed
Appl Microbiol. 1965 Mar;13:190-3 PubMed
J Antibiot (Tokyo). 1957 Sep;10(5):181-8 PubMed
J Biol Chem. 1965 Jul;240:3071-8 PubMed
Investigations of the biological role of antibiotics (some problems and ideas)