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J Bacteriol. 1974 September; 119(3): 923-929
Copyright © 1974 American Society for Microbiology. All Rights Reserved.

Bacterial Metabolism of para- and meta-Xylene: Oxidation of a Methyl Substituent

John F. Davey and David T. Gibson

1 Department of Microbiology, The University of Texas at Austin, Austin, Texas 78712

ABSTRACT

Pseudomonas Pxy was isolated on p-xylene as sole source of carbon and energy. Substrates that supported growth were toluene, p-methylbenzyl alcohol, p-tolualdehyde, p-toluic acid, and the analogous m-methyl derivatives, including m-xylene. Cell extracts prepared from Pseudomonas Pxy after growth with either p-xylene or m-xylene oxidized the p- and m-isomers of tolualdehyde as well as p-methylbenzyl alcohol. The same cell extracts also catalyzed a "meta" fission of both 3- and 4-methylcatechol. Treatment of Pseudomonas Pxy with N-methyl-N'-nitro-N-nitrosoguanidine led to the isolation of two mutant strains. Pseudomonas Pxy-40, when grown on succinate in the presence of p-xylene, accumulated p-toluic acid in the culture medium. Under the same conditions Pseudomonas Pxy-82 accumulated p-toluic acid and also 4-methylcatechol. When Pseudomonas Pxy-82 was grown on succinate in the presence of m-xylene, 3-methylcatechol and 3-methylsalicylic acid were excreted into the culture medium. A pathway is proposed for the initial reactions utilized by Pseudomonas Pxy to oxidize p- and m-xylene.


J Bacteriol. 1974 September; 119(3): 923-929
Copyright © 1974 American Society for Microbiology. All Rights Reserved.




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