Klecka G M, Gibson D T
Appl Environ Microbiol. 1981 May;41(5):1159-65. doi: 10.1128/aem.41.5.1159-1165.1981.
Partially purified preparations of catechol 2,3-dioxygenase from toluene-grown cells of Pseudomonas putida catalyzed the stoichiometric oxidation of 3-methylcatechol to 2-hydroxy-6-oxohepta-2,4-dienoate. Other substrates oxidized by the enzyme preparation were catechol, 4-methylcatechol, and 4-fluorocatechol. The apparent Michaelis constants for 3-methylcatechol and catechol were 10.6 and 22.0 muM, respectively. Substitution at the 4-position decreases the affinity and activity of the enzyme for the substrate. Catechol 2,3-dioxygenase preparations did not oxidize 3-chlorocatechol. In addition, incubation of the enzyme with 3-chlorocatechol led to inactivation of the enzyme. Kinetic analyses revealed that both 3-chlorocatechol and 4-chlorocatechol were noncompetitive or mixed-type inhibitors of the enzyme. 3-Chlorocatechol (Ki = 0.14 muM) was a more potent inhibitor than 4-chlorocatechol (Ki = 50 muM). The effect of the ion-chelating agents Tiron and o-phenanthrolene were compared with that of 3-chlorocatechol on the inactivation of the enzyme. Each inhibitor appeared to remove iron from the enzyme, since inactive enzyme preparations could be fully reactivated by treatment with ferrous iron and a reducing agent.
从以甲苯为生长底物的恶臭假单胞菌细胞中部分纯化得到的儿茶酚2,3-双加氧酶制剂,催化3-甲基儿茶酚按化学计量比氧化为2-羟基-6-氧代庚-2,4-二烯酸酯。该酶制剂氧化的其他底物有儿茶酚、4-甲基儿茶酚和4-氟儿茶酚。3-甲基儿茶酚和儿茶酚的表观米氏常数分别为10.6和22.0 μM。在4位进行取代会降低酶对底物的亲和力和活性。儿茶酚2,3-双加氧酶制剂不能氧化3-氯儿茶酚。此外,该酶与3-氯儿茶酚一起温育会导致酶失活。动力学分析表明,3-氯儿茶酚和4-氯儿茶酚都是该酶的非竞争性或混合型抑制剂。3-氯儿茶酚(Ki = 0.14 μM)比4-氯儿茶酚(Ki = 50 μM)是更强效的抑制剂。将离子螯合剂钛铁试剂和邻菲罗啉与3-氯儿茶酚对酶失活的影响进行了比较。每种抑制剂似乎都从酶中除去了铁,因为失活的酶制剂可以通过用亚铁和还原剂处理而完全重新激活。