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  • 1
    Electronic Resource
    Electronic Resource
    Expression of recombinant protein A from the lac promoter in Escherichia coli JM83 is not subject to catabolite repression when grown under specific conditions of continuous culture (1991)
    New York, NY [u.a.] : Wiley-Blackwell
    Biotechnology and Bioengineering 38 (1991), S. 1050-1058 
    Details
    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.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/bit.260380914
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  • 2
    Electronic Resource
    Electronic Resource
    Sequence of swallow, a gene required for the localization of bicoid message in Drosophila eggs (1991)
    Chichester [u.a.] : Wiley-Blackwell
    Developmental Genetics 12 (1991), S. 333-341 
    Details
    ISSN: 0192-253X
    Keywords: Maternal effect gene ; DNA sequencing ; protein ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: We report the sequence of the Drosophila maternal effect gene swallow, one of the genes whose product is required for the localization of bicoid message during Drosophila oo-genesis. The inferred swallow protein contains a domain that is predicted to be an amphipathic α-helix similar to those implicated in protein:protein associations in other systems. Another part of the predicted protein appears to be a diverged RNA-binding motif. We discuss these structural features in light of the function of the swallow protein in the bicoid message localization process.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/dvg.1020120502
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  • 3
    Electronic Resource
    Electronic Resource
    Mass spectra of trimethylsilyl derivatives of naturally occurring flavonoid aglycones and chalcones (1991)
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 26 (1991), S. 157-160 
    Details
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Electron impact mass spectra of the trimethylsilyl derivatives of a series of flavonoid aglycones and chalcones are reported. The spectra show prominent ions arising from fragmentation of the trimethylsilyl (TMS) groups. Inter-actions between adjacent TMS groups, and between TMS groups in the 3- or 5-position (6′-position for the chalcones) and the C-ring carbonyl, yield structurally significant ions. Few fragments associated with the retro-Diels-Alder cleavage of the C-ring characteristic of the underivatized compounds, are observed. The TMS derivatives thus provide complementary information for the identification of flavonoid aglycones and chalcones in biological systems.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/oms.1210260310
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  • 4
    Electronic Resource
    Electronic Resource
    (E, Z)1-Equilibria, 17 Demonstration of the Nitrogen Inversion Mechanism of Imines in a Schiff Base ModelDedicated to Professor Heinrich Nöth on the occasion of his 65th birthday. (1993)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 747-754 
    Details
    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.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19931260327
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  • 5
    Electronic Resource
    Electronic Resource
    (E,Z) Equilibria, 14. Substituent-Induced Chemical Shifts along the C = N Bond of Schiff Bases (1992)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 125 (1992), S. 2033-2040 
    Details
    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.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19921250911
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  • 6
    Electronic Resource
    Electronic Resource
    Paving: A new approach to automated quadrilateral mesh generation (1991)
    Chichester [u.a.] : Wiley-Blackwell
    International Journal for Numerical Methods in Engineering 32 (1991), S. 811-847 
    Details
    ISSN: 0029-5981
    Keywords: Engineering ; Engineering General
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Mathematics , Technology
    Notes: This paper presents a new mesh generation technique, paving, which meshes arbitrary 2-D geometries with an all-quadrilateral mesh. Paving allows varying element size distributions on the boundary as well as the interior of a region. The generated mesh is well formed (i.e. nearly square elements, elements perpendicular to boundaries, etc.) and geometrically pleasing (i.e. mesh contours tend to follow geometric contours of the boundary). In this paper we describe the theory behind this algorithmic/heuristic technique, evaluate the performance of the approach and present examples of automatically generated meshes.
    Additional Material: 42 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/nme.1620320410
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  • 7
    Electronic Resource
    Electronic Resource
    A fast x-ray counting system (1993)
    New York, NY [u.a.] : Wiley-Blackwell
    X-Ray Spectrometry 22 (1993), S. 58-60 
    Details
    ISSN: 0049-8246
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: An unusually fast x-ray detector and pulse processing counting system has been devised and tested. The overall dead time of the system was determined experimentally to be 42 ns.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/xrs.1300220113
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  • 8
    Electronic Resource
    Electronic Resource
    Substituent-induced chemical shifts (SCS) by the phenyl group in sterically congested styrene derivativesSterically Congested Molecules, Part 7. For Part 6, see R. Knorr et al., Chem. Ber. 126, in press (1993). (1993)
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 31 (1993), S. 388-393 
    Details
    ISSN: 0749-1581
    Keywords: 13C NMR ; 1H NMR ; 9-Methylenefluorenes ; Substituent effects ; Substituent-induced chemical shifts ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The two 13C NMR methyl signals of the sterically congested 9-benzylidene-1,8-dimethylfluorene (1a) have the surprisingly small separation of only 0.37 ppm; for 9-benzylidene-2,7-dimethylfluorene the corresponding methyl separation is 0.04 ppm. An alternative analysis of 1a with respect to 1,8-dimethylfluorene shows that the perturbing syn-phenyl substituent has caused a downfield ( + 0.47 ppm) 13C shift but an upfield 1H shift ( - 0.97 ppm) of the compressed 1-CH3 group. For further comparisons, NMR assignments were also made for 2,7-dimethylfluorene, 1,8-dimethylfluoren-9-one and 2-(1,1-dimethylethyl)-3,3-dimethyl-1-phenylbut-1-ene.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/mrc.1260310415
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  • 9
    Electronic Resource
    Electronic Resource
    Substituent-induced chemical shifts along C=C double bondsSterically Congested Molecules, Part 8. For Part 7, see Ref. 6. (1993)
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 31 (1993), S. 557-565 
    Details
    ISSN: 0749-1581
    Keywords: 13C NMR ; 1H NMR Olefins ; Substituent effects ; Substituent-induced chenical shifts (SCS) ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 1H and 13C NMR signals were assigned and CH coupling constants (1J, 2J, 3J) determined for a series of α-mono-and α,α-disubstituted (1,1,3,3-tetramethyl-2-indanylidene)methanes with the following α-substituents: (mesityl)2B, n-propyl, phenyl, tert-butyl-C(=NH), cyano, (tert-butyl)2C(OH), pivaloyl, H2N-CO, PhNH-CO, carboxy, ritro, acetoxy, Me3SiO, Me3Si, PhS, PhSMe+, PhSO, PhSO2, bromo and trimethylstannyl. The 1J couplings with the olefinic proton span the range 124.3-193.7 Hz. Substituent-induced chemical shifts (SCS) of most of the nuclei with respect to the α-unsubstituted olefin obey simple additivity in the α,α-disubstituted compounds and are very similar to the SCS values along the C=N double bond in the isoelectronic (1,1,3,3-tetramethyl-2-indanylidene)amines within the error limits. The exceptions concern nuclei in the immediate vicinity of the perturbing substituent. A dominant mechanistic contribution of electric field effects appears likely for the more distant aromatic part of the indanylidene moiety. The chemical shifts of two (2,2,5,5-tetramethylcyclopentylidene)methanes are shown to be compatible with the SCS parameters from the indanylidene series.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/mrc.1260310608
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