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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Plant molecular biology 28 (1995), S. 381-389 
    ISSN: 1573-5028
    Keywords: metallothionein ; Oryza sativa ; stress
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract A novel rice genomic sequence encoding coding segments homologous to other metallothionein-like genes was isolated from Oryza sativa genomic library. This sequence, hereby designated as rgMT (rice genomic metallothionein-like gene), consists of two exons and one intron. From the coding sequence, it is predicted that rgMT encodes one protein of 74 amino acids. Differential expression of rgMT in rice plants was observed as mature transcripts were more abundant in roots than in leaves and sheaths. Under different stress conditions, such as excess heavy metals and heat shock, expression of rgMT was significantly elevated. This was especially noticeable with 250 μM CuCl2 for 16 h, 40°C heat for 2 h and 0.06% DMSO for 1 h. Under sucrose starvation, rgMT transcripts also increased with time up to 72 h. During recovery from sucrose starvation, the transcripts declined slightly within 12 h of recovery. rgMT transcripts were also seen to have increased expression in senescent leaves. These results support the notion that rgMT is a stress-inducible gene in rice heretofore unreported.
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Plant molecular biology 32 (1996), S. 525-529 
    ISSN: 1573-5028
    Keywords: metallothionein ; rice ; stress
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract A type 2 metallothionein-like gene from rice, OsMT-2 (Oryza sativa metallothionein-like gene-2), was isolated in its cDNA form and sequenced. By northern analyses OsMT-2 expression was shown to be induced under stress by sucrose starvation, heat shock and, to a lesser extent, abscisic acid, but not excess metals, including copper. Its response to sucrose starvation was transient and different from OsMT-1, a type 1 metallothionein-like gene of rice inducible by copper. These results suggest that while OsMT-2 is also involved in cellular response to stress, its function may be complementary to that of OsMT-1.
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Experimental and applied acarology 20 (1996), S. 215-222 
    ISSN: 1572-9702
    Keywords: Clofentezine ; toxicity ; metabolism ; Acaridae
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Clofentezine was toxic to bulb mite, Rhizoglyphus echinopus (Fumouze and Robin), eggs and larvae; however, it was not toxic to adults alone or in the presence of piperonyl butoxide. When adults were exposed to radioactive clofentezine, the acaricide was absorbed, metabolized and excreted. After 48 h exposure, 49.8% of the recovered radiocarbon was parent compound with 37.1, 9.1 and 3.6% detected in the container rinse, mite rinse and internal fraction, respectively. Homogenates of adults extensively metabolized clofentezine. The most active fraction was the 12 000 g supernatant plus glutathione followed in decreasing order by the supernatant, supernatant plus NADPH and the whole homogenate, each of which metabolized at least 16% of the acaricide. In the presence of piperonyl butoxide, in vitro metabolism of clofentezine by each of these active fractions was increased approximately 10%. Although it is possible that rapid metabolism could have contributed to the lack of toxicity of clofentezine to bulb mite adults, it is more likely that another major mechanism was involved. Perhaps adult bulb mites lack the sensitive target found in immature mites.
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Experimental and applied acarology 22 (1998), S. 343-351 
    ISSN: 1572-9702
    Keywords: Acaricides ; toxicity ; Acaridae
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Using a continuous exposure technique, the toxicity of 35 compounds to the bulb mite, Rhizoglyphus echinopus (Fumouze and Robin) was examined after 48 h. Sixteen acaricides yielded an LC50 of 〈1.0 mg cm2. The highest toxicity was exhibited by cyclodiene GABA antagonists (dieldrin, endrin and aldrin), some organophosphate (chlorpyrifos, diazinon and azinphosethyl) and carbamate (carbofuran) anticholinesterases and a thiazolidine flubenzimine. Oxythioquinox, fenazaflor, fenazaquin and amitraz were less toxic than the cyclodienes, organophosphates and carbamates. The sodium channel agonists (DDT and pyrethroids) and several specific acaricides with other modes of action were inactive (LC50 〉11.0 mg cm-2).
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 27 (1988), S. 1641-1654 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Weight-average molecular weights Mw, second virial coefficients, and z-average radii of gyration 〈S2〉1/2z were determined by light scattering as a function of temperature T for four sodium salt samples of xanthan in 0.01M aqueous NaCl, in which the polysaccharide undergoes an order-disorder conformation change with increasing T. The data for 〈S2〉1/2z and Mw at 25 and 80°C, the lowest and highest temperatures studied, confirmed the previous conclusion that the predominant conformation at the former T, i.e., in the ordered state, is a double helix, while that at the latter T, i.e., in the disordered state, is a dimerized coil expanded by electrostatic repulsions between charged groups of the polymer. As T was increased from 25 to 80°C, 〈S2〉1/2z sigmoidally decreased or increased depending on the dimer's molecular weight. This temperature dependence of 〈S2〉1/2z and that determined elsewhere for a high molecular weight sample were found to be described almost quantitatively by a simple dimer model in which the double helix melts from both ends, when the double-helical fraction in the dimer at a given T estimated previously from optical rotation data was used.
    Additional Material: 7 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 36 (1998), S. 2899-2903 
    ISSN: 0887-624X
    Keywords: cationic ring-opening polymerization ; poly(1,3-dioxepane) triol ; 2,2-bis(hydroxymethyl)butanol ; transacetalization ; activated monomer mechanism ; activated chain mechanism ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Cationic polymerization of 1,3-dioxepane (DOP) initiated by triflic acid was carried out in the presence of 2,2-bis(hydroxymethyl)butanol (BHMB). The structure and molecular weight of the products were characterized by GPC and NMR spectra. The results showed that molecular weight of the polyacetal obtained could be controlled by the initial mole ratio of DOP/BHMB. GPC showed that as the mole ratio of BHMB/DOP increased, the content of cyclic oligomers also increased. Proton, 13C and 2D HMQC-fg NMR demonstrated that no hydroxymethyl group of BHMB appeared as an end group. It was also illustrated by proton NMR that some BHMB units existed in cyclic oligomers. The mechanism of formation of cyclic oligomers was discussed. © 1998 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 36: 2899-2903, 1998
    Additional Material: 4 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Biotechnology and Bioengineering 35 (1990), S. 185-194 
    ISSN: 0006-3592
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: A mathematical model of the tryptophan operon is analyzed to investigate the regulatory effects of feedback repression and the demand for tryptophan in the cell. In this model, feedback repression is considered to be a two-step process. First, the endproduct tryptophan combines with the inactive repressor produced by the regulatory genes to yield an active complex. This complex subsequently binds to the operator and prevents transcription of the structural genes into mRNA. The demand for tryptophan in the cell is modeled by a hyperbolic saturation function of the Michaelis-Menten type. Results are obtained for the expression of the tryptophan operon in Escherichia coli and their applicability to tryptophan production by microbial fermentation is discussed. It is shown that, depending on the strain level of the operon and the rate of utilization of tryptophan in the cell, an overproduction of tryptophan can be achieved under stable operating conditions; in other circumstances, the operon may become stable or unstable, and may lead to a periodic synthesis.
    Additional Material: 5 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 11 (1998), S. 397-406 
    ISSN: 0894-3230
    Keywords: bond dissociation energy ; acidity ; phenylsulfenylamides ; phenylsulfenylanilides ; Chemistry ; Theoretical, Physical and Computational Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Acidities and bond dissociation energies (BDEs) of the N-H bond in two phenylsulfenylamides, PhSNHBz and PhSNH-t-Bu, and four phenylsulfenylanilides, 4-GC6H4NHSPh, where G  =  MeO, H, Br and CN, were measured in order to compare the effects of substituents on acidities and BDEs of N - H bonds with those of C - H bonds. The effects of PhS groups on acidities and BDEs in a series of C - H acids were found to be comparable to those on acidities and BDEs of PhS in a similar series of N - H acids. Comparisons were also made of the effects of changing the oxidation state of sulfur in the series PhS, PhSO and PhSO2 on the acidities and BDEs of adjacent N - H and C - H bonds in weak acids. Hammett-type plots of pKHA values for phenyl benzyl sulfones (4-GC6H4CH2SO2Ph) and phenylsulfenylanilides (4-GC6H4NHSPh) were linear vs σp- values. A linear plot was obtained and explained for a plot of BDE of the N - H bonds in remotely substituted phenylsulfonylanilides with σ+ values. Plots of BDEs vs Eox(A-) were also linear for 4-substituted phenylsulfenylanilides (4-GC6H4NHSPh), phenylsulfonylanilides (4-GC6H4NHSO2Ph) and phenyl benzyl sulfones (4-GC6H4CH2SO2Ph). © 1998 John Wiley & Sons, Ltd.
    Additional Material: 7 Tab.
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  • 9
    ISSN: 1434-1948
    Keywords: Rare earth complexes ; Naphthalocyaninato ligand ; Double-decker complexes ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A series of rare earth(III) double-deckers RE[Nc(tBu)4]2 [RE = La, Ce, Pr, Nd, Eu, Gd, Tb, Y, Er; Nc(tBu)4 = dianion of tetra(tert-butyl)-2,3-naphthalocyanine] (1-9) have been prepared by treating RE(acac)3·n H2O (acac = acetylacetonate) with 6-tert-butylnaphthalonitrile in refluxing n-octanol in the presence of 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU). These novel sandwich-type complexes have been spectroscopically characterized. The electrochemical studies show that the first oxidation and the first reduction potentials increase with the size of the central metal ions with a relatively small separation (0.28-0.33 V), reflecting the narrow HOMO-LUMO gap.
    Additional Material: 5 Ill.
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  • 10
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Six samples of Na xanthan in 0.01M aqueous NaCl containing 0.01 N HCl (pH = 2) were studied by light scattering and viscosity. This study was motivated by the finding that the intrinsic viscosity [η] fairly sharply decreased when the pH of the solvent was lowered from about 6 to 2 by adding HCl to 0.01M aqueous NaCl in which Na xanthan dissolves as rigid dimers having a double-helical structure. The data for weight-average molecular weight, radius of gyration, and [η] showed that Na xanthan at pH = 2 remains a dimer behaving as a semiflexible chain. Data analysis in terms of known theories for unperturbed wormlike chains yielded 0.47 ± 0.02, 2.0 ± 0.6, and 68 ± 7 nm for the contour length h per main-chain residue, diameter d, and persistence length q of the dimer, respectively. these h and d values agreed with the pitch per main-chain residue and the diameter of the double helix of Na xanthan in 0.01 or 0.1M aqueous NaCl. However, the q value, which was close to the intrinsic persistence length q0 ( = q in the absence of electrostatic interaction) of Na xanthan at pH = 2, was much smaller than the q0 (106 nm) of this helix. We concluded that the xanthan dimer at pH = 2 assumes a double-helical structure, which is geometrically the same as, but is more flexible than, that at neutral pH.
    Additional Material: 5 Ill.
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