A Rhodococcus sp. isolated from contaminated river sediment was investigate
d to determine if the isolate could degrade high molecular mass polycyclic
aromatic hydrocarbons. The Rhodococcus sp. was able to utilize anthracene (
53%), phenanthrene (31%), pyrene (13%), and fluoranthene (5%) as sole sourc
e of carbon and energy, but not naphthalene or chrysene. In a study of the
degradation of anthracene by a Rhodococcus sp., the identification of ring-
fission products indicated at least two ring-cleavage pathways. One results
in the production of 6,7-benzocoumarin, previously shown to be produced ch
emically from the product of meta cleavage of 1,2-dihydroxyanthracene, a pa
thway which has been well established in Gram-negative bacteria. The second
is an ortho cleavage of 1,2-dihydroxyanthracene that produces 3-(2-carboxy
vinyl)naphthalene-2-carboxylic acid, a dicarboxylic acid rin.-fission produ
ct. This represents a novel metabolic pathway only identified in Gram-posit
ive bacteria. (C) 2001 Federation of European Microbiological Societies. Pu
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