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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Analytical chemistry 58 (1986), S. 2704-2708 
    ISSN: 1520-6882
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of chemical & engineering data 39 (1994), S. 608-610 
    ISSN: 1520-5134
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Bulletin of environmental contamination and toxicology 45 (1990), S. 228-231 
    ISSN: 1432-0800
    Source: Springer Online Journal Archives 1860-2000
    Topics: Energy, Environment Protection, Nuclear Power Engineering , Medicine
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Bulletin of environmental contamination and toxicology 53 (1994), S. 280-284 
    ISSN: 1432-0800
    Source: Springer Online Journal Archives 1860-2000
    Topics: Energy, Environment Protection, Nuclear Power Engineering , Medicine
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Bulletin of environmental contamination and toxicology 40 (1988), S. 66-68 
    ISSN: 1432-0800
    Source: Springer Online Journal Archives 1860-2000
    Topics: Energy, Environment Protection, Nuclear Power Engineering , Medicine
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Bulletin of environmental contamination and toxicology 43 (1989), S. 505-510 
    ISSN: 1432-0800
    Source: Springer Online Journal Archives 1860-2000
    Topics: Energy, Environment Protection, Nuclear Power Engineering , Medicine
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Environmental management 13 (1989), S. 325-332 
    ISSN: 1432-1009
    Keywords: Hydrocarbon contamination ; Bioreclamation ; Biorestoration ; Oil spill ; Biodegradation of petroleum
    Source: Springer Online Journal Archives 1860-2000
    Topics: Energy, Environment Protection, Nuclear Power Engineering
    Notes: Abstract In the winter months of 1983, approximately 1000 gallons of diesel fuel had flowed along an asphalt parking lot of a commercial establishment towards a surface drain near an open creek. Investigations led to the discovery of an underground storage tank leaking diesel fuel. Exploratory borings showed that contamination was near the surface horizon and the capillary zone of the water table. Hydrocarbon quantities ranged up to 1500 mg/kg of soil. The plume continued to move in an eastward direction toward the surface water of the creek. A laboratory study indicated relatively high numbers of hydrocarbon-oxidizing organisms relative to glucose-utilizing microorganisms in the unsaturated vadose zone. Bioreclamation was initiated in April 1984 by injecting nutrients (nitrogen and phosphorus) and hydrogen peroxide and terminated in October 1984 upon no detection (〈1 mg/kg) of hydrocarbons. A verification boring within the vicinity of the contaminated plume confirmed that residual contamination had attained background levels. The monitoring program was terminated in January 1987.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Biology and fertility of soils 10 (1990), S. 29-34 
    ISSN: 1432-0789
    Keywords: Plant growth regulator ; Biological active substances ; Plant hormones ; Antibiotics ; Waterlogging ; Ethylene
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Geosciences , Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary One of the major factors affecting the production and stability of ethylene (C2H4) in soil is its water content. This study was conducted to determine the effect of unsaturated vs. saturated conditions on the production and stability of C2H4 in soil. L-Methionine and D-glucose were added alone and in combination at 1.0 and 5.0 g kg-1 soil, respectively. The addition of l-methionine significantly promoted C2H4 production at field capacity to a much greater extent than under waterlogged conditions. Glucose was equally effective under both moisture regimes, while the combined application of both amendments (l-methionine and d-glucose) led to the release of significantly higher amounts of C2H4 under saturated conditions. Antibiotic experiments revealed that under aerobic conditions, l-methionine may be more efficiently converted to C2H4 by soil fungi, while in glucose-amended soil, both bacteria and fungi are active in generating C2H4. C2H4 was more stable under saturated conditions. The magnitude of C2H4 removal from the headspace after 3 days of incubation under unsaturated conditions (25.7%) was comparable to that after 6 days under saturated conditions (24.1%). The loss of C2H4 was approximately 10-fold greater in non-sterilized soil than in sterilized (autoclaved) soil, both maintained at field capacity, indicating that a biotic component has a major influence on C2H4 stability. Kinetic analysis revealed that the C2H4 loss/degradation in nonautoclaved soil under aerobic conditions followed a firstorder reaction, with a rate constant (k) of 0.115 day-1 and a half-life (t 1/2) of 6.0 days.
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Biology and fertility of soils 11 (1991), S. 1-5 
    ISSN: 1432-0789
    Keywords: Organic N ; Urease ; Amidase ; Asparaginase ; Soil enzymes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Geosciences , Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary Studies on the distribution of l-asparaginase in soil profile samples revealed that its activity generally decreases with sample depth and is accompanied by a decrease in organic C content. Statistical analyses indicated that l-asparaginase activity was significantly correlated (** P〈0.01) with organic C (r=0.86**) and total N (r=0.78**) in the 26 surface soil samples examined. There was no significant relationship between l-asparaginase activity and the percentage of clay or sand. There was, however, a significant correlation between l-asparaginase activity and amidase (r=0.82**) and urease (r=0.79**) activities in the surface samples studied. The effects of 21 trace elements, 12 herbicides, 2 fungicides, and 2 insecticides on l-asparaginase activity in soils showed that most of the trace elements and pesticides, at the concentrations used, inhibited the reaction catalyzed by this enzyme. The degree of inhibition varied among soils. When the trace elements were compared, at the rate of 5 μmol g-1 soil, the average inhibition of l-asparaginase in three soils showed that Ag(I), Cd(II), Hg(II), Ni(II), Pb(II), and V(IV) were the most effective inhibitors (average inhibition ≥20%). The least effective inhibitors (average ≤10%) included Cu(I), Ba(II), Co(II), Sn(II), Zn(II), Al(III), Se(IV), As(V), and Mo(VI). Other trace elements that inhibited l-asparaginase activity in soils were Cu(II), Mn(II), As(III), B(III), Cr(III), Fe(III), Ti(IV), and W(VI). When the pesticides were compared, at the rate of 10 μg active ingredient g-1 soil, the average inhibition of l-asparaginase activity in three soils ranged from 4% with Merpan to 46% with Malaspray. Other pesticides that inhibited l-asparaginase activity in soils (average inhibition in parentheses) were Aatrex (17%), Alanap (21%), Amiben (18%), Banvel (12%), Bladex (24%), 2,4-D (17%), Dinitramine (19%), Eradicane (16%), Lasso (40%), Paraquat (33%), Sutan (39%), treflan (7%), Menesan (18%), and Diazinon (33%).
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Biology and fertility of soils 11 (1991), S. 6-12 
    ISSN: 1432-0789
    Keywords: Soil enzymes ; Organic N ; Enzyme kinetics ; Asparaginase ; N mineralization
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Geosciences , Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary A simple, precise, and sensitive method to assay l-asparaginase (l-asparagine amidohydrolase, EC 3.5.1.1) activity in soils is described. This method use steam distillation to determine the NH inf4 sup+ produced by l-asparaginase activity when soil is incubated with buffered (0.1 M THAM, pH 10) l-asparagine solution and toluene at 30°C for 2 h. The procedure developed gives quantitative recovery of NH inf4 sup+ -N added to soils and does not cause chemical hydrolysis of l-asparagine. The optimum buffer pH for NH inf4 sup+ -N released by l-asparaginase activity in soils was 10. This enzyme was saturated with 50 mM l-asparagine, and the reaction rate essentially followed zero-order kinetics. The d-isomer of asparagine was also hydrolyzed in soils, but at only 16% of the activity of the l-isomer at a saturating concentration of the substrate. The optimal temperature for the soil l-asparaginase reaction occurred at 60°C and denaturation began at 65°C. The Arrhenius equation plot for l-asparaginase activity in three selected soils was linear between 10 and 50°C. The activation energy values of this enzyme ranged from 20.2 to 34.1 (average 26.6) kJ mol-1. Application of three linear transformations of the Michaelis-Menten equation showed that the K m values of l-asparaginase in nine soils ranged from 2.6 to 10.0 (average 6.1) mM and the V max values ranged from 9 to 131 μg NH inf4 sup+ -N released g-1 soil 2 h-1. The temperature coefficients (Q 10) for soil l-asparaginase activity ranged from 1.12 to 1.70 (average 1.39). Steam sterilization (121°C for 1 h), formaldehyde, and NaF decreased the activity but the presence of toluene increased the amount of NH inf4 sup+ released. Treatment of soils with dimethylsulfoxide completely destroyed l-asparaginase activity. The use of sulfhydryl reagents indicated that a free sulfhydryl moiety was required to maintain the active enzyme. l-Asparaginase activity in soils was increased by 13 to 18% in the presence of THAM buffer prepared to contain 5 mM Ca2+ and Mg2+, respectively.
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