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The above results indicated that the fermentation time for enzyme production under SSF depends on the growth rate of the microorganism and its pattern for enzyme production.
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Cloning of chitinase genes has been carried out for studying aspects of chitinase sequence variations, functional characteristics, changes in enzyme induction pattern, and for enzyme engineering.
We also found a similar overall staining pattern for PGE2-related enzymes irrespectively of NSAID treatment (data not shown).
We also describe a unique localization pattern for these enzymes at septa in live yeast and hyphal cells, and demonstrate that phosphorylation of Chs2 on S222 and specific cell wall stresses independently regulate the amount of Chs2 that is localized to specific sites in cells.
As is apparent from Figure 3, restriction-enzyme specific patterning for individual enzymes is highly conserved even when enzymes are used in different combinations, suggesting that the difference between the fragment numbers per selective PCR is largely the result of the individual restriction enzymes (see above).
The study also showed that elevation pattern of enzyme activity was different for different fish tissues but it revealed that H. fossilis was more sensitive to the changes than A. testudineus.
Next we looked for patterns of enzyme expression that are related to respiration and whether these would be over-represented in one of the enzyme categories that we investigated.
Both variants are physiologically relevant in D. melanogaster, but differences in the expression patterns for each enzyme with respect to tissue distribution and stages of development have been identified.
Enzyme code distributions for each tissue calculated by the main enzyme classes: oxidoreductases, transferases, hydrolases, lysases, isomerases, demonstrated a similar pattern of enzyme activity across tissues.
These include mining the data on structure and function of enzymes for salient patterns of enzyme recruitment.
The induction pattern for both amylolytic enzymes was different in various carbon sources suggesting that these hydrolases are inducible.
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