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1. |
Cultured fish cells for the ecotoxicity testing of aquatic pollutants |
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Toxicity Assessment,
Volume 2,
Issue 2,
1987,
Page 119-133
H. Babich,
E. Borenfreund,
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摘要:
AbstractThe volume of chemicals in everyday use that require ecotoxicity testing, the high‐costs of using whole animals for initial screenings of chemicals for their cyto‐ and genotoxicities, and the need for a ‚biological early warning signal”︁ to detect toxicants in aquatic environments have prompted the development of many microbial‐basedin vitroshort‐term bioassays. An area that has received relatively little study is the application of vertebrate cells, especially fish cells, for ecotoxicity testing of chemicals. From the few studies that are available it has been demonstrated that cultured, established fish cell lines can be used for (1) thein vitrocyto‐ and genotoxicity screening of known aquatic pollutants, (2) thein situmonitoring of natural waters and sediments for chemical cyto‐ and genotoxicants, and (c) elucidating structure‐activity relationships among chemicals, which can thereby serve as a biological adjunct to computer‐based mathematical predictions (QSARs) of chemical c
ISSN:0884-8181
DOI:10.1002/tox.2540020202
出版商:Wiley Subscription Services, Inc., A Wiley Company
年代:1987
数据来源: WILEY
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2. |
The SOS chromotest kit: A rapid method for the detection of genotoxicity |
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Toxicity Assessment,
Volume 2,
Issue 2,
1987,
Page 135-147
F. Fish,
I. Lampert,
A. Halachmi,
G. Riesenfeld,
M. Herzberg,
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摘要:
AbstractThe SOS Chromotest is a bacterial assay for genotoxicity, based on the detection of damage to DNA as measured through the SOS DNA repair system. AnE. colistrain was derived by fusing the structurallacZgene with a promoter of one of the SOS genes, namely thesfiAgene. Auxiliary mutations increase the sensitivity of the Chromotest bacteria to genotoxic materials. In the SOS Chromotest, any damage to the DNA results in the activation of the SOS system, including thesfiAgene promoter. This, in turn, induces thede novotranscription and synthesis of the enzymeB. galactosidase. The enzyme is clearly and easily detected by a chromogenic reaction. We have miniaturized the SOS Chromotest and developed it into a self‐contained kit in the microtitration format. The kit contains all the components of the test, including dried bacteria and a dried liver S‐9 mix in a stable state, allowing on‐site operation. The whole test, including the revival of the bacteria, can be completed in 6–7 hours. In addition to being used as a genotoxics detection and monitoring system in chemical, cosmetics, food and pharmaceutical industries, the advantages of the rapid SOS Chromotest can be exploited in full for environmental and occupational health studies. In order to circumvent tedious concentrations of samples (e.g., urine, water), we have tried to further increase the sensitivity of the Chromotest by exposing the bacteria to relatively large volumes of unconcentrated samples. Employing this approach, we were able to demonstrate genotoxic activity in unconcentrated urine samples obtained from people exposed to environmental genotoxins. It appears, therefore, that the SOS Chromotest kit will allow an economically feasible and efficient monitoring of genotoxics in the envi
ISSN:0884-8181
DOI:10.1002/tox.2540020203
出版商:Wiley Subscription Services, Inc., A Wiley Company
年代:1987
数据来源: WILEY
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3. |
ATP‐TOX system—a new, rapid, sensitive bacterial toxicity screening system based on the determination of ATP |
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Toxicity Assessment,
Volume 2,
Issue 2,
1987,
Page 149-166
Hao Xu,
Wuhan,
Hubei,
B. J. Dutka,
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摘要:
AbstractA new toxicity screening test, based on the inhibition of bacterial growth and luciferase activity by toxicants was developed. In the ATP‐TOX System, chemical toxicity was found to be time‐dependent and increased with increasing exposure time up to 5 hours. Three organisms were evaluated in this study:E. coliK‐12 PQ37,Pseudomonas fluorescensandSalmonella typhimurium. E. coliK‐12 PQ37 was found to be the most sensitive organism. It was also shown thatP. fluorescenswas more sensitive to toxicants when grown in minimal medium than in nutrient broth, suggesting that nutrients may have a protective effect on the bacterium. In comparative studies using selected toxic chemicals the ATP‐TOX System was found to be more sensitive than theSpirillum volutanstest and comparable to the Microtox test. Toxicant activity in sediment samples was found to be time dependent and increased with increasing exposure time in both ATP‐TOX (E. coli) System and Microtox. The ATP‐TOX System is complementary to the Microtox test as it also provides indications of low grade toxicant activity which is only manifested in actively growing cells over several life cycles. Thus, the ATP‐TOX System appears to be an ideal screening test for sediment toxicity. The data indicate that the ATP‐TOX System is sensitive, rapid, reproducible, economical and has great potential i
ISSN:0884-8181
DOI:10.1002/tox.2540020204
出版商:Wiley Subscription Services, Inc., A Wiley Company
年代:1987
数据来源: WILEY
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4. |
Herbicide toxicity and microbial responses in soil |
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Toxicity Assessment,
Volume 2,
Issue 2,
1987,
Page 167-174
P. Mahendru,
P. S. Dubey,
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摘要:
AbstractThe question mark placed on a few herbicides because of their longer persistence in Black Cotton soil made this ecotoxicological assessment necessary. Since microbial responses can be used as an indicator of herbicide toxicity, soil respiration, dehydrogenase, and viable bacterial counts were used as the parameters to assess herbicide toxicity. Basalin, Lasso, and Tafazine are used in Black Cotton Soil of Southwest part of India. Soils treated with 1,5, and 25 ppm (w/w) and assessed 1, ε, 11, 16, and 21 days later, indicated a significant inhibitory effect on microbial activity measured in terms of these parameters. The improvement in soil quality started after 16–21 days in Basalin treated soil only. Further, there exists a correlation between soil respiration and number of bacterial colonies, and soil respiration and dehydrogenase activity. The study warrants a rigorous screening of all the recommended preemergence herbicides in Black Cotton soil of this fertile ar
ISSN:0884-8181
DOI:10.1002/tox.2540020205
出版商:Wiley Subscription Services, Inc., A Wiley Company
年代:1987
数据来源: WILEY
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5. |
Toxicity of lead on microorganisms: Interaction with protein content of culture medium |
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Toxicity Assessment,
Volume 2,
Issue 2,
1987,
Page 175-191
J. Santos Oliveira,
A. Rodrigues,
B. Mendes,
M. Dias,
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摘要:
AbstractLead is a significant environmental pollutant in Portugal, mainly as a consequence of its use as an antidetonant in gasoline. Due to the vast annual gas consumption, evidence of lead emission has been found in the air, soil, plants, and water. Concentrations of lead in Lisbon waste waters average 0.15 mg/L, with occasional levels reaching 1.5 mg/L. The biodegradability of these waste waters is affected by lead. To understand the interaction between lead toxicity and protein concentrations, a study was initiated using selected strains ofProteus mirabilisandKlebsiella pneumoniaeand synthetic effluents. The toxicity of lead to bacteria was noted by an increase in the cell's metabolic activity, and a greater induction of ATP and RNA contents. However, bacterial replication was evidently uninhibited by the lead content in the test medium. While high peptone content in the growth medium caused an increase in the cell's biosynthesis, increased lead concentrations in the growth medium resulted in a substantial loss of metabolic product. This complex interaction was apparently responsible for lead's toxicity to bacteria.
ISSN:0884-8181
DOI:10.1002/tox.2540020206
出版商:Wiley Subscription Services, Inc., A Wiley Company
年代:1987
数据来源: WILEY
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6. |
A new, short term, sensitive, bacterial assay kit for the detection of toxicants |
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Toxicity Assessment,
Volume 2,
Issue 2,
1987,
Page 193-206
A. Reinhartz,
I. Lampert,
M. Herzberg,
F. Fish,
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摘要:
AbstractWe present and evaluate a new bacterial test suitable for the detection of toxicants in water, chemicals, pharmaceuticals, foodstuff, food additives and cosmetics. It is a simple, rapid (1–1.5 hours), colorimetric assay which does not require special equipment, and can easily be carried out under field conditions.The assay is based on the ability of toxicants to inhibit thede novosynthesis of an inducible enzyme, e.g., β‐galactosidase, by a rough mutant ofE. coli, which is highly sensitive to a wide spectrum of toxic substances, such as pesticides, mycotoxins and heavy metals. The test is performed under stress conditions for the bacterium, since under such conditions better sensitivity for low concentrations of analytes is obtained. In the assay, serial dilutions of the sample are mixed with the stressed bacteria and a cocktail containing the specific inducer for the chromogenic enzyme and essential factors, required for the recovery of the bacteria from their‐stressed condition. The ability of cells to synthesize β‐galactosidase under these conditions depends on their ability to recover from the stress. Toxic materials interfere and/or inhibit the recovery process and with it the synthesis of β‐galactosidase. The amount of thede novosynthesized enzyme is determined by a colorimetric reaction.We have developed a commercial kit based on the assay. The kit is field oriented and easy to operate. The kit contains the bacteria in a lyophilized form and all the reagents have been stabilized so that the kit may be stored under normal refrigeration for a long pe
ISSN:0884-8181
DOI:10.1002/tox.2540020207
出版商:Wiley Subscription Services, Inc., A Wiley Company
年代:1987
数据来源: WILEY
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7. |
Assessment for mutagenicity of 10 pharmaceutical products following ames, micronucleus, and sperm morphology testing |
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Toxicity Assessment,
Volume 2,
Issue 2,
1987,
Page 207-215
I. S. Stoyanov,
I. G. Nicolov,
I. N. Chernozemsky,
I. Stoichev,
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摘要:
AbstractTen widely used pharmaceutical agents for which mutagenicity or carcinogenicity data are still lacking were tested in parallel with three methods: Ames' bacterial mutagenicity test (TA1535, TA1537, TA98, and TA100 Salmonella strains), micronucleus (mice BDF1), and sperm morphology abnormality (mice) tests. The groups and generic names of the tested products, all produced by Pharmachim (Bulgaria), were as follows: Psychopharmaca (Loxapinsuccinate, Medazepam hydrochloride, Nomifensinmaleate, Viloxazine hydrochloride), Vasodilatators (Nitroprussid Na, Isosorbid mononitrate, Isosorbid dinitrate), Spasmolytica (Trimetoquinol), Antirheumatica (Diclofenac Na), and the antimycotic agent Lavendotricin. In all tests, negative results were obtained. To avoid false negative results, several suggestions are made.
ISSN:0884-8181
DOI:10.1002/tox.2540020208
出版商:Wiley Subscription Services, Inc., A Wiley Company
年代:1987
数据来源: WILEY
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8. |
Effects of 2,4‐dichlorophenoxyacetic acid onRhizobiumsp. in pure culture |
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Toxicity Assessment,
Volume 2,
Issue 2,
1987,
Page 217-228
A. I. Fabra De Peretti,
G. B. Mori De Moro,
N. E. Ghittoni,
A. M. Evangelista De Duffard,
R. O. Duffard,
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摘要:
AbstractThe effects of 2,4‐Dichlorophenoxyacetic acid on the growth rate, chemical composition,14C‐2,4‐dichlorophenoxyacetic acid and45Ca2+uptake byRhizobiumsp. M 4 able to nodulateArachis hypogaeawere determined. Cellular growth was diminished by the presence of 10−3M 2,4‐dichlorophenoxyacetic acid in the medium. Alterations in cellular chemical composition, in14C‐2,4‐dichlorophenoxyacetic acid and in45Ca2+upta
ISSN:0884-8181
DOI:10.1002/tox.2540020209
出版商:Wiley Subscription Services, Inc., A Wiley Company
年代:1987
数据来源: WILEY
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9. |
Technical Methods Section. A toxicity assay based on oxygen uptake byPseudomonas putida |
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Toxicity Assessment,
Volume 2,
Issue 2,
1987,
Page 229-235
J. L. Slabbert,
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ISSN:0884-8181
DOI:10.1002/tox.2540020210
出版商:Wiley Subscription Services, Inc., A Wiley Company
年代:1987
数据来源: WILEY
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10. |
Meeting announcement |
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Toxicity Assessment,
Volume 2,
Issue 2,
1987,
Page 237-238
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ISSN:0884-8181
DOI:10.1002/tox.2540020211
出版商:Wiley Subscription Services, Inc., A Wiley Company
年代:1987
数据来源: WILEY
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