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Some particular CESA gene expression induction may not lead to significant change of cellulose content.
The fact that a large portion of the cellulosic component had been hydrolytically degraded during DAP could have had large implication on concurrent changes in cellulose ultrastructure, specifically the change of cellulose crystallinity.
Enhancing the enzymatic hydrolysis rate of lignocellulose substrate and altering the crystalline cellulose features, especially the cellulose allomorphs, is often ignored, because a change of cellulose crystal form does not take place for every treatment.
Regarding the bands at 1,160 cm−1, pretreated rachis shows stronger peaks than the untreated, while there are no obvious changes of peaks before and after pretreatment of leaflets, suggesting a more significant compositional change of cellulose and hemicellulose in pretreated rachis.
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The degradation and utilization ability of F. velutipes to ramie stalks substrate were evaluated comprehensively from the content changes of cellulose, hemicellulose and lignin in medium.
Tracking the chemical and structure changes of cellulose, hemicellulose, and lignin by FTIR facilitates mechanical study of the effects of pretreatment on the enzymatic digestibility of biomass.
The changes of cellulose accessibility to cellulase caused by DAP and delignification followed by DAP were also evaluated to further study lignin impact on the accessible surface area of cellulose for downstream enzymatic hydrolysis.
Part of the amorphous cellulose degradation led to a change of the cellulose structure, which increased the surface area with access to cellulase in pretreated corn stover.
Furthermore, fluorescence titration results demonstate that this family of dibenzothiophene derivatives 1 3 is one of potential selective chemosensors for picric acid in aqueous phase and the obvious color change of the cellulose-based dibenzothiophene mixtures is illustrated with the addition of different explosives.
The adsorption of substructure-specific CBMs can be used to accurately quantify the extent of changes to cellulose accessibility induced by non-hydrolytic disruptive proteins.
Pretreatment is also able to change the degree of cellulose crystallinity [ 7].
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