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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 78 (1956), S. 1375-1380 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 77 (1955), S. 1392-1392 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 77 (1955), S. 2662-2663 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 194 (1962), S. 787-788 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] I have been particularly interested in MAP since others have reported that it occurs in some soluble ribonucleic acids5 and since there is considerable evidence that kinetin-type compounds (which may be regarded as derivatives of MAP) may influence growth through effects on ribonucleic acids and ...
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Physiologia plantarum 18 (1965), S. 0 
    ISSN: 1399-3054
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Annals of the New York Academy of Sciences 144 (1967), S. 0 
    ISSN: 1749-6632
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Natural Sciences in General
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1432-2048
    Keywords: Cytokinin and alternative respiration ; Respiration, alternative
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract A disengagement of the cyanide-resistant, alternative respiratory pathway in soybean (Glycine max (L.) Merr.) callus tissue was observed prior to the start of deoxyisoflavone production stimulated by addition of the cytokinin benzyladenine. To test whether this loss of alternativepathway activity was part of the response to cytokinin, inhibitors of the alternative pathway were assayed for their ability to elicit cytokinin-like responses. Salicylhydroxamic acid (SHAM) was found to produce a deoxyisoflavone difference spectrum similar to that observed following treatment of the callus tissue with benzyladenine, while propyl gallate (PG) was without effect. Both SHAM and PG were further tested for cytokinin-like activity in other bioassays. In two anti-senescence bioassays using leaf tissue (of Avena sativa L. and Xanthium pensylvanicum Wallr.) and in the Cucumis sativus L. bioassay which measures stimulation of weight gain by excised cotyledons, both SHAM and PG were effective “cytokinins” at 1 mM and 0.1 mM, respectively. In two other bioassays (betacyanin formation in Amaranthus caudatus L. seedlings and the soybean-callus celldivision assay), SHAM appeared to be toxic. These results substantiate the suggestion that effects on the alternative pathway may play a role in some cytokinin responses and further raise the question of what should be considered a true cytokinin response.
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Planta 87 (1969), S. 26-35 
    ISSN: 1432-2048
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary 1. Callus tissues of Glycine max, cv. Acme, on solid or in liquid media quickly responded to cytokinins by synthesizing two compounds which appear to be glycosides of the deoxyisoflavone, daidzein. Auxin also was necessary for the effect. 2. After a lag, the response could be detected in 24 h or less by reading ultraviolet optical densities of simple acidic or ethanolic extracts of the tissues or of the liquid media and suspended tissues. 3. The effects of different levels or kinds of auxins and cytokinins were parallel to the known growth responses. 4. When 2,4-dichlorophenoxyacetic acid was used, addition of a cytokinin was not required for deoxyisoflavone synthesis. 5. Malonic acid promoted deoxyisoflavone synthesis but only in the presence of an auxin. Addition of a cytokinin was not necessary for this promotion. Citric acid also was effective but acetic, pyruvic, α-ketoglutaric, succinic, malic and fumaric acids were not. 6. The influence by cytokinins and auxins on deoxyisoflavone synthesis offers a system usable for assay of the growth substances and for study of their modes of action.
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  • 9
    ISSN: 1432-2048
    Keywords: Benzylaminopurines, substituted ; Cinnamate ; Coumarate ; Cytokinins ; Glycine ; Tissue culture
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Cells of a soybean tissue strain suspended in an aerated liquid medium caused the disappearance of p-coumaric acid from the medium. The rate of disappearance was modified by cytokinins. When the coumarate and the cytokinin were added to the medium simultaneously, disappearance was increased if the cytokinin was used in the concentration range from 0.05 to 50 μM; higher concentrations inhibited the disappearance. If, however, the cytokinin was added at the beginning of the shaking period (for aeration) and the coumarate added 1 h later, the results were more complex. With this procedure, cytokinins at concentrations from 0.0005 to about 1 μM inhibited, at 50 μM they promoted, and at higher concentrations they inhibited the coumarate disappearance. The promotion was elicited by zeatin, ribosylzeatin, kinetin, 6-benzylaminopurine (BAP), by BAP substituted at the 9-position by methyl, methoxymethyl, cyclohexyl or tetrahydropyran-2-yl groups, by adenine with the amino group substituted by methyl, dimethyl, n-propyl, n-pentyl or n-hexyl groups, by 1,3-diphenylurea and nicotinamide, all at about 50 μM. Adenine and benzimidazole were not effective. The promotion was detected in as little as 12 min. The delayed inhibitory effect required the presence of the cytokinin during the 1 h of shaking before the coumarate was added. This effect was elicited by zeatin, ribosylzeatin, kinetin, BAP, the aforementioned 9-substituted-BAP compounds, 9-glucosyl-BAP, 7-glucosyl-BAP, and 6-isopentenylaminopurine and its ribonucleoside. It was not caused by adenine, cis-ribosylzeatin, diphenylurea, benzimidazole, 6-methylaminopurine, 6,6-dimethylaminopurine or nicotinamide. The chemical specificity for this effect was much the same as that known for promotion of cell division in the soybean tissue.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Planta 146 (1979), S. 503-511 
    ISSN: 1432-2048
    Keywords: Coumarate ; Cytokinin ; Glycine ; Respiration ; Mitochondria
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Cells of a soybean tissue strain, suspended in an aerated liquid medium, caused disappearance of p-coumaric acid from the medium and oxidation of guaiacol, benzidine, pyrogallol, L-dihydroxyphenylalanine and L-epinephrine. Both the disappearance and the oxidations were inhibited by 6-benzylaminopurine (BAP) at a concentration of 0.5 mM. BAP at other concentrations either promoted or inhibited oxidation of epinephrine in precisely the pattern reported earlier for the disappearance of coumarate; therefore, the disappearance of coumarate probably involves its oxidation. The effectiveness of other cytokinins in inhibiting the oxidation was studied. At 0.5 mM, and perhaps even at 0.5 μM, some of the several cytokinins tested inhibited oxygen consumption by the soybean cells. This inhibition, which did not require any of the above metabolizable compounds, was especially marked in the presence of cyanide, azide or Antimycin A, and was detectable in 10 min or less. Either Antimycin A or salicylhydroxamic acid alone promoted O2 consumption but together they were quite inhibitory. The soybean cells apparently have an alternate respiratory pathway and cytokinins may influence its operation. Several cytokinins at 0.5 mM, and perhaps at 0.5 μM, also inhibited oxygen consumption by mitochondrial preparations from the soybean cells, the inhibition being evident in about 20 s. The consumption required a substrate such as malate, succinate or NADH. Cytokinins and related compounds varied in effectiveness as follows: BAP and 6-isopentenyla-minopurine ≥ 9-tetrahydropyranyl-BAP 〉 kinetin, ribosyl-isopentenylaminopurine, 9-methyl-BAP and 9-methoxymethyl-BAP 〉 6,6-dimethylaminopurine and zeatin (slight activity) 〉 6-methylaminopurine, nicotinamide and adenine (ineffective). To a great extent this order parallels the order of effectiveness of the compounds in causing cell division. Mitochondria, therefore, may contain a site for an important cytokinin action.
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