Abstract
The polycyclic aromatic compounds (PAC) produced from the pyrolysis of a bituminous coal at temperatures of 1125 to 1425 degrees K prove to be mutagenic to S. typhimurium, both in the presence and in the absence of postmitochondrial supernatant (PMS) prepared from Aroclor 1254-induced rat liver. Mutagenicity of the PAC samples measured in the absence of PMS exhibits little dependence on pyrolysis temperature; that measured in its presence is higher at the higher pyrolysis temperatures. However, because of the decrease in PAC yield as the temperature is raised, mutagenicity per mass of coal consumed falls with an increase in temperature if measured without PMS (-PMS) and peaks at an intermediate temperature of 1378 degrees K if measured with PMS (+PMS). Using a new chromatographic technique, we have split each coal-derived PAC sample into two fractions: LC1, containing PAC with alkyl and O-containing substitutions and LC2, consisting of unsubstituted PAC. Substituted (LC1) fractions show no significant +PMS mutagenicity, indicating that, as a whole, the alkylated PAC in our coal pyrolysis products are not mutagenic. Only at the higher temperatures do the substituted fractions exhibit significant -PMS mutagenicity, attributed to PAC with carbonyl or etheric functionalities. The extremely low yields of the substituted PAC under the conditions where they show some activity, however, ensure that they contribute little to overall mutagenicity. In contrast to the substituted fractions, the unsubstituted (LC2) fractions display significant mutagenicity under all conditions and appear to be responsible for virtually all of the mutagenicity in these coal-derived PAC samples. In this fraction, -PMS activity is attributed to nitrogen-containing heterocyclic aromatics.
Full text
PDF








Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Alfheim I., Becher G., Hongslo J. K., Ramdahl T. Mutagenicity testing of high performance liquid chromatography fractions from wood stove emission samples using a modified Salmonella assay requiring smaller sample volumes. Environ Mutagen. 1984;6(1):91–102. doi: 10.1002/em.2860060111. [DOI] [PubMed] [Google Scholar]
- Braun A. G., Wornat M. J., Mitra A., Sarofim A. F. Organic emissions from coal pyrolysis: mutagenic effects. Environ Health Perspect. 1987 Aug;73:215–221. doi: 10.1289/ehp.8773215. [DOI] [PMC free article] [PubMed] [Google Scholar]
- El-Bayoumy K., LaVoie E. J., Tulley-Freiler L., Hecht S. S. Effects of ortho-methyl substituents on the mutagenicity of aminobiphenyls and aminonaphthalenes. Mutat Res. 1981 Dec;90(4):345–354. doi: 10.1016/0165-1218(81)90057-4. [DOI] [PubMed] [Google Scholar]
- Kaden D. A., Hites R. A., Thilly W. G. Mutagenicity of soot and associated polycyclic aromatic hydrocarbons to Salmonella typhimurium. Cancer Res. 1979 Oct;39(10):4152–4159. [PubMed] [Google Scholar]
- Lafleur A. L., Wornat M. J. Multimode separation of polycyclic aromatic compounds by size exclusion chromatography with poly(divinylbenzene). Anal Chem. 1988 Jun 1;60(11):1096–1102. doi: 10.1021/ac00162a004. [DOI] [PubMed] [Google Scholar]
- Lao R. C., Thomas R. S., Oja H., Dubois L. Application of a gas chromatography-mass spectrometer-data processor combination to the analysis of the polycyclic aromatic hydrocarbon content of airborne pollutants. Anal Chem. 1973 May;45(6):908–915. doi: 10.1021/ac60328a006. [DOI] [PubMed] [Google Scholar]
- Lavoie E. J., Coleman D. T., Geddie N. G., Rice J. E. Studies on the mutagenicity and tumor-initiating activity of methylated fluorenes. Chem Biol Interact. 1985 Jan;52(3):301–309. doi: 10.1016/0009-2797(85)90025-0. [DOI] [PubMed] [Google Scholar]
- Melikian A. A., Amin S., Huie K., Hecht S. S., Harvey R. G. Reactivity with DNA bases and mutagenicity toward Salmonella typhimurium of methylchrysene diol epoxide enantiomers. Cancer Res. 1988 Apr 1;48(7):1781–1787. [PubMed] [Google Scholar]
- Skopek T. R., Liber H. L., Kaden D. A., Thilly W. G. Relative sensitivities of forward and reverse mutation assays in Salmonella typhimurium. Proc Natl Acad Sci U S A. 1978 Sep;75(9):4465–4469. doi: 10.1073/pnas.75.9.4465. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Skopek T. R., Liber H. L., Krolewski J. J., Thilly W. G. Quantitative forward mutation assay in Salmonella typhimurium using 8-azaguanine resistance as a genetic marker. Proc Natl Acad Sci U S A. 1978 Jan;75(1):410–414. doi: 10.1073/pnas.75.1.410. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wilson B. W., Pelroy R., Cresto J. T. Identification of primary aromatic amines in mutagenically active subfractions from coal liquefaction materials. Mutat Res. 1980 Nov;79(3):193–202. doi: 10.1016/0165-1218(80)90066-x. [DOI] [PubMed] [Google Scholar]
