Literature DB >> 15455137

Nature's many mechanisms for the degradation of oligosaccharides.

Vivian L Y Yip1, Stephen G Withers.   

Abstract

Recent work on the mechanistic elucidation of the polysaccharide lyases, the [small alpha]-1,4-glucan lyases, and the Family 4 glycosidases have demonstrated that nature has evolved to use elimination steps for the degradation of oligosaccharides. The polysaccharide lyases (E.C. 4.2.2.-) have been shown to cleave uronic acid-containing polysaccharides via a stepwise E1cB mechanism. The mechanism of the alpha-1,4-glucan lyases (E.C. 4.2.2.13) is similar to the Family 31 glycosidases, forming a covalent glycosyl-enzyme intermediate, which is subsequently cleaved by an E1-like E2 mechanism. Meanwhile, the Family 4 glycosidases (E.C. 3.2.1.6) are suggested to undergo an oxidation-elimination-addition-reduction sequence. These three groups of enzymes are examples of stark contrast to the vast number of well-characterized glycosidases (E.C. 3.2.1.-), which utilize either the direct or double displacement mechanisms as proposed by Koshland over 50 years ago. Copyright 2004 The Royal Society of Chemistry

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Year:  2004        PMID: 15455137     DOI: 10.1039/B408880H

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  6 in total

1.  Preliminary X-ray analysis of cellobiohydrolase Cel7B from Melanocarpus albomyces.

Authors:  Tarja Parkkinen; Anu Koivula; Jari Vehmaanperä; Juha Rouvinen
Journal:  Acta Crystallogr Sect F Struct Biol Cryst Commun       Date:  2007-08-25

2.  Structural basis of heparan sulfate-specific degradation by heparinase III.

Authors:  Wei Dong; Weiqin Lu; Wallace L McKeehan; Yongde Luo; Sheng Ye
Journal:  Protein Cell       Date:  2012-07-21       Impact factor: 14.870

3.  The retaining β-Kdo glycosyltransferase WbbB uses a double-displacement mechanism with an intermediate adduct rearrangement step.

Authors:  Taylor J B Forrester; Olga G Ovchinnikova; Zhixiong Li; Elena N Kitova; Jeremy T Nothof; Akihiko Koizumi; John S Klassen; Todd L Lowary; Chris Whitfield; Matthew S Kimber
Journal:  Nat Commun       Date:  2022-10-21       Impact factor: 17.694

4.  Crystal structures of Melanocarpus albomyces cellobiohydrolase Cel7B in complex with cello-oligomers show high flexibility in the substrate binding.

Authors:  Tarja Parkkinen; Anu Koivula; Jari Vehmaanperä; Juha Rouvinen
Journal:  Protein Sci       Date:  2008-05-21       Impact factor: 6.725

5.  Crystal and Supramolecular Structure of Bacterial Cellulose Hydrolyzed by Cellobiohydrolase from Scytalidium Candidum 3C: A Basis for Development of Biodegradable Wound Dressings.

Authors:  Lyubov A Ivanova; Konstantin B Ustinovich; Tamara V Khamova; Elena V Eneyskaya; Yulia E Gorshkova; Natalia V Tsvigun; Vladimir S Burdakov; Nikolay A Verlov; Evgenii V Zinovev; Marat S Asadulaev; Anton S Shabunin; Andrey M Fedyk; Alexander Ye Baranchikov; Gennady P Kopitsa; Anna A Kulminskaya
Journal:  Materials (Basel)       Date:  2020-05-01       Impact factor: 3.623

6.  Screening and enzymatic activity of high-efficiency gellan lyase producing bacteria Pseudoalteromonas hodoensis PE1.

Authors:  Ang Li; Hangqi Luo; Tingting Hu; Jingyu Huang; Nafee-Ul Alam; Yuan Meng; Fenbin Meng; Nartey Linda Korkor; Xiufang Hu; Ou Li
Journal:  Bioengineered       Date:  2019-12       Impact factor: 3.269

  6 in total

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