1990
DOI: 10.1007/bf00291275
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Degradation of aniline and monochlorinated anilines by soil-born Pseudomonas acidovorans strains

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Cited by 94 publications
(65 citation statements)
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“…strain SMN-1 degraded 2-nitrotoluene through 3-methylcatechol by a meta-cleavage pathway, with release of nitrite. The results are in agreement with the results of Loidl et al (1990) and Sutherland et al (1981) who found that aniline and benzoic were degraded via ortho pathway. A new UV spectrum at 257 nm which may be β-carboxy -muconate was detected in enzyme reaction products of protocatechuic acid as substrate with catechol 1,2-dioxygenase enzyme (Ornston and Stanier, 1966).…”
Section: Ring Cleavage Enzymesupporting
confidence: 93%
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“…strain SMN-1 degraded 2-nitrotoluene through 3-methylcatechol by a meta-cleavage pathway, with release of nitrite. The results are in agreement with the results of Loidl et al (1990) and Sutherland et al (1981) who found that aniline and benzoic were degraded via ortho pathway. A new UV spectrum at 257 nm which may be β-carboxy -muconate was detected in enzyme reaction products of protocatechuic acid as substrate with catechol 1,2-dioxygenase enzyme (Ornston and Stanier, 1966).…”
Section: Ring Cleavage Enzymesupporting
confidence: 93%
“…Conversion of DNB and AN to brown coloured oxygenated products was reported by Parris (1980). Polymerization of highly reactive catechol or protocatechute was reported also by Loidl et al (1990) and Bachofer et al (1975); it may give a reason for the accumulation of the brownish product.…”
Section: Degradation Of Dnb or An In Shaking Flasksmentioning
confidence: 88%
“…3,7) Recently, many studies on aniline mainly focused on biodegradability, metabolic pathway by pure culture of microorganisms and removal of aniline in wastewater treatment systems. [8][9][10][11][12][13][14] Studies researching into the degradation of aniline by bacteria as the sole source of carbon have been done by many researchers. 4,8) However, few studies have focused on the processes and degradation ability of bacteria to utilize aniline as the sole source of nitrogen.…”
Section: Introductionmentioning
confidence: 99%
“…Anilines are metabolized to the corresponding catechols via one or more oxidative reactions catalyzed by aniline dioxygenases, liberating ammonia and subsequently undergoing metabolic transformations (Liodl et al, 1990;Fuchs et al, 1991). Bacterial degradation of aromatic compounds has frequently been shown to be plasmid encoded (Chakrabarty, 1976).…”
Section: Bacterial Strainsmentioning
confidence: 99%