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These bottlenecks have to be solved to improve the feasibility of the CBP I microorganism.
A prototype model of CBP I is Trichoderma reesei[ 11] or C. thermocellum[ 12], which is one of the widely studied microorganisms because of producing several kinds of cellulases and β-glucosidases.
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The CBP was categorized into CBPs I and II.
For this purpose, a robust CBP database (i.e., high number of sampling locations selected according to system characteristics) corresponding to nine distribution systems was generated.
CBP-BDI deliberative agents collaborate with ARTIS agents in order to solve real-time problems efficiently.
Category I CBP is an engineering method of a cellulase producer to be ethanologenic, while category II CBP of an ethanologen to be cellulolytic.
Some cellulolytic thermophilic bacteria have been described as potential candidates for category I CBP.
In this review, potential of cellulolytic fungi as candidates for category I CBP is discussed.
As an alternative, category I CBP, aimed at engineering a cellulase producer to be ethanologenic, could be pursued, but it is still in its infancy.
In addition, OsHAC701 on average showed 65.3% sequence identity to the monocot CBP proteins of Group I (SbHAC2601, ZmHAC101, and ZmHAC115; see Additional file 1), whereas on average it showed only about 43.0% sequence identity to monocot CBP proteins of Group II (SbHAC2602, SbHAC2603, ZmHAC111, and ZmHAC113).
Adjusted analysis shows that fewer group CBP patients (OR 0.84; 95%CI 0.73-0.96) and fewer network CBP patients (OR 0.92; 95%CI 0.85-1.00) utheizED the ED compared to individual practice.
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CEO of Professional Science Editing for Scientists @ prosciediting.com