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2009 | 58 | 4 |

Tytuł artykułu

Antifungal activity of thionated analogues of Nva-FMDP and Lys-Nva-FMDP

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
The antifungal activity of synthetic endothiopeptdides, i.e. NvaΨ [CSNH]-FMDP and LysΨ [CSNH]-NvaΨ [CSNH]-FMDP was studied in medium containing blood serum, against selected Candida strains; Candida albicans Gu4 (fluconazole sensitive), C. albicans Gu5 (fluconazole resistant), C. albicans ATCC 10231, Candida krusei DSM 6128 and Candidaparapsilosis DSM 5784. Although thiopeptide bonds in the tested peptides increased their stability in blood serum, their antifungal activity, however, drastically decreased in comparison with the peptides containing non-modified peptide bonds. Moreover, the inhibitory activity towards glucosamine-6-phosphate synthase of thionated synthetic analogue of FMDP was performed. The thiopeptdide bond also influenced its inhibitory properties against enzyme from C. albicans.

Wydawca

-

Rocznik

Tom

58

Numer

4

Opis fizyczny

p.295-299,fig.,ref.

Twórcy

autor
  • Gdansk University of Technology, Narutowicza Street 11/12, 80-952 Gdansk, Poland

Bibliografia

  • Andruszkiewicz R., H. Chmara, S. Milewski and E. Borowski. 1987. Synthesis and biological properties of N-3-(4-methoxy-fumaroyl)-L-2,3-diaminopropanoic acid dipeptides, a novel group of antimicrobial agents. J. Med. Chem. 30: 1715-1719.
  • Badet B., P. Vermoote, P.Y. Haumont, F.Lederer and F. Le Goffic. 1987. Glucosamine synthetase from Escherichia coli: purification, properties and glutamine-utilizing site location. Biochemistry 26: 1940-1948.
  • Chmara H., R. Andruszkiewicz and E. Borowski. 1986. Inactivation of glucosamine-6-phosphate synthetase from Salmonella typhimurium Lt2 by fumaroyl diaminopropanoic acid derivatives, a novel group of glutamine analogs. Biochim. Biophys. Acta 870: 357-366.
  • Kenig M., E. Vandamme and E.P. Abraham. 1976. The mode of action of bacilysin and anticapsin and biochemical properties of bacilysin - resistant mutants. J. Gen. Microbiol. 94: 46-54.
  • Kucharczyk N., M.A. Denisot, F. Le Goffic and B. Badet. 1990. Glucosamine-6-phosphate synthase from Escherichia coli - determination of the mechanism of inactivation by (V-3-fumaroyl-L-2,3-diaminopropionic derivatives. Biochemistry 29: 3668-3676.
  • Milewski S., R. Andruszkiewicz, L. Kasprzak, J. Mazerski, F. Mignini and E. Borowski. 1991. Mechanism of action of anticandidal dipeptides containing inhibitors of glucosamine-6-phosphate synthase. Antimicrob. Agents Chemother. 35: 36-43.
  • Milewski S., H. Chmara, R. Andruszkiewicz and E. Borowski. 1992. N³-haloacetyl derivatives of L-2,3-diaminopropanoic acid: novel inactivators of glucosamine-6-phoshate synthase. Biochim. Biophys. Acta 1115: 225-229.
  • Nowak-Jary J. and R. Andruszkiewicz. 2008a. Synthesis and antimicrobial activity of Nva[CSNH]-FMDP. J. Peptide Sci. Suppl. 14: 118-119
  • Nowak-Jary J., R. Andruszkiewicz and J.W. Payne. 2008b. Enzymatic degradation and transport of endothiopeptides into Escherichia coli K12 mutant strains. FEMS Microbiol. Lett. 285: 291-297.
  • Payne J.W. 1995a. Bacterial peptide permeases as a drug delivery target, pp. 341-367. In: M.D. Taylor and G.L. Amidon (eds). Peptide Based Drug Design: Controlling Transport and Metabolism ACS, Washington, D.C.
  • Payne J.W. 1995b. Peptides and microorganisms. Adv. Microbiol. Physiology 13: 55-113.
  • Ringrose P.S. 1980. Peptides as antimicrobial agents, pp. 641-657. In: Payne J. W.(ed) Microorganisms and Nitrogen Sources. John Wiley and Sons Ltd., Chichester, United Kingdom.

Typ dokumentu

Bibliografia

Identyfikatory

Identyfikator YADDA

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