Bacterial Growth Curve Measurements with a Multimode Microplate Reader

Materials and Reagents

1. 96-well clear bottom plates (Corning, catalog number: 3631) (Figure 1)

   
   

   
   Figure 1. Photo of a 96-well microplate with clear bottom and its clear lid.

   
   

2. Polystyrene lids for 96-well microplates (Corning, catalog number: 3931)

3. 1–200 µL pipette tips (VWR, catalog number: 53508-810)

4. 100–1,000 µL pipette tips (VWR, catalog number: 83007-376)

5. 1.5 mL microcentrifuge tubes (VWR, catalog number: 20170-038)

6. 14 mL sterile culture tubes (VWR, catalog number: 60818-725)

7. Escherichia coli strain K-12 MG1655 transformed with plasmid pOEGFP2, encoding ampicillin resistance gene and green fluorescent proteins (Lab collection), which were used previously (Haque et al., 2017; Niyonshuti et al., 2020; Krishnamurthi et al., 2021). (Figure 2)

   Note: Other bacterial strains expressing fluorescent proteins are expected to be compatible with the current protocol.

   
   

   
   Figure 2. Map of the plasmid pOEGFP2 used in this protocol. The plasmid was a gift from Dr. David McMillen at the University of Toronto. The plasmid map was generated using SnapGene Viewer (GSL Biotech LLC).

   
   

8. Tryptone (Bio Basic Inc, catalog number: TG217)

9. Yeast extract (Bio Basic Inc, catalog number: G0961)

10. Sodium chloride (VWR International, LLC, catalog number: 7647-14-5)

11. Ampicillin (VWR, catalog number: AAJ60977-06)

12. Triton X-100 (VWR, catalog number: AAA16046-AP)

13. Ethanol (VWR, catalog number: 89125-188)

14. Deionized water (>17.6 MΩ, from Barnstead ultrapure water purification system [model: D4641])

15. Triton X-100 (VWR, catalog number: AAA16046-AP)

16. Liquid LB medium (200 mL) (see Recipes)

17. Ampicillin stock solution (10 mL) (see Recipes)

18. Python code (see Supplementary file)

Equipment

1. 2–20 µL single channel mechanical pipette (VWR, catalog number: 89079-964)

2. 20–200 µL single channel mechanical pipette (VWR, catalog number: 89079-970)

3. Multimode microplate reader capable of measuring both absorption and fluorescence (BioTek Instruments, model: Synergy H1)

4. Autoclave (Tuttnauer, model: 2540E-B/L)

5. Biosafety cabinet (Labconco, model: Purifier Logic+ Class II Type A2)

Software

1. Gen5 Microplate Reader and Imager Software (BioTek Instruments, https://www.biotek.com/)

2. Microsoft Excel Spreadsheet Software (Microsoft Corporation, https://www.microsoft.com/)

3. Python (https://www.python.org/)

Procedure

Bacteria Growth:

1. Preparation of initial liquid culture of bacteria

   1. Prepare liquid LB medium, followed by autoclaving (120°C, 41 min) and cooling down to room temperature.

   2. Inoculate a single colony of the bacterial strain into 7 mL of LB medium in a culture tube, supplemented with ampicillin or the appropriate antibiotic at a final concentration of 50 µg/mL.
       Note: Several colonies in separate culture tubes may be used if more replicates are desired.

   3. Incubate the liquid culture in a shaking incubator at 37°C with orbital shaking at 250 rpm overnight.

      
      

2. Pre-treatment of 96-well plates and lids

   1. Prepare 10% Triton X-100 in ethanol by mixing 1 mL of Triton X-100 with 9 mL of ethanol.

   2. Pour 10 mL of the diluted Triton X-100 to a new microplate lid.

   3. Incubate the lid with diluted Triton X-100 at room temperature for 15 s.

   4. Take a new 96-well plate and fill each well with 100% ethanol (400 µL per well). Incubate at room temperature for 15 min.

   5. Discard ethanol from the microplate wells and discard the diluted Triton X-100 from the microplate lid.

   6. Air dry the microplate wells and microplate lid at room temperature by leaving them inside the biosafety cabinet for 30 min.

   7. Turn on the UV light of the biosafety cabinet and further disinfect the microplate wells and lid for 15 min.

      Note: Treatment with ethanol and UV is for sterilization, while treatment with Triton X-100 is to prevent water condensation on the lid during the measurements.

      
      

3. Setup of microplate reader and software

   1. Turn on the microplate reader and open the Gen5 software.

   2. Set up a new procedure/protocol in Gen5 (Figure 3).

      1. Plate type: 96-well plate.

      2. Use lid: checked.

      3. Temperature: 37°C.

      4. Shake: orbital for 0:10.

      5. Kinetic measurement for a desired total time (e.g., 16 h, 24 h, or 48 h) and interval of 10 min with continuous orbital shaking.

      6. Reading: absorption at 600 nm, fluorescence at excitation = 488 nm and emission = 525 nm.

      
      

      
      Figure 3. An example for setting up the procedure/protocol in Gen5 software for the growth curve measurements of bacteria using a microplate reader.

      
      

4. Growth curve measurements using microplate reader

   1. Dilute the overnight liquid bacterial culture by 100–500 times in fresh LB supplemented with ampicillin at 50 µg/mL.

      Notes:

      1. If a photometer is available, measure the optical density of the overnight culture and make the dilution to the desired optical density (typically <0.05).

      2. Other media or additional ingredients (such as ions, nanoparticles, and drugs of interest that may affect bacterial growth) can be used if desired. For example, silver ions were added to the LB medium at a final concentration of 40 µg/mL in the sample S2 of the representative data (Figure 4).

   2. Pipette 200 μL of the diluted culture into a single well of the 96-well plate as a sample. Samples should be prepared with at least triplicates.

   3. Pipette 200 µL of LB medium with ampicillin into a single well of the 96-well plate as a blank. Blanks should be prepared with at least triplicates.

   4. After loading all the samples and blanks, cover the 96-well microplate with the prepared lid.

   5. Start the procedure/protocol in Gen5 software. When prompted, place the microplate properly on the microplate holder, and start recording of the bacterial growth curve.

      
      

5. Finishing up

   1. Upon completion of the data acquisition, remove the 96-well plate from the microplate reader.

   2. Disinfect the samples and discard the microplate properly.

   3. Save the results in Gen5 software, and export the data as an Excel spreadsheet file.

   4. Close the Gen5 software, and turn off the microplate reader.

Data analysis

1. Reorganize the data from the Excel spreadsheet as text files so that each text file contains the absorption data (or fluorescence) data of a single sample (or the blank). Note that each column in the text file corresponds to the readings of a single well of the microplate. Fluorescence data and absorption data should be separated into different files.

2. Run the provided Python code (see Supplementary file) to:

   1. Calculate the averaged absorption (or fluorescence) of samples, and plot the results.

   2. Smooth the growth curves, calculate the averaged first-order time derivatives of absorption (or the second-order time derivative of fluorescence) of samples, and plot the results.

   3. Identify the peak locations and heights of the time derivatives.

3. Compare the peak locations (and/or heights) to quantify the relative changes between the samples.

   
   

Representative Data

Figure 4. Representative data for the growth curves of E. coli bacteria measured by a microplate reader and their time derivatives. A. Absorption growth curves. B. Fluorescence growth curves. C. First-order time derivative of absorption growth curves. D. Second-order time derivative of fluorescence growth curves. Sample S1: MG1655 strain with pEOGFP2 plasmid in LB medium. Sample S2: MG1655 strain with pEOGFP2 plasmid in LB medium with silver ions of 40 µg/mL. In all sub-figures, “a.u.” stands for arbitrary units.

Recipes

1. Liquid LB medium (200 mL)

   2 g Tryptone

   1 g yeast extract

   2 g sodium chloride (NaCl)

   Fill up to 200 mL with deionized water and autoclave to sterilize.

2. Ampicillin stock solution (50 mg/mL)

   500 mg of ampicillin powder (sodium salt)

   10 mL of water

   Filter sterilize the ampicillin solution and store 1 mL tubes at -20°C.

Acknowledgments

We thank Dr. David McMillen at the University of Toronto for the generous gift of plasmid encoding the enhanced GFP and ampicillin resistance (pOEGFP2). This work was supported by the University of Arkansas, the Arkansas Biosciences Institute (Grant No. ABI-0189, No. ABI-0226, No. ABI-0277, No. ABI-0326, No. ABI-2021, No. ABI-2022), and the National Science Foundation (Grant No. 1826642). The original protocol was developed and used in Krishnamurthi et al. (2021) and Niyonshuti et al. (2020).

Competing interests

No competing interest is declared.

References

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