The bacterial growth curve and growth rate constants

Microbiology, Immunity and Forensics · Culturing and measuring microorganisms · note 3 of 4

Spec 6.3
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The bacterial growth curve and growth rate constantsSpec 6.3

In short

A bacterial growth curve in a closed culture has four phases: lag, when cells adjust and little division occurs; exponential, when the population doubles each generation; stationary, when divisions equal deaths; and death, when deaths exceed divisions. The exponential growth rate constant is generations per unit time.

When bacteria are inoculated into a fixed volume of broth (a closed culture, with no nutrients added or waste removed) and the number of living cells is plotted against time, the curve has four phases. Cell number is usually plotted as log₁₀ so that the very large range fits on the graph and the exponential phase appears as a straight line.

Phases of the growth curve
PhaseWhat happens to cell numberWhy
Lag phaseLittle or no increaseCells are adjusting to the new medium: they take up nutrients, synthesise enzymes and ribosomes, and grow in size; few cells divide yet
Exponential (log) phaseDoubles every generation: fastest rate of increaseNutrients and space are plentiful and there is little waste; cells divide by binary fission at a constant rate, so the number of cells doubles in each generation time
Stationary phaseConstant: births equal deathsNutrients become limiting, toxic waste (for example acids that lower the pH) accumulates and oxygen may run short, so division slows until the rate of division equals the rate of death
Death (decline) phaseFallsNutrients are exhausted and toxic waste is high, so more cells die than divide
Two graphs of bacterial growth: number of living cells against time on a linear scale (J-shaped curve) and log₁₀ number of living cells against time showing lag, exponential, stationary and death phases, with the gradient of the straight exponential section marked. (opens full size in a new tab)
The growth curve of a closed culture: on the log graph the exponential phase is a straight line whose gradient is the growth rate.

Exponential growth and growth rate constants

In the exponential phase each cell divides once per generation time (the time for the population to double). After n generations a population starting with N₀ cells has Nₙ = N₀ × 2ⁿ cells. Rearranging with logarithms gives the number of generations from the start and end numbers.

number of generations, n = (log₁₀ Nₜ − log₁₀ N₀) ÷ 0.301
exponential growth rate constant, k = n ÷ t (generations per hour) generation time = 1 ÷ k

The constant 0.301 is log₁₀ 2. The growth rate constant k is the number of generations per unit time during the exponential phase; it is the gradient of the straight line on a graph of log₂ (cell number) against time, or the gradient of log₁₀ cell number against time divided by 0.301.

Growth rate constant

A broth culture contained 2.0 × 10³ cells per cm³ at the start of the exponential phase and 1.28 × 10⁵ cells per cm³ 6 hours later. Calculate the exponential growth rate constant.

  1. log₁₀ (1.28 × 10⁵) = 5.107 and log₁₀ (2.0 × 10³) = 3.301, so the difference is 1.806.
  2. Number of generations, n = 1.806 ÷ 0.301 = 6.0.
  3. k = n ÷ t = 6.0 ÷ 6 h = 1.0 generation per hour (generation time 1 hour).

Answer: k = 1.0 generation per hour

Maths skill:

Logarithms on a calculator and reading a log scale are IAL-only skills (A.0.5, A.2.5). If a question does not give the formula, show the doubling idea: 1.28 × 10⁵ ÷ 2.0 × 10³ = 64 = 2⁶, so 6 generations.

Exam tip:

Do not say that cells 'stop dividing' in the stationary phase. The correct idea is that the rate of division equals the rate of death, so the number of living cells is constant.

Written and checked against the Edexcel International A Level Biology (YBI11) specification · Updated October 2026

Frequently asked questions

What is aseptic technique in microbiology?

Aseptic technique is a set of procedures that keeps unwanted microorganisms out of a culture and stops the cultured microorganisms escaping. It includes sterilising equipment, flaming loops and bottle necks, keeping lids on, taping and inverting plates, and disinfecting benches. It protects both the experiment and the worker.

How does dilution plating measure bacterial growth?

Dilution plating counts living bacteria. A culture is serially diluted, a measured volume is spread on agar and incubated, and the colonies are counted. Each colony grew from one colony-forming unit, so colonies divided by the volume plated and multiplied by the dilution factor gives cfu per cm³ of the original culture.

Why does a bacterial growth curve level off?

The curve levels off in the stationary phase because the rate of cell division equals the rate of cell death. Nutrients run short, toxic waste such as acid builds up and oxygen may fall. Cells still divide, but deaths match divisions, so the number of living cells stays constant.

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