Team:UFAM Brazil/Protocol10
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- | <tr><td><h1>Cell growth quantification of mercury resistant <i> Escherichia coli DH5α</i> in differents Hg concentrations by Optical Density</h1></td></tr> | + | <tr><td colspan="3"><h1>Cell growth quantification of mercury resistant <i> Escherichia coli DH5α</i> in differents Hg concentrations by Optical Density</h1></td></tr> |
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Revision as of 14:40, 16 October 2014
Cell growth quantification of mercury resistant Escherichia coli DH5α in differents Hg concentrations by Optical Density | ||
Reagents: - Mercury chloride 20mg/ml; - Chloramphenicol 34 µg/ml; - Luria-Bertani + Mercury (LM) medium. Steps: 1. Pre-inoculum: Inoculate bacteria (DH5α transformed with BBa_K1355004) in Luria-Bertani + Mercury (LM) 0.05µg/ml + chloramphenicol 34µg/ml. Repeat the process for bacteria control with no high Hg resistance. 2. Incubate in shaker overnight at 37 °C. 3. Measure optical density (O.D.) of cultures in spectrophotometer at 600 nm wavelength. 4. Aliquot bacteria suspension in six tubes (50 mL) with 10 mL LM medium in the following concentrations: 0µg/ml, 1 µg/ml; 2.5 µg/ml; 5 µg/ml; 10 µg/ml; and 20 µg/ml. Use aliquots quantity according to the optical density. 5. Incubate in shaker at 37 °C for 48 hours. Measure optical density (O.D.) of cultures in: 2.5 hours – 4.5 hours – 6.5 hours – 17 hours – 24 hours – 43 hours and 48 hours. 6. After 48 hours of growth, measure the final concentration of mercury present in each sample in Direct Mercury Analyzer (DMA-80). | ||
Methods |