Literature DB >> 11530215

Hexuronyl C5-epimerases in alginate and glycosaminoglycan biosynthesis.

S Valla1, J Li, H Ertesvåg, T Barbeyron, U Lindahl.   

Abstract

The sugar residues in most polysaccharides are incorporated as their corresponding monomers during polymerization. Here we summarize the three known exceptions to this rule, involving the biosynthesis of alginate, and the glycosaminoglycans, heparin/heparan sulfate and dermatan sulfate. Alginate is synthesized by brown seaweeds and certain bacteria, while glycosaminoglycans are produced by most animal species. In all cases one of the incorporated sugar monomers are being C5-epimerized at the polymer level, from D-mannuronic acid to L-guluronic acid in alginate, and from D-glucuronic acid to L-iduronic acid in glycosaminoglycans. Alginate epimerization modulates the mechanical properties of seaweed tissues, whereas in bacteria it seems to serve a wide range of purposes. The conformational flexibility of iduronic acid units in glycosaminoglycans promotes apposition to, and thus functional interactions with a variety of proteins at cell surfaces and in the extracellular matrix. In the bacterium Azotobacter vinelandii the alginates are being epimerized at the cell surface or in the extracellular environment by a family of evolutionary strongly related modular type and Ca(2+)-dependent epimerases (AlgE1-7). Each of these enzymes introduces a specific distribution pattern of guluronic acid residues along the polymer chains, explaining the wide structural variability observed in alginates isolated from nature. Glycosaminoglycans are synthesized in the Golgi system, through a series of reactions that include the C5-epimerization reaction along with extensive sulfation of the polymers. The single, Ca(2+)-independent, epimerase in heparin/heparan sulfate biosynthesis and the Ca(2+)-dependent dermatan sulfate epimerase(s) also generate variable epimerization patterns, depending on other polymer-modification reactions. The alginate and heparin epimerases appear unrelated at the amino acid sequence level, and have probably evolved through independent evolutionary pathways; however, hydrophobic cluster analysis indicates limited similarity. Seaweed alginates are widely used in industry, while heparin is well established in the clinic as an anticoagulant.

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Year:  2001        PMID: 11530215     DOI: 10.1016/s0300-9084(01)01313-x

Source DB:  PubMed          Journal:  Biochimie        ISSN: 0300-9084            Impact factor:   4.079


  19 in total

1.  Role of the Pseudomonas fluorescens alginate lyase (AlgL) in clearing the periplasm of alginates not exported to the extracellular environment.

Authors:  Karianne Bakkevig; Håvard Sletta; Martin Gimmestad; Randi Aune; Helga Ertesvåg; Kristin Degnes; Bjørn Erik Christensen; Trond E Ellingsen; Svein Valla
Journal:  J Bacteriol       Date:  2005-12       Impact factor: 3.490

2.  Azotobacter vinelandii lacking the Na(+)-NQR activity: a potential source for producing alginates with improved properties and at high yield.

Authors:  Itzel Gaytán; Carlos Peña; Cinthia Núñez; María S Córdova; Guadalupe Espín; Enrique Galindo
Journal:  World J Microbiol Biotechnol       Date:  2012-06-07       Impact factor: 3.312

3.  Catalytic mechanism and mode of action of the periplasmic alginate epimerase AlgG.

Authors:  Francis Wolfram; Elena N Kitova; Howard Robinson; Marthe T C Walvoort; Jeroen D C Codée; John S Klassen; P Lynne Howell
Journal:  J Biol Chem       Date:  2014-01-07       Impact factor: 5.157

Review 4.  Bacterial polymers: biosynthesis, modifications and applications.

Authors:  Bernd H A Rehm
Journal:  Nat Rev Microbiol       Date:  2010-06-28       Impact factor: 60.633

Review 5.  Iduronic acid in chondroitin/dermatan sulfate: biosynthesis and biological function.

Authors:  Anders Malmström; Barbara Bartolini; Martin A Thelin; Benny Pacheco; Marco Maccarana
Journal:  J Histochem Cytochem       Date:  2012-08-16       Impact factor: 2.479

6.  Construction and analyses of hybrid Azotobacter vinelandii mannuronan C-5 epimerases with new epimerization pattern characteristics.

Authors:  Tonje M Bjerkan; Bjørn E Lillehov; Wenche I Strand; Gudmund Skjåk-Braek; Svein Valla; Helga Ertesvåg
Journal:  Biochem J       Date:  2004-08-01       Impact factor: 3.857

7.  The Pseudomonas fluorescens AlgG protein, but not its mannuronan C-5-epimerase activity, is needed for alginate polymer formation.

Authors:  Martin Gimmestad; Håvard Sletta; Helga Ertesvåg; Karianne Bakkevig; Sumita Jain; Sang-jin Suh; Gudmund Skjåk-Braek; Trond E Ellingsen; Dennis E Ohman; Svein Valla
Journal:  J Bacteriol       Date:  2003-06       Impact factor: 3.490

8.  Structural and mutational characterization of the catalytic A-module of the mannuronan C-5-epimerase AlgE4 from Azotobacter vinelandii.

Authors:  Henriëtte J Rozeboom; Tonje M Bjerkan; Kor H Kalk; Helga Ertesvåg; Synnøve Holtan; Finn L Aachmann; Svein Valla; Bauke W Dijkstra
Journal:  J Biol Chem       Date:  2008-06-23       Impact factor: 5.157

9.  Characterization of three new Azotobacter vinelandii alginate lyases, one of which is involved in cyst germination.

Authors:  Martin Gimmestad; Helga Ertesvåg; Tonje Marita Bjerkan Heggeset; Olav Aarstad; Britt Iren Glaerum Svanem; Svein Valla
Journal:  J Bacteriol       Date:  2009-05-29       Impact factor: 3.490

Review 10.  Opportunities and challenges in three-dimensional brown adipogenesis of stem cells.

Authors:  Andrea M Unser; Yangzi Tian; Yubing Xie
Journal:  Biotechnol Adv       Date:  2015-07-29       Impact factor: 14.227

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