Department of Biological Chemistry, University of Michigan, Ann Arbor, Michigan 48109-5606, USA.
Biochemistry. 2010 Jan 19;49(2):372-85. doi: 10.1021/bi901454u.
There are two known types of microbial two-component flavin-dependent monooxygenases that catalyze oxygenation of p-hydroxyphenylacetate (HPA), and they are distinguished by having structurally distinct reductases and oxygenases. This paper presents a detailed analysis of the properties of the enzyme from Pseudomonas aeruginosa, an example of one group, and compares its properties to those published for the Acinetobacter baumannii enzyme, an example of the alternative group. The reductase and oxygenase from P. aeruginosa were expressed in Escherichia coli. The reductase was purified as a stable C-terminally His-tagged yellow protein containing weakly bound FAD, and the oxygenase was purified as a stable colorless N-terminally His-tagged protein. The reductase catalyzes the reduction of FAD by NADH and releases the FADH(-) product into solution, but unlike the reductase from A. baumannii, this catalysis is not influenced by HPA. The oxygenase binds the released FADH(-) and catalyzes the oxygenation of HPA to form 3,4-dihydroxyphenylacetate, after which the FAD dissociates to be re-reduced by the reductase, a common overall pattern for two-component flavin-dependent oxygenases. With this system, it appears that interactions between the reductase and the oxygenase can facillitate the transfer of FADH(-) to the oxygenase, although they are not required. We show that the P. aeruginosa oxygenase system in complex with FADH(-) reacts with O(2) to form a quasi-stable, unusually high-extinction flavin hydroperoxide species that binds HPA and reacts to form the product. The resultant flavin hydroxide decomposes to FAD and water while still bound to the oxygenase and then releases product and FAD from the protein. Unlike the enzyme from A. baumannii, during normal catalysis involving both the reductase and oxygenase, the rate-determining step in catalysis is the dissociation of FAD from the oxygenase in a process that is independent of the concentration of HPA. Structures for the reductases and oxygenases from A. baumannii and from Thermus thermophilus (similar to the P. aeruginosa system) form a basis for interpreting the molecular origins of the differences between the two groups of flavin-dependent two-component oxygenases.
有两种已知的微生物黄素依赖双组分单加氧酶,它们能够催化对羟基苯乙酸(HPA)的氧化,这两种酶的区别在于它们具有结构不同的还原酶和加氧酶。本文详细分析了铜绿假单胞菌(属于一组)黄素依赖双组分单加氧酶的性质,并将其性质与另一组的鲍曼不动杆菌黄素依赖双组分单加氧酶的性质进行了比较。铜绿假单胞菌的还原酶和加氧酶在大肠杆菌中表达。还原酶被纯化为一种稳定的 C 端带有 His 标签的黄色蛋白,其中含有结合较弱的 FAD,而加氧酶被纯化为一种稳定的无色 N 端带有 His 标签的蛋白。还原酶催化 NADH 还原 FAD,并将 FADH(-)产物释放到溶液中,但与鲍曼不动杆菌的还原酶不同,这种催化作用不受 HPA 的影响。加氧酶结合释放的 FADH(-)并催化 HPA 的氧化形成 3,4-二羟基苯乙酸,之后 FAD 与还原酶解离,这是黄素依赖双组分加氧酶的一种常见的总体模式。使用该系统,似乎还原酶和加氧酶之间的相互作用可以促进 FADH(-)向加氧酶的转移,尽管它们不是必需的。我们表明,与 FADH(-)结合的铜绿假单胞菌加氧酶系统与 O(2)反应形成一种准稳定的、异常高消光的黄素过氧化物物种,该物种结合 HPA 并反应形成产物。生成的黄素氢氧化物在与加氧酶结合的同时分解为 FAD 和水,然后从蛋白质中释放产物和 FAD。与鲍曼不动杆菌的酶不同,在涉及还原酶和加氧酶的正常催化过程中,催化的限速步骤是 FAD 从加氧酶中的解离,该过程独立于 HPA 的浓度。鲍曼不动杆菌和嗜热栖热菌(类似于铜绿假单胞菌系统)的还原酶和加氧酶的结构为解释两种黄素依赖双组分加氧酶之间差异的分子起源提供了基础。