Ensign S A, Small F J, Allen J R, Sluis M K
Department of Chemistry and Biochemistry, Utah State University, Logan, UT 84322-0300, USA.
Arch Microbiol. 1998 Mar;169(3):179-87. doi: 10.1007/s002030050558.
Short-chain aliphatic epoxides and ketones are two classes of toxic organic compounds formed biogenically and anthropogenically. In spite of their toxicity, these compounds are utilized as primary carbon and energy sources or are generated as intermediate metabolites in the metabolism of other compounds (e.g., alkenes, alkanes, and secondary alcohols) by a number of diverse bacteria. One bacterium capable of using both classes of compounds is the gram-negative aerobe Xanthobacter strain Py2. Studies of epoxide and ketone (acetone) metabolism by Xanthobacter strain Py2 have revealed a central role for CO2 in these processes. Both classes of compounds are metabolized by carboxylation reactions that produce beta-keto acids as products. The epoxide- and ketone-converting enzymes are distinct carboxylases with molecular properties and cofactor requirements unprecedented for other carboxylases. Epoxide carboxylase is a four-component multienzyme complex that requires NADPH and NAD+ as cofactors. In the course of epoxide carboxylation, a transhydrogenation reaction occurs wherein NADPH undergoes oxidation and NAD+ undergoes reduction. Acetone carboxylase is a multimeric (three-subunit) ATP-dependent enzyme that forms AMP and inorganic phosphate as ATP hydrolysis products in the course of acetone carboxylation. Recent studies have demonstrated that acetone metabolism in diverse anaerobic bacteria (sulfate reducers, denitrifiers, phototrophs, and fermenters) also proceeds by carboxylation reactions. ATP-dependent acetone carboxylase activity has been demonstrated in cell-free extracts of the anaerobic acetone-utilizers Rhodobacter capsulatus, Rhodomicrobium vannielii, and Thiosphaera pantotropha. These studies have identified new roles for CO2 as a cosubstrate in the metabolism of two classes of important xenobiotic compounds. In addition, two new classes of carboxylases have been identified, the investigation of which promises to reveal new insights into biological strategies for the fixation of CO2 to organic substrates.
短链脂肪族环氧化物和酮是两类通过生物源和人为源形成的有毒有机化合物。尽管它们具有毒性,但这些化合物被多种不同细菌用作主要的碳源和能源,或者在其他化合物(如烯烃、烷烃和仲醇)的代谢过程中作为中间代谢产物产生。一种能够利用这两类化合物的细菌是革兰氏阴性需氧菌黄杆菌属菌株Py2。对黄杆菌属菌株Py2的环氧化物和酮(丙酮)代谢的研究揭示了二氧化碳在这些过程中的核心作用。这两类化合物都通过羧化反应进行代谢,生成β-酮酸作为产物。环氧化物转化酶和酮转化酶是不同的羧化酶,其分子特性和辅因子需求与其他羧化酶前所未有的不同。环氧化物羧化酶是一种四组分多酶复合物,需要NADPH和NAD +作为辅因子。在环氧化物羧化过程中,发生转氢反应,其中NADPH被氧化,NAD +被还原。丙酮羧化酶是一种多聚体(三亚基)ATP依赖性酶,在丙酮羧化过程中形成AMP和无机磷酸作为ATP水解产物。最近的研究表明,多种厌氧细菌(硫酸盐还原菌、反硝化菌、光合细菌和发酵菌)中的丙酮代谢也通过羧化反应进行。在厌氧丙酮利用菌荚膜红细菌、万氏红微菌和泛养硫球菌的无细胞提取物中已证明存在ATP依赖性丙酮羧化酶活性。这些研究确定了二氧化碳作为两种重要的外源性化合物代谢中的共底物的新作用。此外还鉴定出了两类新的羧化酶,对其进行研究有望揭示将二氧化碳固定到有机底物的生物学策略的新见解。