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  • Genetics  (4)
  • Physical Chemistry  (3)
  • Purification
  • 1995-1999  (9)
  • 1985-1989
  • 1998  (4)
  • 1995  (5)
  • 1
    ISSN: 0749-503X
    Keywords: LFH deletion cassette ; functional analysis ; chromosome IV ; Saccharomyces cerevisiae ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: We report here the construction of six deletion mutants and the analysis of their basic phenotype. Deletion cassettes containing the KanMX4 marker module and long flanking regions homologous to the target locus were constructed for each of the six open reading-frames (ORFs YDL088c, YDL087c, YDL086w, YDL085w, YDL084w and YDL082w) located on chromosome IV. Sporulation and tetrad analysis of heterozygous deletant strains revealed that, in the FY1679 genetic background, ORFs YDL088c, YDL087c and YDL084w are essential genes for vegetative growth whereas YDL086w, YDL085w and YDL082w are non-essential. ydl088cΔ and ydl084wΔ haploid strains are viable in the CEN. PK2 genetic background although ydl084wΔ grows at a slower rate than the wild type. Complementation tests by corresponding cognate genes confirmed that gene inactivation was responsible for these growth defects. © 1998 John Wiley & Sons, Ltd.
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  • 2
    ISSN: 0749-503X
    Keywords: Saccharomyces cerevisiae ; chromosome VII ; ribonuclease PH ; HGH1 ; YGR187c ; YGR189c ; YGR194c ; YGR195w ; YGR196c ; YGR198w ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: We have deleted six different ORFs of unknown function located on the right arm of Saccharomyces cerevisiae chromosome VII; namely, YGR187c/HGH1, YGR189c, YGR194c, YGR195w, YGR196c and YGR198w. No basic phenotypes could be attributed to the strains deleted in any of genes YGR187c/HGH1, YGR189c, YGR194c and YGR196c. These deletants did not show mating, sporulation or growth defects under any of the conditions tested. However, spores bearing deletions in either the YGR195w or YGR198w genes were unable to develop into macroscopical colonies. The YGR195w gene product shows significant homology with bacterial ribonuclease PH, an enzyme hitherto undescribed in yeasts, and its deletion causes a loss of viability after one to three rounds of cell division. Overexpression of this gene, using a tetracycline-regulatable promoter system, did not cause any effect on the cells. Contrary to what has been reported for prokaryotic homologs, this enzyme could play an essential role in yeast cell biology. The product encoded by the other essential ORF, YGR198w, shows no significant homology with any protein of known function in the databases. Spores bearing the deletion usually germinate and give rise to microcolonies of 50-100 non-viable cells. © 1998 John Wiley & Sons, Ltd.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Yeast 11 (1995), S. 425-433 
    ISSN: 0749-503X
    Keywords: Yarrowia lipolytica ; orotate phosphoribosyl transferase ; nucleotide sequence ; transcription ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: The URA5 gene of Yarrowia lipolytica encoding the orotate phosphoribosyl transferase (OPRTase, EC2.4.2.10) was isolated by target integration in a mutant strain originally named ura2.21. The nucleotide sequence of the gene predicts a protein with high similarities with the OPRTases from Saccharomyces cerevisiae, Podospora anserina and Escherichia coli and to a lesser extent with that of Dictyostelium discoideum. The transcription start point has been mapped by primer extension analysis and indicates the existence of a long leader sequence in the corresponding mRNA. Northern-blot hybridization revealed the URA5 transcript to be approximately 0·94 kb. Deletion of the URA5 gene in Y. lipolytica produced a leaky phenotype similar to the one described for the ura5 mutation in S. cerevisiae. The URA5 gene of Y. lipolytica was able to complement functionally the ura5 mutation of S. cerevisiae. The sequence presented here has been submitted to the EMBL data library under Accession Number Z22571.
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  • 4
    ISSN: 0749-503X
    Keywords: yeast genome ; chromosome VII ; histidine permease ; glyceraldehyde-3-phosphate dehydrogenase ; pyruvate dehydrogenase ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: We report the sequence of a 9037 bp fragment from the right arm of Saccharomyces cerevisiae chromosome VII. Analysis of the sequence revealed four complete open reading frames (ORFs), namely G7572, G7576, G7579 and G7584. The first three corresponded, respectively, to the previously cloned genes: HIP1, coding for a high-affinity histidine-specific permease, TDH1, one of the known genes coding for glyceraldehyde-3-phosphate dehydrogenase and ODPX, which encodes a precursor of protein X, a component of the pyruvate dehydrogenase complex. The ORF G7584 showed 35·8% identity with a hypothetical protein of Caenorhabditis elegans chromosome 3. The reported sequence has been deposited in the EMBL data library under Accession Number X82408.
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Electrophoresis 19 (1998), S. 1117-1126 
    ISSN: 0173-0835
    Keywords: Purification ; Free-flow electrophoresis ; Transport phenomena ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Free-flow zone electrophoresis may be used to purify biological samples, due to differences in electrophoretic mobility, in absence of a matrix - most frequently a gel - thus enabling the biological integrity of even fragile molecules to be preserved. However, the process is more complicated than its principle suggests due to different transport phenomena interfering with electrophoretic migration, with the resultant separation depending both on separation effects and dispersive phenomena. The physical origin of the main effects involved was identified. Mathematical expressions were proposed to estimate the influence of the crescent effect and electrohydrodynamics on the process. In this paper, these equations are used to determine the minimum difference in electrophoretic mobility required for a separation to be achieved with respect to the processing parameters. A methodology is proposed which defines the conditions under which the difference in electrophoretic mobilities equals that calculated when considering the influence of dispersive phenomena. Optimized separations of the whey proteins lactoferrin and albumin, known to interact strongly, and the purification of a monoclonal antibody from a mouse ascitic fluid illustrate the approach.
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Electrophoresis 19 (1998), S. 1294-1299 
    ISSN: 0173-0835
    Keywords: Isoelectric focusing ; Continuous free flow electrophoresis ; Purification ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: To estimate the feasibility of isoelectric focusing in a continuous mode, the conditions for obtaining stable and linear pH gradients were first investigated, using a mixture of carrier ampholytes. Then the operating parameters allowing the isoelectric focusing of bovine serum albumin as model protein were determined. A theoretical approach was used to find conditions minimizing the electrohydrodynamic effect, mainly responsible for protein dispersion, for the separation of bovine serum albumin and α-lactalbumin from bovine milk.
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  • 7
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction between Co(en)2(2-pzCO2)2+ (bis-ethylenediamine (2-pyrazinecarboxylato)cobalt(III)) and Fe(CN)5H2O3- (aquopentacyanoferrate(II)) to form the binuclear complex [(en)2Co( μ-pzCO2)Fe(CN)5]- has been studied in several isodielectric binary mixtures at 298.2 K (cosolvents: methanol, ethanol, tertbutyl alcohol, ethyleneglycol, and glycerol). Results were rationalized by using a free energy relationship. The importance of correcting the rate constants obtained in the different mixtures from the ionic strength influence has been shown. © 1995 John Wiley & Sons, Inc.
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  • 8
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Time-resolved investigations of the atomic resonance fluorescence Sr(53P1 → 51S0) and the molecular chemiluminescence from SrCl(A2Π1/2,3/2, B2Σ+ → X2Σ+) are reported following the reaction of the electronically excited strontium atom, Sr(5s5p(3PJ)), 1.807 eV above its 5s2(1S0) electronic ground state, with CH2Cl2. The optically metastable strontium atom was generated by pulsed dye-laser excitation of ground state strontium vapor to the Sr(53P1) state at λ = 689.3 nm (Sr(53P1 ← 51S0)) at elevated temperature (850 K) in the presence of excess helium buffer gas in which rapid Boltzmann equilibration within the 53PJ manifold takes place. Sr(53PJ) was then monitored by time-resolved atomic fluorescence from Sr(53P1) at the resonance wavelength together with chemiluminescence from electronically excited SrCl resulting from reaction of the excited atom with CH2Cl2. The molecular systems recorded in the time-domain were SrCl(A2Π1/2 → X2Σ+) (Δν = 0, λ = 674 nm), SrCl(A2Π3/2 → X2Σ+) (Δν = 0, λ = 660 nm), and SrCl(B2Σ+ → X2Σ+) (Δν = 0, λ = 636 nm). Both the A2Π (179.0 kJ mol-1) and (B2Σ+(188.0) kJ mol-1) states of SrCl are energetically accessible on collision between Sr(3P) and CH2Cl2. Exponential decay profiles for both the atomic and molecular (A,B - X) chemiluminescence emission are observed and the first-order decay coefficients characterized in each case. These are found to be equal under identical conditions and hence SrCl(A2Π, B2Σ+) are shown to arise from direct Cl-atom abstractions on reaction with this halogenated species. The combination of integrated molecular and atomic intensity measurements, coupled with optical sensitivity calibration, yields estimations of the branching ratios into the A1/2,3/2, B, and X states arising from Sr(53 PJ) + CH2Cl2 which are found to be as follows: A1/2, 3.0 × 10-3; A3/2, 1.7 × 10-3; B, 4.4 × 10-4 yielding ΣSrCl(A1/2 + A3/2 + B) = 5.1 × 10-3. As only the X, A and B states of SrCl are accessible on reaction, this indicates an upper limit for the branching ratio into the ground state of 0.995. The present results are compared with previous time-resolved measurements on SrF, Cl, Br(A2Π,B2Σ+ - X2Σ+) that we have reported on various halogenated species and with analogous chemiluminescence studies on Sr(3P) with other halides obtained from molecular beam measurements. The results are further compared with those from a series of previous analogous investigations in the time-domain we have presented of molecular emissions from CaF, Cl, Br, I (A,B - X) arising from the collisions of Ca(43PJ) with appropriate halides and with branching ratio data for Ca(43PJ) obtained in beam measurements. © 1995 John Wiley & Sons, Inc.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 27 (1995), S. 525-534 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The oxidation of Fe(bpy)22+ by peroxodisulphate (bpy = 2,2′-bipyridine) has been studied in a variety of sodium bis(2-ethylhexyl)sulfosuccinate(aerosol-OT or AOT)-oil-water microemulsions by changing the nature of the oil phase, the surfactant concentration, and the molar ratio w = [H2O]/[AOT]. Kinetic results show that the influence of surfactant concentration is due to a dilution effect. On the other hand, the comparison between the reaction rate in conventional aqueous solution with that in AOT w/o microemulsions seems to indicate that the iron(II) species is distributed between the aqueous phase and the interphase. © 1995 John Wiley & Sons, Inc.
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