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  • http://hdl.handle.net/10402/era.26801
  • Synthesis and biological evaluation of the lantibiotic peptide lactocin S and its analogues
  • Ross, Avena Clara
  • English
  • peptide synthesis
    lantibiotic
    lactocin S
    antimicrobial
    analogues
  • May 31, 2012 3:24 PM
  • Thesis
  • English
  • Adobe PDF
  • 14216992 bytes
  • Lantibiotics (lanthionine containing antibiotics) are highly post-translationally modified peptides used by bacteria as a form of chemical warfare. In light of the challenges faced today in the field of antibacterial therapy, these potent natural products are useful lead compounds for the development of future antibiotics. Lactocin S (98) is a 37 amino acid lantibiotic peptide isolated from Lactobacillus sakei L45. Due to low levels of production by the natural producer organism, complete structural identification has been challenging. The total chemical synthesis of 98 using a combined solution and solid phase chemistry approach is described. The unusual amino acid lanthionine was synthesized in solution with orthogonal protecting groups (58) so that it could be cyclized on-resin during the solid phase synthesis of the peptide. An N-terminal α-ketoamide precursor was also made in solution. Following coupling to the rest of the peptide on resin, global deprotection of the peptide resulted in the formation of the α-ketoamide containing lactocin S (98). A simplified purification of lactocin S (98) from Lactobacillus sakei L45 was developed. Comparison of the natural and synthetic peptides via activity testing, mass spectrometry and chiral GC/MS analysis confirmed the proposed structure of lactocin S (98). Unfortunately, lactocin S suffers from pH and oxidative instability. This thesis describes the synthesis of analogues developed with a goal of improving stability as well as activity. The lanthionine rings were systematically replaced with diaminopimelate, which contains a methylene carbon in place of the thioether of lanthionine. Orthogonally protected diaminopimelate (137) was synthesized via a key photolysis reaction of diacylperoxide 170 to form the backbone. The solid phase synthesis of the analogues was then accomplished. One of these analogues, A-DAP lactocin S (151), exhibited improved activity compared to the natural peptide (98). A second site of modification was methionine 12. Leucine (181) and norleucine (182) analogues were made that exhibit full retention of activity. A final analogue (183) was synthesized using an oxazole ring to mimic the dehydrobutyrine-α-ketoamide functionality at the N-terminus of lactocin S (98). This compound displayed no biological activity. The methodology described, provides access to potentially stable and active analogues of lantibiotics.
  • Doctoral
  • Doctor of Philosophy
  • Department of Chemistry
  • Spring 2012
  • Vederas, John C. (Chemistry)
  • Vederas, John C. (Chemistry)
    Clive, Derrick L. J. (Chemistry)
    Cairo, Christopher W. (Chemistry)
    Bergens, Steven H. (Chemistry)
    McMullen, Lynn M. (Agricultural, Food and Nutritional Science)
    Dawson, Philip E. (External)