Anaerobic metabolism of aromatic compounds

被引:224
作者
Heider, J [1 ]
Fuchs, G [1 ]
机构
[1] UNIV FREIBURG, INST BIOL 2, D-79104 FREIBURG, GERMANY
来源
EUROPEAN JOURNAL OF BIOCHEMISTRY | 1997年 / 243卷 / 03期
关键词
aromatic metabolism; benzoyl-CoA; anaerobic bacteria; aromatic-ring reduction; phloroglucinol; resorcinol;
D O I
10.1111/j.1432-1033.1997.00577.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Aromatic compounds comprise a wide variety of low-molecular-mass natural compounds (amino acids, quinones, flavonoids, etc.) and biopolymers (lignin, melanin). They are almost exclusively degraded by microorganisms. Aerobic aromatic metabolism is characterised by the extensive use of molecular oxygen. Monoxygenases and dioxygenases are essential for the hydroxylation and cleavage of aromatic ring structures. Accordingly, the characteristic central intermediates of the aerobic pathways (e.g. catechol) are readily attacked oxidatively. Anaerobic aromatic catabolism requires, of necessity, a quite different strategy. The basic features of this metabolism have emerged from studies on bacteria that degrade soluble aromatic substrates to CO2 in the complete absence of molecular oxygen. Essential to anaerobic aromatic metabolism is the replacement of all the oxygen-dependent steps by an alternative set of novel reactions and the formation of different central intermediates (e.g. benzoyl-CoA) for breaking the aromaticity and cleaving the ring; notably, in anaerobic pathways, the aromatic ring is reduced rather than oxidised. The two-electron reduction of benzoyl-CoA to a cyclic diene requires the cleavage of two molecules of ATP to ADP and P-i and is catalysed by benzoyl-CoA reductase. After nitrogenase, this is the second enzyme known which overcomes the high activation energy required for reduction of a chemically stable bond by coupling electron transfer to the hydrolysis of ATP. The alicyclic product cyclohex-1,5-diene-1-carboxyl-CoA is oxidised to acetyl-CoA via a modified beta-oxidation pathway; the ring structure is opened hydrolytically. Some phenolic compounds are anaerobically transformed to resorcinol (1,3-dihydroxybenzene) or phloroglucinol (1,3,5-trihydroxybenzene). These intermediates are also first reduced and then as alicyclic products oxidised to acetyl-CoA. This review gives an outline of the anaerobic pathways which allow bacteria to utilize aromatics even in the absence of oxygen. We focus on previously unknown reactions and on the enzymes characteristic for such novel metabolism.
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页码:577 / 596
页数:20
相关论文
共 177 条
[1]   PURIFICATION AND CHARACTERIZATION OF BENZOATE-COENZYME-A LIGASE AND 2-AMINOBENZOATE-COENZYME-A LIGASES FROM A DENITRIFYING PSEUDOMONAS SP [J].
ALTENSCHMIDT, U ;
OSWALD, B ;
FUCHS, G .
JOURNAL OF BACTERIOLOGY, 1991, 173 (17) :5494-5501
[2]   ANAEROBIC DEGRADATION OF TOLUENE IN DENITRIFYING PSEUDOMONAS SP - INDICATION FOR TOLUENE METHYLHYDROXYLATION AND BENZOYL-COA AS CENTRAL AROMATIC INTERMEDIATE [J].
ALTENSCHMIDT, U ;
FUCHS, G .
ARCHIVES OF MICROBIOLOGY, 1991, 156 (02) :152-158
[3]   NOVEL AEROBIC 2-AMINOBENZOATE METABOLISM - PURIFICATION AND CHARACTERIZATION OF 2-AMINOBENZOATE-COA LIGASE, LOCALIZATION OF THE GENE ON A 8-KBP PLASMID, AND CLONING AND SEQUENCING OF THE GENE FROM A DENITRIFYING PSEUDOMONAS SP [J].
ALTENSCHMIDT, U ;
FUCHS, G .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1992, 205 (02) :721-727
[4]   TAXONOMIC POSITION OF AROMATIC-DEGRADING DENITRIFYING PSEUDOMONAD STRAINS K-172 AND KB-740 AND THEIR DESCRIPTION AS NEW MEMBERS OF THE GENERA THAUERA, AS THAUERA-AROMATICA SP-NOV, AND AZOARCUS, AS AZOARCUS-EVANSII SP-NOV, RESPECTIVELY, MEMBERS OF THE BETA-SUBCLASS OF THE PROTEOBACTERIA [J].
ANDERS, HJ ;
KAETZKE, A ;
KAMPFER, P ;
LUDWIG, W ;
FUCHS, G .
INTERNATIONAL JOURNAL OF SYSTEMATIC BACTERIOLOGY, 1995, 45 (02) :327-333
[5]   CHARACTERIZATION OF A FIXLJ-REGULATED BRADYRHIZOBIUM-JAPONICUM GENE SHARING SIMILARITY WITH THE ESCHERICHIA-COLI FNR AND RHIZOBIUM-MELILOTI FIXK GENES [J].
ANTHAMATTEN, D ;
SCHERB, B ;
HENNECKE, H .
JOURNAL OF BACTERIOLOGY, 1992, 174 (07) :2111-2120
[6]  
ASSINDER SJ, 1990, ADV MICROB PHYSIOL, V31, P1
[7]  
AUBURGER G, 1992, APPL MICROBIOL BIOT, V37, P789, DOI 10.1007/BF00174847
[8]   SELECTIVE ISOLATION OF ACETOBACTERIUM-WOODII ON METHOXYLATED AROMATIC-ACIDS AND DETERMINATION OF GROWTH YIELDS [J].
BACHE, R ;
PFENNIG, N .
ARCHIVES OF MICROBIOLOGY, 1981, 130 (03) :255-261
[9]   ANAEROBIC DEGRADATION OF PHENOL AND PHENOL DERIVATIVES BY DESULFOBACTERIUM-PHENOLICUM SP-NOV [J].
BAK, F ;
WIDDEL, F .
ARCHIVES OF MICROBIOLOGY, 1986, 146 (02) :177-180
[10]   Initial reactions in anaerobic ethylbenzene oxidation by a denitrifying bacterium, strain EB1 [J].
Ball, HA ;
Johnson, HA ;
Reinhard, M ;
Spormann, AM .
JOURNAL OF BACTERIOLOGY, 1996, 178 (19) :5755-5761