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  • Chemistry  (18)
  • 1-Aminocyclopropane-1-carboxylic acid  (5)
  • 1
    ISSN: 1432-2048
    Keywords: 1-Aminocyclopropane-1-carboxylic acid ; Ethylene ; Lycopersicon ; Mutant, rin (tomato) ; Rhizobitoxine analog
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract A simple and sensitive chemical assay was developed for 1-aminocyclopropane-1-carboxylic acid (ACC), a precursor of ethylene. The assay is based on the liberation of ethylene from ACC at pH 11.5 in the presence of pyridoxal phosphate, MnCl2 and H2O2. This assay was used to detect ACC in extracts of tomato fruits (Lycopersicon esculentum Mill.) and to measure the activity of a soluble enzyme from tomato fruit that converted S-adenosylmethionine (SAM) to ACC. The enzyme had a Km of 13 μM for SAM, and conversion of SAM to ACC was competitively and reversibly inhibited by aminoethoxyvinylglycine (AVG), an analog of rhizobitoxine. The Ki value for AVG was 0.2 μM. The level of the ACC-forming enzyme activity was positively correlated with the content of ACC and the rate of ethylene formation in wild-type tomatoes of different developmental stages. Mature fruits of the rin (non-ripening) mutant of tomato, which only produce low levels of ethylene, contained much lower levels of ACC and of the ACC-forming enzyme activity than wild-type tomato fruits of comparable age.
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  • 2
    ISSN: 1432-2048
    Keywords: 1-Aminocyclopropane-1-carboxylic acid ; Elicitor (fungal) ; Ethylene synthesis ; Iron and ethylene synthesis ; Lycopersicon (ethylene synthesis)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The activity of the ethylene-forming enzyme (EFE) in suspension-cultured tomato (Lycopersicon esculentum Mill.) cells was almost completely abolished within 10 min by 0.4 mM of the metal-chelating agent 1,10-phenanthroline. Subsequent addition of 0.4 mM FeSO4 immediately reversed this inhibition. A partial reversion was also obtained with 0.6 mM CuSO4 and ZnSO4, probably as a consequence of the release of iron ions from the 1,10-phenanthroline complex. The inhibition was not reversed by Mn2+ or Mg2+. Tomato cells starved of iron exhibited a very low EFE activity. Addition of Fe2+ to these cells caused a rapid recovery of EFE while Cu2+, Zn2+ and other bivalent cations were ineffective. The recovery of EFE activity in iron-starved cells was insensitive to cycloheximide and therefore does not appear to require synthesis of new protein. The EFE activity in tomato cells was induced by an elicitor derived from yeast extract. Throughout the course of induction, EFE activity was blocked within 10–20 min by 1,10-phenanthroline, and the induced level was equally rapidly restored after addition of iron. We conclude that iron is an essential cofactor for the conversion of 1-aminocyclopropane-1-carboxylic acid to ethylene in vivo.
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  • 3
    ISSN: 1432-2048
    Keywords: 1-Aminocyclopropane-1-carboxylic acid ; Elicitor (fungal) ; Ethylene synthesis ; Iron and ethylene synthesis ; Lycopersicon (ethylene synthesis)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The activity of the ethylene-forming enzyme (EFE) in suspension-cultured tomato (Lycopersicon esculentum Mill.) cells was almost completely abolished within 10 min by 0.4 mM of the metal-chelating agent 1,10-phenanthroline. Subsequent addition of 0.4 mM FeSO4 immediately reversed this inhibition. A partial reversion was also obtained with 0.6 mM CuSO4 and ZnSO4, probably as a consequence of the release of iron ions from the 1,10-phenanthroline complex. The inhibition was not reversed by Mn2+ or Mg2+. Tomato cells starved of iron exhibited a very low EFE activity. Addition of Fe2+ to these cells caused a rapid recovery of EFE while Cu2+, Zn2+ and other bivalent cations were ineffective. The recovery of EFE activity in iron-starved cells was insensitive to cycloheximide and therefore does not appear to require synthesis of new protein. The EFE activity in tomato cells was induced by an elicitor derived from yeast extract. Throughout the course of induction, EFE activity was blocked within 10–20 min by 1,10-phenanthroline, and the induced level was equally rapidly restored after addition of iron. We conclude that iron is an essential cofactor for the conversion of 1-aminocyclopropane-1-carboxylic acid to ethylene in vivo.
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  • 4
    ISSN: 1432-2048
    Keywords: 1-Aminocyclopropane-1-carboxylic acid ; Chitinase ; β-1,3-Glucanase ; Ethylene ; Helianthus cell-suspension cultures
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Auxin-dependent, heterotrophic suspension cells of sunflower (Helianthus annuus L. C.K. Spanners All-zweck) showed, on a cell-protein basis, a seven-fold increase in chitinase activity, which began 5 d after treatment with 10−5 mol·L−1 of the triazole-type growth retardant BAS 111.W. In proportion to this increase, chitinase activity appeared to be excreted into the culture medium. The intracellular activity of β-1,3-glucanase, assayed fluorimetrically with laminarin as the substrate, was only slightly enhanced. Dose-response experiments with BAS 111.W showed that the onset of the induction of chitinase activity coincided with an inhibition of ethylene formation and an accumulation of endogenous 1-aminocyclopropane-1-carboxylic acid (ACC) as a result of blocking the conversion of ACC to ethylene. Other nitrogen-heterocyclic growth retardants (e.g. tetcyclacis, ancymidol), the triazole-type fungicide BAS 480.F, salicylic acid, CoCl2 and 2,4-dichlorophenoxy-acetic acid, which also increased the ACC/ethylene ratio, similarly induced chitinase activity. In contrast, aminoethoxy vinylglycine, which simultaneously lowered endogenous ACC and ethylene formation, did not stimulate chitinase activity. However, after addition of BAS 111.W and ACC, an accumulation of endogenous ACC was accompanied by a strong induction of the enzymatic activity. This effect did not correlate with changes in the cell culture growth nor in the cellular contents of immunoreactive abscisic acid, 3-indoleacetic acid, gibberellins or cytokinins. Furthermore, ethephon, which chemically generates ethylene, led to a slight reduction in ACC levels and tended to decrease chitinase activity relative to the control. In conclusion, it is hypothesized that the induction of chitinase activity in sunflower cell suspensions is antagonistically regulated by ethylene and ACC. At least at higher production rates, ethylene appears to function as an inhibiting factor whereas ACC may be a promoting one. The stimulation of chitinase and β-1,3-glucanase activity, caused by the retardant BAS 111.W and the fungicide BAS 480.F, is discussed as an additional effect of both compounds which possibly leads to an increased resistance of plants to fungal infections.
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  • 5
    ISSN: 1432-2048
    Keywords: 1-Aminocyclopropane-1-carboxylic acid ; 1-Aminocyclopropane-1-carboxylic acid synthase ; Elicitor (fungal) ; Ethylene biosynthesis ; Petroselinum ; Phenylalanine ammonia-lyase
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The biosynthesis of ethylene was examined in suspension-cultured cells of parsley (Petroselinum hortense) treated with an elicitor from cell walls of Phytophthora megasperma. Untreated cells contained 50 nmol g-1 of the ethylene precursor, 1-aminocyclopropane-1-carboxylic acid (ACC), and produced ethylene at a rate of about 0.5 nmol g-1 h-1. Within 2 h after addition of elicitor to the culture medium, the cells started to produce more ethylene and accumulated more ACC. Exogenously added ACC did not increase the rate of ethylene production in control or elicitor-treated cells, indicating that the enzyme converting ACC to ethylene was limiting in both cases. The first enzyme in ethylene biosynthesis, ACC synthase, was very rapidly and transiently induced by the elicitor treatment. Its activity increased more than tenfold within 60 min. Density labelling with 2H2O showed that this increase was caused by the denovo synthesis of the enzyme protein. Cordycepin and actinomycin D did not affect the induction of ACC synthase, indicating that the synthesis of new mRNA was not required. The peak of ACC-synthase activity preceded the maximal phenylalanine ammonia-lyase (PAL) activity by several hours. Exogenously supplied ethylene or ACC did not induce PAL. However, aminoethoxyvinylglycine, an inhibitor of ACC synthase, suppressed the rise in ethylene production in elicitor-treated cells and partially inhibited the induction of PAL. Exogenously supplied ACC reversed this inhibition. It is concluded that induction of the ethylene biosynthetic pathway is a very early symptom of elicitor action. Although ethylene alone is not a sufficient signal for PAL induction, the enhanced activity of ACC synthase and the ethylene biosynthetic pathway may be important for the subsequent induction of PAL.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 78 (1995), S. 403-410 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The preparation of the diastereoisomers of 1-amino-2-bromocyclopropanecarboxylic acid is described using the methyl (1RS, 5SR)-2-oxo-3-oxabicyclo[3.1.0]hexane-1-carboxylate 5 as starting material. The key step is the oxidation of 9 with subsequent radical introduction of bromine according to the Barton procedure. The 2-bromo-cyclopropanecarboxylates cis-11 and trans-11 were obtained as diastereoisomer mixture in a ratio of 3:1. They were converted into cis- and trans-esters 12 and the acids 13.
    Additional Material: 1 Ill.
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  • 7
    ISSN: 0009-286X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 2 Ill.
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  • 8
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Stereospecific syntheses of cycloserine (D-4-amino-3-isoxazolidinone) are described. The same synthetic methods lead to some 5-substituted 4-amino-3-isoxazolidinones. The stereochemical relationship of these compounds to the parent amino acids is discussed.
    Additional Material: 4 Tab.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 43 (1960), S. 887-888 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 48 (1965), S. 94-111 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 1. Es wird gezeigt, dass substituierte Allylbromide Phenol mehr an Kohlenstoff alkylieren als Allylbromid selbst.
    Additional Material: 4 Tab.
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