Escherichia coli GROWN ON MINIMAL SALTS VERSUS COMPLEX MEDIA
Professor of Biology and Chemistry
University of Cincinnati Clermont College,
Batavia OH 45103
grow bacterial cultures
3 August 1992, rvsd 29 June '94, 9 July '95, 3 July '97, 29 June 00, 10 July 00, 17 July 04
used to aerate
Bacteria display a characteristic four-phase pattern of growth in liquid culture. The initial Lag phase is a period of slow growth during which the bacteria are adapting to the conditions in the fresh medium. This is followed by a Log Phase during which growth is exponential, doubling every replication cycle. Stationary Phase occurs when the nutrients become limiting, and the rate of multiplication equals the rate of death. Logarithmic Decline Phase occurs when cells die faster than they are replaced. (This latter occurs over a much longer period of time that the previous three.)
We will study the patterns of aerated growth in minimal salts medium (either Cold Spring Harbor A + 0.1% glucose (CSHA), or Vogel's E + 0.1% glucose (VE)) compared to growth in a complex medium (Tryptic Soy Broth = TSB). Bacterial population in the culture will be estimated by measuring its turbidity, (to which it is proportional) a using spectrophotometer. Turbidity is classically measured as the absorbance at 660 nanometers wavelength. You should record the collected data and make two graphs of it in your notebook: one on a linear scale, and one on a semi-log scale. Labeled the phases and determine the doubling times for each medium.
source or air pump
manifold with spaghetti tubing (be sure the tubing is in good repair
sterile 16 x 150 bubbler tubes
37C hot block, to accept 16 mm tubes
Timex "Triathlon"® watch
sterile pipettes (5 & 1 mL)
two spectrophotometers (one each for CSHA & TSB)
Tryptic Soy Broth
Cold Spring Harbor A minimal medium with 0.1% glucose
10x Cold Spring Harbor A Medium
(NH4)2SO4 10 g
K 2HPO4 105 g
KH2PO4 45 g
dissolve in dH2O, q.s. to 1 L
E. coli stationary overnight culture
|Set up and
GROWTH CURVE APPARATUS (here is a labeled image):
air pump bubbles air through a humidification flask, the humidified air is piped to a valved manifold, which is connected by spaghetti tubing to bubbler tubes, set in the holes of a pre-heated 37C hot block.
To simplify readings, use two spectrophotometers, one blanked to the minimal salts medium, the other blanked to the TSB.
|Inoculate 0.02 mL of an overnight shaken culture (left image) of Escherichia coli into 5.0 mL Tryptic Soy Broth (right image) and into 5.0 mL of minimal salts medium (for instance, Vogel's E or Cold Spring Harbor A) + 0.1% glucose.|
|Mix and determine the resulting A660 of the inoculated cultures, (it shold be between 0.010 and 0.020. This A660 is the time zero reading. Insert the bubbler apparatus, place in 37 C hot block with aeration adjusted, and start the 30 minute count down repeat watch.|
|Read the A660 of the two cultures every 30 minutes. The intervals may be conveniently timed using a Timex Triathlon in its "CDR" mode (Count Down Repeat) set to repeat a signal at 30 minute intervals.|
|Collect the growth data for at least three hours (five if possible). Use a computer for ease and ability to manipulate the data at the end of the experiment.|
|Make two graphs of the A660
of the cultures versus time in minutes:
First, a standard linear-linear graph of a time-course experiment, with minutes incubation on the X axis, and A660 along the Y axis. I have my students construct a graph by hand to develop their graphing skills. If they then wold like to use a spreadsheet program to construct a graph, that is fine.
|Second, produce a semi-log
graph using three cycle semi-log graph
paper. Take care to correctly label the Y axis
values. (First label 0.010, 0.100 and 1.000 lines,
then fill in values between.)
DOUBLING TIME: Use a ruler to draw aline through the linear phases of these curves. This represents their exponential or log phases. Pick an A660 value on the lower end of this straight line, note its time. Then find the point at which the A660 has doubled and note that time. The time elapsed between the two points is the doubling time.
Label the lag and log
phases, and determine the generation time. Mount these
in your notebook.