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  • 1980-1984  (6)
  • 1975-1979  (3)
  • 1960-1964
  • Life and Medical Sciences  (5)
  • Crassulacean acid metabolism  (4)
Materialart
Erscheinungszeitraum
Jahr
  • 1
    Digitale Medien
    Digitale Medien
    Springer
    Planta 161 (1984), S. 71-80 
    ISSN: 1432-2048
    Schlagwort(e): Crassulacean acid metabolism ; Carbon dioxide fixation ; Circadian rhythm ; Kalanchoë
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie
    Notizen: Abstract 14CO2 was applied repeatedly at 3- to 6-h intervals toKalanchoë daigremontiana leaves during continuous light of differing irradiances. The circadian rhythm in net CO2 uptake in gasexchange measurements and its disappearance at high irradiances was confirmed by oscillating rates of14CO2 incorporation. At 10–30 W m-2 a markedly circadian oscillation in the14CO2-uptake rate was measured; with increasing energy fluence rate the oscillation levelled off at a constant high uptake rate. The labelling patterns obtained during the 10 min of14CO2 fixation indicated that the rhythm of CO2 exchange is the consequence of a rhythmic behaviour in the C4 pathway of CO2 fixation. During the mininum of14CO2 uptake no C4 products were labelled; however, substantial amounts of label were transferred to C4 products during the peaks of14CO2 uptake. Metabolism of C3 and C4 products was also studied in pulsechase experiments at different points of the circadian cycle. In bright light (100 W m-2), when the14CO2 uptake was constantly high, the transfer of label into C4 products (malic acid) was high in spite of the fact that the malate pool is known to be reduced to a permanently low level under these conditions. This led us to the conclusion that it is not the capacity of the phosphoenolpyruvatecarboxylase-mediated CO2 fixation but rather the storage of malic acid in the vacuole that is disturbed under bright-light conditions when the circadian oscillation levelled off.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    ISSN: 1432-2048
    Schlagwort(e): Carbon dioxide exchange ; Crassulacean acid metabolism ; Kalanchoë ; Leaf water relations ; Phosphoenolpyruvate carboxylase ; Transpiration
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie
    Notizen: Abstract Gas exchange, leaf water relations, malate content and phosphoenolpyruvate (PEP) carboxylase activity in crude extracts were examined for circadian rhythmicity in the crassulacean acid metabolism plant Kalanchoë daigremontiana. At low irradiance (20 W m-2) the rhythm in CO2 uptake continued for several days with a period length of approx. 22 h, whereas the transpiration rhythm was no longer apparent after 24 h. This shows that the CO2 rhythm in continuous light (LL) is not under stomatal control. Circadian oscillations in malate content were detectable for up to 72 h in LL but were of much reduced amplitude. This was reflected in the changes in leaf water relations, which quickly damped after transfer to LL. The activity of PEP carboxylase assayed immediately after extraction showed a rhythmicity for at least 18 h, but after 36 h, values from different plants were scattered. We suggest that the CO2-uptake rhythm is primarily the result of endogenous changes in the activity of PEP carboxylase, which competes to varying degrees with ribulose-1,5-bisphosphate carboxylase for CO2.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    Springer
    Planta 160 (1984), S. 264-271 
    ISSN: 1432-2048
    Schlagwort(e): Circadian rhythm ; Crassulacean acid metabolism ; Kalanchoë
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie
    Notizen: Abstract Gas exchange in K. blossfeldiana shows a circadian rhythm in net CO2 uptake and transpiration when measured under low and medium irradiances. The period length varies between 21.4 h at 60 W m-2 and 24.0 h at 10 W m-2. In bright light (≧80 W m-2) or darkness there are no rhythms. High leaf temperatures result in a fast dampening of the CO2-uptake rhythm at moderate irradiances, but low leaf temperatures can not overcome the dampening in bright light. The rhythm in CO2 uptake is accompanied by a less pronounced and more rapidly damped rhythm in transpiration and by oscillations in malate levels with the amplitude being highly reduced. The oscillations in starch content, usually observed to oscillate inversely to the acidification in light-dark cycles, disappear after the first cycle in continuous light. The balance between starch and malate levels depends in continuous light on the irradiance applied. Leaves show high malate and low starch content at low irradiance and high starch and low malate in bright light. During the first 12 h in continuous light replacing the usual dark period, malate synthesis decreases with the increasing irradiance. Up to 50 W m-2 starch content decreases; at higher irradiances it increases above the values usually measured at the end of the light period of the 12:12 h light-dark cycle.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 4
    ISSN: 1432-2048
    Schlagwort(e): CO2 dark fixation ; Crassulacean acid metabolism ; Kalanchoë ; PEP-carboxylase ; Temperature (PEP-carboxylase)
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie
    Notizen: Abstract Net CO2 dark fixation of Kalanchoë daigremontiana varies with night temperature. We found an optimum of fixation at about 15° C; with increasing night temperature fixation decreased. We studied the temperature dependence of the activity of phosphoenolpyruvate (PEP)-carboxylase, the key enzyme for CO2 dark fixation. We varied the pH, the substrate concentration (PEP), and the L-malate and glucose-6-phosphate (G-6-P) concentration in the assay. Generally, lowering the pH and reducing the amount of substrate resulted in an increase in activation by G-6-P and in an increase in malate inhibition of the enzyme. Furthermore, malate inhibition and G-6-P activation increased with increasing temperature. Activity measurements between 10° C and 45°C at a given concentration of the effectors revealed that the temperature optimum and maximum activities at that optimum varied with the effector applied. Under the influence of 5 mol m-3 L-malate the temperature optimum and maximum activity dropped drastically, especially when the substrate level was low (at 0.5 mol m-3 PEP from 32° C to 20° C). G-6-P raised the temperature optimum and maximum activity when the substrate level was low. If both malate and G-6-P were present, intermediate values were measured. We suggest that changes in metabolite levels in K. daigremontiana leaves can alter the temperature features of PEP-carboxylase so that the observed in vivo CO2 dark fixation can be explained on the basis of PEP-carboxylase activity.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 5
    Digitale Medien
    Digitale Medien
    New York, N.Y. : Wiley-Blackwell
    Journal of Cellular Biochemistry 20 (1982), S. 71-80 
    ISSN: 0730-2312
    Schlagwort(e): aminoglycoside ; fluorescent paromomycin ; human fibroblasts ; lysosomes ; endocytosis ; exocytosis ; Life and Medical Sciences ; Cell & Developmental Biology
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Biologie , Chemie und Pharmazie , Medizin
    Notizen: Human fetal lung fibroblasts grown in the presence of dansyl-paromomycin (DNS-Pm), a fluorescent derivative of the aminoglycoside antibiotic, paromomycin, probably accumulate DNS-Pm in the lysosomes. The intracellular concentration of DNS-Pm is proportional to the extracellular concentration and to the length of time cells are exposed to the compound. The accumulation of DNS-Pm by human fibroblasts continued to increase for several days, reaching a saturation after 7 days. The kinetic data are consistent with the establishment of a steady state in the cell between fluid-phase pinocytosis and exocytosis of DNS-Pm. About 80% of the intracellular DNS-Pm was released in 24 hr when fresh medium without the analogue was added. The residual 20% remained within the cells, suggesting that it may be irreversibly bound to the lysosomes, endoplasmic reticulum, or ribosonius. The uptake of paromomycin by cells in culture may be a useful means to study error propagation during growth and lifespan of cells in vitro.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 6
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 210 (1984), S. 463-475 
    ISSN: 0003-276X
    Schlagwort(e): Life and Medical Sciences ; Cell & Developmental Biology
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Medizin
    Notizen: Uteri from hibernating bats, Myotis lucifugus, collected periodically from Renfrew County, Ontario, were fixed in 2% glutaraldehyde and processed for electron microscopy or incubated in glyoxylic acid to show adrenergic nerves by fluorescence. The bat uterus is structurally typical of mammalian species; although the right uterine horn is permanently enlarged in parous bats due to hypertrophy of both myometrium and endometrium. Nerves were abundant between both longitudinal and circular layers of muscle cells. Unmyelinated, and some myelinated, axons, ranging from few to many, coursed generally parallel to the uterine long axis. Numerous axonal varicosities containing small dense-cored (adrenergic) vesicles or, less often, small agranular (cholinergic) vesicles, were found forming close nerve-muscle contacts between myometrial cells and blood vessels. Fluorescent microscopy showed a dense network of adrenergic nerves in parous uteri, but a sparse network in nulliparous uteri. A specific adrenergic nerve marker, 5-hydroxydopamine, greatly increased the density and in some instances, the size of granular vesicles, while 6-hydroxydopamine, which depletes adrenergic neutrotransmitter, reduced the number of dense-cored vesicles. Nulliparous uteri appeared unchanged by six daily injections of 0.1 μg estradiol-17β; 0.25 mg progesterone, or both; but parous uteri were greatly enlarged by all regimes. Nerve ultrastructure, however, appeared unaffected by steroid treatment; nor, despite the absolute dextral bias in implantation, were left-right differences observed. Gap junctions were not found between muscle cells in myometria of any bat uteri. Based on this study, we suggest that M. lucifugus may provide a most useful model for examination of neurogenic regulation of the uterus.
    Zusätzliches Material: 15 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 7
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Cellular Physiology 94 (1978), S. 105-115 
    ISSN: 0021-9541
    Schlagwort(e): Life and Medical Sciences ; Cell & Developmental Biology
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Biologie , Medizin
    Notizen: Some properties of the enzyme phosphoglucose isomerase (PGI) from the foetal lung fibroblast strain MRC-5 have been investigated throughout the in vitro lifespan of this cell strain.No significant age-related alterations in specific activity or thermostability of PGI could be detected. Titration of enzymatic activity with antibody directed against purified PGI showed no detectable differences in PGI from extracts of early passage cells compared with enzyme from senescent cells.The effect of p-fluorophenylalanine incorporation on PGI was examined in early passage fibroblasts. Thermostability studies showed increased heat lability of PGI from analogue treated cells when compared with enzyme from control cells at the same passage. However, no inactive PGI protein could be detected by antiserum titration in extracts from analogue-treated cells.The results indicate that no significant amount of altered or inactive PGI is produced in ageing fibroblasts.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 8
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Cellular Physiology 92 (1977), S. 233-239 
    ISSN: 0021-9541
    Schlagwort(e): Life and Medical Sciences ; Cell & Developmental Biology
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Biologie , Medizin
    Notizen: Thrombin may stimulate the proliferation of resting fibroblasts by itself or by potentiating the mitogenic effects of other growth stimulating agents. When added alone to a dense quiescent culture of chick embryo fibroblasts in either a serum-free or a low serum medium, thrombin stimulates these cells to proliferation at a rate comparable to that seen with 5% serum. In the case of rabbit corneal fibroblasts neither fibroblast growth factor nor thrombin is particularly effective as a growth stimulant when added alone but exhibited a pronounced synergism on cell proliferation when present together. Established cell lines in the resting state, including 3T3, SV-3T3, 3T6, BHK-21 and 3T3 injected with avian sarcoma virus strain B77 (B77-3T3), are not responsive to thrombin alone. When the serum concentration in the medium equals or exceeds 2%, thrombin potentiates the mitogenic response of 3T3 cells to serum factors. With the exception of 3T3 and SV3T3 cells, the other cell lines show a potentiation of growth when thrombin is added to a low-serum (0.5%) medium containing epidermal growth factor and prostaglandin F2α. The addition of thrombin to cultures of B77-3T3 cells growing in the presence of epidermal growth factor and prostaglandin F2α does not increase the initial growth rate of these cells but increases significantly the final cell density of these cultures.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 9
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Cellular Physiology 101 (1979), S. 293-309 
    ISSN: 0021-9541
    Schlagwort(e): Life and Medical Sciences ; Cell & Developmental Biology
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Biologie , Medizin
    Notizen: We have investigated the de novo synthesis of intermediates of purine nucleotides in 3T6 fibroblasts and determined the manner by which the activity of this pathway is increased in resting cells by the addition of fresh serum. Within 30 minutes after stimulation, 3T6 cells began to synthesize increased amounts of purines by the de novo pathway as measured by increased amounts of formylglycinamide ribonucleotide, a representative intermediate of this pathway. Within 15 minutes after serum-stimulation 3T6 cells exhibited a substantial increase in their capacity to synthesize ribose compounds, particularly in the form of 5-phosphoribosylpyrophosphate (PRPP). The availability of PRPP appeared to be limiting for the synthesis of purine nucleotides in resting fibroblasts, but not necessarily in serum-stimulated cells.The amount of the enzyme PRPP synthetase as measured in vitro remained constant for at least the first four hours. Therefore, a study was made of various compounds known to activate PRPP synthetase in vitro. No evidence was found that suggested involvement of concentrations of cyclic nucleotides or phosphate. Experiments with methylene blue, an artificial electron acceptor that stimulates the production of ribose 5-phosphate by the hexose monophosphate shunt, indicated that one of the immediate consequences of the addition of serum is increased cycling of the pyridine nucleotide coenzymes, NADP+ and NADPH, and that the rapid increase in formation of ribose compounds and, consequently, purine nucleotides was caused as a result of modulation by this coenzyme. The relative ration of ATP:ADP:AMP as well as their concentrations remain constant in resting and serum-stimulated cells under normal assay conditions. However, there was a substantial decrease in ATP concentrations with a corresponding increase in AMP concentration with methylene blue in the assay buffer. The production of AMP from ATP was 5-fold greater in the serum-stimulated than in the resting fibroblasts. The increased production of AMP is thus serum-dependent and may reflect a basic enzymatic function of proliferative as compared to resting cells.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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