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Exact(10)
MIC (minimal inhibitory concentration) of tested sample against these microorganisms was determined as previous reports [24].
The presence of other microorganisms was determined using PCR technique.
The PCB degradative ability of microorganisms was determined by gas chromatography after 7 days of incubation.
The composition of the airborne microorganisms was determined by cloning and sequencing the 16S rRNA genes.
The number of microorganisms was determined by the successive dilutions method with peptone water, and plated in MRS agar-Rifampicin.
The total number of microorganisms was determined by multiplying the number of CFU by the corresponding dilution factor.
Similar(50)
MICs values, which represented the lowest essential oil concentration that preventing visible growth of microorganisms, were determined as previously described (Ben Bnina et al. [2009]).
In addition, cell counts of iron II), sulfur, and thiosulfate oxidizing, lithotrophic bacteria and chemoorganotrophic microorganisms were determined quantitatively by the most-probable-number technique or by agar-plating.
The soil microbial activity and related coal biosolubilization enzymes mediated by microorganisms were determined along with the chemical variables associated with saline-sodic soils with testing under controlled conditions in a greenhouse.
After 48 h of aerobic incubation at 37 °C, the numbers of surviving microorganisms were determined.
The MICs values of the extract against the test microorganisms were determined by broth microdilution method as recommended by CLSi [ 20].
More suggestions(15)
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microorganisms was found
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