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  • Chemistry  (20)
  • Condensed Matter: Electronic Properties, etc.
  • Imines
  • galactokinase
  • 2010-2014  (2)
  • 1990-1994  (9)
  • 1980-1984  (11)
  • 1965-1969  (2)
  • 1
    ISSN: 1573-4927
    Keywords: galactokinase ; thymidine kinase ; O6-methylguanine-DNA methyltransferase ; gene regulation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Expression of the enzymes galactokinase, thymidine kinase, and O6-methylguanine-DNA methyltransferase is occasionally coordinately regulated in human cell lines. We have measured the activities of these three enzymes in extracts of fibroblasts from individuals with hereditary galactokinase deficiency. These cells do not express measurable galactokinase activity. The levels of O6-methylguanine-DNA methyltransferase were in the normal range in cells from three galactokinase-deficient individuals. The activity of thymidine kinase in the affected cells was in the normal range for two of the three individuals. The reduced thymidine kinase activity in the third individual reflected the extremely poor growth of the cells in culture. Immortalization of one galactokinase-deficient cell line resulted in loss of O6-methylguanine-DNA methyltransferase activity, but the galactokinase and thymidine kinase levels remained unchanged. The data indicate that the loss of galactokinase activity in these individuals is the consequence of an alteration of gene expression which does not involve coordinate silencing with the thymidine kinase and methyltransferase loci.
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  • 2
    ISSN: 1573-4927
    Keywords: galactokinase ; thymidine kinase ; O6-methylguanine-DNA methyltransferase ; gene regulation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Expression of the enzymes galactokinase, thymidine kinase, and O6-methylguanine-DNA methyltransferase is occasionally coordinately regulated in human cell lines. We have measured the activities of these three enzymes in extracts of fibroblasts from individuals with hereditary galactokinase deficiency. These cells do not express measurable galactokinase activity. The levels of O6-methylguanine-DNA methyltransferase were in the normal range in cells from three galactokinase-deficient individuals. The activity of thymidine kinase in the affected cells was in the normal range for two of the three individuals. The reduced thymidine kinase activity in the third individual reflected the extremely poor growth of the cells in culture. Immortalization of one galactokinase-deficient cell line resulted in loss of O6-methylguanine-DNA methyltransferase activity, but the galactokinase and thymidine kinase levels remained unchanged. The data indicate that the loss of galactokinase activity in these individuals is the consequence of an alteration of gene expression which does not involve coordinate silencing with the thymidine kinase and methyltransferase loci.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 125 (1992), S. 2033-2040 
    ISSN: 0009-2940
    Keywords: 13C NMR, SCS ; Substituent effects ; Imines ; Isomerization, (E,Z) Schiff bases ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Sterically congested N-(1,1,3,3-tetraalkyl-2-indanylidene)-amines 8-11, N-(cyclopentylidene)anilines 13-17, and two of their salts are described, together with a short synthesis of 2-imino-1,1,3,3-tetramethylindan (5). Some of these imines show rapid (E,Z) equilibration. Positively and negatively charged nitrogen functions (in 6 and 7) cause opposite 1H- and 13C-NMR chemical shift effects along the C = N bond. Chemical shifts are almost equally affected by the lone electron pair and by the imino N-H bond. Substituent-induced chemical shifts (SCS) have been assigned for all syn and anti positions with respect to methyl, phenyl, and 2,6-dimethylphenyl groups at the imino nitrogen atom. The structurally well-defined, rigid imines recommend themselves as new models for the calibration of theoretical approaches to syn/anti-differentiating SCS.
    Additional Material: 3 Tab.
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  • 4
    ISSN: 0009-2940
    Keywords: Diastereotopomerization, (E, Z) ; Imines ; Inversion, nitrogen ; Permethylation ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Experimental differentiation between pure C=N double bond rotation and nitrogen inversion in N1-arylimines is possible with a single compound (13b) under the proviso of slow rotation about the N-aryl single bond. Labelling by 1H and 13C nuclei at the diastereotopic faces of the C=N moiety as well as of the N-aryl group is the clue to a successful stereodynamic analysis, as performed by variable-temperature NMR spectroscopy of 13b, a sterically congested and chiral model compound. Interpretation of similar measurements on a second model (13d) is less straightforward. The experimental observation of time-averaged Cs symmetry by NMR coalescences is only compatible with a mechanism of (E/Z) stereomutation either by pure inversion at sp2 nitrogen or by a contribution from C=N rotation together with a synchronized (geared) controtation about the N-aryl single bond. However, the latter combination is concluded to be predominantly inversion-like by comparisons with related imines.
    Additional Material: 1 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 116 (1983), S. 1623-1630 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Synthesis and Properties of New Perhalogenated 1,3-Dithietane S-OxidesNew perchlorinated and perfluorinated 1,3-dithietanes (4, 6, 7, 12, 14, 15), which are partially oxidized at the sulfur atoms, are described. Pyrolysis of the 1,3-dioxides 7 and 15 leads to the sulfoxides 8 and 16, X2C = S = O (X = Cl, F). respectively. Two new oxidizing agents are used: trifluoromethane- and nonafluorobutanepersulfonic acid.
    Notes: Die neuen perchlorierten und perfluorierten, am Schwefel partiell oxidierten 1,3-Dithietane 4, 6, 7, 12, 14 und 15 werden beschrieben. Pyrolysen der 1,3-Dioxide 7 und 15 führen zu den Sulfoxiden 8 bzw. 16, X2C = S = O (X = Cl, F). Zwei neue Oxidationsmittel werden angewendet: Trifluormethan- und Nonafluorbutanpersulfonsäure.
    Additional Material: 1 Ill.
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  • 6
    ISSN: 0006-3592
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Proline excretion from proline overproducing strains of E. coli K12 has been studied as a model chemical production system. We have isolated proline overproducing mutants of E. coli and have shown that uncontrolled synthesis is not sufficient to cause excretion of this amino acid. An episomal mutation causing proline over production has been introduced into a series of otherwise isogenic strains that bear well defined, chromosomal lesions affecting the active uptake and catabolism of L-proline. A syntropism test reveals that L-proline is excreted by overproducing strains only if transport and/or catabolism are impaired. Dansyl derivatization and chromatographic analysis of culture supernatants shows that proline is the only amino acid excreted. Batch cultures of an excreting strain in an amino acid production medium yield culture supernatants containing 1 g proline/L, whereas no proline is detectable in supernatants derived from cultures of an overproducing strain with normal transport and catabolic activities. These data reveal that genetic lesions eliminating active uptake can be used to specifically enhance metabolite excretion.
    Additional Material: 1 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Biotechnology and Bioengineering 26 (1984), S. 1140-1140 
    ISSN: 0006-3592
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
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  • 8
    ISSN: 0006-3592
    Keywords: catabolite repression ; protein A ; membrane proteins ; continuous culture ; protein expression ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Although widely used in experimental and industrial situations, genetically engineered plasmids containing the lac promoter from Escherichia coli are subject to catabolite repression when grown in glucose-containing media. Several methods of overcoming this problem have been investigated by studying the expression of the protein A gene from Staphylococcus aureus under the control of the Escherichia coli lac promoter. When glycerol is used as a sole carbon source, the plasmid is unstable and is rapidly lost from the culture. When the bacteria are grown in chemostats under glucose limitation, the plasmid is maintained, even at high dilution rates, and the expression of protein A is similar to that observed when glycerol was used. The balance between metabolic load and protein A expression seems to be maintained by reducing the gene dose to a tolerable level. Depending on the metabolic conditions prevailing in the culture, this is achieved, either by reducing the copy number of the plasmid or in extreme cases by removing the plasmid altogether.
    Additional Material: 10 Ill.
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  • 9
    ISSN: 0170-2041
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: 4-Alkyl(Aryl)-λ5-phosphorins; 1,4-Dihydrophosphorin/λ5-Phosphorin4 RearrangementThe 1-R'-4-R-4-methoxy-1,4-dihydrophosphorins11-17, the 1H- and 13C-NMR spectra and stereochemistry of which are discussed, are formed by reaction of (1 Z, 4Z)-1,5-dilithio-3-R-3-methoxy-1,4-pentadienes9 with R'PCl2 [R' = aryl, alkyl, N(C2H5)2, OC4H9, SC6H5] at - 78°C. Addition of catalytic amounts of acid causes rearrangement of the 1,4-dihydrophosphorins and yields the 1-R'-1-methoxy-4-R-λ5-phosphorins23 - 29 which represent the most simple derivatives of this class of compounds. - The mechanism of this 1,4-dihydrophosphorin/λ5-phosphorin rearrangement has been studied; according to that a direct H+-catalyzed 1,4-migration of the methoxy group is assumed concerning the trans-isomers, while the 1-R'-phosphorinium cations are intermediates in the case of the cis-isomers. - Acid-catalyzed hydrolysis of the λ5-phosphorins yields the 1-R'-4-R-1,2-dihydrophosphorin oxides35. The 1,1-dimethoxy-4-R-λ5-phosphorins28 have been prepared by direct oxidative alkoxylation of the λ3-phosphorins with Hg(OAc)2/methanol.
    Notes: Durch Umsetzung der (1 Z,4Z)-1,5-Dilithio-3-R-3-methoxy-1,4-pentadiene9 mit R'PCl2 [R' = Aryl, Alkyl, N(C2H5)2, OC4H9, SC6H5] bei - 78°C werden die 1-R'-4-R-4-methoxy-1,4-dihydrophosphorine11 - 17 erhalten, deren 1H- und 13C-NMR-Spektren und cis/trans-Stereochemie diskutiert werden. - Die 1,4-Dihydrophosphorine lagern sich bei der Einwirkung von katalytischen Mengen Säure in die entsprechenden 1-R'-1-methoxy-4-R-λ5-phosphorine23-29 als bisher einfachste Vertreter dieser Verbindungsklasse um. Ihre 1H-NMR-, 13C-NMR-, UV-, IR- und Massenspektren werden diskutiert. - Der Mechanismus dieser 1,4-Dihydrophosphorin/λ5-Phosphorin-Umlagerung wird untersucht; danach muβ angenommen werden, daβ sich die trans-Isomeren in einer direkten H + -katalysierten 1,4-Verschiebung der Methoxygruppe umlagern, während bei den cis-Isomeren die 1-R'-phosphoriniumkationen Zwischenstufe sind. - Bei der säure-katalysierten Hydrolyse der λ5-Phosphorine entstehen die 1-R'-4-R-1,2-dihydrophosphorinoxide35. Die 1,1-Dimethoxy-4-R-λ5-phosphorine28 lassen sich direkt durch oxidative Alkoxylierung der λ3-Phosphorine mit Hg(OAc)2/Methanol darstellen.
    Additional Material: 10 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 14 (1980), S. 226-233 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In recent publications we have described a novel method of analysis for high-resolution NMR spectra of compounds in isotropic solution which differs from conventional procedures in that it exploits the full information content of a spectrum and does not require assignments of energy levels or transitions. We now present a further development of this technique which also makes it applicable to the NMR spectra of molecules partially oriented in liquid crystal solvents. Illustrative applications are reported for the nematic phase spectra of allyl fluoride, allyl chloride and allyl bromide. The results are discussed in terms of various theoretical models of the interplay between the internal and overall rotations of the conformationally mobile solutes.
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