Development of an expression platform, based on E. coli, for the production of enzymes used for lignocellulosic biomass hydrolysis.

• Grant number: 10/08089-2
• Support Opportunities: Research Grants - Young Investigators Grants
• Start date: October 01, 2010
• End date: September 30, 2015
• Field of knowledge: Engineering - Chemical Engineering - Chemical Process Industries
• Principal Investigator: Sindelia Freitas Azzoni
• Grantee: Sindelia Freitas Azzoni
• Host Institution: Centro Nacional de Pesquisa em Energia e Materiais (CNPEM). Campinas , SP, Brazil
• City of the host institution: Campinas
• Associated researchers: Jose Geraldo da Cruz Pradella ; Marcelo Brocchi ; Roberto Ruller

Abstract

Biomass conversion by enzymatic hydrolysis still represents a high cost step for production of second generation ethanol. To overcome this drawback it is important increase the enzyme efficiency, obtaining balanced cocktails tailored made for each pretreated biomass and decrease production costs by using genetics tools for enzyme engineering and by production process optimization. The objective of this project is study and develops a recombinant protein expression platform based on modified strains of E. coli by using genetic engineering and new vectors and strains recently available. Two major drawbacks of E. coli large-scale protein production will be addressed: 1) the intracellular expression; and 2) the need of antibiotic as a selection marker. To reach this objective, E. coli mutants strains, BL21DE3 and SE1 will be modified in order to achieve membrane permeability. The mutation will be done by gene knock out of the lpp gene which codifies to a Braun´s lipoprotein. The efficacy of these systems will be evaluated by performing high cell densities fermentations for the production of three model enzymes (endoglicanase, xylanase, feruloyl esterase). Critical fermentation parameters will be obtained in bioreactors such as cellular growth rate and enzyme biosynthesis rate. Special attention will be dedicated to the induction phase by optimizing parameters such as inducer type and concentration, inducer feeding rate, carbon and nitrogen sources concentration by using a factorial design. We expect develop a robust and economic process to enzymes production in order to make enzymatic complex tailored made for several pretreated biomass in study in the CTBE. (AU)

Scientific publications

(The scientific publications listed on this page originate from the Web of Science or SciELO databases. Their authors have cited FAPESP grant or fellowship project numbers awarded to Principal Investigators or Fellowship Recipients, whether or not they are among the authors. This information is collected automatically and retrieved directly from those bibliometric databases.)

BUSSAMRA, BIANCA CONSORTI; FREITAS, SINDELIA; DA COSTA, ALINE CARVALHO. Improvement on sugar cane bagasse hydrolysis using enzymatic mixture designed cocktail. Bioresource Technology, v. 187, p. 173-181, JUL 2015. (08/57873-8, 10/08089-2, 12/23223-2)

FERREIRA, RAFAEL DA GAMA; AZZONI, ADRIANO RODRIGUES; FREITAS, SINDELIA. Techno-economic analysis of the industrial production of a low-cost enzyme using E. coli: the case of recombinant beta-glucosidase. BIOTECHNOLOGY FOR BIOFUELS, v. 11, MAR 29 2018. (10/08089-2, 14/13974-6)

MARINO, M. A.; FREITAS, S.; MIRANDA, E. A.. ETHANOL PRECIPITATION OF GLYCOSYL HYDROLASES PRODUCED BY Trichoderma harzianum P49P11. Brazilian Journal of Chemical Engineering, v. 32, n. 2, p. 325-333, APR-JUN 2015. (10/08089-2)