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Detailed dissection of a new mechanism for glycoside cleavage: ?-1,4-glucan lyase

Detailed dissection of a new mechanism for glycoside cleavage: ?-1,4-glucan lyase
Detailed dissection of a new mechanism for glycoside cleavage: ?-1,4-glucan lyase
The unusual enzyme, Gracilariopsis ?-1,4-glucan lyase of the sequence-related glycoside hydrolase family 31, cleaves the glycosidic bond of ?-1,4-glucans via a ?-elimination reaction involving a covalent glycosyl?enzyme intermediate (Lee, S. S., Yu, S., and Withers, S. G. (2002) J. Am. Chem. Soc. 124, 4948?4949). The classical bell-shaped pH dependence of kcat/Km indicates two ionizable groups in the active site with apparent pKa values of 3.05 and 6.66. Brønsted relationships of log kcat versus pKa and log(kcat/Km) versus pKa for a series of aryl glucosides both show a linear monotonic dependence on leaving group pKa with low ?lg values of 0.32 and 0.33, respectively. The combination of these low ?lg values with large secondary deuterium kinetic isotope effects (kH/kD = 1.161.19) on the first step indicate a glycosylation step with substantial glycosidic bond cleavage and proton donation to the leaving group oxygen at the transition state. Developed oxocarbenium ion character of the transition state is also suggested by the potent inhibition afforded by acarbose and 1-deoxynojirimycin (Ki = 20 and 130 nM, respectively) and by the substantial rate reduction afforded by adjacent fluorine substitution. For only one substrate, 5-fluoro-?-d-glucopyranosyl fluoride, was the second elimination step shown to be rate-limiting. The large ?-secondary deuterium kinetic isotope effect (kH/kD = 1.23) at C-1 and the small primary deuterium kinetic isotope effect (kH/kD = 1.92) at C-2 confirm an E2 mechanism with strong E1 character for this second step. This considerable structural and mechanistic similarity with retaining ?-glucosidases is clear evidence for the evolution of an enzyme mechanism within the family.
13081-13090
Lee, Seung Seo
ee34fa26-5fb6-48c8-80c2-1f13ec4ccceb
Yu, Shukun
bbd9599a-fdff-4d07-93fc-76105bfc5f44
Withers, Stephen G.
2fa507a8-6772-41a0-97a0-a33f443bbcc1
Lee, Seung Seo
ee34fa26-5fb6-48c8-80c2-1f13ec4ccceb
Yu, Shukun
bbd9599a-fdff-4d07-93fc-76105bfc5f44
Withers, Stephen G.
2fa507a8-6772-41a0-97a0-a33f443bbcc1

Lee, Seung Seo, Yu, Shukun and Withers, Stephen G. (2003) Detailed dissection of a new mechanism for glycoside cleavage: ?-1,4-glucan lyase. Biochemistry, 42 (44), 13081-13090. (doi:10.1021/bi035189g).

Record type: Article

Abstract

The unusual enzyme, Gracilariopsis ?-1,4-glucan lyase of the sequence-related glycoside hydrolase family 31, cleaves the glycosidic bond of ?-1,4-glucans via a ?-elimination reaction involving a covalent glycosyl?enzyme intermediate (Lee, S. S., Yu, S., and Withers, S. G. (2002) J. Am. Chem. Soc. 124, 4948?4949). The classical bell-shaped pH dependence of kcat/Km indicates two ionizable groups in the active site with apparent pKa values of 3.05 and 6.66. Brønsted relationships of log kcat versus pKa and log(kcat/Km) versus pKa for a series of aryl glucosides both show a linear monotonic dependence on leaving group pKa with low ?lg values of 0.32 and 0.33, respectively. The combination of these low ?lg values with large secondary deuterium kinetic isotope effects (kH/kD = 1.161.19) on the first step indicate a glycosylation step with substantial glycosidic bond cleavage and proton donation to the leaving group oxygen at the transition state. Developed oxocarbenium ion character of the transition state is also suggested by the potent inhibition afforded by acarbose and 1-deoxynojirimycin (Ki = 20 and 130 nM, respectively) and by the substantial rate reduction afforded by adjacent fluorine substitution. For only one substrate, 5-fluoro-?-d-glucopyranosyl fluoride, was the second elimination step shown to be rate-limiting. The large ?-secondary deuterium kinetic isotope effect (kH/kD = 1.23) at C-1 and the small primary deuterium kinetic isotope effect (kH/kD = 1.92) at C-2 confirm an E2 mechanism with strong E1 character for this second step. This considerable structural and mechanistic similarity with retaining ?-glucosidases is clear evidence for the evolution of an enzyme mechanism within the family.

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More information

e-pub ahead of print date: 15 October 2003
Published date: 11 November 2003
Organisations: Organic Chemistry: SCF

Identifiers

Local EPrints ID: 345658
URI: http://eprints.soton.ac.uk/id/eprint/345658
PURE UUID: 27252b89-3f6d-4e9c-b858-d768b9282c73
ORCID for Seung Seo Lee: ORCID iD orcid.org/0000-0002-8598-3303

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Date deposited: 12 Feb 2013 16:47
Last modified: 15 Mar 2024 03:46

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Contributors

Author: Seung Seo Lee ORCID iD
Author: Shukun Yu
Author: Stephen G. Withers

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