Literature DB >> 26422370

Crystal structures of halohydrin hydrogen-halide-lyases from Corynebacterium sp. N-1074.

Fumiaki Watanabe1, Fujio Yu1, Akashi Ohtaki2, Yasuaki Yamanaka2, Keiichi Noguchi3, Masafumi Yohda2, Masafumi Odaka2,4.   

Abstract

Halohydrin hydrogen-halide-lyase (H-Lyase) is a bacterial enzyme that is involved in the degradation of halohydrins. This enzyme catalyzes the intramolecular nucleophilic displacement of a halogen by a vicinal hydroxyl group in halohydrins to produce the corresponding epoxides. The epoxide products are subsequently hydrolyzed by an epoxide hydrolase, yielding the corresponding 1, 2-diol. Until now, six different H-Lyases have been studied. These H-Lyases are grouped into three subtypes (A, B, and C) based on amino acid sequence similarities and exhibit different enantioselectivity. Corynebacterium sp. strain N-1074 has two different isozymes of H-Lyase, HheA (A-type) and HheB (B-type). We have determined their crystal structures to elucidate the differences in enantioselectivity among them. All three groups share a similar structure, including catalytic sites. The lack of enantioselectivity of HheA seems to be due to the relatively wide size of the substrate tunnel compared to that of other H-Lyases. Among the B-type H-Lyases, HheB shows relatively high enantioselectivity compared to that of HheBGP1 . This difference seems to be due to amino acid replacements at the active site tunnel. The binding mode of 1, 3-dicyano-2-propanol at the catalytic site in the crystal structure of the HheB-DiCN complex suggests that the product should be (R)-epichlorohydrin, which agrees with the enantioselectivity of HheB. Comparison with the structure of HheC provides a clue for the difference in their enantioselectivity.
© 2015 Wiley Periodicals, Inc.

Entities:  

Keywords:  NAD(P)H-dependent short-chain dehydrogenases/reductase; Rossmann fold; crystal structure; enantioselectivity; halohydrin; lyase

Mesh:

Substances:

Year:  2015        PMID: 26422370     DOI: 10.1002/prot.24938

Source DB:  PubMed          Journal:  Proteins        ISSN: 0887-3585


  3 in total

1.  Exploiting distant homologues for phasing through the generation of compact fragments, local fold refinement and partial solution combination.

Authors:  Claudia Millán; Massimo Domenico Sammito; Airlie J McCoy; Andrey F Ziem Nascimento; Giovanna Petrillo; Robert D Oeffner; Teresa Domínguez-Gil; Juan A Hermoso; Randy J Read; Isabel Usón
Journal:  Acta Crystallogr D Struct Biol       Date:  2018-04-03       Impact factor: 7.652

2.  Position 123 of halohydrin dehalogenase HheG plays an important role in stability, activity, and enantioselectivity.

Authors:  Jennifer Solarczek; Thomas Klünemann; Felix Brandt; Patrick Schrepfer; Mario Wolter; Christoph R Jacob; Wulf Blankenfeldt; Anett Schallmey
Journal:  Sci Rep       Date:  2019-03-25       Impact factor: 4.379

Review 3.  Recent advances on halohydrin dehalogenases-from enzyme identification to novel biocatalytic applications.

Authors:  Anett Schallmey; Marcus Schallmey
Journal:  Appl Microbiol Biotechnol       Date:  2016-08-08       Impact factor: 4.813

  3 in total

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