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Difference between revisions of "Carbohydrate-active enzymes"

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* [[Author]]s: ^^^Stephen Withers^^^ and ^^^Spencer Williams^^^
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* [[Author]]s: [[User:Steve Withers|Stephen Withers]], [[User:Spencer Williams|Spencer Williams]], and [[User:Harry Brumer|Harry Brumer]]
* [[Responsible Curator]]:  ^^^Spencer Williams^^^
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* [[Responsible Curator]]:  [[User:Spencer Williams|Spencer Williams]]
 
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Individual monosaccharide units have the potential to be joined together to form oligo- and polysaccharides, with the glycosidic linkage occurring between the anomeric position of one sugar with the hydroxyl group of another. Owing to the many hydroxy groups on each sugar, the potential for two possible anomeric configurations, and the possibility of different ring sizes (pyranose and furanose are the most common), there is a combinatorially-large number of structures possible. Further, carbohydrates can be linked to other, non-carbohydrate molecules to generate a wide range of glycoconjugates. Reflecting this structural diversity, there is a large diversity of enzymes involved in the biosynthesis, modification, binding and catabolism of carbohydrates.
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Individual monosaccharide units have the potential to be joined together to form oligo- and polysaccharides, with the glycosidic linkage occurring between the anomeric position of one sugar with the hydroxyl group of another <cite>StickWilliams2009 Sinnott2007</cite>. Owing to the many hydroxy groups on each sugar, the potential for two possible anomeric configurations, and the possibility of different ring sizes (pyranose and furanose are the most common), there is a combinatorially-large number of structures possible <cite>Laine1994</cite>. Further, carbohydrates can be linked to other, non-carbohydrate molecules to generate a wide range of glycoconjugates <cite>TaylorDrickamer2011</cite>. Reflecting this structural diversity, there is a large diversity of enzymes involved in the biosynthesis, modification, binding and catabolism of carbohydrates.
  
==The CAZy classification==
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==The <U>C</U>arbohydrate <U>A</U>ctive En<U>Zy</U>me ("CAZy") classification==
The <U>C</U>arbohydrate <U>A</U>ctive En<U>Zy</U>me (CAZy) classification is a sequence-based classification of enzymes that are active on carbohydrate structures (''see <cite>DaviesSinnott2008 Cantarel2009 Lombard2013</cite> for key reviews''). The creation of a family requires at least one biochemically-characterized member, and is based on the concept that sequence defines protein structure, and protein structure defines function. Generally, but not exclusively, functional properties often extend to other members of the family, and provides a framework upon which to base testable hypotheses of enzyme structure and function <cite>Davies1995</cite>.
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The <U>C</U>arbohydrate <U>A</U>ctive En<U>Zy</U>me (CAZy) classification is a [[sequence-based classification]] of enzymes that synthesize or break-down saccharides, which originated with the seminal grouping of glycoside hydrolases by [[User:Bernard Henrissat|Bernard Henrissat]] (<cite>Henrissat1989 Henrissat1991 Henrissat1993 Henrissat1996</cite>; see <cite>DaviesSinnott2008</cite> for a lucid historical review). The creation of a family requires at least one biochemically-characterized member, and is based on the concept that sequence defines protein structure, and protein structure defines function. Generally, but not exclusively, functional properties often extend to other members of the family, and provides a framework upon which to base testable hypotheses of enzyme structure and function <cite>DaviesHenrissat1995</cite>.  Since its inception, the CAZy classification and associated database has undergone continually active curation, including the addition of new enzyme and associated module classes <cite>Cantarel2009 Lombard2013 Drula2022</cite>.  Hence, the CAZy classification presently comprises the following modules:
 +
* [[Glycosyltransferase Families]] <cite>Campbell1997 Coutinho2003 Coutinho2009</cite>
 +
* [[Glycoside Hydrolase Families]] <cite>Henrissat1991 Henrissat1993 Henrissat1996</cite>
 +
* [[Polysaccharide Lyase Families]] <cite>Lombard2010 Garron2010</cite>
 +
* [[Carbohydrate Esterase Families]] <cite>Davies2005 Biely2012</cite>
 +
* [[Auxiliary Activity Families]] <cite>Levasseur2013</cite>
 +
* [[Carbohydrate Binding Module Families]] (non-catalytic; included due to their association with catalytic modules) <cite>Cantarel2009</cite>.
  
===Glycoside hydrolases (GH)===
+
Further information on the composition of the families and mechanistic details can be obtained via these pages and the corresponding [[Lexicon]] entries.
Strictly speaking, the term '[[glycoside hydrolase]]' or 'glycosidase' refers to enzymes that catalyze the hydrolytic cleavage of the glycosidic bond to give the carbohydrate hemiacetal. However, it is found that sequence-based classification methods often group in enzymes that have non-hydrolytic activities into the same families as hydrolytic enzymes.
 
 
 
* [[Transglycosidases]]: Sequence analysis classifies [[transglycosidases]] with [[retaining]] [[glycoside hydrolases]]. According to all available evidence[[transglycosidases]] and [[glycoside hydrolases]] use the same mechanism, except that a sugar or some other group, rather than water, acts as the nucleophile.
 
 
 
* [[Phosphorylases]]: Sequence similarly classifies many, but all (see Glycosyltransferases, below) [[phosphorylases]] with [[retaining]] and [[inverting]] [[glycoside hydrolases]]. Enzymatic cleavage of the bond between two sugars or between a sugar and another group by reaction with phosphate is termed phosphorolysis, and yields the sugar-1-phosphate, and the reaction is reversible, allowing synthesis of glycosidic linkages form sugar-1-phosphates. Again, GH-like [[phosphorylases]] share mechanistic similarities with [[glycoside hydrolases]].
 
 
 
* [[Alpha-glucan lyases]]: An unusual group of enzymes has been found within family [[GH31]] termed [[alpha-glucan lyases]] that degrade starch via an elimination mechanism, rather than via hydrolysis, forming an unsaturated (enol) product that tautomerises to its keto form, 1,5-anhydro fructose. Again, there are mechanistic similarities between [[alpha-glucan lyases]] and [[glycoside hydrolases]].
 
 
 
* [[NAD-dependent hydrolysis|NAD-dependent glycoside hydrolases]]: Another unusual group of enzymes use an NAD-cofactor to hydrolyze through a mechanism involving a redox reaction. These enzymes are found within familes [[GH4]] and [[GH109]].
 
 
 
''Seminal publications on GH classification: <cite>Henrissat1991 Henrissat1993 Henrissat1996</cite>.''
 
 
 
''Key reviews on GH and related mechanisms (''e.g.'' GH4 enzymes and GH31 lyases): <cite>VocadloDavies2008 YipWithers2006</cite>.''
 
 
 
===Polysaccharide lyases (PL)===
 
Polysaccharide lyases (PLs) cleave uronic acid-containing polysaccharides via a β-elimination mechanism to generate an unsaturated hexenuronic acid residue and a new reducing end at the point of cleavage. These enzymes are distinct from [[alpha-glucan lyases]], which are classified within the GH modules, as described above.
 
 
 
''Formal introduction of the PL classification:  <cite>Lombard2010</cite>.''
 
 
 
''Reviews of PL mechanisms: <cite>YipWithers2006 Lombard2010 Garron2010</cite>.''
 
 
 
===Auxiliary activities (AA)===
 
The original CAZy classification scheme aimed to describe the families of enzymes that cleave or build complex carbohydrates and the associated carbohydrate binding modules. The discovery that members of families [[CBM33]] and family [[GH61]] are lytic polysaccharide monooxygenases (LPMO), gave impetus to a reclassification of these families into a
 
new category, the "Auxiliary Activities" <cite>Levasseur2013</cite>. The auxiliary activities are familes of catalytic proteins that are potentially involved in plant cell degradation through an ability to help the original [[GH]], [[PL]] and [[CE]] enzymes gain access to the carbohydrates comprising the plant cell wall. Currently, the AA families contain redox active enzymes.
 
 
 
''Introduction of the AA classification: <cite>Levasseur2013</cite>.''
 
 
 
===Glycosyltransferases (GT)===
 
The principal enzymes that catalyze glycoside synthesis are [[glycosyltransferases]]. Glycosyltransferases utilize various sugar-1-phosphate derivatives including:
 
* Sugar mono- or diphosphonucleotides, in which case the resulting enzymes are referred to as Leloir glycosyltransferases.
 
* Non-nucleotide carbohydrate donors including various sugar polyprenol mono- or diphosphates, in which case the enzymes are referred to as non-Leloir glycosyltransferases.
 
* Sugar-1-phosphates and -pyrophosphates, in which case the enzymes are referred to as phosphorylases or pyrophosphorylases. Only some of such enzymes are classified as GTs on the basis of sequence (''e.g.'' glycogen phosphorylase of [[GT35]]), others are classified as GHs.
 
 
 
''Seminal publications on GT classification: <cite>Campbell1997 Coutinho2003</cite>.''
 
 
 
''Key GT review: <cite>Lairson2008</cite>.''
 
  
 
== References ==
 
== References ==
 
<biblio>
 
<biblio>
#DaviesSinnott2008 Davies, G.J. and Sinnott, M.L. (2008) Sorting the diverse: the sequence-based classifications of carbohydrate-active enzymes. ''Biochem. J.'' (A BJ Classics review, online only). [http://dx.doi.org/10.1042/BJ20080382 DOI: 10.1042/BJ20080382]
+
#StickWilliams2009 isbn=9780240521183
 +
#Laine1994 pmid=7734838
 +
#TaylorDrickamer2011 isbn=9780199569113
 +
#Henrissat1991 pmid=1747104
 +
#Henrissat1993 pmid=8352747
 +
#Henrissat1996 pmid=8687420
 +
#DaviesHenrissat1995 pmid=8535779
 +
#DaviesSinnott2008 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. [https://doi.org/10.1042/BIO03004026 DOI:10.1042/BIO03004026].
 
#Cantarel2009 pmid=18838391
 
#Cantarel2009 pmid=18838391
 
#Lombard2013 pmid=24270786
 
#Lombard2013 pmid=24270786
#Lairson2008 pmid=18518825
 
 
#Lombard2010 pmid=20925655
 
#Lombard2010 pmid=20925655
 +
#Campbell1997 pmid=9334165
 +
#Coutinho2003 pmid=12691742
 +
#Coutinho2009 isbn=9780470016671 // ''Chapter 5:'' Coutinho PM, Rancurel C, Stam M, Bernard T, Couto FM, Danchin EGJ, Henrissat B. "Carbohydrate-active Enzymes Database: Principles and Classification of Glycosyltransferases."
 
#Garron2010 pmid=20805221
 
#Garron2010 pmid=20805221
 
#Levasseur2013 pmid=23514094
 
#Levasseur2013 pmid=23514094
#Boraston2004 pmid=15214846
+
#Henrissat1989 pmid=2806912
#Shoseyov2006 pmid=16760304
+
#Sinnott2007 isbn=9780854042562
#Hashimoto2006 pmid=17131061
+
#Davies2005 pmid=16263268
#Guillen2010 pmid=19908036
+
#Biely2012 pmid=22580218
#Gilbert2013 pmid=23769966
+
 
#VocadloDavies2008 pmid=18558099
+
#Drula2022 pmid=34850161
#YipWithers2006 pmid=16495121
 
#Henrissat1991 pmid=1747104
 
#Henrissat1993 pmid=8352747
 
#Henrissat1996 pmid=8687420
 
#Davies1995 pmid=8535779
 
#Levasseur2013 pmid=23514094
 
#Campbell1997 pmid=9334165
 
#Coutinho2003 pmid=12691742
 
 
</biblio>
 
</biblio>
  
 
[[Category:Definitions and explanations]]
 
[[Category:Definitions and explanations]]

Latest revision as of 12:28, 4 July 2023

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Individual monosaccharide units have the potential to be joined together to form oligo- and polysaccharides, with the glycosidic linkage occurring between the anomeric position of one sugar with the hydroxyl group of another [1, 2]. Owing to the many hydroxy groups on each sugar, the potential for two possible anomeric configurations, and the possibility of different ring sizes (pyranose and furanose are the most common), there is a combinatorially-large number of structures possible [3]. Further, carbohydrates can be linked to other, non-carbohydrate molecules to generate a wide range of glycoconjugates [4]. Reflecting this structural diversity, there is a large diversity of enzymes involved in the biosynthesis, modification, binding and catabolism of carbohydrates.

The Carbohydrate Active EnZyme ("CAZy") classification

The Carbohydrate Active EnZyme (CAZy) classification is a sequence-based classification of enzymes that synthesize or break-down saccharides, which originated with the seminal grouping of glycoside hydrolases by Bernard Henrissat ([5, 6, 7, 8]; see [9] for a lucid historical review). The creation of a family requires at least one biochemically-characterized member, and is based on the concept that sequence defines protein structure, and protein structure defines function. Generally, but not exclusively, functional properties often extend to other members of the family, and provides a framework upon which to base testable hypotheses of enzyme structure and function [10]. Since its inception, the CAZy classification and associated database has undergone continually active curation, including the addition of new enzyme and associated module classes [11, 12, 13]. Hence, the CAZy classification presently comprises the following modules:

Further information on the composition of the families and mechanistic details can be obtained via these pages and the corresponding Lexicon entries.

References

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  1. Robert V. Stick and Spencer J. Williams. (2009) Carbohydrates. Elsevier Science. [StickWilliams2009]
  2. Michael Sinnott. (2007) Carbohydrate Chemistry and Biochemistry. Royal Society of Chemistry. [Sinnott2007]
  3. Error fetching PMID 7734838: [Laine1994]
  4. Maureen E. Taylor and Kurt Drickamer. (2011-04-21) Introduction to Glycobiology. Oxford University Press, USA. [TaylorDrickamer2011]
  5. Error fetching PMID 2806912: [Henrissat1989]
  6. Error fetching PMID 1747104: [Henrissat1991]
  7. Error fetching PMID 8352747: [Henrissat1993]
  8. Error fetching PMID 8687420: [Henrissat1996]
  9. 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. DOI:10.1042/BIO03004026.

    [DaviesSinnott2008]
  10. Error fetching PMID 8535779: [DaviesHenrissat1995]
  11. Error fetching PMID 18838391: [Cantarel2009]
  12. Error fetching PMID 24270786: [Lombard2013]
  13. Error fetching PMID 34850161: [Drula2022]
  14. Error fetching PMID 9334165: [Campbell1997]
  15. Error fetching PMID 12691742: [Coutinho2003]
  16. Claus-Wilhelm von der Lieth, Thomas Luetteke, and Martin Frank. (2010-01-19) Bioinformatics for Glycobiology and Glycomics: An Introduction. Wiley. [Coutinho2009]

    Chapter 5: Coutinho PM, Rancurel C, Stam M, Bernard T, Couto FM, Danchin EGJ, Henrissat B. "Carbohydrate-active Enzymes Database: Principles and Classification of Glycosyltransferases."

  17. Error fetching PMID 20925655: [Lombard2010]
  18. Error fetching PMID 20805221: [Garron2010]
  19. Error fetching PMID 16263268: [Davies2005]
  20. Error fetching PMID 22580218: [Biely2012]
  21. Error fetching PMID 23514094: [Levasseur2013]

All Medline abstracts: PubMed