PubMed Health⌕ Search

Biomedical subjects

R Bartha

Publications and source records attributed to R Bartha.

83 records · Page 5Linked to original sources

Pesticide transformations: production of chloroazobenzenes from chloroanilines.

Aniline and 11 different chloroanilines were added to soil. No azo compound was formed from aniline, but all monochloro-and some dichloroanilines were transformed to their corresponding dichloro-and tetrachloroazobenzenes. Other dichloroanilines and the trichloroanilines were stable in soil. Peroxidase catalyzed the formation of azo compounds by some chloroanilines. Correspondence in the range of substrates used and products formed in the two systems suggests a peroxidatic mechanism for the synthesis of azo compounds residues in soil.

Aniline Compounds↗

Pesticide transformation to aniline and azo compounds in soil.

The herbicide 3',4'-dichloropropionanilide decomposes in soil to carbon dioxide and 3,4-dichloroaniline. and two molecules of the latter compound are condensed to form 3,3',4,4'-tetrachloroazobenzene. Soil microorganisms are involved in both transformations.

Anilides↗

Stability and effects of some pesticides in soil.

The influence of 29 pesticides on CO(2) production and nitrification by soil microorganisms was determined. A few compounds were stable but without significant effect in soil (chlorinated hydrocarbons), some persisted and depressed respiration and nitrification (carbamates, cyclodienes, phenylureas, thiolcarbamates), and others displayed toxicity but were transformed by soil microorganisms (amides, anilides, organophosphates, phenylcarbamates, triazines). Some compounds of the last type induced an initial increase and subsequent decrease in CO(2) production by soil. No simple explanation of this effect is possible, but the results of studies of model systems having established activities suggest that in soil any one or a combination of the following mechanisms is responsible for the observed complex relation of CO(2) production to time: (i) a pesticide acts to uncouple oxidative phosphorylation in a manner analogous to 2,4-dinitrophenol; (ii) a pesticide lacking antimicrobial action is oxidized in part and transformed to a stable and toxic product; (iii) a pesticide that is selectively toxic inhibits CO(2) production by sensitive microorganisms but is subject to oxidation without detoxification by other members of the microbial population that are resistant to its initial action. Pesticide concentrations greatly in excess of those recommended for agricultural and home use were required to produce an effect, and supplementary organic matter (glucose) tended to reduce pesticide toxicity and increase the microbial degradation of pesticides in soil.

Bacteria↗

Fecapentaene causes sister-chromatid exchanges in human lymphocytes.

Fecapentaenes are potent mutagenic compounds found in human feces that are considered as potential colon carcinogens. It is demonstrated that a synthetic racemic all-trans fecapentaene-12 (fec-12) causes a strong dose-dependent increase in the frequency of sister-chromatid exchanges (SCE) in human lymphocytes exposed at different stages of the cell cycle. The SCE-inducing capacity is consistent with published results on the DNA-damaging activity of fec-12 such as formation of DNA single-strand breaks and interstrand cross-links.

Cell Cycle↗