Seyfried B, Tschech A, Fuchs G
Angewandte Mikrobiologie, Universität Ulm, Germany.
Arch Microbiol. 1993;159(6):563-73. doi: 10.1007/BF00249036.
Anaerobic degradation of (4-hydroxy)phenylacetate in denitrifying Pseudomonas sp. was investigated. Evidence is presented for alpha-oxidation of the coenzyme A (CoA)-activated carboxymethyl side chain, a reaction which has not been described. The C6-C2 compounds are degraded to benzoyl-CoA and furtheron to CO2 via the following intermediates: Phenylacetyl-CoA, phenylglyoxylate, benzoyl-CoA plus CO2; 4-hydroxyphenylacetyl-CoA, 4-hydroxyphenylglyoxylate, 4-hydroxybenzoyl-CoA plus CO2, benzoyl-CoA. Trace amounts of mandelate possibly derived from mandelyl-CoA were detected during phenylacetate degradation in vitro. The reactions are catalyzed by (i) phenylacetate-CoA ligase which converts phenylacetate to phenylacetyl-CoA and by a second enzyme for 4-hydroxyphenylacetate; (ii) a (4-hydroxy)-phenylacetyl-CoA dehydrogenase system which oxidizes phenylacetyl-CoA to (4-hydroxy)phenylglyoxylate plus CoA; and (iii) (4-hydroxy)phenylglyoxylate: acceptor oxidoreductase (CoA acylating) which catalyzes the oxidative decarboxylation of (4-hydroxy)phenylglyoxylate to (4-hydroxy)benzoyl-CoA and CO2. (iv) The degradation of 4-hydroxyphenylacetate in addition requires the reductive dehydroxylation of 4-hydroxybenzoyl-CoA to benzoyl-CoA, catalyzed by 4-hydroxybenzoyl-CoA reductase (dehydroxylating). The whole cell regulation of these enzyme activities supports the proposed pathway. An ionic mechanism for anaerobic alpha-oxidation of the CoA-activated carboxymethyl side chain is proposed.
研究了反硝化假单胞菌中(4-羟基)苯乙酸的厌氧降解。本文提供了辅酶A(CoA)激活的羧甲基侧链α-氧化的证据,该反应尚未见报道。C6-C2化合物通过以下中间体降解为苯甲酰辅酶A并进一步降解为二氧化碳:苯乙酰辅酶A、苯乙二醛、苯甲酰辅酶A加二氧化碳;4-羟基苯乙酰辅酶A、4-羟基苯乙二醛、4-羟基苯甲酰辅酶A加二氧化碳、苯甲酰辅酶A。在体外苯乙酸降解过程中检测到痕量可能源自扁桃酰辅酶A的扁桃酸。这些反应由以下酶催化:(i)苯乙酸-CoA连接酶,将苯乙酸转化为苯乙酰辅酶A,以及另一种作用于4-羟基苯乙酸的酶;(ii)一种(4-羟基)苯乙酰辅酶A脱氢酶系统,将苯乙酰辅酶A氧化为(4-羟基)苯乙二醛加辅酶A;(iii)(4-羟基)苯乙二醛:受体氧化还原酶(CoA酰化),催化(4-羟基)苯乙二醛氧化脱羧为(4-羟基)苯甲酰辅酶A和二氧化碳。(iv)4-羟基苯乙酸的降解还需要由4-羟基苯甲酰辅酶A还原酶(脱羟基)催化将4-羟基苯甲酰辅酶A还原脱羟基为苯甲酰辅酶A。这些酶活性的全细胞调节支持了所提出的途径。提出了CoA激活的羧甲基侧链厌氧α-氧化的离子机制。