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Difference between revisions of "Glycoside Hydrolase Family 75"

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== Substrate specificities ==
 
== Substrate specificities ==
Glycoside hydrolases of family 75 include both eukaryotic (essentially fungal) and prokaryotic proteins. They have so far been characterized only from filamentous fungi. They are primarily of beta-1,4-chitosanases with endo-splitting activity <cite>Shimosaka1993 Cheng2000</cite>. The analysis of the final product of hydrolysis of partially ''N''-deacetylated chitosan by the GH75 chitosanase from ''Aspergillus fumigatus'' suggests that this enzyme cleaves preferentially GlcN-GlcN and GlcNAc-GlcN links in the polysaccharide chain <cite>Cheng2006</cite>.
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Glycoside hydrolases of family 75 include both eukaryotic (essentially fungal) and prokaryotic proteins. They have so far been characterized only from filamentous fungi. They are beta-1,4-chitosanases with endo-splitting activity <cite>Shimosaka1993 Cheng2000</cite>. The analysis of the final product of hydrolysis of partially ''N''-deacetylated chitosan by the GH75 chitosanase from ''Aspergillus fumigatus'' suggests that this enzyme cleaves preferentially GlcN-GlcN and GlcNAc-GlcN links in the polysaccharide chain <cite>Cheng2006</cite>.
  
 
== Kinetics and Mechanism ==
 
== Kinetics and Mechanism ==
 
Family GH46 enzymes are classified as inverting enzymes. This has been shown by <sup>1</sup>H NMR for the enzyme from ''Aspergillus fumigatus'' using chitosan as substrate  <cite>Cheng2006</cite>.
 
Family GH46 enzymes are classified as inverting enzymes. This has been shown by <sup>1</sup>H NMR for the enzyme from ''Aspergillus fumigatus'' using chitosan as substrate  <cite>Cheng2006</cite>.
 
 
  
 
== Catalytic Residues ==
 
== Catalytic Residues ==
A site-directed mutagenesis study performed on the enzyme from ''Fusarium solani'' (expressed as a recombinant protein in ''Saccharomyces cerevisiae'') showed that Asp175 and Glu188 are essential for catalysis <cite>Shimosaka2005</cite>. This was confirmed by a study on the chitosanase from ''Aspergillus fumigatus'' (expressed as a recombinant protein in ''Escherichia coli'') showing that the corresponding residues Asp160 and Glu169 are essential for catalysis <cite>Cheng2006</cite>. Both residues are strictly conserved among eukaryotic and prokaryotic GH75 family members
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A site-directed mutagenesis study performed on the enzyme from ''Fusarium solani'' (expressed as a recombinant protein in ''Saccharomyces cerevisiae'') showed that Asp175 and Glu188 are essential for catalysis <cite>Shimosaka2005</cite>. This was confirmed by a study on the chitosanase from ''Aspergillus fumigatus'' (expressed as a recombinant protein in ''Escherichia coli'') showing that the corresponding residues Asp160 and Glu169 are essential for catalysis <cite>Cheng2006</cite>. Both residues are strictly conserved among eukaryotic and prokaryotic GH75 family members.
 
 
  
 
== Three-dimensional structures ==
 
== Three-dimensional structures ==
 
No three-dimensional structure has been solved for this family.
 
No three-dimensional structure has been solved for this family.
 
 
  
 
== Family Firsts ==
 
== Family Firsts ==

Latest revision as of 13:16, 18 December 2021

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Glycoside Hydrolase Family GH75
Clan Not assigned
Mechanism Inverting
Active site residues Inferred
CAZy DB link
https://www.cazy.org/GH75.html


Substrate specificities

Glycoside hydrolases of family 75 include both eukaryotic (essentially fungal) and prokaryotic proteins. They have so far been characterized only from filamentous fungi. They are beta-1,4-chitosanases with endo-splitting activity [1, 2]. The analysis of the final product of hydrolysis of partially N-deacetylated chitosan by the GH75 chitosanase from Aspergillus fumigatus suggests that this enzyme cleaves preferentially GlcN-GlcN and GlcNAc-GlcN links in the polysaccharide chain [3].

Kinetics and Mechanism

Family GH46 enzymes are classified as inverting enzymes. This has been shown by 1H NMR for the enzyme from Aspergillus fumigatus using chitosan as substrate [3].

Catalytic Residues

A site-directed mutagenesis study performed on the enzyme from Fusarium solani (expressed as a recombinant protein in Saccharomyces cerevisiae) showed that Asp175 and Glu188 are essential for catalysis [4]. This was confirmed by a study on the chitosanase from Aspergillus fumigatus (expressed as a recombinant protein in Escherichia coli) showing that the corresponding residues Asp160 and Glu169 are essential for catalysis [3]. Both residues are strictly conserved among eukaryotic and prokaryotic GH75 family members.

Three-dimensional structures

No three-dimensional structure has been solved for this family.

Family Firsts

First primary structure determination
Chitosanase from Fusarium solani f. sp. phaseoli [5].
First stereochemistry determination
Chitosanase from Aspergillus fumigatus [3].
First catalytic nucleophile identification
Not yet identified.
First general acid/base residue identification
Not yet identified.
First 3-D structure
Not yet determined.

References

Error fetching PMID 11115392:
Error fetching PMID 16330537:
Error fetching PMID 16384794:
  1. Shimosaka M, Nogawa M, Ohno Y, and Okazaki M. Chitosanase from the pathogenic fungus, Fusarium solani f.sp. phaseoli - purification and some properties. Biosci. Biotech. Biochem. 1993 57, 231-235.

    [Shimosaka1993]
  2. Error fetching PMID 11115392: [Cheng2000]
  3. Error fetching PMID 16330537: [Cheng2006]
  4. Error fetching PMID 16384794: [Shimosaka2005]
  5. Shimosaka M, Kumehara M, Zhang X-Y, Nogawa M, and Okazaki M. Cloning and characterization of a chitosanase gene from the plant pathogenic fungus Fusarium solani. J. Ferment. Bioeng. 1996 82, 426-431.

    [Shimosaka1996]

All Medline abstracts: PubMed