Glycoside Hydrolase Family 66

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• Author: ^^^Ryuichiro Suzuki^^^
• Responsible Curator: ^^^Zui Fujimoto^^^

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Glycoside Hydrolase Family GH66
Clan	none, (β/α)8
Mechanism	retaining
Active site residues	known
CAZy DB link
http://www.cazy.org/GH66.html

Substrate specificities

    Glycoside hydrolases of GH66 contains exo-acting dextranases (Dex; EC 3.2.1.11) and cycloisomaltooligosaccharide glucanotransferase (CITase; EC 2.4.1.248). Dexs hydrolyze a-1,6 linkage of dextran and produce isomaltooligosaccharides (IGs) of varying length. Dexs are classified into GH49 and GH66. In contrast to inverting GH49 enzymes, GH66 enzymes are retaining enzymes. CITases catalyze intramolecular transglucosylation to produce cycloisomaltooligosaccharides (CIs; cyclodextrans) with degree of polymerization of 7-17   Normal  0        0  2    false  false  false    EN-US  JA  X-NONE                                                                                                                                                                                                                                                                                                                                                                                  [1].        Normal  0        0  2    false  false  false    EN-US  JA  X-NONE

CITases produce CIs from IG4 and larger IGs[2].

Some Dexs displaying strong dextranolytic activity and low cyclization activity have been discovered [3, 4]. The GH66 enzymes are classified into the following three types: (i) Dexs, (ii) Dex with low CITase activity, and (iii) CITases.

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Kinetics and Mechanism

GH66 enzymes are retaining enzymes, as first shown by structural [5, 6]and chemical rescue studies [3]. .

Catalytic Residues

To date, catalytic residues of four GH66 enzymes were identified by mutational and structural studies [2, 3, 6]. In Dex from Streptococcus mutans (SmDex), Asp385 and Glu453 are nucleophile and acid/base catalyst, respectively[6]. In Dex from Paenibacillus sp. (PsDex), Asp340 and Glu412 are nucleophile and acid/base catalyst, respectively [3]. In CITase from Bacillus circulans T-3040 (CITase-T3040), Asp270 and Glu342 are nucleophile and acid/base catalyst, respectively[2]. In CITase from Paenibacillus sp. 598K (CITase-598K), Asp269 and Glu341 are nucleophile and acid/base catalyst, respectively [2].

Three-dimensional structures

The crystal structures of truncated mutant of SmDex (lacking the N-terminal 99 and C-terminal 118 residues) have been reported as the first three-dimensional structure of GH66 enzymes [5, 6]. Ligand free (PDB code 3VMN), in compex with IG3 (PDB code 3VMO), and in complex with 4’,5’-epoxypentyl-a-D-glucopyranoside (PDB code 3VMP). The catalytic domain of the enzyme is a (b/a)8-barrel fold. The enzyme consists of at least three domains.

Family Firsts

First stereochemistry determination

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First catalytic nucleophile identification

SmDex and PsDex by structural study and chemical rescue approach, respectively [2, 3] Normal 0 0 2 false false false EN-US JA X-NONE .

First general acid/base residue identification

SmDex and PsDex by structural study and chemical rescue approach, respectively [2, 3].

First 3-D structure

Truncated mutant of SmDex [5, 6] .

References

1. pmid=

7. . Funane K, Terasawa K, Mizuno Y, Ono H, Gibu S, Tokashiki T, Kawabata Y, Kim YM, Kimura A, Kobayashi M.(2008) Isolation of Bacillus and Paenibacillus bacterial strains that produce large molecules of cyclic isomaltooligosaccharides. Biosci Biotechnol Biochem. 72, 3277-3280. Normal 0 0 2 false false false EN-US JA X-NONE [http: DOI: ]

8. pmid=

9. . Suzuki, R., Terasawa, K., Kimura, K., Fujimoto, Z., Momma, M., Kobayashi, M., Kimura, A., and Funane, K. (2012) Biochemical characterization of a novel cycloisomaltooligosaccharide glucanotransferase from Paenibacillus sp. 598K. Biochim. Biophys. Acta Normal 0 0 2 false false false EN-US JA X-NONE [http: DOI: ]

3. pmid=

10. . Kim, Y. M., Kiso, Y., Muraki, T., Kan, M. S., Nakai, H., Saburi, W., Lang, W., Kang, H. K., Okuyama, M., Mori, H., Suzuki, R., Funane, K., Suzuki, N., Momma, M., Fujimoto, Z., Oguma, T., Kobayashi, M., Kim, D., and Kimura, A. (2012) Novel dextranase catalyzing cycloisomaltooligosaccharide formation and identification of catalytic amino acids and their functions using chemical rescue approach. J. Biol. Chem. 287, 19927-19935 Normal 0 0 2 false false false EN-US JA X-NONE [http: DOI: ]

4. pmid=

11. . Kim, YM, Yamamoto, E, Kang, MS, Nakai, H, Saburi, W, Okuyama, M, Mori, H, Funane, K, Momma, M, Fujimoto, Z, Kobayashi, M, Kim, D and Kimura, A (2012) Bacteroides thetaiotaomicron VPI-5482 glycoside hydrolase family 66 homolog catalyzes dextranolytic and cyclization reactions. FEBS J. 279, 3185-3191 Normal 0 0 2 false false false EN-US JA X-NONE [http: DOI: ]

5. pmid=

12. . Suzuki, N., Kim, Y. M., Fujimoto, Z., Momma, M., Kang, H. K., Funane, K., Okuyama, M., Mori, H., and Kimura, A. (2011) Crystallization and preliminary crystallographic analysis of dextranase from Streptococcus mutans. Acta Crystallogr. F Struct. Biol. Cryst. Commun. 67, 1542–1544 Normal 0 0 2 false false false EN-US JA X-NONE [http: DOI: ]

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5. pmid=

13. . Suzuki N, Kim YM, Fujimoto Z, Momma M, Okuyama M, Mori H, Funane K & Kimura A (2012) Structural elucidation of dextran degradation mechanism by Streptococcus mutans dextranase belonging to glycoside hydrolase family 66. J Biol Chem 287, 19916-19926. Normal 0 0 2 false false false EN-US JA X-NONE [http: DOI: ]