Nitroaromatic Compounds, from Synthesis to Biodegradation

被引:738
作者
Ju, Kou-San [1 ]
Parales, Rebecca E. [1 ]
机构
[1] Univ Calif Davis, Coll Biol Sci, Dept Microbiol, Davis, CA 95616 USA
基金
美国国家科学基金会;
关键词
PSEUDOMONAS-PSEUDOALCALIGENES [!text type='JS']JS[!/text]45; SP STRAIN DNT; 2,4,6-TRINITROPHENOL PICRIC ACID; NOCARDIOIDES-SIMPLEX FJ2-1A; RADICAL-INITIATED REACTIONS; META-CLEAVAGE PATHWAY; ACTIVE-SITE RESIDUES; N-OXYGENASE AURF; P-NITROPHENOL; SUBSTRATE-SPECIFICITY;
D O I
10.1128/MMBR.00006-10
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Nitroaromatic compounds are relatively rare in nature and have been introduced into the environment mainly by human activities. This important class of industrial chemicals is widely used in the synthesis of many diverse products, including dyes, polymers, pesticides, and explosives. Unfortunately, their extensive use has led to environmental contamination of soil and groundwater. The nitro group, which provides chemical and functional diversity in these molecules, also contributes to the recalcitrance of these compounds to biodegradation. The electron-withdrawing nature of the nitro group, in concert with the stability of the benzene ring, makes nitroaromatic compounds resistant to oxidative degradation. Recalcitrance is further compounded by their acute toxicity, mutagenicity, and easy reduction into carcinogenic aromatic amines. Nitroaromatic compounds are hazardous to human health and are registered on the U. S. Environmental Protection Agency's list of priority pollutants for environmental remediation. Although the majority of these compounds are synthetic in nature, microorganisms in contaminated environments have rapidly adapted to their presence by evolving new biodegradation pathways that take advantage of them as sources of carbon, nitrogen, and energy. This review provides an overview of the synthesis of both man-made and biogenic nitroaromatic compounds, the bacteria that have been identified to grow on and completely mineralize nitroaromatic compounds, and the pathways that are present in these strains. The possible evolutionary origins of the newly evolved pathways are also discussed.
引用
收藏
页码:250 / +
页数:24
相关论文
共 222 条
[1]  
ALIDSADAT S, 1995, FEMS MICROBIOL ECOL, V17, P169
[2]  
[Anonymous], 2000, Biodegradation of Nitroaromatic Compounds
[3]   PYRROLNITRIN NEW ANTIBIOTIC SUBSTANCE PRODUCED BY PSEUDOMONAS [J].
ARIMA, K ;
FUKUTA, A ;
IMANAKA, H ;
KOUSAKA, M ;
TAMURA, G .
AGRICULTURAL AND BIOLOGICAL CHEMISTRY, 1964, 28 (08) :575-&
[4]   KINETICS AND PRODUCTS OF THE GAS-PHASE REACTIONS OF OH RADICALS AND N2O5 WITH NAPHTHALENE AND BIPHENYL [J].
ATKINSON, R ;
AREY, J ;
ZIELINSKA, B ;
ASCHMANN, SM .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1987, 21 (10) :1014-1022
[5]   FORMATION OF RING-RETAINING PRODUCTS FROM THE OH RADICAL-INITIATED REACTIONS OF BENZENE AND TOLUENE [J].
ATKINSON, R ;
ASCHMANN, SM ;
AREY, J ;
CARTER, WPL .
INTERNATIONAL JOURNAL OF CHEMICAL KINETICS, 1989, 21 (09) :801-827
[6]   STRUCTURE OF FERROVERDIN [J].
BALLIO, A ;
VITTORIO, VD ;
CHAIN, EB ;
BERTHOLDGODEFROY, H .
NATURE, 1962, 194 (4830) :769-&
[7]  
Behrend C, 1999, APPL ENVIRON MICROB, V65, P1372
[8]   One-step reductive amidation of nitro arenes:: application in the synthesis of Acetaminophen™ [J].
Bhattacharya, A ;
Purohit, VC ;
Suarez, V ;
Tichkule, R ;
Parmer, G ;
Rinaldi, F .
TETRAHEDRON LETTERS, 2006, 47 (11) :1861-1864
[9]   Metabolism of 3-nitrotyrosine induces apoptotic death in dopaminergic cells [J].
Blanchard-Fillion, Beatrice ;
Prou, Delphine ;
Polydoro, Manuela ;
Spielberg, David ;
Tsika, Elpida ;
Wang, Zeneng ;
Hazen, Stanley L. ;
Koval, Michael ;
Przedborski, Serge ;
Ischiropoulos, Harry .
JOURNAL OF NEUROSCIENCE, 2006, 26 (23) :6124-6130
[10]   3-nitroadipate, a metabolic intermediate for mineralization of 2,4-dinitrophenol by a new strain of a Rhodococcus species [J].
Blasco, R ;
Moore, E ;
Wray, V ;
Pieper, D ;
Timmis, K ;
Castillo, F .
JOURNAL OF BACTERIOLOGY, 1999, 181 (01) :149-152