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1.
Bioengineered ; 4(2): 97-102, 2013.
Artigo em Inglês | MEDLINE | ID: mdl-22989992

RESUMO

Consolidated bioprocessing (CBP), which integrates enzyme production, saccharification and fermentation into a one step process, is a promising strategy for the effective ethanol production from cheap lignocellulosic and starchy materials. CBP requires a highly engineered microbial strain able to both hydrolyze biomass with enzymes produced on its own and convert the resulting simple sugars into high-titer ethanol. Recently, heterologous production of cellulose and starch-degrading enzymes has been achieved in yeast hosts, which has realized direct processing of biomass to ethanol. However, essentially all efforts aimed at the efficient heterologous expression of saccharolytic enzymes in yeast have involved laboratory strains and much of this work has to be transferred to industrial yeasts that provide the fermentation capacity and robustness desired for large scale bioethanol production. Specifically, the development of an industrial CBP amylolytic yeast would allow the one-step processing of low-cost starchy substrates into ethanol. This article gives insight in the current knowledge and achievements on bioethanol production from starchy materials with industrial engineered S. cerevisiae strains.


Assuntos
Biomassa , Biotecnologia/métodos , Etanol/metabolismo , Saccharomyces cerevisiae/metabolismo , Amido/metabolismo , Fermentação , Saccharomyces cerevisiae/crescimento & desenvolvimento
2.
Appl Microbiol Biotechnol ; 95(4): 957-68, 2012 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-22450569

RESUMO

The development of a yeast that converts raw starch to ethanol in one step (called consolidated bioprocessing) could yield large cost reductions in the bioethanol industry. The aim of this study was to develop an efficient amylolytic Saccharomyces cerevisiae strain suitable for industrial bioethanol production. A native and codon-optimized variant of the Aspergillus awamori glucoamylase gene were expressed in the S. cerevisiae Y294 laboratory strain. Codon optimization resulted to be effective and the synthetic sequence sGAI was then δ-integrated into a S. cerevisiae strain with promising industrial fermentative traits. The mitotically stable recombinant strains showed high enzymatic capabilities both on soluble and raw starch (2425 and 1140 nkat/g dry cell weight, respectively). On raw corn starch, the engineered yeasts exhibited improved fermentative performance with an ethanol yield of 0.42 (g/g), corresponding to 75 % of the theoretical maximum yield.


Assuntos
Aspergillus/enzimologia , Códon , Glucana 1,4-alfa-Glucosidase/metabolismo , Amido/metabolismo , Aspergillus/genética , Sequência de Bases , Primers do DNA , Eletroforese em Gel de Poliacrilamida , Fermentação , Mitose , Plasmídeos , Reação em Cadeia da Polimerase , Recombinação Genética
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