The physiology of aromatic hydrocarbon degrading bacteria
The physiology of aromatic hydrocarbon degrading bacteria
复制标题
芳香烃降解菌的生理学
DOI:
10.1007/978-94-011-1687-9_11
复制
发表时间:
1994
期刊:
影响因子:
--
通讯作者:
Mark R. Smith
中科院分区:
文献类型:
--
作者:
Mark R. Smith
Aromatic hydrocarbons are ubiquitous in nature. Indeed, next to glucosyl residues, the benzene ring is the most widely distributed unit of chemical structure in nature (Dagley 1981). The amount and variety of aromatic hydrocarbons generated by commercial and industrial activities has continued to increase over the years. The occurrence of such compounds is a cause for great concern due to their potential hazard to the well being of both plants and animals. Benzene, toluene, ethylbenzene, styrene and the xylenes are among the 50 largest-volume industrial chemicals produced, with production figures of the order of millions of tonnnes per year. These compounds are widely used as fuels and industrial solvents. In addition, they and the polynuclear aromatic compounds provide the starting materials for the production of pharmaceuticals, agrochemicals, polymers, explosives and many other everyday products (Smith 1990). The use of man-made aromatic hydrocarbons has inevitably led to their release (either accidental or otherwise) into the environment and this problem is still escalating in spite of governmental intervention.The biodegradation of aromatic compounds can be considered, on the one hand as part of the normal process of the carbon cycle and as the removal of man-made pollutants from the environment, on the other. Over the last decades this topic has been extensively reviewed (Hopper 1978; Cripps and Watkinson 1978; Gibson and Subramanian 1984; Cerniglia 1984; Dagley 1986; Smith 1990, as examples). The majority of the recent advances made have consolidated previous findings, tying up some of the loose ends. The purpose of this current review is to examine the present status of our understanding of the physiology of aromatic hydrocarbon degradation, using examples from a selected range of key compounds (benzene, alkylbenzenes, alkenylbenzenes, tetralin, biphenyl, naphthalene and polycyclic aromatic hydrocarbons-see Fig. 1).