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Type: Artigo de periódico
Title: Assembling a xylanase-lichenase chimera through all-atom molecular dynamics simulations
Author: Cota, J
Oliveira, LC
Damasio, ARL
Citadini, AP
Hoffmam, ZB
Alvarez, TM
Codima, CA
Leite, VBP
Pastore, G
de Oliveira-Neto, M
Murakami, MT
Ruller, R
Squina, FM
Abstract: Multifunctional enzyme engineering can improve enzyme cocktails for emerging biofuel technology. Molecular dynamics through structure-based models (SB) is an effective tool for assessing the tridimensional arrangement of chimeric enzymes as well as for inferring the functional practicability before experimental validation. This study describes the computational design of a bifunctional xylanase-lichenase chimera (XylLich) using the xynA and bglS genes from Bacillus sub fills. In silico analysis of the average solvent accessible surface area (SAS) and the root mean square fluctuation (RMSF) predicted a fully functional chimera, with minor fluctuations and variations along the polypeptide chains. Afterwards, the chimeric enzyme was built by fusing the xynA and bglS genes. XylLich was evaluated through small-angle X-ray scattering (SAXS) experiments, resulting in scattering curves with a very accurate fit to the theoretical protein model. The chimera preserved the biochemical characteristics of the parental enzymes, with the exception of a slight variation in the temperature of operation and the catalytic efficiency (k(cat)/K-m). The absence of substantial shifts in the catalytic mode of operation was also verified. Furthermore, the production of chimeric enzymes could be more profitable than producing a single enzyme separately, based on comparing the recombinant protein production yield and the hydrolytic activity achieved for XylLich with that of the parental enzymes. (C) 2013 Elsevier B.V. All rights reserved.
Subject: Multifunctional enzyme
Small-angle X-ray scattering
Molecular dynamics
Computational characterization
Experimental validation
Country: Holanda
Editor: Elsevier Science Bv
Citation: Biochimica Et Biophysica Acta-proteins And Proteomics. Elsevier Science Bv, v. 1834, n. 8, n. 1492, n. 1500, 2013.
Rights: fechado
Identifier DOI: 10.1016/j.bbapap.2013.02.030
Date Issue: 2013
Appears in Collections:Unicamp - Artigos e Outros Documentos

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