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F Korte

Publications and source records attributed to F Korte.

At least 19 recordsLinked to original sources
PubMed2000

Organic toxicants and plants.

Organic xenobiotics absorbed by roots and leaves of higher plants are translocated by different physiological mechanisms. The following pathways of xenobiotic detoxication have been observed in higher plants: conjugation with such endogenous compounds as peptides, sugars, amino acids, and organic acids; oxidative degradation and consequent oxidation of xenobiotics with the final participation of their carbon atoms in regular cell metabolism. The small parts of xenobiotics are excreted maintaining their original structure and configuration. Enzymes catalyze oxidative degradation of xenobiotics from the initial hydroxylation to their deep oxidation. The wide intracellular distribution and inductive nature of oxidative enzymes lead to the high detoxication ability. With plant aging, transformation of the monooxygenase system into peroxidase takes place. Once in the cells, xenobiotics are incorporated into different cell organelles. All xenobiotics examined are characterized by a negative effect on cell ultrastructure. The penetration of high doses of xenobiotics into plant cells leads to significant deviations from the norm and, in some cases, even to the complete cell destruction and plant death.

Oxidation-Reduction↗
PubMed1998

Editorial

Explore the source record for details and available documents.

Journal Article↗
PubMed1997

Plant monooxygenases: participation in xenobiotic oxidation.

The induction of individual components of the plant microsomal monooxygenase system have been studied. Quantitative distribution of NADPH reducible equivalents at monooxygenase and oxidase reactions and rereduction of coenzyme have been exhibited when there is deficiency of oxygen. Xenobiotic oxidation specificity in NADPH and NADH synergism with NADPH have been detected. The dependence of hydroxylation rate on the degree of hydrophobicity of xenobiotic molecules has been established. The possibility of cytochrome P-450 switching over from biosynthetic into detoxication pathway and transformation of monooxigenase mechanism of oxidation into peroxidase according to plant age have been demonstrated.

Cytochrome P-450 Enzyme System↗
PubMed1997

Uptake and transformation of benzene and toluene by plant leaves.

The [1-6(14)C]benzene and [1-(14)C]toluene vapors penetrate into hypostomatous leaves of Acer campestre, Malus domestica, and Vitis vinifera from both sides, whereas hydrocarbons are more intensively absorbed by the stomatiferous side and more actively taken up by young leaves. Benzene and toluene conversion in leaves occurs with the aromatic ring cleavage and their carbon atoms are mainly incorporated into nonvolatile organic acids, while their incorporation into amino acids is less intensive. Intact spinach chloroplasts oxidize benzene, and this process is strongly stimulated in light. Oxidation of benzene by spinach chloroplasts or by enzyme preparation from spinach leaves is almost completely inhibited by 8-oxyquinoline or sodium diethyldithiocarbamate, and slightly affected by alpha, alpha'-dipyridyl. Benzene oxidation by enzyme preparation is significantly stimulated by NADH and NADPH; in their presence, the benzene hydroxylation product, phenol, is formed in a determinable amount. It is supposed that the enzyme performing the first step of oxidative transformation of benzene in plant leaves contains copper as the prosthetic group.

Absorption↗
PubMed1995

From single-substance evaluation to ecological process concept: the dilemma of processing gold with cyanide.

In the past decades, limit concentration values for environmentally dangerous synthetic and natural chemical substances have been established in industrialized countries. Depending on the range of application, state of aggregation, propagation velocity, specific action on living organisms, long- or short-time effect, etc., different terms are used to specify these limit concentrations (acceptable daily intakes, TLV, LD50, emission values, water quality standards, etc.). Several parameters (e.g., range of application, ethic and social valuation, environmental factors, scientific knowledge) have led to nationally and internationally varying values depending on the region and time. The accuracy of this system of evaluation cannot necessarily be improved by listing further analytical data, but rather by furnishing sufficiently secured scientific data for a serious discussion, with the public concepts influenced more and more by the mass media. The best-established scientific knowledge has been acquired by the chemical industry. National and international groups demand that ecological-chemical problems in other fields of industry be dealt with as well; this research should, without doubt, be intensified. The example of the mining industry, which must employ chemical methods to isolate small concentrations (ppm), demonstrates the environmental conflict caused by the increasing world population, requiring the adaptation of the process by industry to the modern environmental concept. This is illustrated by the evolution of the gold recovery process.

Animals↗
PubMed1994

Uptake pathways of chlorobenzenes in plants and their correlation with N-octanol/water partition coefficients.

The bioconcentration factors of 14C-labeled chlorinated benzenes in plants from soil were quantified in short-term laboratory experiments and correlated to Kow. The correlation was negative for barley and positive for cress. In order to interpret these opposite results, the log/log correlation between partition coefficients and Kow of the chemicals was established also for each step of the uptake, via both roots and leaves. For the first step of root uptake--the partition of the chemicals from soil solids into soil water--the correlation with Kow was negative, whereas it was positive for the second step, the partition roots/soil water, of both plant species. Similarly, the correlation between the first step of foliar uptake--the partition of the chemical from soil into air--and Kow was negative, and that between the second step--the partition between aerial plant parts and air--and Kow was positive for both plant species. The slopes of the regression lines differed between plant species. It may be concluded that Kow can be used as a parameter to predict the uptake of chemicals from soil by plants only if the same class of chemicals and the same plant species is considered.

Chlorobenzenes↗
PubMed1992

Effects of short-term inhalation exposure to 1-nitropropane and 2-nitropropane on rat liver enzymes.

Male Sprague-Dawley rats were exposed to vapors of 1-nitropropane (1-NP) and 2-nitropropane (2-NP) at air concentrations of 100 ppm for 7 hours per day on four consecutive days. Livers were analyzed for enzymatic activities after 1-, 2-, and 4-day inhalation periods. Liver microsomal cytochrome P450 was depressed by 2-NP and elevated following exposure to 1-NP. Levels of cytochrome b5 were slightly increased in rats exposed to 1-NP and remained unchanged after inhalation of 2-NP. Total glutathione (GSH), GSH S-transferase, and UDP-glucuronosyltransferase activities were enhanced by 2-NP. 1-NP induced GSH peroxidase while 2-NP did not. Glutathione reductase was not altered after exposure to either isomer. No changes in the microsomal malondialdehyde content as a measure of lipid peroxidation and in the levels of serum aspartate transferase and serum glutamic oxaloacetic transaminase were observed during a 4-day exposure period in either of the exposed groups compared to control animals.

Animals↗
PubMed1991

QSAR for organic chemical bioconcentration in Daphnia, algae, and mussels.

Prediction of the bioconcentration of organic chemicals from water by aquatic organisms has important applications in the management of hazardous chemicals. This study gives a compilation of bioconcentration factors on a wet weight basis (BCFw) of 52 organic chemicals by Daphnia magna from aqueous solution. The bioconcentration factors for the chemicals in Daphnia were successfully correlated with their n-octanol/water partition coefficients (log Kow) using a linear regression analysis. In addition to the ordinary least-square regression technique, the geometric mean regression technique is also used because this takes into account deviations in Kow values. Both results show that the Kow value of a chemical is a good predictor of the BCF in Daphnia. The BCF-Kow relationships between Daphnia, algae (Chlorella), and mussels (Mytilus edulis) are compared with each other.

Animals↗
PubMed1990

Correlation between acute toxicity of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) and total body fat content in mammals.

Single oral 30-day LD50s of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) were correlated with total body fat (TBF) content in various species and strains of laboratory mammals. LD50 values and TBF contents were either obtained from the literature or determined by experiments. A log (LD50) vs. log (TBF) plot yielded a highly significant linear regression equation (r2 = 0.834, P less than 0.001, n = 20). It is suggested that this correlation exists for at least two reasons: (1) increasing TBF content in organisms represents an enhanced capacity to remove TCDD from the systemic circulation and (2) different TBF content reflects a differential role and regulation of fat metabolism for various organisms. Extrapolation of this correlation to man suggests that adult humans are among the less sensitive species to the acute toxicity of TCDD.

Adipose Tissue↗
PubMed1989

Kinetics of the uptake of 14C-labeled chlorinated benzenes from soil by plants.

[14C]Benzene, [14C]1,2,4-trichlorobenzene, [14C]pentachlorobenzene, and [14C]hexachlorobenzene were applied to soils in outdoor lysimeters to a 10-cm depth (2 mg/kg dry soil); barley and cress plants were grown for one vegetation period and analyzed after varying time intervals. The bioaccumulation factors (concentration of radioactive substances in plants divided by that in soils) of barley were higher than those of cress, except for hexachlorobenzene. In barley, bioaccumulation factors increased with decreasing chlorine content of the molecules, except for benzene, whereas in cress hexachlorobenzene exhibited the highest bioaccumulation factor. The conversion ratios of chlorinated benzenes (percentage of conversion products based on total radioactivity in plants) were negatively correlated to the chlorine content of the molecules and, in barley, positively correlated with time; in general, they were higher in barley than in cress. The concentration of radioactive substances in the plants, as well as bioaccumulation factors, decreased with time, except for a slight increase in benzene-derived residues in barley after 125 days. This effect is due to growth dilution. The percentage of radioactivity in barley seeds, based on that in the whole plant, was negatively correlated to the chlorine content of the molecule.

Benzene Derivatives↗
PubMed1989

Disposition and metabolism of 1-nitropropane in rats and chimpanzees.

The metabolic fate of 1-nitropropane (1-NP) has not been previously reported. In this study male rats and chimpanzees were given single doses of 40 mg/kg ip and 5 mg/kg iv 1-[1-14C]NP, respectively. The quantitative extent of urinary and fecal elimination was similar in both species. The rats excreted 16.5% of the dose in urine and 1.7% in feces. For chimpanzees the respective values were 14.8 and 1.2%. Experiments with rats demonstrated that the major route of elimination was by exhalation. With a total elimination via the lungs of 72.6%, rats expired 10.3% of the dose as unchanged 1-NP. Five polar metabolites were isolated from the urine of chimpanzees. The two major metabolites were identified as 3-hydroxypropionic acid and N-methyl-N-2-(methylsulfinyl)ethylpropionic acid amide (NMPA). Both substances were also excreted in rat urine. The two identified metabolites indicate that 1-NP was degraded to propionic acid, part of which was modified to 3-hydroxypropionic acid or NMPA. A hypothetical pathway for the biochemical generation of NMPA is suggested.

Alkanes↗