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  • Acetaldehyde  (1)
  • Petrocoptis
  • Springer  (2)
  • 2005-2009
  • 1990-1994  (2)
  • 1975-1979
  • 1994  (2)
  • 1
    Electronic Resource
    Electronic Resource
    Isolation and characterization of two new N-glycosidase type-1 ribosome-inactivating proteins, unrelated in amino-acid sequence, fromPetrocoptis species (1994)
    Springer
    Planta 194 (1994), S. 487-491 
    Details
    ISSN: 1432-2048
    Keywords: Petrocoptis ; Petroglaucin ; Petrograndin ; Ribosome-inactivating protein ; rRNA N-glycosidase ; Translation (inhibition)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Two new N-glycosidase type-1 ribosome-inactivating proteins (RIPs), denoted petroglaucin 1 and petrograndin, respectively, were isolated from the plantsPetrocoptis glaucifolia (Lag.) Boiss sp.viscosa (Rothm.) Laínz andPetrocoptis grandiflora Rothm. These new RIPs do not share H2N-terminal amino-acid sequence homology with petroglaucin (now denoted as petroglaucin 2), the only other type-1 RIP to be isolated fromP. glaucifolia (Arias et al. (1992) Planta186, 532–540). Petroglaucin 1 shares amino-acid sequence homology with RIPs from Cucurbitaceae while petroglaucin 2 and petrograndin do so with saporins and dianthin 30 (Caryophyllaceae). The new RIPs strongly inhibited protein synthesis at subnanomolar concentrations in rabbit reticulocyte lysates and other eukaryotic cell-free systems, but they were inactive on bacterial ribosomes.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00714460
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  • 2
    Electronic Resource
    Electronic Resource
    On the origin of the barriers and the structures of acetaldehyde in its ground and first singlet excited state (1994)
    Springer
    Theoretical chemistry accounts 88 (1994), S. 299-310 
    Details
    ISSN: 1432-2234
    Keywords: Hyperconjugation ; Origin of barriers ; Acetaldehyde ; Internal rotation ; Wagging
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Anab initio study of the ground and the first singlet excited states of acetaldehyde has been performed to analyze the molecular properties as a function of the methyl torsion and the aldehydic hydrogen wagging angles. The structural characteristics and the conformational behaviour in both electronic states have been determined. The important structural changes between the two states have been analyzed by a decomposition of the total energy into its components. It was found that the methyl torsion barriers arise mainly from attractive interactions. Evidence is presented which shows that these barriers arise from in-plane and out-of-plane hyperconjugative effects involving the oxygen atom. It is also shown that the pyramidalization experienced by the carbonyl carbon in the first singlet excited state has two sources, namely, a decrease in the electronic repulsion and an increase in the electron-nucleus attraction.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF01113453
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