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Difference between revisions of "Glycoside Hydrolase Family 115"
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| − | * [[Author]]: | + | * [[Author]]: [[User:Satoshi Kaneko|Satoshi Kaneko]] |
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|- | |- | ||
|'''Clan''' | |'''Clan''' | ||
| − | | | + | |none |
|- | |- | ||
|'''Mechanism''' | |'''Mechanism''' | ||
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== Substrate specificities == | == Substrate specificities == | ||
| − | Glycoside hydrolases of | + | [[Glycoside hydrolases]] of GH115 display α-glucuronidase activity. In particular, members of this family catalyze the cleavage of 4-''O''-methyl D-glucuronic acid sidechains from native xylan polysaccharides (EC [{{EClink}}3.2.1.131 3.2.1.131)]. In contrast to [[GH67]] enzymes, which only cleave glucuronosyl linkages at the non-reducing ends of xylooligosaccharides, GH115 enzymes remove glucuronic acid from the both terminal and internal regions of xylooligosaccharides and xylans <cite>Ryabova2009</cite>. This substrate specificity was first demonstrated by an α-glucuronidase purified from ''Thermoascus aurantiacus'' <cite>Khandke1989</cite>, and later for a ''Schizophyllum commune'' α-glucuronidase <cite>Tenkanen2000</cite>. Although GH115 was established on the basis of biochemical and sequence analysis of ''Pichia stipitis'' (4-''O''-methyl)-α-glucuronidase <cite>Ryabova2009</cite>, available N-terminal protein sequence of the ''S. commune'' enzyme <cite>Tenkanen2000</cite> allowed the tentative assignment of this enzyme to GH115 <cite>Ryabova2009</cite>, which was later confirmed by the full protein sequence <cite>Chong2011</cite>. A GH115 member from ''Streptomyces pristinaespiralis'' produces both 4-''O''-methyl-D-glucuronic acid and non-methylated D-glucuronic acid from xylan and xylo-oligosaccharides <cite>Fujimoto2011</cite>. |
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== Kinetics and Mechanism == | == Kinetics and Mechanism == | ||
| − | Using | + | Using reduced aldopentauronic acid (MeGlcA3Xyl4-ol) as a substrate, analysis by <sup>1</sup>H-NMR spectroscopy revealed that the enzymes from both ''S. commune'' and ''P. stipitis'' release the β-anomer of 4-O-methyl-D-glucuronic acid (MeGlcA) as the first-formed product, thus suggesting a one step, [[inverting]] mechanism <cite>Kolenova2010</cite>. |
| − | |||
== Catalytic Residues == | == Catalytic Residues == | ||
| − | + | The catalytic residues have not yet been identified in a member of this family. | |
| − | |||
== Three-dimensional structures == | == Three-dimensional structures == | ||
| − | No 3D | + | No 3D structure has been solved for this family at present, although crystallization of a ''Streptomyces pristinaespiralis'' homolog has been reported <cite>Fujimoto2011</cite>. |
| − | |||
== Family Firsts == | == Family Firsts == | ||
| − | ; | + | ;First stereochemistry determination: Release of the β-anomer of 4-methyl-D-glucuronic acid by both the ''Schizophyllum commune'' and ''Pichia stipitis'' enzymes using <sup>1</sup>H NMR <cite>Kolenova2010</cite>. |
| − | ;First | + | ;First [[general acid]] residue identification: Not yet identified. |
| − | ;First general | + | ;First [[general base]] residue identification: Not yet identified. |
| − | ;First 3-D structure: | + | ;First 3-D structure: Crystallization of the ''Streptomyces pristinaespiralis'' family member has been reported <cite>Fujimoto2011</cite>. |
== References == | == References == | ||
<biblio> | <biblio> | ||
| − | #Khandke1989 pmid= | + | #Khandke1989 pmid=2802623 |
| − | # | + | #Tenkanen2000 pmid=10725538 |
| − | # | + | #Ryabova2009 pmid=19344716 |
| − | # | + | #Kolenova2010 pmid=20804758 |
| − | # | + | #Fujimoto2011 pmid=21206027 |
| + | #Chong2011 pmid=21442271 | ||
</biblio> | </biblio> | ||
| + | |||
[[Category:Glycoside Hydrolase Families|GH115]] | [[Category:Glycoside Hydrolase Families|GH115]] | ||
Latest revision as of 13:16, 18 December 2021
This page has been approved by the Responsible Curator as essentially complete. CAZypedia is a living document, so further improvement of this page is still possible. If you would like to suggest an addition or correction, please contact the page's Responsible Curator directly by e-mail.
| Glycoside Hydrolase Family GH115 | |
| Clan | none |
| Mechanism | inverting |
| Active site residues | not known |
| CAZy DB link | |
| https://www.cazy.org/GH115.html | |
Substrate specificities
Glycoside hydrolases of GH115 display α-glucuronidase activity. In particular, members of this family catalyze the cleavage of 4-O-methyl D-glucuronic acid sidechains from native xylan polysaccharides (EC 3.2.1.131). In contrast to GH67 enzymes, which only cleave glucuronosyl linkages at the non-reducing ends of xylooligosaccharides, GH115 enzymes remove glucuronic acid from the both terminal and internal regions of xylooligosaccharides and xylans [1]. This substrate specificity was first demonstrated by an α-glucuronidase purified from Thermoascus aurantiacus [2], and later for a Schizophyllum commune α-glucuronidase [3]. Although GH115 was established on the basis of biochemical and sequence analysis of Pichia stipitis (4-O-methyl)-α-glucuronidase [1], available N-terminal protein sequence of the S. commune enzyme [3] allowed the tentative assignment of this enzyme to GH115 [1], which was later confirmed by the full protein sequence [4]. A GH115 member from Streptomyces pristinaespiralis produces both 4-O-methyl-D-glucuronic acid and non-methylated D-glucuronic acid from xylan and xylo-oligosaccharides [5].
Kinetics and Mechanism
Using reduced aldopentauronic acid (MeGlcA3Xyl4-ol) as a substrate, analysis by 1H-NMR spectroscopy revealed that the enzymes from both S. commune and P. stipitis release the β-anomer of 4-O-methyl-D-glucuronic acid (MeGlcA) as the first-formed product, thus suggesting a one step, inverting mechanism [6].
Catalytic Residues
The catalytic residues have not yet been identified in a member of this family.
Three-dimensional structures
No 3D structure has been solved for this family at present, although crystallization of a Streptomyces pristinaespiralis homolog has been reported [5].
Family Firsts
- First stereochemistry determination
- Release of the β-anomer of 4-methyl-D-glucuronic acid by both the Schizophyllum commune and Pichia stipitis enzymes using 1H NMR [6].
- First general acid residue identification
- Not yet identified.
- First general base residue identification
- Not yet identified.
- First 3-D structure
- Crystallization of the Streptomyces pristinaespiralis family member has been reported [5].
References
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- Error fetching PMID 10725538:
- Error fetching PMID 21442271:
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