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Each bacterial isolate was also tested against a panel of six antibiotics using Kirby-Bauer disk diffusion method following CLSI guidelines [ 28].
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The metabolic pathway of BPA degradation by the bacterial isolates was also designed in today's analysis.
Radiation death of the bacterial isolates was also obtained by the linear regression equations.
The bacterial isolates were also identified using the VITEK 2 microbial identification system.
The bacterial isolates were also physiologically characterized on the basis of their growth at different temperatures, NaCl concentrations, and pH.
The bacterial isolates were also characterized on the basis of 16S rRNA gene sequencing to verify the recorded conventional characterizations of the isolates.
Two gene cassettes that encode proteins of unknown function, that have also been identified by other workers in class 1 integrons from a variety of clinical bacterial isolates, were also identified, orfF and orfC.
These bacterial isolates were also resistant to ampicillin, teicoplanin, and aminoglycosides but susceptible to linezolid, quinupristin/dalfopristin, and tetracycline.
Each bacterial isolate was classified as susceptible, intermediate, or resistant, depending on the growth inhibition diameter.
Bacterial isolate was grown in nutrient broth at 35 °C overnight.
A single bacterial isolate was cultured in 36% of wounds.
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