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  • About
  • The Global ETD Search service is a free service for researchers to find electronic theses and dissertations. This service is provided by the Networked Digital Library of Theses and Dissertations.
    Our metadata is collected from universities around the world. If you manage a university/consortium/country archive and want to be added, details can be found on the NDLTD website.
1

Actinomycetes and fungi associated with marine invertebrates : a potential source of bioactive compounds : a thesis submitted in partial fulfilment of the requirements for the degree of Doctor of Philosophy in Microbiology at the University of Canterbury /

Mahyudin, Nor Ainy. January 1900 (has links)
Thesis (Ph. D.)--University of Canterbury, 2008. / Typescript (photocopy). "January 2008." Includes bibliographical references (leaves 201-215). Also available via the World Wide Web.
2

Chemical investigations of marine filamentous and zoosporic fungi and studies in marine microbial chemical ecology /

Jenkins, Kelly Matthew, January 1998 (has links)
Thesis (Ph. D.)--University of California, San Diego, 1998. / Vita. Includes bibliographical references (p. 169-179).
3

Biomimetic apporaches to the synthesis of polyketide derived marine natural products (-)-Maurenone and the spiculoic acids /

Crossman, Julia Stephanie, January 2007 (has links)
Thesis (Ph.D.)--Flinders University, Dept. of Chemistry. / Typescript bound. Includes bibliographical references: (p. 360-369) Also available online.
4

Potential study of chemical and pharmacological of secundary metabolites of coast cearense fungi: Aspergillus sp. / Estudo do potencial quÃmico e farmacolÃgico de metabÃlitos secundÃrios de fungos da costa cearense: Aspergillus sp.

JoÃo Evangelista de Ãvila dos Santos 25 September 2015 (has links)
CoordenaÃÃo de AperfeiÃoamento de Pessoal de NÃvel Superior / This study aimed to the chemical and pharmacological research of biodiversity of marine fungi associated with sediment from the coastline of northeastern Brazil, especially the state of CearÃ. From the collection of marine sediments at the beach Pecem - SÃo GonÃalo do Amarante-CE, were cultivated various fungi, of which the strain identified as Aspergillus sp. (BRF 087), showed a preliminary cytotoxic activity. The methodology has been directed in finding secondary metabolites with cytotoxic activity using a kinetic fungus study was grown in four different media, BD (potato dextrose), BDL (potato dextrose and yeast), MPD (malt, peptone and dextrose ) and MntPL (mannitol, peptone and yeast) and in different culture periods (7, 14, 21, 28 days). This procedure resulted in the isolation of nine diketopiperazines two tetrapeptides cycle, 3 derivatives of succinic acid and p-hydroxyphenylacetic acid, characterized as cyclo (L-Pro-L-Leu) (A-1), cyclo (L-Pro-L -Phe) (A-2), cyclo (4-OH-Pro-Leu) (A-3), cyclo (4-OH-Pro-Phe) (A-4), cyclo (L-Pro-L-tyr ) (A-5), cyclo (L-Leu-L-Val) (A-6), cyclo (L-Phe-L-Val) (A-7), cyclo (L-Phe-L-Leu) (A-8), cyclo (L-Leu-L-Ile) (A-9), cyclo (L-Ile-L-Pro-L-Leu-L-Pro) (A-10), cyclo (Leu-Ile Leu-Phe) (A-11), 2-metilenosuccinic acid (A-12), 3-Methyl-2-metilenosuccinic (A-13), 4-metoxy-2-methylidene-4-oxobutanoic acid (A-14) and p-hydroxyphenylacetic acid (A-15). The isolation of secondary metabolites was conducted by using usual chromatographic techniques, including chromatography on reverse phase C18 column and high-performance liquid chromatography (HPLC). For structural characterization of the compounds were used customary spectrometric techniques like IR, mass spectrometry and nuclear magnetic resonance (NMR), one and two dimensional, and compared with literature data. / O presente trabalho teve como objetivo principal a investigaÃÃo quÃmico-farmacolÃgica da biodiversidade dos fungos marinhos associados a sedimentos da costa litorÃnea do Nordeste do Brasil, e em especial do estado do CearÃ. A partir da coleta de sedimentos marinhos na praia do PecÃm - SÃo GonÃalo do Amarante-CE, foram cultivados vÃrios fungos, dos quais a cepa identificada como Aspergillus sp. (BRF 087), mostrou uma atividade citotÃxica preliminar. A metodologia empregada foi direcionada na busca de metabÃlitos secundÃrios com atividade citotÃxica, atravÃs de um estudo cinÃtico do fungo que foi cultivado em quatro meios diferentes, BD (batata dextrose), BDL (batata dextrose e levedura), MPD (malte, peptona e dextrose) e MntPL (manitol, peptona e levedura) e em diferentes perÃodos de cultivo (7, 14, 21, 28 dias). Este procedimento resultou no isolamento de nove dicetopiperazinas, dois ciclo tetrapeptÃdeos, 3 derivados do Ãcido succinio e o Ãcido p-hidroxifenilacÃtico, caracterizados como ciclo (L-Pro-L-Leu) (A-1), ciclo (L-Pro-L-Fen) (A-2),ciclo (4-OH-Pro-Leu) (A-3), ciclo (4-OH-Pro-Fen) (A-4), ciclo (L-Pro-L-Tyr) (A-5), ciclo (L-Leu-L-Val) (A-6), ciclo (L-Fen-L-Val) (A-7), ciclo (L-Fen-L-Leu) (A-8), ciclo (L-Leu-L-Ile) (A-9), ciclo (L-Ile-L-Pro-L-Leu-L-Pro) (A-10), ciclo (Leu-Ile-Leu-Fen) (A-11), Ãcido 2-metilenosuccinio (A-12), Ãcido 3-metil-2-metilenosuccinio (A-13), Ãcido 4-metoxi-2-metileno-4-oxobutanÃico (A-14) e o Ãcido p-hidroxifenilacÃtico (A-15). O isolamento dos metabÃlitos secundÃrios foi realizado atravÃs do uso de tÃcnicas cromatogrÃficas usuais, incluindo cromatografia em coluna de fase reversa C18 e cromatografia lÃquida de alta eficiÃncia (CLAE). Para a caracterizaÃÃo estrutural dos compostos foram utilizadas tÃcnicas espectromÃtricas usuais como infravermelho, espectrometria de massa e ressonÃncia magnÃtica nuclear (RMN), uni e bidimensional, alÃm de comparaÃÃo com dados da literatura.

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