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  • Organic Chemistry  (2)
  • 1-aminocyclopropane-1-carboxylic acid (ACC) oxidase  (1)
  • ACC synthase  (1)
Materialart
Erscheinungszeitraum
Schlagwörter
  • 1
    Digitale Medien
    Digitale Medien
    Springer
    Plant molecular biology 34 (1997), S. 89-97 
    ISSN: 1573-5028
    Schlagwort(e): 1-aminocyclopropane-1-carboxylic acid (ACC) oxidase ; ACC synthase ; Dianthus caryophyllus ; ethylene ; flower senescence ; organ-specific gene expression
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie
    Notizen: Abstract Ethylene production and expression patterns of an 1-aminocyclopropane-1-carboxylic acid (ACC) oxidase (CARAO1) and of two ACC synthase (EC 4.4.1.14) genes (CARACC3 and CARAS1) were studied in floral organs of cut carnation flowers (Dianthus caryophyllus L.) cv. White Sim. During the vase life and after treatment of fresh flowers with ethylene, production of ethylene and expression of ethylene biosynthetic genes first started in the ovary followed by the styles and the petals. ACC oxidase was expressed in all the floral organs whereas, during the vase life, tissue-specific expression of the two ACC synthase genes was observed. After treatment with a high ethylene concentration, tissue specificity of the two ACC synthase genes was lost and only a temporal difference in expression remained. In styles, poor correlation between ethylene production and ACC synthase (CARAS1) gene expression was observed suggesting that either activity is regulated at the translational level or that the CARAS1 gene product requires an additional factor for activity. Isolated petals showed no increase in ethylene production and expression of ethylene biosynthetic genes when excised from the flower before the increase in petal ethylene production (before day 7); showed rapid cessation of ethylene production and gene expression when excised during the early phase of petal ethylene production (day 7) and showed a pattern of ethylene production and gene expression similar to the pattern observed in the attached petals when isolated at day 8. The interorgan regulation of gene expression and ethylene as a signal molecule in flower senescence are discussed.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    ISSN: 0947-3440
    Schlagwort(e): Thermotropic and lyotropic phase behavior ; Amphotropes ; Surfactants ; Liquid crystals ; Chromophores ; Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: New ammonium amphiphiles having a N,N-dimethyl-N-hydroxyethylammonium headgroup and various azobenzene mesogenic units connected by a decyl or dodecyl spacer have been synthesized. The azobenzene unit is functionalized at the 4-position with a cyano, methoxy or fluoro substituent. For the cyano-substituted amphotropes and the fluoro compound with a dodecyl spacer a smectic phase is formed as was observed by differential scanning calorimetry and polarization microscopy. Complexation with sodium dodecyl sulfate, SDS, in a 1:1 molar ratio induces the formation of a smectic phase for the compounds with a decyl spacer. The compounds with a dodecyl spacer showed rather complex behavior attributed to different crystal morphologies. The ammonium amphotropes form aggregates in water when heated above their Krafft temperature. However, these aggregates are not stable and crystallize upon cooling. The ion pair amphiphiles with SDS as second component form vesicles in water as observed by optical and electron microscopy. The observed blue shift in the UV absorption maximum of the amphotropes upon addition of SDS indicates π-π stacking between mesogenic units resulting from aggregation.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 3
    ISSN: 0947-3440
    Schlagwort(e): Mesogenic unit ; Monomer exchange ; “Gel-to-liquid crystalline” phase transition ; Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Novel double-chained ammonium amphiphiles carrying one azobenzene moiety (I) have been synthesized. The bilayer-stabilizing effect of different azobenzenes (ABs) has been investigated by measuring the “gel-to-liquid crystalline” phase transition temperatures of the formed bilayers in water using differential scanning calorimetry. It is found that the stabilizing effect of the azobenzenes strongly depends on the substituents at the aromatic ring. The stabilizing effect increases in the sequence F 〈 H 〈 NO2 〈 CN 〈 OCH3 〈 N=N-Ph, which cannot be correlated with the electron-withdrawing or -donating properties of the substituents. It is concluded that dipole-dipole interactions between the ABs are of minor importance for the overall stabilization of the bilayer. Instead, other factors determine the strength of the van der Waals interactions between the ABs. In the bilayers the ABs form H-aggregates as is observed by the blue shift of the UV absorption maximum. This blue shift is not affected by the “gel-to-liquid crystalline” phase transition. Bilayers of I-N=N-Ph do not exchange monomers with vesicles of didodecyldimethylammonium bromide, whereas all other investigated bilayers do. Compound I-N=N-Ph forms monolayers at the water-air interface, which are much more stable than the monolayers of the other investigated compounds.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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