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1

Doege, Maria. "Photoprotektive Mechanismen der Alge Euglena gracilis in Abhängigkeit vom Carotinoidgehalt Untersuchungen zur nichtphotochemischen Löschung der Chlorophyll a - Fluoreszenz /." [S.l. : s.n.], 1999. http://deposit.ddb.de/cgi-bin/dokserv?idn=96085844X.

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2

Javed, Q. "Regulation of enzyme synthesis in Euglena gracilis." Thesis, Swansea University, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.637408.

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The expression of NADPH-specific glutamate dehydrogenase (NADPH-GDH) was examined in <i>Euglena gracilis</i> Klebs strain z Pringsheim in relation to light and available nitrogen source. The exposure of dark-grown resting cells to white or red light caused a transient increase in NADPH-GDH specific activity over the first 12 hours of regreening. Nitrogen-starved or cells grown on glutamate had high NADPH-GDH activity but activity was completely repressed in cells grown on ammonium bicarbonate as sole nitrogen source. These characteristics of the dehydrogenase suggest that the enzyme has a cata
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3

Rotte, Carmen. "Molekulare Biochemie ausgewählter Enzyme des anaeroben Energiestoffwechsels in den fakultativ anaeroben Mitochondrien von Euglena gracilis." [S.l. : s.n.], 2003. http://deposit.ddb.de/cgi-bin/dokserv?idn=968538150.

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4

Hoffmeister, Meike. "Anaerober Energiestoffwechsel und Fettsäurebiosynthese im fakultativ anaeroben Mitochondrium von Euglena gracilis." [S.l. : s.n.], 2004. http://deposit.ddb.de/cgi-bin/dokserv?idn=971748764.

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5

Parker, J. E. "Developmental regulation of protein synthesis in Euglena gracilis." Thesis, Swansea University, 1987. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.638412.

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The expression of mitochondrial citrate synthase (CS) and the cytosolic enzyme NADP-dependent glutamate dehydrogenase (NADPH-GDH) was examined in <i>Euglena gracilis</i> Klebs strain z Pringsheim in relation to light and glutamate provision. Exposure of dark grown cells to white or red light but not blue light caused a transient increase in CS and NADPH-GDH specific activity over the first 12 hours of regreening. Illumination with white or red light but not blue light also initiated efficient chloroplast development over 72 hours. Provision of L-glutamate as sole nitrogen source caused an incr
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6

Ebenezer, ThankGod Echezona. "The genome of Euglena gracilis : annotation, function and expression." Thesis, University of Cambridge, 2018. https://www.repository.cam.ac.uk/handle/1810/275885.

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Euglena gracilis is a species of unicellular photosynthetic flagellate that inhibits aquatic ecosystems. E. gracilis belongs to the supergroup Excavata, and are an important component of the global biosphere, have biotechnological potential and is useful biological model due to their evolutionary history and complex biology. Whilst the evolutionary position of E. gracilis is now clear, their relationship with other protists such as Naegleria, Giardia, and Kinetoplastids, remains to be investigated in detail. Investigating and understanding the biology of this complex organism is a promising wa
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7

Tucker, Margie M. "Purification and Characterization of Enoyl-acp Reductase From Euglena Gracilis." Digital Commons @ East Tennessee State University, 1990. https://dc.etsu.edu/etd/2812.

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Enoyl-(acyl-carrier-protein) reductase was purified from the phytoflagellate Euglena gracilis. Its purification employed DEAE-Sephacel chromatography, Matrex Orange chromatography, and affinity chromatography using acyl carrier protein (ACP) covalently bound to Sepharose as the affinity ligand. Matrex Orange chromatography resolved two different enoyl-ACP reductases having different characteristics. Euglena gracilis appears to resemble higher plants in the possession of two isoforms of this enzyme. Antibodies specific for the cofactor binding site of NADP (H)-requiring dehydrog
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8

Van, der Merwe Laurianne. "UDP-glucose: [beta]-(1-3)-glucan (paramylon) synthase from Euglena gracillis /." Link to the online version, 2007. http://hdl.handle.net/10019/722.

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9

Copertino, Donald Woodward. "Twintrons: Introns-within-introns in the chloroplast genes of Euglena gracilis." Diss., The University of Arizona, 1992. http://hdl.handle.net/10150/186052.

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The chloroplast genes of Euglena gracilis contain more than 100 introns. A comparison of intron content and position among plastid and prokaryote genes has led to the hypothesis that introns have been inserted into chloroplast genes during evolution. Several Euglena loci contain unusual introns. These introns have been characterized by direct primer extension cDNA sequencing, cDNA cloning and sequencing, and northern hybridization. The psbF locus has a 1042 nt intron that appears to be one group II intron inserted into domain V of another group II intron. It was determined that a 618 nt intern
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10

Cholewa, Dominik [Verfasser], Karl [Akademischer Betreuer] Friehs, and Anant [Akademischer Betreuer] Patel. "Ein Bioraffineriekonzept mit Euglena gracilis / Dominik Cholewa ; Karl Friehs, Anant Patel." Bielefeld : Universitätsbibliothek Bielefeld, 2017. http://d-nb.info/1125626119/34.

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11

Van, der Merwe Laurianne. "UDP-glucose: β-(1-3)-glucan (paramylon) synthase from Euglena gracilis". Thesis, Stellenbosch : University of Stellenbosch, 2007. http://hdl.handle.net/10019.1/1560.

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Thesis (MSc (Plant Biotechnology))--University of Stellenbosch, 2007.<br>The photosynthetic protist Euglena gracilis synthesizes a storage carbohydrate named paramylon, a glucan consisting only of β-(1-3)-glycosidic linkages. The enzyme that produces paramylon is a glycosyltransferase commonly known as paramylon synthase (EC 2.4.1.34; UDP-glucose: 1,3-β-D-glucan 3-β-D-glucosyl transferase). This enzyme uses UDP-glucose as its main substrate. In 2001, Bäumer et al. isolated and partially purified paramylon synthase, but never presented any sequence information. Hence, the main aim of this proje
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12

Carvalho, Juliana Maria Andrade. "Produção de bioetanol de terceira geração a partir de Euglena gracilis." Universidade Federal da Bahia, 2018. http://repositorio.ufba.br/ri/handle/ri/27079.

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Submitted by Juliana Carvalho (juma.andrade@gmail.com) on 2018-08-16T12:56:38Z No. of bitstreams: 1 Dissertação Digital.pdf: 1627062 bytes, checksum: 67f59becf12b9f50517eaaff5f564782 (MD5)<br>Approved for entry into archive by Vanessa Reis (vanessa.jamile@ufba.br) on 2018-08-27T11:51:11Z (GMT) No. of bitstreams: 1 Dissertação Digital.pdf: 1627062 bytes, checksum: 67f59becf12b9f50517eaaff5f564782 (MD5)<br>Made available in DSpace on 2018-08-27T11:51:11Z (GMT). No. of bitstreams: 1 Dissertação Digital.pdf: 1627062 bytes, checksum: 67f59becf12b9f50517eaaff5f564782 (MD5)<br>FAPESB/CNPq<br>Atua
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13

Strauch, Sebastian M. "Euglena gracilis als Sauerstoffproduzent eines bioregenerativen Lebenserhaltungssystems und ihre physiologische Reaktion auf Änderungen der Schwerkraft." kostenfrei, 2009. http://d-nb.info/999863657/34.

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14

Kolba, Clifford Andrew. "Intracellular and extracellular acid phosphatase activity in axenically cultured phosphate-deprived achlorophyllous euglena gracilis /." Access Digital Full Text version, 1994. http://pocketknowledge.tc.columbia.edu/home.php/bybib/11714372.

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Thesis (Ed.D.)--Teachers College, Columbia University, 1994.<br>Typescript; issued also on microfilm. Sponsor: O. Roger Anderson. Dissertation Committee: Patricia L. Dudley. Includes tables. Includes bibliographical references (leaves 119-129).
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15

ABAHAMID, ABDELOUAHAB. "Adaptation de cellules d'euglena gracilis au pentachlorophenol et au cadmium : modulations de l'expression de proteines de stress et d'enzymes de detoxication apparentees aux cytochromes p-450 (doctorat : structure et fonctionnement des systemes biologiques integres)." Paris 11, 1998. http://www.theses.fr/1998PA114825.

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16

Jenkins, Joanne M. "Biochemical analysis of the early steps in tetrapyrrole biosynthesis in Euglena gracilis." Thesis, University of Cambridge, 1992. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.284208.

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17

Stevenson, Jennifer Kaye. "Transcription and intercistronic RNA processing of polycistronic operons of Euglena gracilis chloroplast." Diss., The University of Arizona, 1994. http://hdl.handle.net/10150/186765.

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The Euglena chloroplast genome contains 3 sets of genes for ribosomal RNAs 16S, 23S and 5S, and an additional 16S gene; 31 tRNA genes; 25 protein coding genes for transcription and translation; 27 protein coding genes for photosynthesis; and 15 open reading frames. The majority of these genes are transcribed as polycistronic operons. Using primer extension RNA sequencing, in vitro capping and S1 nuclease protection, I have determined 6 transcription start sites for operons of protein coding genes. These are found upstream of chlI, psbD, psbA, rpl20, psbI and rpoB. Sequence upstream of the chlI
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18

Bonavia-Fisher, Bruna. "Evidence that a chloroplast membrane protein is located in the mitochondria of photosynthetic and non-photosynthetic euglenoids." Thesis, McGill University, 2000. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=36755.

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1. Distribution of the two photosystems (PS I and PS II) in the thylakoid membranes of the alga Euglena gracilis. The distribution of photosystem I and II (PS I and PS II) in the alga Euglena gracilis Z strain was studied by electron microscopic immunocytochemistry. In this alga, the thylakoids are not organized in gram structures, as they are in higher plants. Two different antibodies were used to identify PS I. One is directed against particles of PS I from maize and the other against the 60 and 62 kDa PS I reaction centre proteins of the cyanobacterium Synechococcus elongatus. Both antibodi
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19

Radebaugh, Catherine Ann 1956. "Characterization of the structure and expression of the Euglena gracilis chloroplast rpoC1 and rpoC2 gene loci." Diss., The University of Arizona, 1990. http://hdl.handle.net/10150/185057.

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In order to expand our understanding of the expression of chloroplast genes, the structure and expression of the Euglena gracilis rpoC1 and rpoC2 loci were studied. The rpoC1 and rpoC2 gene products are similar to the amino- and carboxyl-terminal regions of the $\beta\sp\prime$ subunit of E. coli RNA polymerase. The nucleotide sequence (7,270 bp) was determined for 100% of both strands encoding these two genes. The rpoC1 and rpoC2 genes are located downstream and in the same polarity as the rpoB gene. The organization of the Euglena rpoB-rpoC1-rpoC2 genes is conserved in plant chloroplasts and
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20

Yepiz, Plascencia Gloria Martina. "Characterization of the structure and expression of the Euglena gracilis chloroplast rpoB and 23S ribosomal-RNA genes." Diss., The University of Arizona, 1990. http://hdl.handle.net/10150/282094.

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The rpoB gene coding for a β-like subunit (homologous to the E. coli DNA-dependent RNA polymerase β subunit) of the chloroplast DNA-dependent RNA polymerase was located on the chloroplast genome of Euglena gracilis distal to the rrnC ribosomal RNA operon. The complete nucleotide sequence of the gene was determined. The sequence includes 97 bp of the 5S rRNA gene, an intergenic spacer of 1264 bp, the rpoB gene of 4249 bp, 84 bp spacer and 67 bp of the rpoC1 gene. The rpoB gene is of the same polarity as the rRNA operons. The organization of the rpoB and rpoC genes resemble the E. coli rpoB-rpoC
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21

Shashidhara, L. S. "Porphobilinogen deaminase from Euglena gracilis : expression, subcellular localization, regulation, and targeting to plastids." Thesis, University of Cambridge, 1991. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.239204.

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22

Tamponnet, Christian. "Rôle du calcium dans la conservation d'une algue unicellulaire immobilisée, Euglena gracilis Z." Grenoble 2 : ANRT, 1986. http://catalogue.bnf.fr/ark:/12148/cb376014461.

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23

Hong, Ling. "Gene structure and expression of the Euglena gracilis chloroplast psbB and petB operons." Diss., The University of Arizona, 1994. http://hdl.handle.net/10150/186930.

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Euglena gracilis has been used as a model for studying the chloroplast genome and gene expression during chloroplast biogenesis. My graduate research has been focused on the following two areas: (1) DNA sequencing of part of the Euglena gracilis chloroplast genome, (2) Euglena chloroplast RNA metabolism, such as intercistronic RNA processing and intron splicing. The region that I characterized is between the psbB and rbcL loci on the Euglena gracilis chloroplast genome. Three photosystem II genes (psbT, psbN and psbH), one cytochrome b6 gene (petB) and two ATPase subunit genes (atpB and atpE)
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24

Ryll, Joachim. "Fermentative Gewinnung von Paramylon aus Euglena gracilis auf Nebenprodukten der Stärkeindustrie in einer Pilotanlage." [S.l. : s.n.], 2005. http://deposit.ddb.de/cgi-bin/dokserv?idn=974970581.

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25

Gumpel, Nicola Jane. "Characterisation of uroporphyrinogen III synthase and a novel calcium binding protein from Euglena gracilis." Thesis, University of Cambridge, 1991. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.386737.

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26

JULISTIONO, HEDDY. "Metabolisation de l'ethanol chez euglena gracilis z : similarites entre l'euglene et la cellule hepatique." Paris 7, 1992. http://www.theses.fr/1992PA077094.

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La metabolisation de l'ethanol chez l'euglene implique l'alcool deshydrogenase (adh) et le meos (systeme microsomal d'oxydation de l'ethanol). L'exces de formation de nadh serait vraisemblablement la cause principale des perturbations physiologiques lors de la metabolisation de l'ethanol. La cellule s'adapte a l'ethanol en diminuant l'activite de l'adh et en augmentant l'activite du meos. La cinetique d'activite de l'alcool deshydrogenase montre la presence de plusieurs isoenzymes. La presence dans la fraction microsomale: 1) d'activites nad(p)h cytochrome c reductases; 2) de cytochrome p-450
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27

Thuillier-Bruston, Francine. "Culture photoorganotrophique sur milieu glycolate et metabolisme photorespiratoire de ce substrat chez euglena gracilis z." Paris 7, 1987. http://www.theses.fr/1987PA077086.

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Les euglenes cultivees en presence du substrat glycolate utilisent le systeme chloroplastique pour synthetiser leurs reserves carbonees et s'apparentent aux euglenes photoautotrophes par leur photochimie du psii, leurs activites carboxylasiques et leur ultrastructure
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28

LARHRISSI, ZAKIA. "Importance de la dismutation de l'eau oxygenee dans l'energetique cellulaire chez euglena gracilis z etiolee." Paris 7, 1994. http://www.theses.fr/1994PA077052.

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Euglena gracilis cultivee a l'obscurite en presence du lactate comme seule source carbonee montre un parallelisme entre les activites respiratoires et les activites catalatiques au cours du vieillissement de la culture cellulaire, c'est a dire qu'elles sont fortes toutes les deux en phase exponentielle et deviennent faibles en phase stationnaire. L'utilisation de deux inhibiteurs specifiques de l'adenosine triphosphase, le dinitrophenol et le dicyclohexylcarbodiimide a permis de montrer que: la photoconsommation d'oxygene en presence des rayonnements ultraviolets diminue jusqu'a s'annuler sous
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29

Thuillier-Bruston, Francine. "Culture photoorganotrophique sur milieu glycolate et métabolisme photorespiratoire de ce substrat chez Euglena gracilis Z." Grenoble 2 : ANRT, 1987. http://catalogue.bnf.fr/ark:/12148/cb37610429d.

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30

Ripley, Scott James. "Biochemical characterisation and subcellular localisation of the ARP : a novel calcium-binding protein from Euglena gracilis." Thesis, University of Cambridge, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.627242.

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31

Regnault, Annie. "Effets de contraintes trophiques : manque ou exces en phosphate d'ammonium chez euglena gracilis cultivee en photoheterotrophie." Paris 7, 1991. http://www.theses.fr/1991PA077197.

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Des euglenes photoheterotrophes sont adaptees a differentes concentrations en phosphate d'ammonium: 0,125; 0,5; 1,5 g/l. Quatre conditions metaboliques ont ete definies: photoheterotrophie sans limitation nutritive; photoheterotrophie limitee en azote; autotrophie limitee ou non en azote. En photoheterotrophie sans limitation le developpement des plastes et leur structure dependent peu de la concentration en azote du milieu. L'intensite de la photosynthese determine la teneur cellulaire en paramylon. Le passage de ce type metabolique aux autres types est marque par une grande variation dans le
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32

Christopher, David Alan. "Structure and expression of a Euglena gracilis chloroplast transcription unit encoding 11 ribosomal protein genes, a tRNA gene and a 2.8 kb intergenic region." Diss., The University of Arizona, 1989. http://hdl.handle.net/10150/184937.

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The structure and expression of a novel Euglena gracilis chloroplast ribosomal protein operon was studied by gene mapping, molecular cloning, nucleotide sequencing primer extension and Northern analyses. The nucleotide sequence (12,240 bp) was determined for 100% of both strands encoding the 12 genes, rpl23 - rpl2 - rps19 - rpl22 - rps3-(2.8 kb region)- rpl16 - rpl14 - rpl5 - rps8 - rpl36 - trnI - rps14. The gene organization resembles the S10 and spc ribosomal protein operons of E. coli. The rpl5 gene was a new chloroplast gene not previously reported for any chloroplast genome nor described
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33

Tamponnet, Christian. "Rôle du calcium dans la conservation d'une algue unicellulaire immobilisée : Euglena gracillis Z." Compiègne, 1986. http://www.theses.fr/1986COMPD029.

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La potentialité biotechnologique des cellules photosynthétiques est très importante. L'immobilisation de telles cellules semble prometteuse à la fois dans leur utilisation comme "sacs à enzymes" et comme méthode de conservation des souches. Ce travail explore la seconde voie. Euglena gracilis Klebs souche Z a été le matériel photosynthétique sélectionné et l'inclusion dans une matrice d'alginate de calcium a été la technique d'immobilisation la mieux adaptée à ce matériel. Cette étude montre qu'une telle immobilisation stabilise non seulement les structures cellulaires (chloroplastes, mitochon
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34

Mackay, Stephen. "Identification of the genes encoding enzymes involved in the synthesis of the biopolymer paramylon from Euglena gracilis." Thesis, Stellenbosch : University of Stellenbosch, 2010. http://hdl.handle.net/10019.1/5420.

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Thesis (MSc (Plant Biotechnology))--University of Stellenbosch, 2010.<br>Includes bibliography.<br>Title page: Dept. of Genetics, Faculty of Science<br>ENGLISH ABSTRACT: Recent advances in medical pharmacology have identified the immune-potentiating effects of β-1,3-glucans on mammalian immune systems. Extensive research has identified and described the mechanisms of action and receptor binding specificity of different β-1,3-glucans as well as their structural and functional relationships. Molecular mass, solubility, structural order, degree of branching as well as chemical modification all de
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35

Tokuta, Yuya [Verfasser]. "Negative Phototaxis of Euglena Gracilis and Resulting Bioconvection Patterns under Stationary or Rapidly Periodic Illumination / Yuya Tokuta." Berlin : Freie Universität Berlin, 2020. http://d-nb.info/1219904813/34.

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36

Williams, Sande G. "Probing Protein-protein Interactions Among Proteins of a Nonaggregated Fatty Acid Synthetase From Euglena Gracilis Variety Bacillaris." Digital Commons @ East Tennessee State University, 1993. https://dc.etsu.edu/etd/2830.

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Enoyl-acyl carrier protein (ACP) reductase from chloroplast nonaggregated fatty acid synthetase (FAS) of Euglena gracilis variety bacillaris was purified to a single band on a denaturing polyacrylamide gel. The enzyme was partially characterized with respect to substrate specificity, reduced nucleotide requirement, and the effect of ACP and Ca$\sp{++}$ on enzyme activity. Antibodies against the purified protein were raised in hens and isolated from eggs. ACP was purified from Euglena in yields of about 1mg/100g (wet weight) of cells. Antibodies were raised against the purified
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37

Drager, Robert Gray. "Structure and transcript processing of a Euglena gracilis chloroplast operon encoding genes rps2, atpI, atpH, atpF, atpA and rps18." Diss., The University of Arizona, 1993. http://hdl.handle.net/10150/186334.

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A 9.8 kbp region of the Euglena gracilis chloroplast genome has been cloned, sequenced and analyzed. This region contains six genes, rps2, rps18, atpI, atpH, atpF and atpA which encode ribosomal proteins S2 and S18 and ATP synthase subunits CFₒIV, CFₒIII, CFₒI and CF₁α, respectively. The linear order of these genes, 5'-rps2-atpI-atpH-atpF-atpA-rps18-3', is similar to that of land plant chloroplasts. These six genes are co-transcribed with two tRNA genes which are 5' to rps2. A fully spliced, 5.5 kb transcript containing all six genes accumulates. The spliced hexa-cistronic transcript is proces
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38

Nasir, Adeel [Verfasser], Michael [Gutachter] Lebert, and Robert [Gutachter] Slany. "Analysis of signal transduction chains of gravity and light sensing in Euglena gracilis / Adeel Nasir ; Gutachter: Michael Lebert, Robert Slany." Erlangen : Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), 2016. http://d-nb.info/1121303765/34.

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39

Benichou, Pierre. "Etude des proprietes physiologiques et du metabolisme energetique chez euglena gracilis zheterotrophe ayant developpe une respiration resistance a l'antimycine a." Paris 6, 1990. http://www.theses.fr/1990PA066400.

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L'antimycine a provoque un arret de la croissance d'euglena gracilis en culture aerobie heterotrophe, et inhibe fortement, mais non completement, la respiration. L'activite residuelle est sensible au sham. Apres plusieurs heures, cette respiration resistante au cyanure augmente, et la croissance reprend. Les cellules ainsi adaptees ont ete cultivees en presence d'antimycine pendant des mois. L'euglene possede deux voies respiratoires principales dont les contributions relatives ont ete evaluees pour les deux types cellulaires. De plus, une oxydase stimulee par le sham a faible concentration a
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40

Houlné, Guy. "Structure et expression des genes codant pour les apoproteines des antennes collectrices de photons ps2 et ps1 chez euglena gracilis." Université Louis Pasteur (Strasbourg) (1971-2008), 1988. http://www.theses.fr/1988STR13169.

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41

Houlné, Guy. "Structure et expression des gènes codant pour les apoprotéines des antennes collectrices de photons PS2 et PS1 chez Euglena gracilis." Grenoble 2 : ANRT, 1988. http://catalogue.bnf.fr/ark:/12148/cb376143878.

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42

WITTEMER, GROTZINGER CHRISTIANNE. "Etude de genes nucleaires codant pour des proteines chloroplastiques d'euglena gracilis." Strasbourg 1, 1987. http://www.theses.fr/1987STR13229.

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43

Stoltze, Julia [Verfasser], Andreas [Akademischer Betreuer] Burkovski, and Michael [Gutachter] Lebert. "Untersuchung von Gravitaxis-abhängigen Proteinen in Euglena gracilis, unter besonderer Berücksichtigung einer Proteinkinase A / Julia Stoltze ; Gutachter: Michael Lebert ; Betreuer: Andreas Burkovski." Erlangen : Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), 2019. http://d-nb.info/1188466798/34.

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44

Krüger, Julia [Verfasser], Michael [Akademischer Betreuer] Lebert, and Michael [Gutachter] Lebert. "Analysis of Gene Expression Changes Induced by Differential Acceleration and Swimming Behavior in Euglena gracilis / Julia Krüger ; Gutachter: Michael Lebert ; Betreuer: Michael Lebert." Erlangen : Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), 2019. http://d-nb.info/1229194142/34.

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45

Télolahy, Paul. "Contribution à l'étude de la déshydratase de l'acide delta aminolilévulinique (E. C. 4. 2. 1. 24. ) de l'Euglene (Euglena gracilis) : son intérêt en toxicologie." Paris 11, 1989. http://www.theses.fr/1989PA114805.

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46

WEISS, CATHERINE. "Etude de la photoregulation de la biosynthese des proteines d'origine chloroplastique impliquees dans les centres reactionnels des ps 1 et ps 2 chez euglena gracilis." Université Louis Pasteur (Strasbourg) (1971-2008), 1989. http://www.theses.fr/1989STR13025.

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Etude de la regulation de la biosynthese des proteines (d1, d2, apoproteines du cp1) pendant la maturation du chloroplaste chez euglena gracilis. Ces proteines sont presentes a l'etat de trace dans le protoplaste et leur taux augmente de 10 a 30 fois pendant les premieres 24 heures d'exposition des cellules a la lumiere. La maturation du plaste est etudie en milieu nutritionnel, une regulation post-transcriptionnelle par mobilisation des messagers sur les polysomes est mise en evidence. La regulation de l'expression du gene codant pour la proteine d1 se fait essentiellement au niveau transcrip
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47

Keller, Mario. "Etude des genes de trna chloroplastiques et du gene de la proteine thylakoidale de 32 kd du photosysteme ii chez euglena gracilis : localisation et sequence nucleotidique." Université Louis Pasteur (Strasbourg) (1971-2008), 1986. http://www.theses.fr/1986STR13007.

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Le fractionnement des trna chloroplastiques d'euglena gracilis d'une part par electrophorese bidimensionnelle sur gel de polyacrylamide et d'autre part, par chromatographie sur sepharose 4b a permis d'identifier 24 isoaccepteurs specifiques de 18 aminoacides. Plusieurs de ces trna ont ete purifies et utilises pour localiser leur gene sur le dna chloroplastique. Les genes de trna sont dissemines tout au long de la molecule circulaire du genome plastidial; deux d'entre eux, les genes de trna**(ala) et trna**(ile) sont localises dans la region intercistronique separant les genes des rrna 23s et 1
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48

Keller, Mario. "Etude des gènes de tRNA chloroplastiques et du gène de la protéine thylakoïdale de 32 kd du photosystème II chez Euglena gracilis localisation et séquence nucléotidique." Grenoble 2 : ANRT, 1986. http://catalogue.bnf.fr/ark:/12148/cb37598669m.

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49

Nowitzki, Ulrich. "Studien zum Gentransfer aus Organellen nach Endosymbiose anhand der Chloroplast-Cytosol-Isoenzyme von Glucose-6-phosphat-Isomerase aus Spinacia oleracea und der 3-Phosphoglycerat-Kinase aus Euglena gracilis." [S.l.] : [s.n.], 2002. http://deposit.ddb.de/cgi-bin/dokserv?idn=964591677.

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50

Vignoles, Philippe. "Toxicite du benzamido-2 nitro-5 thiazole et de onze derives sur lymnaea peregra ovata muller, gammarus pulex pulex l. Et euglena gracilis klebs. Relations structure-activite quantitatives." Limoges, 1990. http://www.theses.fr/1990LIMO0107.

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L'efficacite in vitro de douze derives du benzamido-2 nitro-5 thiazole substitues sur le cycle benzenique a ete etudiee sur trois especes: lymnaea peregra ovata, gammarus pulex pulex et euglena gracilis. Les resultats obtenus ont ete compares a ceux obtenus avec un produit de reference, le niclosamide. La determination: 1) de la cl50 (concentration de toxique pour laquelle on obtient 50% de mortalite) chez l. P. Ovata et g. P. Pulex, et 2) de la cl50, de la ci50 (concentration de toxique reduisant de 50% la croissance) et de la camax (concentration provoquant une activation maximale de la croi
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