This lab provides a valuable opportunity to teach microbiology techniques, population growth dynamics, molecular genetics and basic synthetic biology concepts in a meaningful, real world way. As can be seen in the discussion questions for the lab report, the analysis of the lab will provide the students with a chance to do meaningful error analysis and examine the difference between quantitative results and qualitative results. If time allows the students can carry out all parts of the procedure. This will take about 5 class periods in a typical High School AP Biology or Biotechnology class. If instead the teacher prepares in advance the samples as outlined in Part 1 of the procedure, the students can conduct the smell tests and population measurements over two or three days. In a college lab course, most of the bacterial growth curve can be conducted in a typical three to four hour lab period. The procedure includes instructions for using a spectrophotometer to measure the population growth. If a spectrophotometer is not available, the population can be easily measured using the McFarland Turbidity methodology, as explained below.
Needed Materials
Teacher Provides
Innoculating loop or sterile toothpicks and bunsen burner
Sterile tubes for growing liquid cultures of cells
Cuvettes to measure absorbances if spectrophotometer is not fitted for glass tubes
4 x 100 ml erlenmeyer flasks per lab group
Stir plates and stir bars
Pipetmen and tips (P1000, P200, P20)
Pipets (10 ml and 5 ml) and bulbs
Timers or stopwatches
Sharpies
Nitrile or Latex gloves
If available, rollerwheel at 37° for growing overnight cultures of bacteria (if available)
If available, vortex for mixing cells prior to additions
If available, fume hood for measuring isoamyl alcohol (aka isopentyl alcohol) if available
Kit Provides
4 strains (see table below)
Store stabs at room temp
Store plates and liquid cultures at room temp or 4° (= fridge) for longer times.
Day 2: grow strains from plates as liquid overnights
Day 3: subculture bacteria in larger volumes, collect data through lag phase
Day 4: subculture continues, collect data through log phase
Day 5: finish growth curve, collect data for stationary phase
When you are done with this lab, here is a link to survey that you can offer the students. Thank you for helping us improve this content.
Annotated Procedure
Day 1:
TO DO
I. Streak out strains from stabs to plates
II. Prepare banana extract standards
I. Streak out strains from stabs to plates
We will be receiving our bacteria with the plasmid already inserted. This culture will come in the form of a "stab" or "slant", a test tube with a small amount of bacteria on a slanted media. To continue the experiment we will have to further culture the bacteria by streaking out the stabs onto LB+amp plates. The plates will be incubated 37° overnight.
Using a sterile toothpick or inoculating loop, gather a small amount of bacteria from the stab and transfer it to a petri dish containing Luria Broth (LB) agar plus ampicillin medium.
Repeat with the remaining stab samples, streaking out each onto a different petri dish.
Place these cultures in a 37°C incubator overnight.
This video illustrates the technique used for this transfer. TEACHERS: You may wish to conduct this procedure yourself. However, if time allows, the students will enjoy learning these microbiological techniques. If your class will test the whole set, there will be 4 strains to streak out. Strains can also be streaked out on LB+Amp+Cam if you'd like to verify the indole- strain background.
II. Prepare banana extract standards
The banana extract is provided in the kit. It will be necessary to make up the standards following the table. TEACHERS: The banana extract is an oil and will not dissolve in water. However, the concentrations are low and as long as the standard is given a shake before smelling, a suspension is sufficient.
Day 2:
TO DO:
I. Grow liquid overnights of bacterial strains
II. Prepare Turbidity standards (if no spectrophotometer is available)
I. Grow liquid overnights of bacterial strains
1. Using a sterile inoculating loop, transfer a bacterial colony from one of the petri dishes to a large sterile culture tube containing 5 ml of Luria Broth and 5 μl of ampicillin. TEACHERS: Colonies can be inoculated into the media with a toothpick, a loop, or a pipet tip.
2. Repeat for each strain you will inoculate. TEACHERS: Each group will need 2 mls of each sample for the next day of this procedure. If you conducting this part of the procedure for your students, you'll have to scale up the amounts in order to prepare enough for each group.
3. Place the culture tubes in the roller wheel in the incubator at 37°C overnight. Be sure to balance the tubes across from each other to minimize stress on the roller wheel.
This video illustrates the general technique for setting up overnight liquid cultures, though you’ll be transferring cells from the petri dish to the Luria Broth. TEACHERS: If you do not have a roller wheel and an incubator, you can prepare these cultures in small erlenmeyer flasks (with stir bars) placed on a stir plate at a slow pace. Cultures are stable and active for a week at least (stored at room temp or in the fridge) but will take considerably longer to start growing on the day you subculture (~3 hours rather than 1).
2. Prepare turbidity standards
As the populations of bacteria increase, the culture media gets increasingly turbid. Using the McFarland Turbidity Scale, it is possible to estimate the changes in turbidity. The results will not be as precise as what you would measure with a spectrophotometer, but the changes over time will be detected and the results can be graphed.
TEACHERS: these standards can be prepared well in advance of lab and are useful if you are running the protocols without access to a spectrophotometer.
Day 3: Measuring bacterial population growth in lag phase
TO DO:
Innoculate large volumes and collect data for lag phase TEACHERS: The procedure assumes each lab group will measure all 4 cultures. Due to equipment constraints, you may wish to vary this experiment so larger "class size" cultures are grown. In that case, increase the solutions and the amount of bacteria added by a factor equal to the number of lab groups. Students can then remove aliquots from these larger cultures for analysis.
Procedure, if using a spectrophotometer
1. Prepare a stock growth solution with
300 ml Luria broth
300 μl Ampicillin
250 μl isoamyl alcohol
TEACHERS: While isoamyl alcohol is safe enough for lab use, it is best if this is added by the teacher.
2. Mix this stock growth solution, by swirling the bottle or vortexing gently.
3. Set aside 2 ml of this mixture for each student group into a small sterile culture tube. This aliquot will serve as the blank for the spectrophotometer. TEACHERS: If you are using a small plastic cuvette, a 1 ml sample will be sufficient.
4. Move 50 ml of the broth solution to 100ml sterile erlenmeyer flask and add 2ml of bacteria from one of the overnight cultures, e.g. strain 1-1.
5. Repeat the addition of 2ml of bacteria to 50 ml of broth in the erlenmeyer flasks for each of the overnight cultures.
6. Cover the flasks with foil and start them gently stirring on the stir plates.
7. Remove 2 ml from each sample to read the starting density of each. If you are testing all 4 samples you should now have 5 small test tubes (4 with bacterial dilutions and one blank).
8. Prepare the spectrophotometer by setting it to OD600.
9. Note the time and take an "initial" density reading for the bacterial samples. Please note that your teacher may have carried out the preceding steps in advance of the lab. If that is the case, the teacher will tell you how much time has elapsed. That time will be your T0. TEACHERS: Given time constraints in most lab classes, it is OK for the students to prepare these samples and then place them in the refrigerator. The teacher can them place the samples on the room temperature stir plate the next morning and note the time. This may not be necessary during an extended lab period. At room temperature, it will take around three hours for the cultures to enter log phase. Initial readings will have an OD 600 around 0.05.
10. Add a stir bar to each culture flask and place onto stir plates. Stir slowly. Cover the flasks with foil.
11. After 20 minutes, remove 1-2 ml from each sample and place in a cuvette. Note: the volume you use here will depend on the size of the cuvette appropriate for your spectrophotometer. Please follow the teacher's instructions. TEACHERS: 1 ml is sufficient for a small plastic cuvette, while 2 mls will be needed for a small test tube that fits into most Spec 20 spectrophotometers
12. Read the blank and adjust the % Absorbance to zero.
13. Read the sample tubes and record the % Absorbance.
14. Sniff the flask for any evidence of a banana smell, comparing the smell with the banana extract standards. Be sure to shake the standards and the cultures before sniffing. Record your data.
15. At 20 minute intervals repeat steps 11-14.
16. Between time points, you can calculate the bacterial population: 1 OD600 unit = 1 x 109 bacteria. TEACHERS: If the entire growth curve (i.e. days 3, 4 and 5) is to be done in one class, you may have to start the early time points in advance. If you are dividing the growth curve into several short lab periods, be sure to store the cells in the fridge (~4°) until the next session.
Procedure, if no spectrophotometer is available
Error creating thumbnail: Unable to save thumbnail to destinationTurbidity comparisons for some bacterial cultures (left) and McFarland standards (right)The turbidity of the bacterial populations can be estimated using the McFarland Turbidity Scale. This method uses suspensions of a 1% BaCl2 in 1% H2SO4 that are visually similar to suspensions of various populations of E. coli.
1. Following your teacher's instructions, obtain small clear test tubes containing the turbidity standards. The tubes should contain enough standard in each to fill the tube to a height of about 1 inch (2.5 cm) from the bottom. Make sure each tube is properly labeled with its turbidity standard number. If you are filling the tubes from stock bottles of the standards, use small tubes and place enough standard in each to fill the tube to a height of about 1 inch (2.5 cm) from the bottom. TEACHERS: The size of the tubes and the volume of sample and standard used is flexible. The important things are that the volume can obscure the thick black lines and that the samples and standards are prepared in the same fashion, as shown in the photo.
2. Place the samples in a test tube rack that allows you to view them from the side. Use small tubes and place enough standard in each to fill the tube to a height of about 1 inch (2.5 cm) from the bottom.
3. On a blank index card or paper use a marker to draw two thick black lines. These lines should be within the height of the standards.
4. Place the card with the lines behind the standards.
5. To compare your bacterial cultures to the standards, you will need to place the bacterial sample in a test tube of the same size and equal volume as the standards. be sure to label these sample tubes.
6. Place the sample tube next to the standard tubes. You should move the sample to compare it to the standard tubes with the most similar turbidity. You can make this assessment more precise by looking for a standard that most similarly obscures the black lines on the background card.
7. Use the table below to determine the comparable OD 600.
8. 1 OD 600 unit equals approximately 1 x 109 cells.
Day 4: Measuring bacterial population growth in log phase
TO DO:
Restart cultures and collect data for lag phase
TEACHERS: A successful time course for Day 4 could be: Start the samples up in the morning for a class later in the day. These hours will allow the population to reach log phase. At this point, the students can take 2 or 3 more readings, as described for Day 3. The culture can be run overnight at room temperature to reach stationary phase for Day 5
Day 5: Measuring bacterial population growth in stationary phase
TO DO:
Collect data for stationary phase
TEACHERS: Two or three readings from each phase will provide sufficient data points for construction of the population growth curve. Just make sure that the students are tracking the time accurately from the initial reading.
TEACHERS: Note that the original strain is supposed to smell like bananas only during stationary phase but we have found that it actually smells throughout the measurements we've made...perhaps because stationary phase activity starts earlier than we think. Similarly, we have seen the strain 1-2, which has the stationary phase promoter and the inverter, is more active throughout the growth curve and generates a stronger banana smell than strain 1-3, which has the log phase promoter.
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Variations to try
Next version of this series will have BBa_J45400, a 3-methylbutanal generator to allow the strain to convert its own leucine into the ATF1 precursor.
Try growing the cells at different temperatures?
If you are using the McFarland standard, would more precise or subtle standards be useful?
Feedback
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