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  • Chemistry  (8)
  • Brassica oxyrrhina  (2)
  • Gnetum ula  (2)
  • 1
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Phytochemistry 20 (1981), S. 1455-1456 
    ISSN: 0031-9422
    Keywords: Gnetaceae ; Gnetum ula ; acetophenones ; bergenin ; isocoumarin. ; stilbene
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Phytochemistry 24 (1985), S. 622-624 
    ISSN: 0031-9422
    Keywords: Gnetaceae ; Gnetum ula ; stilbenes ; structure ; structure revision. ; synthesis
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Theoretical and applied genetics 79 (1990), S. 285-287 
    ISSN: 1432-2242
    Keywords: Cytoplasmic male sterility ; Brassica oxyrrhina ; B. campestris ; B. juncea ; Alien gene transfer
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Synthetic alloploid Brassica oxyrrhina (2n = 18, OO) x B. campestris (2n = 20, AA) was repeatedly backcrossed with B. campestris to place B. campestris nucleus in the cytoplasm of B. oxyrrhina. Alloplasmic plants, obtained in BC5 generation, were stably male sterile but mildly chlorotic during initial development. Synthetic alloploid B. oxyrrhina-campestris was also hybridized with B. juncea to transfer B. oxyrrhina cytoplasm. Segregation for green and chlorotic plants was observed in BC1 and BC2 generations. By selection, however, normal green male sterile B. juncea was obtained in BC3. Pollen abortion in both B. campestris and B. juncea is post-meiotic.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1432-2242
    Keywords: Key words Chromosome addition line ; Synteny group ; Brassica campestris ; Brassica oxyrrhina ; Monosomic ; Alloplasmic ; RAPD
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract  Monosomic chromosome addition lines of Brassica oxyrrhina in the background of alloplasmic B. campestris carrying B. oxyrrhina cytoplasm were generated and characterised through morphology, cytology and molecular (RAPD) analysis. Four successive backcrosses of the synthetic alloploid B. oxycamp with B. campestris yielded 24 monosomic addition plants that were grouped into seven different synteny groups based on morphological similarity and RAPD patterns. Each synteny group exhibited morphological features diagnostic for the presence of individual B. oxyrrhina chromosomes including some novel phenotypes. Meiotic studies of the addition lines revealed the homoeology of four B. oxyrrhina chromosomes (synteny groups 1, 3, 5 and 6 ) with B. campestris chromosomes as indicated by trivalent associations, with the highest homoeology (44.23%) in synteny group 1 and the lowest (6.1%) in synteny group 3. Seed fertility of the addition lines ranged from 94.85% (synteny group 1) to 56.98% (synteny group 5). All of the addition lines were male-sterile except synteny group 6 which had 12–16% stainable pollen. Ovule transmission of the B. oxyrrhina chromosomes added to the progenies of addition lines ranged from 23.52% (synteny group 6) to 14% (synteny group 7). RAPD analysis confirmed the validity of synteny grouping based on morphological observations. Approximately 45% of the primers studied were informative, giving B. oxyrrhina-specific RAPD bands unique for each synteny group, except group 6.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The lone-pair orbital interactions arising in a phosphodiester are incorporated into semiempirical conformational energy calculations using a unifold “torsional potential” around the virtual bond linking the ester oxygen atoms. The results explain the observed experimental data better than other methods.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Biotechnology and Bioengineering 46 (1995), S. 621-626 
    ISSN: 0006-3592
    Keywords: microencapsulation ; urea ; ammonia ; alginate-poly-L-lysine-alginate (APA) ; artificial cells ; mechanical strength ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: This article describes a novel method of urea and ammonia removal using microencapsulated, genetically engineered Escherichia coli DH5 cells. Optimization of bacterial cell encapsulation was carried out. The optimal method consists of alginate 2.00% (w/v) at a flow rate of 0.0724 mL/min and a coaxial air flow rate of 2.00 L/min. This produces spherical, alginate-poly-L-lysine-alginate (APA) microcapsules of an average 500 ± 45 μm diameter. Increasing the concentration of alginate from 1.00% to 1.75% improves the quality of the microcapsules, while cell viability remains unaffected. The APA microcapsules are mechanically stable up to 210-rpm agitation with no bacterial cell leakage. The in vitro performance of urea and ammonia removal by encapsulated bacteria is assessed. One hundred milligrams of bacterial cells in APA microcapsules, in their log phase state of growth, can lower 87.89 ± 2.25% of the plasma urea within 20 min and 99.99% in 30 min. The same amount of encapsulated bacteria can also lower ammonia from 975.14 ± 70.15 μM/L to 81.151 ± 7.37 μM/L in 30 min. There are no significant differences in depletion profiles by free and encapsulated bacteria for urea and ammonia removal. This novel approach using microencapsulated, genetically engineered E. coli cells is significantly more efficient than presently available methods of urea and ammonia removal. For instance, it is 30 times more efficient than the standard urease-ammonium adsorbent system. © 1995 John Wiley & Sons, Inc.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 36 (1967), S. 24-28 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Reactions of tantalum pentaalkoxides (ethoxide, isopropoxide and tertiarybutoxide with acetyl bromide give the products: Ta(OEt)4Br; Ta(OEt)3Br2; Ta(OEt)2Br3 · MeCO2Et; Ta(OEt)Br4 · MeCO2Et; Ta(OPr1)4Br; Ta(OPr1)3Br2; Ta(OPr1)2Br3 · MeCO2Pr1; TaOBr3. MeCo2Pr1; Ta(OBut)4Br and TaOBr3 · MeCO2But. These products were found to be viscous liquids or solids. All these bromide alkoxides except the tertiarybutoxide derivatives were found to be soluble in benzene. The tetraalkoxide monobromide derivatives could either be distilled or sublimed unchanged under reduced pressure. The tetraalkoxide monobromide derivative was found to be dimeric in boiling benzene.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Existing data on the self-reactions of tertiary peroxy radicals RO2 has been reanalyzed and corrected to deduce Arrhenius parameters for both termination and nontermination paths. For R = t-Butyl, these are logkt(M-1sec-1) = 7.1 - (7.0/θ) and logknt(M-1sec-1) = 9.4 - (9.0/θ), respectively, different from those recommended by other authors. The higher magnitudes observed for termination processes of tertiary peroxy radicals like those of cumyl and 1,1-diphenylethyl have been discussed in terms of a much greater cage recombination of cumyloxy radicals as contrasted with t-butoxy radicals. It is shown that for benzyl peroxy radicals, the R - O·2 bond dissociation energy is sufficiently low (18-20 kcal) that reversible dissociation into R· + O2 opens a competing second-order path to fast recombination R· + RO·22 → ROOR. This path is probably not important for cumyl peroxy radicals under usual experimental conditions but can become important for 1,1-diphenyl ethyl peroxy radicals at (O2) 〈 10-3M. At very low RO·2 concentrations (〈10-5M), in the absence of added O2, an apparent first-order disappearance of RO·2 can occur reflecting the rate determining breaking of the cumyl - O·2 bond followed by the second step above. The thermochemistry of RO·n is used to show that the reaction of R2O4 → 2RO + O2 must be concerted and cannot proceed via RO·3 which is too unstable and cannot form even from RO· + O2.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A chain mechanism is proposed to account for the very rapid termination reactions observed between alkyl peroxy radicals containing α-C - H bonds which are from 104 to 106 faster than the termination of tertiary alkyl peroxy radicals. The new mechanism is with termination by. \documentclass{article}\pagestyle{empty}\begin{document}$ {\rm R}\overline {{\rm CHOO}} $\end{document} is the zwitterion originally postulated by Criegee to account for the chemistry of O3-olefin addition. Heats of formation are estimated for \documentclass{article}\pagestyle{empty}\begin{document}$ \overline {{\rm CH}_2 {\rm OO,}} {\rm }\overline {{\rm RCHOO}} $\end{document}, and \documentclass{article}\pagestyle{empty}\begin{document}$ ({\rm C}\overline {{\rm H}_3 )_2 {\rm COO}} $\end{document} and it is shown that all steps in the mechanism are exothermic. The second step can account for (1Δ)O2 which has been observed. k1 is estimated to be 109-2/θ liter/M sec where θ = 2.303RT in kcal/mole. The second and third steps constitute a chain termination process where chain length is estimated at from 2 to 10. This mechanism for the first time accounts for minor products such as acid and ROOH found in termination reactions. Trioxide (step 3) is shown to be important below 30°C or in very short time observations (〈10 s at 30°C). Solvent effects are also shown to be compatible with the new mechanism.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 12 (1980), S. 169-181 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Data on the liquid-phase oxidation of isobutane at 50 and 100°C have been reexamined, using a modified mechanism to take into account the termination by isobutylperoxy radicals. Algebraic expressions are derived from steady-state methods. Using Arrhenius parameters fitted by transition-state A factors and activation energies derived from observed “best” rate constants, new sets of parameters are derived for the rate constants for propagation by t—BuO2 + t—BuH → t-BuO2H + t—Bu⋅: \documentclass{article}\pagestyle{empty}\begin{document}$$ k_4 \, = \,1 \times 10^{8 - 14.5/{\rm \theta }} {\rm M}^{{\rm - 1}} \sec ^{ - 1} $$\end{document} where θ = 2.303RT in kcal/mol. This, together with new values for the termination parameters and rates of i-butyl production by k4B, is shown to give good agreement with the published data. An important reaction:\documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm R}'{\rm O}_{2}^{.} + {\rm RO}_{2} {\rm H}\mathop{{\buildrel{-\!\!\longrightarrow}\over{\longleftarrow}}}\limits^{{\rm 12}}{\rm R'O}_{\rm 2} {\rm H} + {\rm RO}_{2}^{.} $$\end{document} is shown to quench the possible contributions to termination of adventitious radicals such as CH3O⋅2.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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