Glycoside Hydrolase Family 36

Glycoside Hydrolase Family GH36
Clan	GH-D
Mechanism	retaining
Active site residues	known
CAZy DB link
http://www.cazy.org/fam/GH36.html

Substrate specificities

Alpha-galactosidase and alpha-N-acetylgalactosaminidase activity has been demonstrated in archaeal, bacterial, and eukaryotic members of this family. Additionally, certain plant members of this family possess stachyose synthase or raffinose synthase activity.

Kinetics and Mechanism

Family GH36 alpha-galactosidases are anomeric configuration-retaining enzymes, as first shown by NMR studies on the alpha-galactosidase GalA from Thermotoga maritima [1]. Correspondingly, GH36 enzymes use a classical Koshland double-displacement mechanism [2], like their Glycoside Hydrolase Family GH27 (GH27) relatives in Clan GH-D. This mechanism involves the formation of a covalent glycosyl-enzyme intermediate [3] that partitions predominantly to water in hydrolytic enzymes and to saccharide acceptor substrates in transglycosylating enzymes, such as stachyose and raffinose synthases.

Catalytic Residues

Detailed phylogenetic analysis of archaeal GH36 alpha-galactosidases within Clan GH-D originally highlighted likely candidates for the catalytic nucleophile and general acid/base residues in this family, based on protein sequence similarity with those identified in GH27 [4]. Mutagenesis of the corresponding residues in Sulfolobus solfataricus alpha-galactosidase GalS dramatically reduced enzyme activity: the D367G (nucleophile) and D425G (acid/base) mutant had <1 x 10^–3 and 5 x 10^–3 lower activity than the wild type enzyme when assayed against p-nitrophenol-alpha-D-galactopyranoside [4]. Rescue of the catalytic function of both enzyme mutants was unsuccessful with both azide and formate anions [4].

The identities for the catalytic residues in GH36 were also confirmed in the Thermotoga maritima alpha-galactosidase GalA, guided by structural homology with GH27 enzymes [1]. Site-directed mutation of Asp327 to Gly yielded a variant that had a 200-800-fold lower catalytic rate on aryl galactosides compared with the WT enzyme. Addition of azide was shown to rescue the ability of the enzyme to hydrolyze p-nitrophenol-alpha-D-galactopyranoside and resulted in formation of beta-galactopyranosyl azide, confirming Asp327 as the nucleophilic residue. Mutation of the predicted acid/base residue, Asp387, to Gly reduced activity 1500-fold on p-nitrophenol-alpha-D-galactopyranoside, while addition of azide resulted in formation of alpha-galactopyranosyl azide by nucleophilic attack on the beta-linked glycosyl enzyme.

Three-dimensional structures

In June 2005, the first three-dimensional structural coordinates for a member of this family, alpha-galactosidase TmGalA from Thermotoga maritima, were deposited by the Joint Center For Structural Genomics (JCSG) (X-ray, 2.34 Å, PDB 1zy9) [5]. Subsequent analysis of this data by an American/Russian/Swedish consortium, in the context of existing structures of GH27 enzymes, revealed homologous active site residues, including two key catalytic Asp residues and a number of conserved substrate-binding residues [1]. The active sites of both GH27 and GH36 enzymes are presented by (alpha/beta)8 (TIM) barrel domains. Both GH36 and GH27 enzymes contain a C-terminal beta-sheet domain of unknown function, although this domain is structurally different and more disordered in TmGalA compared with the homologous domain in GH27 (e.g., Oryza sativa alpha-galactosidase). Notably, an extra N-terminal, primarily beta-sheet domain, which is not found in GH27 enzymes, contributes a key substrate-binding residue (Trp65) to the active site of TmGalA (Trp65, replacing Trp164 in the O. sativa enzyme). Another notable active site substitution, this time within the TIM barrel itself, is the replacement of the aromatic residues Phe328 and Trp 291 in TmGalA with Ser102 and the Cys101-Cys132 disulfide in the O. sativa enzyme [1].

Phylogeny: [4]

Family Firsts

First sterochemistry determination

Thermotoga maritima alpha-galactosidase, by NMR [1].

First catalytic nucleophile identification

Sulfolobus solfataricus alpha-galactosidase GalS, by sequence homology with GH27 enzymes and mutagenesis [4]. Subsequently confirmed in Thermotoga maritima alpha-galactosidase by structural homology, mutagenesis, and azide rescue [1].

First general acid/base residue identification

Sulfolobus solfataricus alpha-galactosidase GalS, by sequence homology with GH27 enzymes and mutagenesis [4]. Subsequently confirmed in Thermotoga maritima alpha-galactosidase by structural homology, mutagenesis, and azide rescue [1].

First 3-D structure

Thermotoga maritima alpha-galactosidase by X-ray crystallography. Coordinates (PDB 1zy9) deposited in 2005 as part of a high-throughput functional genomics project [5], first structural analysis reported in 2007 [1].

References

1. Comfort DA, Bobrov KS, Ivanen DR, Shabalin KA, Harris JM, Kulminskaya AA, Brumer H, and Kelly RM. (2007). Biochemical analysis of Thermotoga maritima GH36 alpha-galactosidase (TmGalA) confirms the mechanistic commonality of clan GH-D glycoside hydrolases. Biochemistry. 2007;46(11):3319-30. DOI:10.1021/bi061521n |

2. Sinnott, M.L. (1990) Catalytic mechanisms of enzymatic glycosyl transfer. Chem. Rev. 90, 1171-1202. DOI: 10.1021/cr00105a006

3. Vocadlo DJ, Davies GJ, Laine R, and Withers SG. (2001). Catalysis by hen egg-white lysozyme proceeds via a covalent intermediate. Nature. 2001;412(6849):835-8. DOI:10.1038/35090602 |
4. Brouns SJ, Smits N, Wu H, Snijders AP, Wright PC, de Vos WM, and van der Oost J. (2006). Identification of a novel alpha-galactosidase from the hyperthermophilic archaeon Sulfolobus solfataricus. J Bacteriol. 2006;188(7):2392-9. DOI:10.1128/JB.188.7.2392-2399.2006 |
5. Lesley SA, Kuhn P, Godzik A, Deacon AM, Mathews I, Kreusch A, Spraggon G, Klock HE, McMullan D, Shin T, Vincent J, Robb A, Brinen LS, Miller MD, McPhillips TM, Miller MA, Scheibe D, Canaves JM, Guda C, Jaroszewski L, Selby TL, Elsliger MA, Wooley J, Taylor SS, Hodgson KO, Wilson IA, Schultz PG, and Stevens RC. (2002). Structural genomics of the Thermotoga maritima proteome implemented in a high-throughput structure determination pipeline. Proc Natl Acad Sci U S A. 2002;99(18):11664-9. DOI:10.1073/pnas.142413399 |