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The activity and functional diversity of soil microorganisms were tested using the BIOLOG technique in laboratory.
These recombinant reporter microorganisms were tested for bioluminescence response to relevant phenol concentrations in the laboratory and to phenolic-containing effluents generated by an industrial wastewater treatment plant.
All microorganisms were tested separately: Micro plates were inoculated with one test organism, each, and used to either test five fungal extracts at 8 concentrations, or 10 fungal extracts at 4 concentrations.
The antimicrobial activities of cathelicidin BF against forty strains of microorganisms were tested.
Amplicons of desired size (463-bp) were obtained when purified genomic DNA of different serovars of C. trachomatis (A, D and L2) were used as templates for the in-house PCR, while no amplicon was detected when genomic DNA from humans as well as other STD causing and related microorganisms were tested as templates.
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The efficiency of two bioremediation treatments namely biostimulation (BS) by the addition of nutrients, and bioaugmentation (BA) by addition of indigenous microorganisms was tested in comparison with hydrocarbon natural attenuation in un-colonized and with rhizoremediation in colonized sediments.
80% methanol leaf extract of C. aurea inhibiting growth of one or more microorganisms was tested for MIC.
Moreover, in order to improve specificity, targeting photosensitizers specifically to a certain type of microorganisms was tested.
In the following work, the antifungal activity of these extracts against oil field microorganism was tested under the concentrations of 1,000 mg/L and 500 mg/L, and the results are summarized in Table 4.
Cetylpyridinium chloride disks were tested against microorganisms commonly found in oro-dental infections namely Candida albicans, Staphylococcus aureus, Escherichia coli and Streptococcus mutans.
Several microorganisms commonly used for fermentation were tested for their microbial growth on heat-treated OPF juice such as Bacillus cereus, Bacillus subtilis, Escherichia coli, Staphylococcus aureus, Saccharomyces cerevisiae, Mucor, Penicillium, and Trichoderma.
Related(20)
bodies were tested
organizations were tested
bacteria were tested
media were tested
charges were tested
pathogens were tested
agents were tested
plants were tested
samples were tested
microorganisms were isolated
microorganisms were found
microorganisms were cultured
microorganisms were activated
microorganisms were identified
microorganisms were normalized
microorganisms were observed
microorganisms were immobilized
microorganisms were presumed
microorganisms were sampled
microorganisms were performed
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