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dc.contributor.advisorHaug, Tor
dc.contributor.authorTadesse, Margey
dc.date.accessioned2010-10-06T07:12:07Z
dc.date.available2010-10-06T07:12:07Z
dc.date.issued2010-09-17
dc.description.abstractInfectious diseases are a leading cause of death world-wide and there is a growing need for new anti-infective agents to combat multi-resistant strains of bacteria and fungi. Marine natural products are promising sources of novel antimicrobial compounds. In the present thesis, an investigation into the antimicrobial metabolites of Arctic and sub-Arctic marine invertebrate species is presented. Extracts of seven ascidian species, six sponge species, a soft-alcyonid coral and a bryozoan species, were screened for their antimicrobial activities. The extracts were pre-fractionated by solid phase extraction (SPE) and purified by reversephase high-performance liquid chromatography (RP-HPLC). Active metabolites were characterized by electrospray ionization mass spectrometry (ESI-MS) and nuclear magnetic resonance (NMR) techniques. <br>The antibacterial tyrosine-derived guanidines, 3-dihydroxy-tubastrine and tubastrine, have been isolated from the ascidian Dendrodoa aggregata. This is the first report on the isolation of active metabolites from D. aggregata. 3-dihydroxy-tubastrine has previously been isolated from the Australian sponge species Spongosorites sp. The compound was present in high concentrations in extracts of the ascidian and could serve as a chemotaxonomic marker for the species. <br>Extracts of the ascidian Synoicum pulmonaria displayed the highest antimicrobial activities in our assays. Bio-guided fractionation of the extract, revealed the presence of three novel compounds, named synoxazolidinones A, B and C. The structures of the compounds were elucidated by spectroscopic methods including 1D and 2D NMR techniques, and analysis of mass spectrometric data. The absolute configuration of the compounds was also established by computational methods. The synoxazolidinones contain a unique 4-oxazolidinone core rarely encountered in natural products. Biogenetically, the compounds appear to be derived from arginine and tyrosine. This is the first report on the chemistry of S. pulmonaria. Synoxazolidinones also displayed anticancer activities and provide novel chemical scaffolds for structure-activity relationship studies which are currently being carried out. <br>The dibrominated tryptophan-derived metabolite, eusynstyelamide B, and three new derivatives, eusynstyelamides D, E and F, have been isolated from the bryozoan Tegella cf. spitzbergensis. The structures of the compounds were elucidated by mass spectrometry and, 1D and 2D NMR techniques. All four compounds displayed potent antibacterial activities in our assays. This is the first report of bioactive metabolites from T. spitzbergensis. Eusynstyelamide B has previously been isolated from the Australian ascidian Eusynstyela latericius. The presence of the same metabolites in different organisms and environments, suggests biosynthesis by symbiotic microorganisms. <br>In addition, this thesis provides background information on natural product research and current antimicrobial investigations of marine invertebrate species. The potential of Arctic and sub-Arctic marine invertebrates as sources of structurally novel, bioactive metabolites is demonstrated.en
dc.description.doctoraltypeph.d.en
dc.descriptionThe papers of the thesis are not available in Munin due to publisher's restrictions: <br>1. Margey Tadesse, Bjørn Gulliksen, Morten B. Strøm, Olaf B. Styrvold, Tor Haug: «Screening for antibacterial and antifungal activities in marine benthic invertebrates from northern Norway», Journal of Invertebrate Pathology, 99(2008), 286-293 (Elsevier). Available at <a href=http://dx.doi.org/10.1016/j.jip.2008.06.009>http://dx.doi.org/10.1016/j.jip.2008.06.009</a> <br>The accepted version of the article is avalable in Munin at <a href=http://hdl.handle.net/10037/2728>http://hdl.handle.net/10037/2728</a> <br>2. Margey Tadesse, Veronika Tørfoss, Morten B. Strøm, Espen Hansen, Jeanette Hammer Andersen, Klara Stensvåg, Tor Haug: «Isolation and biological activity of (E)-1-(4-hydroxystyryl)guanidine from the sub-Arctic ascidian, Dendrodoa aggregata», Biochemical Systematics and Ecology (2010) - in press-version (Elsevier). Available at <a href=http://dx.doi.org/10.1016/j.bse.2010.04.002>http://dx.doi.org/10.1016/j.bse.2010.04.002</a> <br>3. Margey Tadesse, Morten B. Strøm, Johan Svenson, Marcel Jaspars, Bruce F. Milne, Veronika Tørfoss, Jeanette H. Andersen, Espen Hansen, Klara Stensvåg and Tor Haug: «Synoxazolidinones A, B, and C; novel bioactive alkaloids from the ascidian Synoicum pulmonaria». Manuscript, published version available in Organic Letters at <a href=http://dx.doi.org/10.1021/ol101707u>http://dx.doi.org/10.1021/ol101707u</a> <br>4. Margey Tadesse, Jioji N. Tabudravu, Marcel Jaspars, Morten B. Strøm, Espen Hansen, Jeanette H. Andersen and Tor Haug: «The antibacterial eusynstelamides B, D, E and F, from the Arctic bryozoan Tegella cf. spitzbergensis» (manuscript)en
dc.format.extent960536 bytes
dc.format.mimetypeapplication/pdf
dc.identifier.isbn978-82-9108-695-8
dc.identifier.urihttps://hdl.handle.net/10037/2702
dc.identifier.urnURN:NBN:no-uit_munin_2445
dc.language.isoengen
dc.publisherUniversitetet i Tromsøen
dc.publisherUniversity of Tromsøen
dc.rights.accessRightsopenAccess
dc.rights.holderCopyright 2010 The Author(s)
dc.subjectVDP::Mathematics and natural science: 400::Chemistry: 440::Pharmaceutical chemistry: 448en
dc.subjectVDP::Matematikk og naturvitenskap: 400::Kjemi: 440::Legemiddelkjemi: 448en
dc.subjectArctic and sub-Arctic marine invertebratesen
dc.subjectantimicrobialen
dc.subjectcold-water spongesen
dc.subjectascidiansen
dc.subjectcoralsen
dc.subjectbryozoansen
dc.subjectDendrodoa aggregataen
dc.subjectSynoicum pulmonariaen
dc.subjectTegella cf spitzbergensisen
dc.subjecttubastrineen
dc.subject3-dehydroxytubastrineen
dc.subjectsynoxazolidinones A, B and Cen
dc.subjecteusynstyelamides B, D, E and Fen
dc.subject1D and 2D NMRen
dc.subjectESI-MSen
dc.titleAntimicrobial natural products from Arctic and sub-Arcticmarine invertebratesen
dc.typeDoctoral thesisen
dc.typeDoktorgradsavhandlingen


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