Artículos de revistas
Assembling a xylanase-lichenase chimera through all-atom molecular dynamics simulations
Registro en:
Biochimica Et Biophysica Acta-proteins And Proteomics. Elsevier Science Bv, v. 1834, n. 8, n. 1492, n. 1500, 2013.
1570-9639
WOS:000321802200005
10.1016/j.bbapap.2013.02.030
Autor
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
Institución
Resumen
Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) 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. 1834 8 1492 1500 Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) LNLS Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) FAPESP [2008/58037-9, 2011/13242-7, 2010/11499-1, 2011/02169-7] CNPq [475022/2011-4, 310177/2011-1, 140420/2009-6]