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Differential expression of enzyme activities initiating anoxic metabolism of various aromatic compounds via benzoyl-CoA
Authors:Werner Dangel  Ruth Brackmann  Achim Lack  Magdy Mohamed  Jürgen Koch  Brigitte Oswald  Birgit Seyfried  Andreas Tschech  Georg Fuchs
Affiliation:(1) Abteilung Angewandte Mikrobiologie, Universität Ulm, Postfach 4066, W-7900 Ulm, Federal Republic of Germany
Abstract:The regulation of the expression of enzyme activities catalyzing initial reactions in the anoxic metabolism of various aromatic compounds was studied at the whole cell level in the denitrifying Pseudomonas strain K 172. The specific enzyme activities were determined after growth on six different aromatic substrates (phenol, 4-hydroxybenzoate, benzoate, p-cresol, phenylacetate, 4-hydroxyphenylacetate) all being proposed to be metabolized anaerobically via benzoyl-CoA. As a control cells were grown on acetate, or aerobically on benzoate. The expression of the following enzyme activities was determined.ldquoPhenol carboxylaserdquo, as studied by the isotope exchange between 14CO2 and the carboxyl group of 4-hydroxybenzoate; 4-hydroxybenzoyl-CoA reductase (dehydroxylating); p-cresol methylhydroxylase; 4-hydroxybenzyl alcohol dehydrogenase; 4-hydroxybenzaldehyde dehydrogenase; coenzymeA ligases for the aromatic acids benzoate, 4-hydroxybenzoate, phenylacetate, and 4-hydroxyphenylacetate; phenylglyoxylate: acceptor oxidoreductase and 4-hydroxyphenylglyoxylate: acceptor oxidoreductase; aromatic alcohol and aldehyde dehydrogenases.The formation of most active enzymes is strictly regulated; they were only induced when required, the basic activities being almost zero. The observed whole cell regulation pattern supports the postulate that the enzyme activities play a role in anoxic aromatic metabolism and that the compounds are degraded via the following intermediates: Phenol rarr 4-hydroxybenzoate rarr 4-hydroxybenzoyl-CoA rarr benzoyl-CoA; 4-hydroxybenzoate rarr 4-hydroxybenzoyl-CoA rarr benzoyl-CoA; benzoate rarr benzoyl-CoA; p-cresol rarr 4-hydroxybenzaldehyde rarr 4-hydroxybenzoate rarr 4-hydroxybenzoyl-CoA rarr benzoyl-CoA; phenylacetate rarr phenylacetyl-CoA rarr phenylglyoxylate rarr benzoyl-CoA plus CO2; 4-hydroxyphenylacetate rarr 4-hydroxyphenylacetyl-CoA rarr 4-hydroxyphenylglyoxylate rarr 4-hydroxybenzoyl-CoA plus CO2 rarr benzoyl-CoA.
Keywords:Aromatic compounds  Anaerobic aromatic metabolism  Pseudomonas K 172  Phenol  4-Hydroxybenzoate  p-Cresol  Phenylacetate  Benzoate  Coenzyme A thioester
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