Literature DB >> 21371261

A kinetic model for the burst phase of processive cellulases.

Eigil Praestgaard1, Jens Elmerdahl, Leigh Murphy, Søren Nymand, K C McFarland, Kim Borch, Peter Westh.   

Abstract

Cellobiohydrolases (exocellulases) hydrolyze cellulose processively, i.e. by sequential cleaving of soluble sugars from one end of a cellulose strand. Their activity generally shows an initial burst, followed by a pronounced slowdown, even when substrate is abundant and product accumulation is negligible. Here, we propose an explicit kinetic model for this behavior, which uses classical burst phase theory as the starting point. The model is tested against calorimetric measurements of the activity of the cellobiohydrolase Cel7A from Trichoderma reesei on amorphous cellulose. A simple version of the model, which can be solved analytically, shows that the burst and slowdown can be explained by the relative rates of the sequential reactions in the hydrolysis process and the occurrence of obstacles for the processive movement along the cellulose strand. More specifically, the maximum enzyme activity reflects a balance between a rapid processive movement, on the one hand, and a slow release of enzyme which is stalled by obstacles, on the other. This model only partially accounts for the experimental data, and we therefore also test a modified version that takes into account random enzyme inactivation. This approach generally accounts well for the initial time course (approximately 1 h) of the hydrolysis. We suggest that the models will be useful in attempts to rationalize the initial kinetics of processive cellulases, and demonstrate their application to some open questions, including the effect of repeated enzyme dosages and the 'double exponential decay' in the rate of cellulolysis.
© 2011 The Authors Journal compilation © 2011 FEBS.

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Year:  2011        PMID: 21371261     DOI: 10.1111/j.1742-4658.2011.08078.x

Source DB:  PubMed          Journal:  FEBS J        ISSN: 1742-464X            Impact factor:   5.542


  23 in total

1.  Pre-steady-state kinetics for hydrolysis of insoluble cellulose by cellobiohydrolase Cel7A.

Authors:  Nicolaj Cruys-Bagger; Jens Elmerdahl; Eigil Praestgaard; Hirosuke Tatsumi; Nikolaj Spodsberg; Kim Borch; Peter Westh
Journal:  J Biol Chem       Date:  2012-04-09       Impact factor: 5.157

2.  Slow Off-rates and Strong Product Binding Are Required for Processivity and Efficient Degradation of Recalcitrant Chitin by Family 18 Chitinases.

Authors:  Mihhail Kurašin; Silja Kuusk; Piret Kuusk; Morten Sørlie; Priit Väljamäe
Journal:  J Biol Chem       Date:  2015-10-14       Impact factor: 5.157

3.  Systems-level modeling with molecular resolution elucidates the rate-limiting mechanisms of cellulose decomposition by cellobiohydrolases.

Authors:  Barry Z Shang; Rakwoo Chang; Jhih-Wei Chu
Journal:  J Biol Chem       Date:  2013-08-15       Impact factor: 5.157

4.  A distinct model of synergism between a processive endocellulase (TfCel9A) and an exocellulase (TfCel48A) from Thermobifida fusca.

Authors:  Maxim Kostylev; David Wilson
Journal:  Appl Environ Microbiol       Date:  2013-10-25       Impact factor: 4.792

5.  Temperature Effects on Kinetic Parameters and Substrate Affinity of Cel7A Cellobiohydrolases.

Authors:  Trine Holst Sørensen; Nicolaj Cruys-Bagger; Michael Skovbo Windahl; Silke Flindt Badino; Kim Borch; Peter Westh
Journal:  J Biol Chem       Date:  2015-07-16       Impact factor: 5.157

6.  Systematic deletions in the cellobiohydrolase (CBH) Cel7A from the fungus Trichoderma reesei reveal flexible loops critical for CBH activity.

Authors:  Corinna Schiano-di-Cola; Nanna Røjel; Kenneth Jensen; Jeppe Kari; Trine Holst Sørensen; Kim Borch; Peter Westh
Journal:  J Biol Chem       Date:  2018-12-11       Impact factor: 5.157

7.  Endo-exo synergism in cellulose hydrolysis revisited.

Authors:  Jürgen Jalak; Mihhail Kurašin; Hele Teugjas; Priit Väljamäe
Journal:  J Biol Chem       Date:  2012-06-25       Impact factor: 5.157

8.  Origin of initial burst in activity for Trichoderma reesei endo-glucanases hydrolyzing insoluble cellulose.

Authors:  Leigh Murphy; Nicolaj Cruys-Bagger; Heidi Delcomyn Damgaard; Martin J Baumann; Søren Nymand Olsen; Kim Borch; Søren Flensted Lassen; Matt Sweeney; Hirosuke Tatsumi; Peter Westh
Journal:  J Biol Chem       Date:  2011-11-22       Impact factor: 5.157

9.  The predominant molecular state of bound enzyme determines the strength and type of product inhibition in the hydrolysis of recalcitrant polysaccharides by processive enzymes.

Authors:  Silja Kuusk; Morten Sørlie; Priit Väljamäe
Journal:  J Biol Chem       Date:  2015-03-12       Impact factor: 5.157

10.  Cellulase processivity.

Authors:  David B Wilson; Maxim Kostylev
Journal:  Methods Mol Biol       Date:  2012
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