de Jong R M, Tiesinga J J W, Rozeboom H J, Kalk K H, Tang L, Janssen D B, Dijkstra B W
Department of Biophysical Chemistry, Groningen Biomolecular Sciences and Biotechnology Institute, University of Groningen, Nijenborgh 4, NL-9747 AG Groningen, The Netherlands.
EMBO J. 2003 Oct 1;22(19):4933-44. doi: 10.1093/emboj/cdg479.
Haloalcohol dehalogenases are bacterial enzymes that catalyze the cofactor-independent dehalogenation of vicinal haloalcohols such as the genotoxic environmental pollutant 1,3-dichloro-2-propanol, thereby producing an epoxide, a chloride ion and a proton. Here we present X-ray structures of the haloalcohol dehalogenase HheC from Agrobacterium radiobacter AD1, and complexes of the enzyme with an epoxide product and chloride ion, and with a bound haloalcohol substrate mimic. These structures support a catalytic mechanism in which Tyr145 of a Ser-Tyr-Arg catalytic triad deprotonates the haloalcohol hydroxyl function to generate an intramolecular nucleophile that substitutes the vicinal halogen. Haloalcohol dehalogenases are related to the widespread family of NAD(P)H-dependent short-chain dehydrogenases/reductases (SDR family), which use a similar Ser-Tyr-Lys/Arg catalytic triad to catalyze reductive or oxidative conversions of various secondary alcohols and ketones. Our results reveal the first structural details of an SDR-related enzyme that catalyzes a substitutive dehalogenation reaction rather than a redox reaction, in which a halide-binding site is found at the location of the NAD(P)H binding site. Structure-based sequence analysis reveals that the various haloalcohol dehalogenases have likely originated from at least two different NAD-binding SDR precursors.
卤代醇脱卤酶是一类细菌酶,可催化邻位卤代醇(如具有遗传毒性的环境污染物1,3 - 二氯 - 2 - 丙醇)的非辅因子依赖性脱卤反应,从而生成环氧化物、氯离子和质子。在此,我们展示了来自放射形土壤杆菌AD1的卤代醇脱卤酶HheC的X射线晶体结构,以及该酶与环氧化物产物和氯离子、与结合的卤代醇底物类似物的复合物结构。这些结构支持了一种催化机制,即丝氨酸 - 酪氨酸 - 精氨酸催化三联体中的酪氨酸145使卤代醇的羟基去质子化,生成一个分子内亲核试剂,以取代邻位卤素。卤代醇脱卤酶与广泛存在的依赖NAD(P)H的短链脱氢酶/还原酶家族(SDR家族)相关,后者使用类似的丝氨酸 - 酪氨酸 - 赖氨酸/精氨酸催化三联体来催化各种仲醇和酮的还原或氧化转化反应。我们的研究结果揭示了一种与SDR相关的酶催化取代脱卤反应而非氧化还原反应的首个结构细节,其中在NAD(P)H结合位点的位置发现了一个卤化物结合位点。基于结构的序列分析表明,各种卤代醇脱卤酶可能起源于至少两种不同的结合NAD的SDR前体。