ALBERT

All Library Books, journals and Electronic Records Telegrafenberg

X
feed icon rss

Ihre E-Mail wurde erfolgreich gesendet. Bitte prüfen Sie Ihren Maileingang.

Leider ist ein Fehler beim E-Mail-Versand aufgetreten. Bitte versuchen Sie es erneut.

Vorgang fortführen?

Exportieren
Filter
  • Chemistry  (4)
  • Expression analysis  (1)
  • Genetics  (1)
  • 1995-1999  (2)
  • 1985-1989  (3)
  • 1950-1954  (1)
  • 1
    Digitale Medien
    Digitale Medien
    Isolation and expression analysis of two yeast regulatory genes involved in the derepression of glucose-repressible enzymes (1987)
    Springer
    Molecular genetics and genomics 209 (1987), S. 366-373 
    Details
    ISSN: 1617-4623
    Schlagwort(e): Glucose repression ; Glucose derepression ; Regulatory genes ; Expression analysis ; Saccharomyces cerevisiae
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie
    Notizen: Summary Yeast strains carrying one of the two regulatory mutations cat1 and cat3 are defectve in derepression of several glucose-repressible enzymes that are necessary for utilizing non-fermentable carbon sources. Hence, these strains fail to grow on ethanol, glycerol or acetate. The synthesis of isocitrate lyase, malate synthase, malate dehydrogenase and fructose-1,6-bisphosphatase is strongly affected in cat1 and cat3 strains. Genes CAT1 and CAT3 have been isolated by complementation of the cognate, mutations after transformation with an episomal plasmid gene library. The restriction map of CAT1 proved its allelism to the earlier isolated SNF1 gene. Both genes appear to exist as single-copy genes per haploid genome as indicated by Southern hybridization. Northern analysis has shown that the 1.35 kb CAT3 mRNA is constitutively expressed, independent of the carbon source in the medium. Derepression studies with CAT3 transformants using a multi-copy plasmid showed over-expression of glyoxylate cycle enzymes. This result would be consistent with a direct effector function for the CAT3 gene product.
    Materialart: Digitale Medien
    URL: http://dx.doi.org/10.1007/BF00329667
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
    Artikel (Nationallizenzen)
    Volltext
  • 2
    Digitale Medien
    Digitale Medien
    Fabrication of glassy carbon microstructures by pyrolysis of microfabricated polymeric precursorsThis work has been supported in part by the Office of Naval Research and the Defense Advanced Research Projects Agency. It used MRSEC Shared Facilities supported by the National Science Foundation (DMR-9400396). The authors thank Xiao-Mei Zhao for demonstrating microtransfer molding. (1997)
    Weinheim : Wiley-Blackwell
    Advanced Materials 9 (1997), S. 477-480 
    Details
    ISSN: 0935-9648
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
    URL: http://dx.doi.org/10.1002/adma.19970090604
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
    Artikel (Nationallizenzen)
    Volltext
  • 3
    Digitale Medien
    Digitale Medien
    Grundlagen der Werkstoffchemie. Ein Überblick über die Struktur und Konstitution der Werkstoffe von Prof. Dr. E. Brandenberger. Rascher-Verlag, Zürich, 1947. Form. 8º 298 S. mit 98 Abb (1950)
    Weinheim [u.a.] : Wiley-Blackwell
    Materials and Corrosion/Werkstoffe und Korrosion 1 (1950), S. 430-430 
    Details
    ISSN: 0947-5117
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Maschinenbau
    Materialart: Digitale Medien
    URL: http://dx.doi.org/10.1002/maco.19500011017
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
    Artikel (Nationallizenzen)
    Volltext
  • 4
    Digitale Medien
    Digitale Medien
    Bausteine von Oligosacchariden, LXXVIII. Synthese von KDO-haltigen Lipoid-A-Analoga (1987)
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1987 (1987), S. 249-258 
    Details
    ISSN: 0170-2041
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: Building Units of Oligosaccharides, LXXVIII. - Synthesis of KDO-Containing Lipid A AnaloguesThe non-neighbouring group supported glycosidation of 12 with the suitably protected glycosyl bromide 9 of 2-azido-2-deoxy-D-glucose leads - in the presence of a heterogeneous silver catalyst - to the formation of the β-(1→6)-glycosidically linked disaccharide 14. It consists of two 2-azido-2-deoxy-D-glucose units. Partial deblocking of 14 furnishes 15. On glycosidation with KDO bromide this compound yields the trisaccharide 16, which contains a KDO unit in an α-(2→6) ketosidic bond. Reduction of the two azido groups followed by amidation with (R)-3-hydroxymyristic acid and further deblocking generates the trisaccharide α-KDO-(2→6)-β-D-GlcA-(1→6)-D-GlcA 20 with two 3-hydroxy fatty acid residues in an amidic linkage.
    Notizen: Die Umsetzung des Pyranosylbromids 9 der 2-Azido-2-desoxy-D-glucose mit dem Akzeptor 12 führt bei Gegenwart eines heterogenen Silberkatalysators ohne Nachbargruppenbeteiligung unter Inversion zum β-(1→6)-glycosidisch verknüpften Disaccharid 14 aus zwei 2-Azido-2-desoxy-D-glucose-Einheiten. Nach partieller Entblockierung zu 15 ist die Anknüpfung eines KDO-Restes unter Bildung einer α-(2→6)-ketosidischen Bindung zum Trisaccharid 16 möglich. Nach Reduktion der Azidogruppen und Anknüpfung von (R)-3-Hydroxymyristinsäure-Resten gelangt man nach Entblockierung zum Trisaccharid α-KDO-(2→6)-β-D-GlcA-(1→6)-D-GlcA 20, das amidartig zwei 3-Hydroxyfettsäure-Reste gebunden enthält.
    Materialart: Digitale Medien
    URL: http://dx.doi.org/10.1002/jlac.198719870316
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
    Artikel (Nationallizenzen)
    Volltext
  • 5
    Digitale Medien
    Digitale Medien
    A search in the genome of Saccharomyces cerevisiae for genes regulated via stress response elements (1998)
    New York, NY [u.a.] : Wiley-Blackwell
    Yeast 14 (1998), S. 1041-1050 
    Details
    ISSN: 0749-503X
    Schlagwort(e): Saccharomyces cerevisiae ; STRE ; stress response ; genomics ; bioinformatics ; Life and Medical Sciences ; Genetics
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Biologie
    Notizen: Stress response elements (STREs, core consensus AG4 or C4T) have been demonstrated previously to occur in the upstream region of a number of genes responsive to induction by a variety of stress signals. This stress response is mediated by the homologous transcription factors Msn2p and Msn4p, which bind specifically to STREs. Double mutants (msn2 msn4) deficient in these transcription factors have been shown to be hypersensitive to severe stress conditions. To obtain a more representative overview of the set of yeast genes controlled via this regulon, a computer search of the Saccharomyces cerevisiae genome was carried out for genes, which, similar to most known STRE-controlled genes, exhibit at least two STREs in their upstream region. In addition to the great majority of genes previously known to be controlled via STREs, 69 open reading-frames were detected. Expression patterns of a set of these were examined by grid filter hybridization, and 14 genes were examined by Northern analysis. Comparison of the expression patterns of these genes demonstrates that they are all STRE-controlled although their detailed expression patterns differ considerably. © 1998 John Wiley & Sons, Ltd.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
    Artikel (Nationallizenzen)
  • 6
    Digitale Medien
    Digitale Medien
    Verzweigte und kettenverlängerte Zucker, XXX. Diastereoselektive Synthese von L-glycero-D-manno-Heptose, einem Baustein der inneren Core-Region von Lipopolysacchariden (1986)
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1986 (1986), S. 675-686 
    Details
    ISSN: 0170-2041
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: Branched and Chain-extended Sugars, XXX.  -  Diastereoselective Synthesis of L-glycero-D-manno-Heptose, a Constituent of the Inner Core Region of LipopolysaccharidesReaction of 2,3;5,6-di-O-isopropylidene-D-mannofuranose (1) with 2-lithio-1,3-dithiane affords diastereoselectively the 3,4;6,7-di-O-isopropylidene-D-glycero-D-galacto-heptose trimethylene dithioacetal (3). Conversion of compound 3 by a sequence of steps gives the tri-O-isopropylidene-D-glycero-D-galacto-heptit 16 which is oxidized with 1,1′-(azodicarbonyl)-dipiperidine to give the tri-O-isopropylidene-L-glycero-D-manno-heptose 17. Finally, compound 17 is transferred via the acetate 19 into the L-glycero-D-manno-heptopyranose 18.
    Notizen: 2,3;5,6-Di-O-isopropyliden-D-mannofuranose (1) reagiert diastereoselektiv mit 2-Lithio-1,3-dithian zum 3,4;6,7-Di-O-isopropyliden-D-glycero-D-galacto-heptose-trimethylendithioacetal (3). Nach Umwandlung von 3 über eine Reihe von Zwischenstufen zum Tri-O-isopropyliden-D-glycero-D-galacto-heptit 16 läßt sich dieser mit 1,1′-(Azodicarbonyl)dipiperidin zur Tri-O-isopropyliden-L-glycero-D-manno-heptose 17 oxidieren. Hieraus ist über das Acetat 19 die freie L-glycero-D-manno-heptopyranose 18 zu gewinnen.
    Materialart: Digitale Medien
    URL: http://dx.doi.org/10.1002/jlac.198619860409
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
    Artikel (Nationallizenzen)
    Volltext
Schließen ⊗
Diese Webseite nutzt Cookies und das Analyse-Tool Matomo. Weitere Informationen finden Sie hier...