Relatively high enzyme loadings are required for the bioconversion of lignocellulosic biomass, impeding the economical production of cellulosic sugars. The relative stability and robustness of these enzymes make enzyme recycling an attractive cost-reduction strategy. However, the efficiency of enzyme recycling has been limited by the complexity of enzyme-substrate interactions, which are influenced by enzyme, substrate, and physical factors. A lack of techniques to probe specific enzyme adsorption further limits our understanding of these interactions. Therefore, overcoming these challenges to better understand enzyme-substrate interactions is crucial if we are to improve the effectiveness of enzyme recycling strategies. Initial work compa...
Abstract Background It is necessary to develop efficient methods to produce renewable fuels from lig...
The adsorption of purified Trichoderma reesei cellulases (TrCel7A, TrCel6A and TrCel5A) and xylanase...
The adsorption of purified Trichoderma reesei cellulases (TrCel7A, TrCel6A and TrCel5A) and xylanase...
Relatively high enzyme loadings are required for the bioconversion of lignocellulosic biomass, imped...
In the past, two main approaches have been used to try to enhance the enzymatic hydrolysis step of ...
Producing ethanol from the bioconversion of lignocellulosic substrates is one of the most promising ...
Producing ethanol from the bioconversion of lignocellulosic substrates is one of the most promising ...
The enzymatic hydrolysis of cellulose is a thermodynamically challenging catalytic process that is i...
Abstract Background Although various pre-treatment methods have been developed to disrupt the struct...
The cost-effective production of sugars from biomass continues to remain challenging, partly due to ...
The cost-effective production of sugars from biomass continues to remain challenging, partly due to ...
The objective of this research was to investigate cellulase adsorption and recycling during enzymati...
Background: It is widely recognised that fast, effective hydrolysis of pretreated l...
Background: It is widely recognised that fast, effective hydrolysis of pretreated l...
The potential of enzymes recycling after hydrolysis and fermentation of wheat straw under a variety ...
Abstract Background It is necessary to develop efficient methods to produce renewable fuels from lig...
The adsorption of purified Trichoderma reesei cellulases (TrCel7A, TrCel6A and TrCel5A) and xylanase...
The adsorption of purified Trichoderma reesei cellulases (TrCel7A, TrCel6A and TrCel5A) and xylanase...
Relatively high enzyme loadings are required for the bioconversion of lignocellulosic biomass, imped...
In the past, two main approaches have been used to try to enhance the enzymatic hydrolysis step of ...
Producing ethanol from the bioconversion of lignocellulosic substrates is one of the most promising ...
Producing ethanol from the bioconversion of lignocellulosic substrates is one of the most promising ...
The enzymatic hydrolysis of cellulose is a thermodynamically challenging catalytic process that is i...
Abstract Background Although various pre-treatment methods have been developed to disrupt the struct...
The cost-effective production of sugars from biomass continues to remain challenging, partly due to ...
The cost-effective production of sugars from biomass continues to remain challenging, partly due to ...
The objective of this research was to investigate cellulase adsorption and recycling during enzymati...
Background: It is widely recognised that fast, effective hydrolysis of pretreated l...
Background: It is widely recognised that fast, effective hydrolysis of pretreated l...
The potential of enzymes recycling after hydrolysis and fermentation of wheat straw under a variety ...
Abstract Background It is necessary to develop efficient methods to produce renewable fuels from lig...
The adsorption of purified Trichoderma reesei cellulases (TrCel7A, TrCel6A and TrCel5A) and xylanase...
The adsorption of purified Trichoderma reesei cellulases (TrCel7A, TrCel6A and TrCel5A) and xylanase...