The document outlines key concepts related to bacterial growth, including definitions, importance, growth phases, and measurement methods. It describes the phases of bacterial growth—lag, exponential, stationary, and death—along with various factors affecting growth, such as culture media types and environmental conditions. Measurement techniques are detailed, emphasizing direct and indirect methods for assessing bacterial populations and their viability.

1. BACTERIAL GROWTH
MUNDIA KANGONGWE

2. LECTURE OBJECTIVES
Define growth in relation to bacteria
Know the importance of growth in bacteria
Know how bacteria grow and also the growth
phases in bacteria growth
Know the methods used to measure bacterial
growth
Know the different types of culture media & their
uses
Know the factors affecting bacterial growth

3. Bacterial growth
In clinical perspective bacterial growth can be used
for:
Detection
Identification
Assessment of antibiotic effects.

4. Bacterial growth
Growth is an orderly increase in the quantity of cellular
constituents.
It depends upon the ability of the cell to form new
protoplasm from nutrients available in the environment.
In most bacteria, growth involves:
increase in cell mass and number of ribosomes,
duplication of the bacterial chromosome,
synthesis of new cell wall and plasma membrane.
partitioning of the two chromosomes,
septum formation, and cell division.
This asexual process of reproduction is called binary fission.

5. Binary fission

6. Four phases of Bacterial Growth Curve

7. Lag Phase
1.. Immediately after inoculation of the cells into
fresh medium, the population remains
temporarily unchanged.
There is no apparent cell division occurring,
cells may be growing in volume or mass,
synthesizing enzymes, proteins, RNA, etc., and
 increasing in metabolic activity.

8. Lag phase
The length of the lag phase is apparently dependent on
a wide variety of factors including
◦ the size of the inoculum;
◦ time necessary to recover from physical damage or
shock in the transfer;
◦ time required for synthesis of essential coenzymes or
division factors;
◦ time required for synthesis of new (inducible)
enzymes that are necessary to metabolize the
substrates present in the medium.

9. 2. Exponential (log) Phase
is a pattern of balanced growth wherein all
the cells are dividing regularly by binary
fission, and are growing by geometric
progression.
The cells divide at a constant rate depending
upon the composition of the growth medium
and the conditions of incubation.

10. Exponential (log) Phase
The rate of exponential growth of a bacterial
culture is expressed as generation time, also
known as the doubling time of the bacterial
population.
Measured to be anything between 13min for V.
cholerae to days or weeks for M. tuberculosis.

11. Stationary Phase
Exponential growth cannot be continued forever in a
batch culture (e.g. a closed system such as a test tube or
flask).
Population growth is limited by one of the factors:
1. Exhaustion of available nutrients;
2. Accumulation of inhibitory metabolites or end products;
3. Exhaustion of space, in this case called a lack of
"biological space".
4. Acidic pH of media
5. Insufficient oxygen supply

12. Stationary Phase
The stationary phase, like the lag phase, is not
necessarily a period of quiescence.
◦Bacteria that produce secondary metabolites,
such as antibiotics, do so during the stationary
phase of the growth cycle
◦(Secondary metabolites are defined as
metabolites produced after the active stage of
growth).
It is during the stationary phase that spore-
forming bacteria have to induce or unmask the
activity of dozens of genes that may be involved in
sporulation process.

13. Death Phase
If incubation continues after the population
reaches stationary phase, a death phase follows, in
which the viable cell population declines.
◦(Note, if counting by turbidometric measurements
or microscopic counts, the death phase cannot be
observed.).
During the death phase, the number of viable cells
decreases geometrically (exponentially), essentially
the reverse of growth during the log phase.

14. Measurement of Growth
For unicellular organisms such as the
bacteria, growth can be measured in terms
of two different parameters:
changes in cell mass and
changes in cell numbers.

15. Methods for Measurement of Cell Mass
Methods for measurement of the cell mass
involve both direct and indirect techniques.

16. Direct Techniques.
1. Direct physical measurement of
◦ weight
◦ volume of cells after centrifugation.
2. Direct chemical measurement of some chemical
component of the cells such as
◦ total protein, or
◦ total DNA content.

17. Indirect Techniques.
3. Indirect measurement of chemical activity such as
◦ rate of O2 production or consumption,
◦ CO2 production or consumption, etc.

18. Indirect Techniques….
4. Turbidity measurements employ a variety of
instruments to determine the amount of light
scattered by a suspension of cells.
◦Particulate objects such as bacteria scatter light
in proportion to their numbers.
◦The turbidity or optical density of a suspension
of cells is directly related to cell mass or cell
number, after construction and calibration of a
standard curve.

19. Measuring Microbial Growth
Indirect Methods of Measurement
Turbidity:
As bacteria multiply in media, it becomes turbid.
Use a spectrophotometer to determine % transmission or
absorbance.
Multiply by a factor to determine concentration.
Advantages:
•No incubation time required.
Disadvantages:
•Cannot distinguish between live and dead bacteria.
•Requires a high concentration of bacteria (10 to 100
million cells/ml).

20. Methods for Measurement of Cell Numbers
Measuring techniques involve:
Direct counts, visually or instrumentally, and
Indirect viable cell counts.

21. 1. Plate count:
Most frequently used method of measuring bacterial
populations.
 Inoculate plate with a sample and count number of
colonies.
Assumptions:
 Each colony originates from a single bacterial
cell.
 Original inoculum is homogeneous.
Measuring Microbial Growth
Direct Methods of Measurement

22. Colonies

23. Advantages:
◦ Measures viable cells
Disadvantages:
◦ Takes 24 hours or more for visible colonies to appear.
◦ Only counts between 25 and 250 colonies are accurate.
◦ Must perform serial dilutions to get appropriate
numbers/plate.

24. Measuring Microbial Growth
Direct Methods of Measurement
-Plate count
◦The sample or cell suspension can be diluted in
a non-toxic diluents (e.g. saline) before plating.
◦Each colony that can be counted is called a
colony forming unit (cfu) and the number of
cfu's is related to the viable number of bacteria
in the sample.

25. Serial Dilutions are Used with the Plate Count
Method to Measure Numbers of Bacteria

26. Methods for Measurement of Cell Numbers
Advantages of the technique are its sensitivity
(theoretically, a single cell can be detected), and it
allows for inspection and positive identification of
the organism counted.
Disadvantages are :
1. only living cells develop colonies that are
counted;
2. clumps or chains of cells develop into a single
colony;
3. colonies develop only from those organisms for
which the cultural conditions are suitable for
growth.

27. Measuring Microbial Growth
Direct Methods of Measurement
2. Direct Microscopic Count:
A specific volume of a bacterial suspension (0.01 ml) is placed
on a microscope slide with a special grid.
Stain is added to visualize bacteria.
Cells are counted and multiplied by a factor to obtain
concentration.
Advantages:
•No incubation time required.

28. Disadvantages:
•Cannot always distinguish between live and dead
bacteria.
•Motile bacteria are difficult to count.
•Requires a high concentration of bacteria (10
million/ml).
•samples may require to be concentrated by
centrifugation or filtration to increase sensitivity

29. Measuring Microbial Growth
Direct Methods of Measurement
Filtration:
Used to measure small quantities of bacteria.
•Example: Fecal bacteria in a lake or in ocean
water.
 A large sample (100 ml or more) is filtered to
retain bacteria.
Filter is transferred onto a Petri dish.
Incubate and count colonies.

30. Culture Media

31. Types of culture media
i. Defined media: Nutrient material whose exact
chemical composition is known.
 For chemoheterotrophs, must contain organic source
of carbon and energy (e.g.: glucose, starch, etc.).
 May also contain amino acids, vitamins, and other
important building blocks required by microbe.
 Not widely used.
 Expensive.

32. Types of culture media
ii. Complex media: Nutrient material whose exact
chemical composition is not known.
 contains digests of heart, brain, blood, yeast, milk,
etc;
Widely used for heterotrophic bacteria and fungi.

33. Types of culture media
Two forms of complex media:
•Nutrient broth: Liquid media
•Nutrient agar: Solid media

34. Liquid media

35. Solid Media

36. Types of culture media
iii. Selective media: substances are present
that encourage growth of the desired microbe,
or inhibit the growth of undesired ones; ex:
Campylobacter media

37. Types of culture media
iv. Differential media: appearance of the
growing colonies are not the same;
example: presence and type of hemolysis in
blood agar plates, carbohydrate utilization
broths and ability to ferment lactose in
MacConkey agar

38. Different appearance on solid media

39. Different types of haemolysis

40. Types of culture media
iv. Anaerobic Growth Media: Used to grow anaerobes that
might be killed by oxygen
Contain ingredients that chemically combine with oxygen
and remove it from the medium.
Example: Sodium thioglycolate
Tubes are heated shortly before use to drive off oxygen.
Plates must be grown in oxygen free containers (anaerobic
chambers).

41. Equipment for producing CO2 rich
environment

42. v. Transport media
- Support survival of delicate pathogens outside
of the body e.g. Stuarts transport media.
◦Keep anaerobes alive

43. Factors affecting bacterial
growth
On basis of O2 requirements, organisms can be
classified as:
Aerobes
Anaerobes
1. Aerobes:
Obligate Aerobes - Absolutely requires O2
Microaerophiles – Requires only a low
concentration of O2.

44. 2. Anaerobes:
Obligate Anaerobes – Do not require O2
i.e. cannot withstand the presence of O2
Facultative Anaerobes – do not require its
presence but can survive its presence and
can even use it for respiration

45. Environmental Factors Affecting Bacterial
Growth-pH
pH-Organisms can be classified as:
• Acidophiles
◦ Neutrophiles
◦ Alkaliphiles
•The range of pH over which an organism grows is defined by
three cardinal points:
◦ minimum pH, below which the organism cannot grow,
◦ maximum pH, above which the organism cannot grow, and
◦ optimum pH, at which the organism grows best.

46. Growth rate vs pH for three environmental classes of procaryotes. Most free-
living bacteria grow over a pH range of about three units. Note the symmetry of
the curves below and above the optimum pH for growth.

47. Environmental Factors Affecting Bacterial
Growth - Temperature
Psychrophilic bacteria (Psychrophiles) are
adapted to their cool environment by having
largely unsaturated fatty acids in their plasma
membranes.
Saturated fatty acids, as in the membranes of
thermophilic bacteria, are stable at high
temperatures.

48. Environmental Factors Affecting Bacterial
Growth-Temperature

49. Environmental Factors Affecting Bacterial
Growth-Temperature
Temperature for growth (degrees C)
Group Minimum Optimum Maximum Comments
Psychrophile Below 0 10-15 Below 20 Grow best at relatively low T
Psychrotroph 0 15-30 Above 25
Able to grow at low T but
prefer moderate T
Mesophile 10-15 30-40 Below 45
Most bacteria esp. those living
in association with warm-
blooded animals
Thermophile* 45 50-85
Above
100
(boiling)
Among all thermophiles is wide
variation in optimum and
maximum T

50. Environmental Factors Affecting Bacterial
Growth-Salt concentration
•The only common solute in nature that occurs over a wide
concentration range is salt [NaCl], and some microorganisms are
named based on their growth response to salt.
•Microorganisms that require some NaCl for growth are halophiles.
•Mild halophiles require 1-6% salt,
•Moderate halophiles require 6-15% salt;
Extreme halophiles that require 15-30% NaCl for growth are found
among the archaea.
•Bacteria that are able to grow at moderate salt concentrations,
even though they grow best in the absence of NaCl, are called
halotolerant.

51. Environmental Factors Affecting Bacterial
Growth
•The term osmophiles is usually used for organisms
that are able to live in environments high in sugar.
•Organisms which live in dry environments (made dry
by lack of water) are called xerophiles.
•The concept of lowering water activity in order to
prevent bacterial growth is the basis for preservation
of foods by drying (in sunlight or by evaporation) or by
addition of high concentrations of salt or sugar.

52. Effects of lower water levels
•Longer lag, slower growth
•Loss of membrane fluidity
•Impaired transportation across membrane

53. Environmental Factors Affecting Bacterial
Growth - Pressure
1. Most organisms exist at 1 atm
2. In deep sea à higher pressures
a) Barotolerant organisms (barophiles) – survive at high
pressures but grows better at 1 atm.
b) Moderate barophiles – grow at high pressures but still
grow at 1 atm.
c) Extreme (obligate) barophiles – only grows at high
pressures

54. Environmental Factors Affecting Bacterial
Growth - Radiation
Ionizing radiation (radiation that is very short wavelength/high
energy)
a) Types
(1) Gamma
(2) X-rays
Low levels of these radiations - may cause mutations and may
indirectly
result in death.
High levels - may directly cause death of the microbes.
b) Effects that damage cell components and DNA
(1) break H bonds
(2) oxidize double bonds
(3) formation of hydroxyl radical