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- 1 Overview
- 2 Mechanism of glycoside hydrolase-like phosphorylases
- 3 Mechanism of glycosyltransferase-like phosphorylases
- 4 References
Phosphorylases are enzymes that catalyze the cleavage of a glycosidic bond through substitution with phosphate (formally referred to as phosphorolysis). Phosphorylases are usually named using a combination of the ‘substrate name’ and ‘phosphorylase’ [1, 2]
Phosphorolysis of a glycosidic bond can occur with retention or inversion of configuration and always occurs in an exo-fashion leading to formation of a monosaccharide or disaccharide 1-phosphate.
The energy content of the sugar 1-phosphate product means that the cleavage reaction is often in a practical sense reversible and, in Nature, these enzymes may be involved in either synthesis or cleavage of the glycosidic bond. As such there is a relatively fine distinction among sugar phosphorylases, glycoside hydrolases and classical sugar nucleoside (di)phosphate dependent glycosyltransferases. In the last case the synthetic reaction is normally, but not always, irreversible because of the higher energy of a sugar nucleoside (di)phosphate.
The phosphorylases are classified into various glycoside hydrolase (GH) and glycosyltransferase (GT) families on the basis of sequence similarity . Glycoside phosphorylases have been found in a total of 7 GH and GT families (see below).
The classical example of phosphorylases are the glycogen/starch phosphorylases . These enzymes catalyze the cleavage of individual glucosyl residues from glycogen/amylopectin (up to five residues (or up to four for hyperthermophilic bacterial and archael forms) from a branchpoint), forming sequentially deglycosylated glycogen/amylopectin and glucose 1-phosphate. Glycogen/starch phosphorylases have a complex mechanism that is not fully understood and requires pyridoxal phosphate (PLP) as a cofactor. All glycogen/starch phosphorylases are classified into the same sequence-related glycosyltransferase family as starch phosphorylases (GT35), which also require a PLP cofactor. Trehalose phosphorylase (retaining) is classified as a glycosyltransferase and belongs to GT4. There is no evidence that trehalose phosphorylase (retaining) uses a PLP cofactor.
- Family GT4 contains trehalose phosphorylase, a retaining enzyme.
- Family GT35 contains glycogen and starch phosphorylases.
Glycoside hydrolase-like phosphorylases
Most sugar phosphorylases act on glucosides and many cleave simple disaccharides such as sucrose, trehalose, cellobiose and maltose leading to glucose-1-phosphate and the reducing end sugar (glucose or fructose in these specific cases). Other sugar phosphorylases are known that act on N,N'-diacetylchitobiose, laminaribiose, 1,3-β-glucan and nucleosides. A phosphorylase from GH13 has been reported that acts on α-1,4-glucans to release the disaccharide maltose 1-phosphate .
- Family GH3 contains NagZ enzymes, which are N-acetyl-β-D-glucosaminide/β-glucoside hydrolases/phosphorylases.
- Family GH13 contains sucrose phosphorylase and α-1,4-glucan:maltose 1-phosphate maltosyltransferase.
- Family GH65 contains maltose phosphorylase, trehalose phosphorylase, kojibiose (Glc-α-1,2-Glc) phosphorylase, nigerose (Glc-α-1,3-Glc) phosphorylase, and trehalose 6-phosphate phosphorylase.
- Family GH94 contains cellobiose phosphorylase, cellodextrin phosphorylase, and chitobiose phosphorylase.
- Family GH112 contains β-galactoside phosphorylases such as β-1,3-D-galactosyl-D-hexososamine phosphorylase, and β-1,4-D-galactosyl-L-rhamnose phosphorylase.
- Family GH130 contains β-mannoside phosphorylases such as β-mannosyl-1,4-glucose phosphorylase and β-1,4-mannooligosaccharide phosphorylase.
Mechanism of glycoside hydrolase-like phosphorylases
Sequence and structural analysis of sugar phosphorylases reveal that some have sequences and structures (and likely mechanisms) similar to glycosyltransferases, whereas others have sequences and structures that more closely resemble glycoside hydrolases.
Inverting phosphorylase mechanism
All inverting phosphorylases are GH-like in their sequence classification. Phosphorolysis of a glycoside by a GH-like phosphorylase with net inversion of anomeric configuration is achieved via a one step, single-displacement mechanism involving oxocarbenium ion-like transition states, as shown below. The reaction occurs with acid/base assistance from a suitably positioned carboxylate residue. This mechanism has clear parallels with the mechanism for inverting glycoside hydrolases.
Retaining phosphorylase mechanism
Phosphorolysis of a glycoside with net retention of configuration by the GH-like retaining phosphorylases is achieved via two step, double-displacement mechanisms involving a nucleophilic participation and a covalent intermediate. The mechanism of these enzymes involves a covalent glycosyl-enzyme intermediate, as shown in the figure below. Reaction occurs with acid/base and nucleophilic assistance provided by two amino acid side chains, typically glutamate or aspartate, but occasionally histidine (for family GH3 NagZ enzymes). In the first step (called the glycosylation step), one residue plays the role of a nucleophile, attacking the anomeric centre to displace the aglycon and form a glycosyl enzyme intermediate. At the same time the other residue functions as an acid catalyst and protonates the glycosidic oxygen as the bond cleaves. In the second step (termed the deglycosylation step), the glycosyl enzyme is cleaved by phosphate, with the other residue now acting as a base catalyst deprotonating the phosphate as it attacks. Each step passes through an oxocarbenium ion-like transition state. An alternative mechanism for retention of anomeric configuration has been proposed involving direct front-side nucleophilic displacement (SNi). Both of these mechanisms bear considerable analogy to those proposed for retaining glycosyltransferases [3, 5].
Mechanism of glycosyltransferase-like phosphorylases
Only retaining enzymes have been identified within the currently known glycosyltransferase-like phosphorylases
Retaining phosphorylase mechanism
As in the case for retaining glycosyltransferases, the evidence supporting the specific molecular details are meagre. Two mechanistic proposals remain in contention. The first proposes a mechanism that is essentially identical to the two-step double displacement mechanism of a retaining GH-like phosphorylase drawn above. However, limited evidence is available to support the existence of a nucleophilic residue in the active site, and a front-side displacement mechanism termed an SNi (substitution, nucleophilic, internal return) has been posited as an alternative.
- Kitaoka M, Hayashi K: Carbohydrate-processing phosphorolytic enzymes. Trends Glycosci. Glycotechnol. 2002, 14, 35-50.
- Nakai H, Kitaoka M, Svensson B, and Ohtsubo K. (2013) Recent development of phosphorylases possessing large potential for oligosaccharide synthesis. Curr Opin Chem Biol. 17, 301-9. DOI:10.1016/j.cbpa.2013.01.006 |
- Lairson LL, Henrissat B, Davies GJ, and Withers SG. (2008) Glycosyltransferases: structures, functions, and mechanisms. Annu Rev Biochem. 77, 521-55. DOI:10.1146/annurev.biochem.76.061005.092322 |
- Elbein AD, Pastuszak I, Tackett AJ, Wilson T, and Pan YT. (2010) Last step in the conversion of trehalose to glycogen: a mycobacterial enzyme that transfers maltose from maltose 1-phosphate to glycogen. J Biol Chem. 285, 9803-12. DOI:10.1074/jbc.M109.033944 |
- Lairson LL and Withers SG. (2004) Mechanistic analogies amongst carbohydrate modifying enzymes. Chem Commun (Camb)., 2243-8. DOI:10.1039/b406490a |