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Microbial cellulose utilization: fundamentals and biotechnology.

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TLDR
A concluding discussion identifies unresolved issues pertaining to microbial cellulose utilization, suggests approaches by which such issues might be resolved, and contrasts a microbially oriented cellulose hydrolysis paradigm to the more conventional enzymatically oriented paradigm in both fundamental and applied contexts.
Abstract
Fundamental features of microbial cellulose utilization are examined at successively higher levels of aggregation encompassing the structure and composition of cellulosic biomass, taxonomic diversity, cellulase enzyme systems, molecular biology of cellulase enzymes, physiology of cellulolytic microorganisms, ecological aspects of cellulase-degrading communities, and rate-limiting factors in nature. The methodological basis for studying microbial cellulose utilization is considered relative to quantification of cells and enzymes in the presence of solid substrates as well as apparatus and analysis for cellulose-grown continuous cultures. Quantitative description of cellulose hydrolysis is addressed with respect to adsorption of cellulase enzymes, rates of enzymatic hydrolysis, bioenergetics of microbial cellulose utilization, kinetics of microbial cellulose utilization, and contrasting features compared to soluble substrate kinetics. A biological perspective on processing cellulosic biomass is presented, including features of pretreated substrates and alternative process configurations. Organism development is considered for "consolidated bioprocessing" (CBP), in which the production of cellulolytic enzymes, hydrolysis of biomass, and fermentation of resulting sugars to desired products occur in one step. Two organism development strategies for CBP are examined: (i) improve product yield and tolerance in microorganisms able to utilize cellulose, or (ii) express a heterologous system for cellulose hydrolysis and utilization in microorganisms that exhibit high product yield and tolerance. A concluding discussion identifies unresolved issues pertaining to microbial cellulose utilization, suggests approaches by which such issues might be resolved, and contrasts a microbially oriented cellulose hydrolysis paradigm to the more conventional enzymatically oriented paradigm in both fundamental and applied contexts.

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Journal ArticleDOI

Synthesis of transportation fuels from biomass: chemistry, catalysts, and engineering.

TL;DR: Hydrogen Production by Water−Gas Shift Reaction 4056 4.1.
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Biomass recalcitrance: engineering plants and enzymes for biofuels production.

TL;DR: Here, the natural resistance of plant cell walls to microbial and enzymatic deconstruction is considered, collectively known as “biomass recalcitrance,” which is largely responsible for the high cost of lignocellulose conversion.
Journal ArticleDOI

Toward an aggregated understanding of enzymatic hydrolysis of cellulose: noncomplexed cellulase systems.

TL;DR: It is suggested that it is timely to revisit and reinvigorate functional modeling of cellulose hydrolysis and that this would be highly beneficial if not necessary in order to bring to bear the large volume of information available on cellulase components on the primary applications that motivate interest in the subject.
Journal ArticleDOI

Trends in biotechnological production of fuel ethanol from different feedstocks.

TL;DR: The different technologies for producing fuel ethanol from sucrose-containing feedstocks (mainly sugar cane, starchy materials and lignocellulosic biomass) are described along with the major research trends for improving them.
Journal ArticleDOI

Ethanol from lignocellulosic biomass: techno-economic performance in short-, middle- and long-term

TL;DR: In this paper, the state of the art of hydrolysis-fermentation technologies to produce ethanol from lignocellulosic biomass, as well as developing technologies, are evaluated.
References
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Journal ArticleDOI

Production of cellulases by Trichoderma reesei QM 9414 in fed-batch and continuous-flow culture with cell recycle.

TL;DR: In fed‐batch cultures, slow addition of cellulose at high concentrations can improve enzyme productivity by as much as 33% over a batch process.
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Expression of Aspergillus aculeatus No. F-50 cellobiohydrolase I (cbhI) and β-glucosidase 1 (bgl1) genes by Saccharomyces cerevisiae

TL;DR: By the combination of three different types of cellulases, FI-CMCase, CBHI, and BGL1, the authors could hydrolyze Avicel up to 59% under experimental conditions and had the same enzymatical properties as the native enzyme except for the specific activity toward cellulosic substrates.
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Construction of brewer's yeasts secreting fungal endo-ß-glucanase

TL;DR: Barley β-glucans present in wort were efficiently hydrolyzed by the recombinant brewer's yeast using the yeast copper chelatin gene CUP1 as a selection marker in the transformation.
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Conversion of pretreated lignocellulosic substrates to ethanol by Clostridium thermocellum in mono- and co-culture with Clostridium thermosaccharolyticum and Clostridium thermohydrosulphuricum

TL;DR: Two strains of Clostridium thermocellum demonstrated different product yields and cellulase activities when grown on solka floc, steam-exploded aspen wood, and wheat straw fractions, while higher substrate concentrations resulted in a decrease in ethanol production.
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Kinetic analysis of Clostridium cellulolyticum carbohydrate metabolism: importance of glucose 1-phosphate and glucose 6-phosphate branch points for distribution of carbon fluxes inside and outside cells as revealed by steady-state continuous culture.

TL;DR: It appears that the properties of the G1P-G6P branch points have been selected to control excretion of carbon surplus and to dissipate excess energy, whereas the pyruvate-acetyl coenzyme A branch points chiefly regulate the redox balance of the carbon catabolism.
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