Glycoside Hydrolase Family 172

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• Author: Toma Kashima
• Responsible Curator: Shinya Fushinobu

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Glycoside Hydrolase Family GH172
Clan	None
Mechanism	retaining
Active site residues	known
CAZy DB link
https://www.cazy.org/GH172.html

Substrate specificities

Glycoside hydrolase family 172 (GH172) includes α-D-arabinofuranosidases and α-D-fructofuranosidases. This family was established following the discovery of αFFase1 from Bifidobacterium dentium by Kashima et al. in 2021 [1]. αFFase1 hydrolyzes the alkylated glycosides Me-α-D-Araf and Me-α-D-Fruf. In nature, it catalyzes the dehydrating condensation reaction of inulobiose (β-D-Fruf-(2→1)-α-D-Fruf) to difructose dianhydride I (DFA I, α-D-Fruf-1,2′:2,1′-β-D-Fruf). The dehydrating condensation reaction reaches equilibrium when the ratio of DFA and inulobiose is 9:1. αFFase1 is less specific for D-Fru at the non-reducing end and is able to catalyze the dehydrating condensation of β-D-Frup-(2→1)-α-D-Fruf to diheterolevulosan II (DHL II, α-D-Frup-1,2′:2,1′-β-D-Fruf). Physiologically, it is believed that after degradation of DFA I to inulobiose, inulobiose is degraded to D-Fru by GH32 β-D-fructofuranosidase, and then the produced monosaccharides are metabolized by the microorganism. DFA I is an oligosaccharide found in caramel, and since the degradation system of DFA I by bifidobacteria has been clarified, DFA I has attracted a certain attention in the food industry.

Also, some GH172 enzymes which physiologically functions as α-D-arabinofuranosidase, was reported in 2023 by Al-Jourani et al. (DgGH172a, DgGH172b, DgGH172c [2]) and Shimokawa et al. (ExoMA1 [3]). In particular, ExoMA1 was compared in detail with αFFase1, and it was found that its α-D-fructofuranosidase activity is extremely weak. These enzymes are believed to be involved in the degradation system of d-arabinan in the cell walls of Mycobacteria and other acid-fast bacteria, and are expected to be applied to the development of therapeutic, preventive, and diagnostic agents for infectious diseases.

Kinetics and Mechanism

As of 2023, all of the enzymes reported in GH172 catalyze reactions by an anomer-retaining mechanism. When pNP-D-Araf is hydrolyzed by αFFase1 [1] or ExoMA1 [3], the initial product was identified by ¹H NMR to have the same anomeric conformation as the substrate. In addition, when pNP-α-D-Araf was enzymatically treated in the presence of organic solvents, transglycosylation products were detected by TLC. These are characteristic to GH with an anomer-retaining mechanism, and therefore, both enzymes are considered to have such kind of mechanism. Enzyme kinetic experiments with this substrate were first reported for αFFase1, with K_m and k_cat values of 2.71 ± 0.21 mM and 127.5 ± 4.0 s^-1, respectively; kinetic constants for ExoMA1 were comparable.

A similar reaction mechanism is employed in the dehydrating condensation reaction of inulobiose to DFA I by αFFase1. Specifically, the reaction proceeds as follows (Figure 1).

(i) The reducing end sugar of inulobiose changes its furanose/pyranose and α/β forms in the internal cavity of αFFase1 as well as in solution because of mutarotation.

(ii) The active site of αFFase1 selectively accommodates the α-furanose form in the −1 subsite. The +1 subsite can also accommodate the pyranose moiety of Frupβ2,1Fru. The Glu270 is located at an appropriate position for proton donation (general acid catalysis) to the O2 hydroxy group of α-Fruf at the −1 subsite, and Glu291 is placed at a position working as a nucleophile to the anomeric carbon (C2). After this step, the O2 hydroxy group is released from the substrate as a water molecule.

(iii) Rotations of the glycosidic bond and the C1–C2 bond of the +1-subsite sugar are required for the intramolecular transfer reaction to occur.

(iv) When the C1 hydroxy group of fructose at the +1 subsite is appropriately positioned for proton acceptance (general base catalysis) by Glu270, deglycosylation of Glu291 is facilitated.

(v) After the reaction at the active site, DFA I is released through the channel to the inner cavity of the hexamer of αFFase1.

The opposite reaction from DFA I (v) to inulobiose (i) is expected to be similar to the standard retaining reaction mechanism of GHs. The k_cat/K_m were 0.813 ± 0.016 mM^-1.s^-1 and 0.0378 ± 0.0032 mM^-1.s^-1 for inulobiose dehydration and DFA I hydrolysis, respectively.

Catalytic Residues

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Three-dimensional structures

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Family Firsts

First stereochemistry determination

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First catalytic nucleophile identification

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First general acid/base residue identification

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First 3-D structure

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References

1. Kashima T, Okumura K, Ishiwata A, Kaieda M, Terada T, Arakawa T, Yamada C, Shimizu K, Tanaka K, Kitaoka M, Ito Y, Fujita K, and Fushinobu S. (2021). Identification of difructose dianhydride I synthase/hydrolase from an oral bacterium establishes a novel glycoside hydrolase family. J Biol Chem. 2021;297(5):101324. DOI:10.1016/j.jbc.2021.101324 |
2. Al-Jourani O, Benedict ST, Ross J, Layton AJ, van der Peet P, Marando VM, Bailey NP, Heunis T, Manion J, Mensitieri F, Franklin A, Abellon-Ruiz J, Oram SL, Parsons L, Cartmell A, Wright GSA, Baslé A, Trost M, Henrissat B, Munoz-Munoz J, Hirt RP, Kiessling LL, Lovering AL, Williams SJ, Lowe EC, and Moynihan PJ. (2023). Identification of D-arabinan-degrading enzymes in mycobacteria. Nat Commun. 2023;14(1):2233. DOI:10.1038/s41467-023-37839-5 |

3. Shimokawa, M., Ishiwata, A., Kashima, T. et al. (2023) Identification and characterization of endo-α-, exo-α-, and exo-β-D-arabinofuranosidases degrading lipoarabinomannan and arabinogalactan of mycobacteria. Nature Communications 14, 5803. DOI:10.1038/s41467-023-41431-2

4. Cantarel BL, Coutinho PM, Rancurel C, Bernard T, Lombard V, and Henrissat B. (2009). The Carbohydrate-Active EnZymes database (CAZy): an expert resource for Glycogenomics. Nucleic Acids Res. 2009;37(Database issue):D233-8. DOI:10.1093/nar/gkn663 |

5. Davies, G.J. and Sinnott, M.L. (2008) Sorting the diverse: the sequence-based classifications of carbohydrate-active enzymes. The Biochemist, vol. 30, no. 4., pp. 26-32. Download PDF version.