Busca avançada
Ano de início
Entree
(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

Xanthomonas campestris expansin-like X domain is a structurally disordered beta-sheet macromolecule capable of synergistically enhancing enzymatic efficiency of cellulose hydrolysis

Texto completo
Autor(es):
Tomazini Junior, Atilio [1] ; Dolce, Luciano Graciani [1] ; de Oliveira Neto, Mario [2] ; Polikarpov, Igor [1]
Número total de Autores: 4
Afiliação do(s) autor(es):
[1] Univ Sao Paulo, Inst Fis Sao Carlos, Dept Fis & Ciencia Interdisciplinar, BR-13560970 Sao Carlos, SP - Brazil
[2] Univ Estadual Paulista, Inst Biociencias, BR-18618970 Botucatu, SP - Brazil
Número total de Afiliações: 2
Tipo de documento: Artigo Científico
Fonte: Biotechnology Letters; v. 37, n. 12, p. 2419-2426, DEC 2015.
Citações Web of Science: 4
Resumo

Objectives To biochemically characterize an expansin-like X protein domain from Xanthomonas campestris (XcEXLX1) and to study its synergy with cellulases in cellulose depolymerization. Results The protein was purified using a combination of ion exchange and size exclusion chromatography rendering about 30 mg pure protein/l culture medium. Circular dichroism spectroscopy and small-angle X-ray scattering studies of XcEXLX1 reveal that it is a strongly disordered beta-sheet protein. Its low resolution envelope fits nicely the crystallographic structure of the homologous protein EXLX1 from Bacillus subtillis. Furthermore, we demonstrate that XcEXLX1 shows a synergistic, pH-dependent effect when combined with a commercial enzymatic preparation (Accellerase 1500), enhancing its hydrolytic activity on a cellulosic substrate. The strongest effect was observed in acid pHs with an increase in sugar release of up to 36 %. Conclusion The synergistic effect arising from the action of the expansin-like protein was considerable in the presence of significantly larger amounts of the commercial enzymatic cocktail then previously observed (0.35 FPU of Accellerase 1500/g substrate). (AU)

Processo FAPESP: 08/56255-9 - Structure and function of enzymes and auxiliary proteins from Trichoderma, active in cell-wall hydrolysis
Beneficiário:Igor Polikarpov
Modalidade de apoio: Auxílio à Pesquisa - Programa BIOEN - Temático
Processo FAPESP: 10/52362-5 - Targeted analysis of microbial lignocellulolytic secretomes: a new approach to enzyme discovery
Beneficiário:Igor Polikarpov
Modalidade de apoio: Auxílio à Pesquisa - Regular
Processo FAPESP: 07/08706-9 - ESTUDOS MOLECULARES E ESTRUTURAIS DE ENZIMAS DO COMPLEXO CELULOLÍTICO DO FUNGO Trichoderma harzianum COM POTENCIAL NA TRANSFORMAÇÃO ENZIMÁTICA DA BIOMASSA
Beneficiário:Viviane Isabel Serpa
Modalidade de apoio: Bolsas no Brasil - Doutorado
Processo FAPESP: 09/05349-6 - Expressão e purificação da celobiohidrolase I do fungo filamentoso Trichoderma harzianum
Beneficiário:Bruno Luan Soares Paula de Mello
Modalidade de apoio: Bolsas no Brasil - Iniciação Científica