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  • 1
    ISSN: 1399-3054
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: The changes in several metabolic parameters induced in thermosensitive seeds of Phacelia tanacetifolia Benth. (cv. Bleu Clair) by an inhibitory temperature of 30°C were evaluated and compared to those occurring at the optimum temperature for germination (16°C). The severe inhibition of germination (70%) at 30°C was accompanied by an inhibition of the increase in total RNA and glucose-6-phosphate followed by an inhibition of the increase in DNA, reducing sugars and ATP. Both transcriptional and translational activities occurred at the two temperatures, but with substantial differences. They were higher at 30 than at 16°C after 9 h of imbibition. With time, translational activity became much lower at 30°C, as indicated by the inhibition of the increases in the polysome/monosome ratio and of the levels of activities, evaluated in vitro, of glucose-6-phosphate dehydrogenase, pyruvate kinase, glucokinase and malate dehydrogenase. Transport also occurred at 30°C, as indicated by the positive net flux of K+ into the cells and by the electrochemical equilibrium of mobile K+ between the outside and inside of the cells. There was much less mobile K+ inside the cells at 30 than at 16°C (50 and 13%, respectively, after 24 and 72 h of imbibition). The values of cytoplasmic pH were the same at 16 and 30°C. At 30°C, the vacuolar pH did not change, whereas at 16°C it became more acidic at 72 h. The possible roles of cytoplasmic K+ concentration and pH in the control of the reactivation of metabolism during germination of Phacelia tanacetifolia seeds are discussed.
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Physiologia plantarum 93 (1995), S. 0 
    ISSN: 1399-3054
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: 31 P nuclear magnetic resonance spectroscope (NMR) was used to study the response of Phacelia tanacetifolia seeds to dark and light conditions during the first 72 h of incubation. Changes in the chemical shifts (δ) of the pH-dependent 31P-NMR signals from the vacuolar and the cytoplasmic orthophosphate pools were correlated with the different incubation conditions. In the dark (favorable to germination), the cytoplasmic pH remained nearly constant over the whole period considered, while the vacuolar pH shitted to more acidic values after the 24th h of incubation. In the light (inhibiting germination), the values of cytoplasmic pH tended to become more acidic than in the dark after the 24th h of incubation, while the vacuolar pH remained practically constant. When seed germination was inhibited in the dark by butyric acid (BA). a permeant weak acid, the values of cytoplasmic and vacuolar pH were similar to those of the ungerminated seeds incubated in the light. When, vice versa, seed germination was promoted in the light by fusicoccin (FC), the values of cytoplasmic and vacuolar pH were similar to those of the dark-germinated seeds. A progressive augmentation of P, metabolism occurred both in the dark and in the light up to the 24th h of incubation. Subsequently, light blocked any further evolution of this parameter. Treatment with butyric acid in the dark again mimicked the effect of light, while FC reversed the negative effect of light. The data show that in Phacelia tanacetifolia seeds germination is linked to a more alkaline cytoplasmic pH. The finding that the light-dependent metabolic inhibition occurs after an early activation of metabolism, i.e. after the first 24 h. suggests that the effects of light on the cytoplasmic and vacuolar pH depend on the early metabolic processes involved in the control of the homeostasis of cell pH and/or on the inhibition of the reactivation of the transport mechanisms.
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  • 3
    ISSN: 1399-3054
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: To elucidate the inhibitory effect of light on the germination of the negatively photo-blastic seeds of Phacelia tanacetifolia Benth. (cv. Bleu Clair). we have compared the changes that occur during the first 24 h of imbibition in the dark and in the light. Here, we give data on transcription products, translation activity, activities of some enzymes involved in the metabolic reactivation of seeds (glucose-6-phosphate dehydrogenase, pyruvate kinase, glucokinase and malate dehydrogenase), and the capability to absorb L-[U-14C]-leucine. During the first stages of imbibition, the changes in the protein pattern and in the mRNA populations that occurred were not related to the light/dark regimes. Differences due to the light treatment did not appear until after 24 h. when new microsomal proteins appeared in the dark and some mRNA populations encoding low molecular mass polypeptides were increased in the light. The translation activity, measured as L-[U-14C]-leucine incorporated into proteins and as the ratio polysomes/monosomes, increased with time in both darkness and light, but to a much higher extent in the dark. The activities of the four enzymes tested were higher in the light than in the dark before 16 h, then decreased in the light and increased sharply in the dark. Together with the behaviour of the increase in the ratio polysomes/monosomes in the dark, this suggests an increased rate of protein degradation in the dark during the period 0–16 h. The absorption of L-[U-14C]-leucine was severely inhibited by light during the whole period studied, as expected since light inhibits the reactivation of the transport mechanisms at the plasma membrane. In seeds imbibed in the dark and then transferred to light, the inhibition by light of absorption and of incorporation into proteins of L-[U-14C]-leucine, as well as the inhibition of the increase in the ratio poly-somes/monosornes, was effective before the 22nd h; after which time the control exerted by light disappeared.
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  • 4
    ISSN: 1432-2048
    Keywords: Key words: H+-ATPase ; Plasma membrane ; Protein phosphorylation ; Zea
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract. Phosphorylation/dephosphorylation of the plasma-membrane H+-ATPase (EC 3.6.1.35) could act as a regulatory mechanism to control its activity. In this work, a plasmalemma-enriched fraction from maize roots and a partially purified H+-ATPase were used to investigate the effects of Ca2+ and calmodulin on the H+-ATPase activity and on its phosphorylation status. Both the hydrolytic and the proton-pumping activities were reduced approximately 50% by micromolar Ca2+ concentrations while calmodulin did not show any effect either alone or in the presence of Ca2+. The lack of effect of calmodulin antagonists indicated that calmodulin was not involved in this response. The addition of staurosporine, a kinase inhibitor, abolished the inhibitory effect of Ca2+. Phosphorylation of plasma membrane and partially purified H+-ATPase showed the same behavior. In the presence of Ca2+ a polypeptide of 100 kDa was phosphorylated. This polypeptide cross-reacted with antibodies raised against the H+-ATPase of maize roots. The autoradiogram of the immunodetected protein clearly showed that this polypeptide, which corresponds to the H+-ATPase, was phosphorylated. Additional clear evidence comes from the immunoprecipitation experiments: the data obtained show that the H+-ATPase activity is indeed influenced by its state of phosphorylation.
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  • 5
    ISSN: 1573-5028
    Keywords: gene expression ; b-ZIP motif ; seed storage proteins ; trans-acting factors ; transcription factors ; transcriptional regulation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The Opaque-2 (O2) gene from maize encodes a transcriptional activator of the b-ZIP class. We have isolated and characterized a gene from sorghum, related in sequence to the O2 gene from maize. A single copy of the gene is present in sorghum. Both genomic and cDNA sequences of the O2-related sorghum gene were determined. The sequence is highly homologous to maize O2 both in the promoter and in the coding region. The most closely related sequences contain the b-ZIP domain with only 11 amino acid substitutions in a total of 122 residues. In transient expression assays, the sorghum O2-related coding sequence, expressed from a CaMV 35S promoter, activates expression from the maize b-32 promoter as effectively as that obtained with the maize O2 sequence.
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  • 6
    Publication Date: 1999-08-12
    Print ISSN: 0032-0935
    Electronic ISSN: 1432-2048
    Topics: Biology
    Published by Springer
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  • 7
    Publication Date: 1996-10-01
    Print ISSN: 0014-2956
    Electronic ISSN: 1432-1033
    Topics: Biology , Chemistry and Pharmacology , Medicine
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