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  • 1
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 4 (1971), S. 270-270 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 5 (1972), S. 442-443 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    World journal of surgery 10 (1986), S. 892-894 
    ISSN: 1432-2323
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Chromosoma 46 (1974), S. 121-144 
    ISSN: 1432-0886
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract Transcribing ribosomal RNA genes in primary spermatocyte nucleoli of Drosophila hydei have been visualized by electron microscopy using a microspreading technique. The length of the transcribing unit is in agreement with the length of the ribosomal RNA precursor as determined by acrylamide gel electrophoresis (2.6×106 daltons). The length of the non-transcribed spacer is approximately 1.0×106 daltons. The maximum number of active cistrons in wild type (XY) males only approaches one half the estimated number of ribosomal cistrons of the replicated diploid genome (∼300) of D. hydei and is found to vary between 120 and 320 cistrons in different developmental stages of spermatocytes. There is also some variation between different males. In a few cases a variation in the transcriptional activity of different cistrons has been observed. The synthesis of ribosomal RNA therefore seems to be regulated primarily by the activation or inaetivation of varying numbers of ribosomal cistrons. Groups of adjacent cistrons seem to be under coordinated control. Inhibition of RNA synthesis by actinomycin, in contrast, follows a random pattern. The frequent observation of a bipartite nucleolus indicates that the nucleolus organizer regions of the two sex chromosomes are both active in transcription. The number of active ribosomal eistrons found in some X-Y translocation stocks and in XO males deviates considerably from that expected on the basis of DNA/RNA hybridization data. We conclude that, in agreement with the observations of other authors, a mechanism adjusting the number of ribosomal cistrons may be operating in these cases.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1432-203X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract ATP-dependent H+ transport in microsomes from zucchini hypocotyls is stimulated by the ether lipid 1-0-alkyl-2-acetyl-sn-glycero-3-phosphocholine (platelet-activating factor = PAF) known as a hormone-like substance from mammals. The stimulation can only be observed when soluble cytosolic proteins are present. A soluble protein mediating the PAF-dependent H+ transport and a PAF-stimulated protein kinase are coeluted by DEAE-Sephacel chromatography. Stimulation of phosphorylation by PAF of a 55 kDa polypeptide without Ca2+ and, additionally, of a 35 kDa polypeptide in the presence of Ca2+ is observed in zucchini microsomal membranes. This is evidence for a novel phospholipid-stimulated protein kinase in plants. Phosphorylation of regulatory proteins may be involved in the stimulation of in vitro H+ transport by PAF.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1432-203X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Addition of the animal ether phospholipid platelet-activating factor, 1-0-alkyl-2-acetyl-sn-glycero-3-phosphocholine, (PAF) stimulates medium acidification in cultured soybean (Glycine max L.) cells. The pH of the medium after 8–10 hours is on the average one pH unit lower than in controls. With fusicoccin an average pH difference of 1.7 units is reached. Phospholipids, glycerol, 1-oleyl-2-acetyl-sn-glycerol, 1-0-hexadecyl-sn-glycerol, and triolein at the same concentrations as PAF had no stimulatory effect on medium acidification. The detergents CHAPS and deoxycholate lead to alkalinization of the medium whereas lysophosphatidylcholine (LPC), a detergent with structural similarity to PAF, shows no effect.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 1432-0886
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract Initial observations of low fertility, reduced sexual activity of males, and a high frequency of abnormalities in sperm differentiation of the wild type strain (Sevelen, Zürich) of Drosophila melanogaster, normally used in this laboratory, have lead to a study of this phenomenon and its causes. The abnormalities occur during all spermiogenetic stages and are not unique but are found with much lower frequency in normally fertile flies (Oregon R). Growth of Sevelen flies at high but sublethal temperatures (30°C) results in complete sterility, highly abnormal sperm differentiation, and a failure to recover fertility after return to normal temperatures (25° C) in the time period in which normal flies recover. — The principal factor, or factors, controlling normal sperm differentiation are located on the Y chromosome, but are thus far not precisely localized. Expression of the phenotype is modified by genetic background in which the Y chromosome is found.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1432-2048
    Keywords: Cucurbita (phospholipid) ; Ether phospholipid ; H+ transport ; Platelet activating factor
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract A plant lipid was isolated from zucchini (Cucurbita pepo L.) membranes and from soybean (Glycine max [L.] Merr) phospholipids by thinlayer chromatography and further purified by high-performance liquid chromatography. This plant lipid was chromatographically very similar to the platelet-activating factor, an ether phospho-lipid with hormone-like properties found in mammals. Both the plant lipid and the platelet-activating factor stimulated ATP-dependent H+ transport in isolated membrane vesicles from zucchini hypocotyls.
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 1432-2048
    Keywords: H+-ATPase ; Cucurbita ; Plasma membrane ; Platelet-activating factor ; Phospholipid ; Protein kinase, phospholipid-activated ; Tonoplast
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract 1-O-alkyl-2-acetyl-sn-glycero-3-phosphocholine, an ether phospholipid from mammals known as platelet-activating factor (PAF), specifically stimulates proton transport in zucchini (Cucurbita pepo L.) microsomes (G.F.E. Scherer, 1985, Biochem. Biophys. Res. Commm. 133, 1160–1167). When plant lipids were analyzed by two-dimensional thin-layer chromatography a lipid was found with chromatographic properties very similar to the PAF (G.F.E. Scherer and B. Stoffel, 1987, Planta, 172, 127–130). This lipid was isolated from zucchini hypocotyls, red beet root, lupin root, maize seedlings and crude soybean phospholipids. It had biological activity similar to that of the PAF, based on phosphorus content, and stimulated the steady-state ΔpH in zucchini hypocotyl microsomes about twofold. Other phospholipids, monoglyceride, diglyceride, triglyceride, oleic acid, phorbol ester, and 1-O-alkylglycerol did not stimulate proton transport. When microsomes were washed the PAF was ineffective but when soluble protein was added the PAF stimulation of H+ transport was reconstituted. The soluble protein responsible for the PAF-dependent stimulation of transport activity could be partially purified by diethylaminoethyl Sephacel column chromatography. In the same fractions where the PAF-dependent transport-stimulatory protien was found, a protein kinase was active. This protein kinase was stimulated twofold either by the PAF or by Ca2+. When Ca2+ was present the PAF did not stimulate protein-kinase activity. When either the PAF, protein kinase, or both were added to membranes isolated on a linear sucrose gradient, ATPase activity was stimulated up to 30%. Comparison with marker enzymes indicated the possibility that tonoplast and plasma-membrane H+-ATPase might be stimulated by the PAF and protein kinase. We speculate that a PAF-dependent protein kinase is involved in the regulation of proton transport in plants in vitro and in vivo.
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