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  • Arabidopsis thaliana  (3)
  • IR spectroscopy  (2)
  • Springer  (5)
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  • Springer  (5)
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  • 1
    Electronic Resource
    Electronic Resource
    Indole-3-butyric acid in Arabidopsis thaliana III. In vivo biosynthesis (1994)
    Springer
    Plant growth regulation 14 (1994), S. 7-14 
    Details
    ISSN: 1573-5087
    Keywords: Arabidopsis thaliana ; IBA biosynthesis ; indole-3-acetic acid ; indole-3-butyric acid ; α-naphthylacetic acid ; phenylacetic acid
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract Indole-3-butyric acid (IBA) was identified by HPLC and GC-MS as one of the reaction products after incubation of sterile cultures of Arabidopsis thaliana seedlings with labeled indole-3-acetic acid (IAA). This is the first demonstration of IBA biosynthesis in a dicotyledonous plant. After 1 h of incubation most of the IBA was found in the free form, while after longer periods of incubation most of it was detected in conjugated forms. Formation of IBA conjugates was inhibited by the addition of unlabeled IBA. The biosynthesis of IBA and its conjugates was followed throughout the development of the seedlings and at different pH values. All parts of the plant (isolated roots, leaves, shoots and flowers) were able to convert IAA to IBA to the same extent. IAA was more readily transported than IBA in mature Arabidopsis plants. Feeding of labeled phenylacetic acid (PAA) and α-naphthylacetic acid (NAA) to Arabidopsis seedlings resulted in a new small peak which was hydrolyzed by 7N NaOH, but the formation of compounds with longer side chains (analogous to IBA) could not be detected.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00024135
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  • 2
    Electronic Resource
    Electronic Resource
    Indole-3-butyric acid in Arabidopsis thaliana (1993)
    Springer
    Plant growth regulation 13 (1993), S. 189-195 
    Details
    ISSN: 1573-5087
    Keywords: Arabidopsis thaliana ; autofluorography ; auxin conjugates ; IBA-glucose synthase ; indole-3-butyric acid
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract Indole-3-butyric acid (IBA) was metabolized by seedlings of Arabidopsis thaliana cultivated in liquid medium under sterile conditions to two major metabolites. One metabolite was hydrolyzed by 1 N NaOH and β-glucosidase and was tentatively identified as IBA-glucose and the other was hydrolyzed by 7 N NaOH and amidase and was identified as an amide-linked conjugate. IBA-glucose synthase activity was found in a soluble enzyme fraction after incubation of 3H-IBA, IBA and UDP-glucose. The labelled reaction product had an Rf value comparable to IBA glucose and stained positive with Ehmann reagent.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00024261
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  • 3
    Electronic Resource
    Electronic Resource
    Indole-3-butyric acid in Arabidopsis thaliana (1993)
    Springer
    Plant growth regulation 13 (1993), S. 179-187 
    Details
    ISSN: 1573-5087
    Keywords: Arabidopsis thaliana ; auxin conjugates ; ethylene ; indole-3-acetic acid ; indole-3-butyric acid
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract Indole-3-butyric acid (IBA) was identified by HPLC and GC-MS as an endogenous compound in plantlets of the crucifer Arabidopsis thaliana (L.) Heynh. A. thaliana was cultivated under sterile conditions as shaking culture in different liquid media with and without supply of hormones. Free and total IBA and indole-3-acetic acid (IAA) were determined at different stages of development during the culture period as well as in culture media of different initial pH values. The results showed that IAA was present in higher concentrations than IBA, but both hormones seemed to show the same behaviour under the different experimental conditions. Differences were found in the mode of conjugation of the two hormones. While IAA was mostly conjugated via amide bonds, the main IBA conjugates were ester bound. The ethylene concentration derived from the seedlings, when they were grown in flasks of different size, seemed not to influence the auxin content in the same cultures.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00024260
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  • 4
    Electronic Resource
    Electronic Resource
    The structure ofO-arylmercury derivatives of dihydroxy-9,10-anthraquinones and their reactions with anions (1996)
    Springer
    Russian chemical bulletin 45 (1996), S. 2784-2791 
    Details
    ISSN: 1573-9171
    Keywords: IR spectroscopy ; electron spectroscopy ; hydroxyanthraquinone derivatives
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The structure of mono- and di-O-arylmercury-derivatives of quinizarin (1,4-dihydroxy-9, 10-anthraquinone) and anthrarufin (1,5-dihydroxy-9, 10-anthraquinone) and their reactions with Br−, Cl−, OH−, andtBuO− anions in the solid state and in aprotic solvents were examined by vibrational and electron spectroscopy. These reactions result in cleavage of the O-Hg bond. The formation of ions or contact ion pairs depends on the size and nature of the counterion; quinizarin dianions give very strong ion pairs with K+ cations, which do not cleave in DMSO. The electronic structure of mono- and dianions of the compounds studied is discussed.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF01430643
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  • 5
    Electronic Resource
    Electronic Resource
    Visualization of solid-state reactions of anisylmercury and triphenylphosphinegold derivatives of phthaleins with bromides (1993)
    Springer
    Russian chemical bulletin 42 (1993), S. 2028-2030 
    Details
    ISSN: 1573-9171
    Keywords: phthaleins ; electronic reflectance spectroscopy ; IR spectroscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The visualization of solid-state reactions of bis-O-metallated phenolphthaleins and xylenolphthaleins (M=HgC6H4OMe, AuPPh3) with bromides, which has been discovered for the first time, was studied by IR and electronic reflectance spectroscopy. The appearance of intense coloration (purple, violet, or blue) after short-term grinding of colorless or faintly colored solid samples with salts is due to their ionization with the formation of ion pairs or dianions depending on the nature of the counterion. The reaction affects only a small fraction of the molecules in the surface layers of the metallocomplexes.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00698891
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