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Engineering the Exo-loop of Cellobiohydrolase, Cel7A. A comparison with Cel7D

Von Ossowski, Ingemar, Stahlberg, Jerry, Koivula, Anu, Piens, Kathleen, Becker, Dieter, Boer, Harry, Harle, Raija, Harris, Mark, Divine, Christina, Mahdi, Sabah, Zhao, Yongxin, Driguez, Hugues, Claeyssens, Marc, Sinnott, Michael L. and Teeri, Tuula T. (2003) Engineering the Exo-loop of Cellobiohydrolase, Cel7A. A comparison with Cel7D. Journal of Molecular Biology, 333 (4). pp. 817-829. ISSN 00222836

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Abstract

The exo-loop of Trichoderma reesei cellobiohydrolase Cel7A forms the roof of the active site tunnel at the catalytic centre. Mutants were designed to study the role of this loop in crystalline cellulose degradation. A hydrogen bond to substrate made by a tyrosine at the tip of the loop was removed by the Y247F mutation. The mobility of the loop was reduced by introducing a new disulphide bridge in the mutant D241C/D249C. The tip of the loop was deleted in mutant Δ(G245-Y252). No major structural disturbances were observed in the mutant enzymes, nor was the thermostability of the enzyme affected by the mutations.

The Y247F mutation caused a slight kcat reduction on 4-nitrophenyl lactoside, but only a small effect on cellulose hydrolysis. Deletion of the tip of the loop increased both kcat and KM and gave reduced product inhibition. Increased activity was observed on amorphous cellulose, while only half the original activity remained on crystalline cellulose. Stabilisation of the exo-loop by the disulphide bridge enhanced the activity on both amorphous and crystalline cellulose. The ratio Glc2/(Glc3+Glc1) released from cellulose, which is indicative of processive action, was highest with Tr Cel7A wild-type enzyme and smallest with the deletion mutant on both substrates. Based on these data it seems that the exo-loop of Tr Cel7A has evolved to facilitate processive crystalline cellulose degradation, which does not require significant conformational changes of this loop.

Item Type: Article
Subjects: Q Science > Q Science (General)
Q Science > QH Natural history > QH301 Biology
Schools: School of Applied Sciences
School of Applied Sciences > Biomolecular Sciences Research Centre
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Depositing User: Sara Taylor
Date Deposited: 11 Aug 2008 12:25
Last Modified: 25 Mar 2010 09:32
URI: http://eprints.hud.ac.uk/id/eprint/1451

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