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In this paper, three models describing the population balance of microorganisms based on the assumption of symmetric cell division are discussed in terms of whether it is possible or not to use them to explain the dynamic behavior of the RBC.
Similarly, GC-FAME-based identification was also considered rapid and reliable technique for the identification of microorganisms based on the pattern of cellular fatty acid in bacteria, which is unique signature and aids in their identification and classification.
Antibody-based immunoassays such as the enzyme-linked immunosorbent assay (ELISA) and the Western blot have also been used for detection of microorganisms based on the antibody-antigen interaction[4].
For example, microbiologists tried to classify microorganisms based on the structures of their cell walls, their shapes, and the substances they consume.
A global multispecies biofilm development model for a biofilm formed from these three microorganisms based on the collected information is then proposed.
That means on a global view that there is a selection of the fittest microorganisms based on the presence of resistance determinants and their stable inheritance.
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In the second place, we classified the assays into cell-free, cell-based and microorganism based on the biological object of the experiments (Fig. 2a) (see Section 2).
On the other hand, some other functions are sparsely dispersed across distant clades, which would make it difficult to predict the presence or absence of these functions in a microorganism based on the functions of its phylogenetic neighbors.
Recently, genetically engineered microorganisms based on fusing of the lux, gfp or lacZ gene reporters to an inducible gene promoter have been widely applied to assay toxicity and bioavailability.
The detection and identification of microorganisms based on traditional culture-based methods make time-critical decision-making rather difficult because of the significant time lags between patient sampling and results.
Data on the initial site of infection and the infecting microorganisms (based on infection site and blood culture) were collected periodically.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com