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  • 2020-2023  (1)
  • 1960-1964  (21)
  • 1950-1954  (2)
  • 1
    Publication Date: 2022-05-26
    Description: © The Author(s), 2020. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Rodenfels, J., Sartori, P., Golfier, S., Nagendra, K., Neugebauer, K. M., & Howard, J. Contribution of increasing plasma membrane to the energetic cost of early zebrafish embryogenesis. Molecular Biology of the Cell, 31(7), (2020): 520-526, doi:10.1091/mbc.E19-09-0529.
    Description: How do early embryos allocate the resources stored in the sperm and egg? Recently, we established isothermal calorimetry to measure heat dissipation by living zebra­fish embryos and to estimate the energetics of specific developmental events. During the reductive cleavage divisions, the rate of heat dissipation increases from ∼60 nJ · s−1 at the two-cell stage to ∼90 nJ · s−1 at the 1024-cell stage. Here we ask which cellular process(es) drive this increasing energetic cost. We present evidence that the cost is due to the increase in the total surface area of all the cells of the embryo. First, embryo volume stays constant during the cleavage stage, indicating that the increase is not due to growth. Second, the heat increase is blocked by nocodazole, which inhibits DNA replication, mitosis, and cell division; this suggests some aspect of cell proliferation contributes to these costs. Third, the heat increases in proportion to the total cell surface area rather than total cell number. Fourth, the heat increase falls within the range of the estimated costs of maintaining and assembling plasma membranes and associated proteins. Thus, the increase in total plasma membrane associated with cell proliferation is likely to contribute appreciably to the total energy budget of the embryo.
    Description: The analysis of these data was initiated in the 2019 Physical Biology of the Cell course at the Marine Biological Laboratory in Woods Hole, MA. We acknowledge the support and feedback from the course directors and participants. This work was supported by funding from EMBO Long-Term Fellowship ALTF 754–2015 (to J.R.), the Eric and Wendy Schmidt Membership in Biology at the Institute for Advanced Study (to P.S.), National Institutes of Health (NIH) R21 HD094013 (to K.M.N.), and NIH R01 GM110386 (to J.H.). Its contents are solely the responsibility of the authors and do not necessarily represent the official views of the NIH.
    Repository Name: Woods Hole Open Access Server
    Type: Article
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of organic chemistry 26 (1961), S. 3152-3155 
    ISSN: 1520-6904
    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
    Chemical reviews 63 (1963), S. 279-296 
    ISSN: 1520-6890
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 76 (1964), S. 376-377 
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 76 (1964), S. 603-603 
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 75 (1963), S. 417-417 
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Chemie Ingenieur Technik - CIT 36 (1964), S. 9-14 
    ISSN: 0009-286X
    Keywords: Chemistry ; Industrial Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Bei der Elektrofluorierung werden die Substanzen in flüssigem, wasserfreiem Fluorwasserstoff an Metall-Elektroden fluoriert, ohne daß dabei elementares Fluor frei wird. Durch Abändern der Apparatur nach Simons gelingt es nun auch, Gase, z. B. CH4, C2H6, C3H8 und H2S, zu fluorieren; die Reaktionsprodukte werden anschlie-end durch fraktioniertes Ausfrieren getrennt.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 61 (1963), S. 46-62 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die aus dem systematischen kinetischen Studium der Äthylen-Propylen-Copolymerisation in Anwesenheit von Katalysatoren aus Al(C6H13)3 und VCl4 erhaltenen und schon in einer früheren Arbeit mitgeteilten Ergebnisse werden zunächst kurz zusammengefaßt.Die bemerkenswerte Zunahme der Brutto-Copolymerisationsgeschwindigkeit, die man beobachtet, wenn das Äthylen-Propylen-Verhältnis in der flüssigen Reaktionsmischung zunimmt, kann nicht nur auf Grund der kinetischen Wachstumskonstanten erklärt werden, sondern es ist auch nötig, eine Änderung der Konzentration der wachsenden Ketten anzunehmen. Es werden einige experimentelle Beweise erbracht, die eine solche Annahme unterstützen.Dieses Ergebnis kann nicht auf die Äthylen-Propylen-Copolymerisation in Anwesenheit von anderen, mit anionisch-koordinativem Mechanismus wirkenden Katalysatoren übertragen werden, bei denen das Verhältnis zwischen der Äthylen- und der Propylenhomopolymerisationsgeschwindigkeit sehr nahe bei dem Copolymerisationsparameter des Äthylens liegt.Schließlich wird eine Gleichung vorgeschlagen, die mit guter Näherung den Werten der Brutto-Copolymerisationsgeschwindigkeit in Anwesenheit des Katalysatorsystems Al(C6H13)3 + VCl4 entspricht.
    Notes: The results obtained from a systematic kinetic study of ethylene-propylene copolymerization in the presence of catalysts prepared from Al(C6H13)3 and VCl4, already reported are briefly summarized.The considerable increase of the overall copolymerization rate, observed with the increase of the ratio of ethylene to propylene in the reacting liquid phase, cannot be explained only on the basis of the values of the kinetic constants of propagation, but it is also necessary to admit a variation in the concentration of the number of growing chains. Some experimental evidences are indicated proving this hypothesis.This result cannot be extended to the ethylene-propylene copolymerization in the presence of other catalytic systems acting through an anionic co-ordinated mechanism, for which the ratio between the rates of ethylene and propylene homopolymerization is very close to the value of the reactivity ratio of ethylene.Finally, an equation is proposed which interprets, to a good approximation, the values of the overall rate of the copolymerization process in the presence of the catalytic system Al(C6H13)3 - VCl4.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 51 (1961), S. 429-454 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The values of the reactivity ratios for ethylene-propylene and ethylene-1-butene copolymerization, described in previous papers, and the distribution of monomer units in different length sequences are discussed. In this paper the kinetics of ethylene-propylene copolymerization in the presence of catalysts prepared from trialkylaluminum and vanadium tetrachloride is studied. Having adopted the conditions leading to the formation of catalysts having an activity independent of time, we were able to determine that the copolymerization rate is first order with respect to the catalyst concentration and to the sum of the concentrations of the two monomers. With the total concentration of the monomers constant, the copolymerization rate increases very rapidly as the ethylene concentration increases. The activation energies of the four chain growth reactions of the copolymerization proved to be practically equal.
    Additional Material: 17 Ill.
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Ethylene-propylene copolymerization in the presence of catalysts prepared from vanadium halides was described in our previous papers. Linear, high molecular weight, completely amorphous copolymers, having an ethylene molar content up to 80%, can also be von 0°C weitaus höhere Copolymerausbeuten als bei Raumtemperatur. Die höhere Bruttopolymerisationsgeschwindigkeit bei tiefen Temperaturen ist spezifisch für dieses besonder katalytische System und tritt bei Katalysatoren, die aus Vanadinchloriden dargestellt wurden, nicht auf. Bei -20°C ist die Zusammensetzung der Copolymeren von der Polymerisationsdauer, dem Molverhältnis Al(C2H5)2Cl/VAc3, der Katalysator-konzentration oder der Gesamtkonzentration der Monomeren unabhängig. Das mittlere Molekulargewicht der Copolymeren nimmt mit steigendem Al(C2H5)2Cl/VAc3Verhältnis und steigender Katalysatorkonzentration ab, was für das Auftreten eines Ubertragungsprozesses zwischen den wachsenden Ketten und den im System vorhandenen organometallischen Verbindungen spricht. Bei konstantem Verhältnis zwischen den Monomerkonzentrationen und zwischen den Katalysatorkomponenten ist die Bruttopolymerisationsgeschwindigkeit in bezug auf die Katalysator- und Monomerkonzentrationen von erster Ordnung. Die Reaktivitätsverhältnisse der Monomeren, r(C2H4) = 15.0, r(C3H6) = 0.04, sind zwischen -20°C und +25°C von der Temperatur unabhängig. Das Produkt der beiden Werte (0,6) weist darauf hin, dass eine Abwechslung der Monomereinheiten in den Ketten wahrscheinlicher ist als eine statistische Verteilung, bei der das Produkt dieser Verhältnisse gleich 1 ist.
    Additional Material: 11 Ill.
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