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  • ASTROPHYSICS  (30)
  • Analytical Chemistry and Spectroscopy  (15)
  • Biochemistry and Biotechnology  (9)
  • 1990-1994  (54)
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Year
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Biotechnology and Bioengineering 37 (1991), S. 627-638 
    ISSN: 0006-3592
    Keywords: solubility parameters ; hydrophobicity index ; Hansen parameter ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Widespread commercial application of enzymes as catalysts for specialty or commodity chemical synthesis will require their use in nonaqueous systems. While a number of non-aqueous enzyme applications have been demonstrated, the lack of useful rules for predicting enzyme-solvent interactions has hindered the development of this technology. Both Hildebrand and solvent hydrophobicity (octanol-water partition coefficient) parameters have been used previously to correlate and predict enzyme activity in nonaqueous systems, with some success, but any single-parameter approach is inherently limited in its ability to reflect the spectrum of possible enzyme-solvent interactions. Therefore, this study evaluates the three-dimensional solubility parameter space, as proposed by Hansen, to correlate and predict enzyme activity in microaqueous, miscible, and biphasic nonaqueous systems. Preliminary results suggest that Hansen parameters may be useful for correlating nonaqueous enzyme activity, and that the dispersive and polar parameters may be disproportionately important in single-phase microaqueous systems. The Hansen hydrogen-bonding parameter appears to be the only parameter yet evaluated capable of correlating the water requirement for enzyme activity in microaqueous systems, suggesting that water affects protein structure through enthalpic rather than entropic processes in nonaqueous systems. Insufficient data are available for miscible and biphasic systems, but it is proposed that enzyme activity may correlate with the average solubility parameters of miscible systems and of the aqueous phase in biphasic systems.
    Additional Material: 15 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 26 (1991), S. 1057-1060 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: It is shown that the position of the double bond close to the hydrocarbon end of an aliphatic diene functionalized at C(1) can readily be determined by chemical ionization with NO+. Owing to the low abundance of the ions characteristic for the position of the other double bond, its localization may be difficult. Measurement of the chemical ionization (nitric oxide as reagent gas) spectra of the corresponding epoxides or collision activation studies can help.
    Additional Material: 5 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 28 (1993), S. 1353-1361 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS) has the potential for providing a rapid alternative to gel electrophoresis for DNA sequence analysis provided that an intense mass spectrometric response can be obtained from mixtures of DNA fragments containing up to 300 nucleotides. MALDI-MS has not yet proved viable for such analyses because the MS response falls off rapidly for mixed-base DNA fragments containing more than 20-30 nucleotides. Previous studies have demonstrated that base composition is a critical factor in the MALDI-MS response of oligodeoxyribonucleotides. This paper describes an investigation of the physical roots of the observed influence of base composition on the mass spectrometric response, focusing on homopolymer oligodeoxyribonucleotides (dT7, dT10, dT18, dT36, dG7, dG10, dG18, dI18 and dU18) and dT5G5. Forty-eight different matrix compounds were tested for their ability to produce laser desorption masses spectra from such homopolymer oligodeoxyribonucleotides. Considerably stronger mass spectrometric responses were obtained from polydeoxythymidines than from polydeoxyguanosines, polydeoxycytidines and polydeoxyadenosines. Although mass spectral peaks corresponding to dT18 were observed from 20 of the matrices studied, no discernible response was observed for dG18 from any of these matrices. To elucidate the physical basis for origins of the observed differences in response, a number of factors were investigated including the ionization efficiency, the tendency towards fragmentation and the extent to which the oligodeoxyribonucleotides were incorporated into the matrix crystals. The results of these experiments indicate that low ionization efficiency is not a likely main contributor to the low response to polydeoxyguanosines, fragmentation is a likely main contributor to the low response to polydeoxyguanosines, the overall incorporation of polydeoxyguanosines into matrix crystals is comparable to that for polydeoxythymidines and the exocyclic amino group of guanosine, adenosine and cytidine has a strong inhibitory effect on the mass spectrometric response.
    Additional Material: 8 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 21 (1992), S. 554-559 
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Non-derivatized gibberellin glucosyl conjugates were analysed by capillary reversed-phase high-performance liquid chromatography/mass spectrometry. Positive as well as negative ion mass spectra were obtained by frit fast atom bombardment. The spectra were found to provide useful information for the identification and structural elucidation of the glucosyl conjugates.
    Additional Material: 6 Ill.
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  • 5
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Some partial synthetic amino acid ((S)-alanine, (S)-leucine, (S)-isoleucine, (S)-aspartic acid, (S)-glutamic acid, (S)-phenylalanine, (S)- and (R)-valine) conjugates of the plant growth regulator (-)-jasmonic acid (JA) were investigated as methyl esters by capillary gas chromatography/mass spectrometry. By gas chromatographic data (retention indices) as well as by mass spectral behaviour all these substances can be differentiated unequivocally. In addition, the distinction between the leucine and isoleucine JA conjugates was carried out by mass-analysed ion kinetic energy spectroscopy (tandem mass spectrometry). Based on this some naturally occurring (S)-isoleucine conjugates of (-)-JA, (+)-7-iso-JA and related compounds as well as the (S)-leucine and (S)-phenylalanine conjugates of (-)-JA could be identified from extracts of the broad bean Vicia faba L.
    Additional Material: 16 Ill.
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  • 6
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A specific assay is described for the confirmatory identification of danofloxacin residues in edible tissues of cattle and chicken. The assay utilizes on-line microbore high-performance liquid chromatography and pneumatically assisted electrospray tandem mass spectrometry (MS/MS). Collision-induced dissociation of the danofloxacin protonated molecule results in two significant daughter ions. Monitoring both ions provides the specificity required for this confirmatory assay. Optimum electrospray and MS/MS operating conditions permitted the specific monitoring of danofloxacin and the confirmation of its residues in chicken and cattle liver extracts down to 50 ppb. The analysis of control liver or the commercially available antibacterial quinolones enrofloxacin and its metabolite ciprofloxacin gave no response under the assay conditions. The ratios of the two daughter ions were similar for danofloxacin standard solutions, fortified tissues and incurred tissues.
    Additional Material: 3 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Microcolumn Separations 6 (1994), S. 115-125 
    ISSN: 1040-7685
    Keywords: gas chromatography ; stationary phases ; liquid crystal polysiloxane ; C18 polysiloxane ; shape selectivity ; polycyclic aromatic hydrocarbons ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Column selectivity is examined for a series of smectic liquid crystalline columns and is compared with methyl and C18 polysiloxane columns for the separation of polycyclic aromatic hydrocarbon (PAH) isomers. A set of extended and condensed solute probes is described that provides a sensitive indication of variations in column shape selectivity. Examples of shape selectivity differences are presented for smectic liquid crystalline columns and 5% phenyl polysiloxane columns using various PAH isomer sets. Variations in selectivity have been observed among different smectic liquid crystalline columns, and this problem appears more significant than for methyl polysiloxane columns. The selectivity ration for tetraphenylmethane and p-terphenyl provides a sensitive indication of column shape selectivity, with a change in elution order occurring between ordered (smectic liquid crystalline) columns and non-ordered (methyl polysiloxane) columns. Shape selectivity differences indicated by this test mixture are apparent for more complex PAH isomer mixtures. Despite stationary phase selectivity variability, smectic liquid crystalline columns offer considerable potential for solving difficult separation problems involving structured solutes.
    Additional Material: 10 Ill.
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  • 8
    ISSN: 0951-4198
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: Olefinic aliphatic compounds can be transformed on a microscale into the corresponding epoxides by reaction with m-chloroperbenzoic acid. The crude reaction mixture can be analysed without further work-up, by gas chromatography followed by chemical ionization mass spectrometry or desorption chemical ionization mass spectrometry with nitric oxide as the chemical ionization gas.
    Additional Material: 3 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Rapid Communications in Mass Spectrometry 4 (1990), S. 24-29 
    ISSN: 0951-4198
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: A simple method for off-line coupling of desorption mass spectrometry and capillary-zone electrophoresis (CZE) is described. Use of a “porous glass joint”, near the cathodic end of the CZE column, facilitates fraction collection in a manner similar to that used with liquid chromatography. This method allows independent optimization of both the CZE and mass spectrometry parts of the experiment. It is directly applicable to a number of desorption mass spectrometry methods (including plasma desorption (PD) and UV laser desorption (LD)). In the present study, PD mass spectrometry was used for eluant characterization. The fraction collection procedure is described, as is mass transfer through the porous glass joint. Detection limits are discussed and the approach is illustrated by analysis of a simple mixture of bradykinin derivatives. Finally, a brief comparison to current on-line CZE/mass spectrometric methods is presented.
    Additional Material: 8 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Cell Biochemistry and Function 8 (1990), S. 227-232 
    ISSN: 0263-6484
    Keywords: Energy-consuming processes ; rat hepatocytes ; oxygen consumption ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: A method for the quantification of energy consuming processes described by Siems et al.6 for reticulocytes and by Müller et al.10 for ascites tumour cells was applied to balance the ATP-consumption of isolated rat hepatocytes. On the basis of decreased coupled respiration rates following the specific inhibition of energy-requiring reactions, the energy demands of protein turnover, nucleic acid synthesis, Na+/K+-ATPase and Ca2+-transport of hepatocytes in different incubation media were assessed. These processes together with urea synthesis account for about 60 per cent of the total energy consumption in a glucose and amino acid-enriched Eagle/Borsook medium. The metabolic flux rates of total ATP-consumption and ATP-consumption of single energy-requiring processes in hepatocytes are compared with those in reticulocytes and different tumour cell types.
    Additional Material: 3 Ill.
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