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T. reesei is an important model organism of lignocellulosic biomass degradation and it can, remarkably, produce over 100 g = l yields of extracellular protein in industrial cultivations [ 28].
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However, recent research studies have shown that the production of cellulases from actinomycetes could also be significantly improved by employing different types of strain improvement methods, thus achieving high yields of extracellular proteins.
The specific extracellular cellulase production rates and the yield of extracellular protein correlated strongly with SPPR and the specific sulphate consumption rate with specific lactose consumption rate and hence, are not shown in Figure 1.
a, b TEM images showing capping protein layer (arrows) around AuNPs. c SDS-PAGE of extracellular protein secreted from T. crassum and protein associated with nanoparticles.
The heterologous expression of extracellular proteins (e.g. cellulases or hemicellulases) is the key feature of recombinant cellulolytic strategies, conferring cellulolytic ability to microorganisms exhibiting high product yields and titers.
Here we discuss, also on the basis of experimental evidences based on SMFS, the possibility that disulfide bond switching and mechanical deformation of extracellular proteins can be coupled, thus leading to an efficient and highly tuned switch for protein function.
This observation suggests the involvement of extracellular proteins of fungus in the formation and stability of the nanoparticles.
Pathogenic streptococcal species produce an extensive array of extracellular proteins and use several protein export mechanisms.
The cultivation yielded 223 mg L−1 of recombinant protein, which corresponds to 52% of total extracellular protein.
Fig. 4 SDS-PAGE analysis of total extracellular protein in culture supernatants.
Notably, we found that deletion of Ncap3m (NCU03998) in N. crassa achieved the highest extracellular protein yield among all screened mutants, with amounts of secreted proteins comparable to Δ cre- 1.
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