Schlömann M, Fischer P, Schmidt E, Knackmuss H J
Institut für Mikrobiologie, Universität Stuttgart, Federal Republic of Germany.
J Bacteriol. 1990 Sep;172(9):5119-29. doi: 10.1128/jb.172.9.5119-5129.1990.
Enzymatic conversion of 4-fluorocatechol in the simultaneous presence of partially purified preparations of catechol 1,2-dioxygenase from Pseudomonas cepacia and muconate cycloisomerase from Alcaligenes eutrophus 335 yielded a product that was unambiguously identified as (+)-4-fluoromuconolactone [(+)-4-carboxymethyl-4-fluoro-but-2-en-4-olide]. This compound was shown to be the only major product formed from 3-fluoro-cis,cis-muconate by the action of muconate cycloisomerases from A. eutrophus 335, A. eutrophus JMP134, and P. cepacia as well as by the action of dichloromuconate cycloisomerase from A. eutrophus JMP134. This finding implies that dichloromuconate cycloisomerase, like the muconate cycloisomerases, catalyzes primarily a cycloisomerization reaction, which only in the case of chloro- and bromo-substituted substrates is connected to a dehalogenation. 4-Fluoromuconolactone at pH 7 decomposes by spontaneous reactions mainly to maleylacetate, which then decarboxylates to give cis-acetylacrylate. Although significant amounts of an unidentified compound are also formed from the fluorolactone, HF elimination to the two isomeric dienelactones (4-carboxymethylenebut-2-en-4-olides) is negligible. However, all spontaneous reactions proceed so slowly that an enzymatic conversion of 4-fluoromuconolactone must be assumed. Participation of dienelactone hydrolases in this reaction is indicated by their induction during growth of various strains with 4-fluorobenzoate. However, experiments with cell extracts of P. putida A3.12 suggest that at least one other hydrolytic enzyme is able to contribute to 4-fluoromuconolactone conversion. In light of these observations, earlier proposals for a 4-fluorobenzoate degradative pathway are discussed.
在洋葱伯克霍尔德氏菌的儿茶酚1,2 -双加氧酶和真养产碱菌335的粘康酸环异构酶的部分纯化制剂同时存在的情况下,4 -氟儿茶酚的酶促转化产生了一种产物,该产物被明确鉴定为(+)-4 -氟粘康酸内酯[(+)-4 -羧甲基-4 -氟-2 -丁烯-4 -内酯]。该化合物被证明是真养产碱菌335、真养产碱菌JMP134和洋葱伯克霍尔德氏菌的粘康酸环异构酶以及真养产碱菌JMP134的二氯粘康酸环异构酶作用于3 -氟-顺,顺-粘康酸形成的唯一主要产物。这一发现意味着二氯粘康酸环异构酶与粘康酸环异构酶一样,主要催化环异构化反应,只有在氯代和溴代取代底物的情况下才与脱卤反应相关。pH 7时的4 -氟粘康酸内酯通过自发反应主要分解为马来酰乙酸,然后马来酰乙酸脱羧生成顺式乙酰丙烯酸。尽管从氟内酯也形成了大量未鉴定的化合物,但向两种异构二烯内酯(4 -羧甲基亚甲基-2 -丁烯-4 -内酯)的氢氟酸消除可以忽略不计。然而,所有自发反应进行得都非常缓慢,因此必须假定存在4 -氟粘康酸内酯的酶促转化。各种菌株在以4 -氟苯甲酸生长期间二烯内酯水解酶的诱导表明它们参与了该反应。然而,恶臭假单胞菌A3.12细胞提取物的实验表明,至少还有一种其他水解酶能够促进4 -氟粘康酸内酯的转化。鉴于这些观察结果,讨论了早期关于4 -氟苯甲酸降解途径的提议。