CLS 311: Basic Microbiology

MICROBIAL GROWTH

Mrs. Amany Ahmed Niazy

HISTORY

• The greatest contributor to methods of cultivating bacteria was Robert Koch (1843-1910).

• Koch initially experimented with growing bacteria on the cut surfaces of potatoes.

• Then gelatin was used initially to solidify the media. But it has a 2 major drawback: It melts at the temperature preferred by many

medically important organisms. Many bacteria digest it.

ROBERT KOCH

THE MARVELOUS BACTERIA.

• Bacteria can live in environment that no unprotected human could survive (e.g. ocean depths, volcanic vents …..etc).

• However, each species of bacteria has a limited set of environmental conditions in which it can grow; even then , it will grow only if specific nutrients are available.

What Do We Mean By Bacterial Growth?

• When we are talking about bacterial growth we are really referring to the number of cells, not the size of the cells.

• Bacteria that are growing are increasing in number, accumulating into colonies of hundred of thousands of cells, or population of billion of cells.

• A colony should have millions of bacterial cells to be seen by naked eye.

DOUBLING TIME (GENERATION TIME)

• The time taken by a bacteria to double in number.• It varies greatly according to :

Type of organism Temperature Nutrients Other conditions.

• 10 cells of a food-borne pathogen in a potato salad, sitting for 4 hours in the warm sun at a picnic, may multiply to more than 40,000 cells.

N1 = N0 X 2n

N1 number of bacterial cells at a given time.N0 original number of cells in a population. n number of divisions those cells have undergone during that time.

PROBLEM

• E.coli have a generation time of 20 minutes. If you start with 1 E.coli cell how many do you have after 2 hours.

• N1 = N0 X 2n.

• 64 = 1 x 26

• 120 minutes / 20 minutes = 6• If it is 2 hours then 6 generations

BACTERIAL GROWTH IN NATURE

• Bacterial growth and behavior in natural environment differ than its growth and behavior in the laboratory.

E.g. when prokaryotes grow in a running stream, it frequently synthesize slime layers or other

structures that allow them to attach to rocks.

BACTERIAL GROWTH IN NATURE BIOFILMS

• Biofilms: are communities of bacteria that attach to surfaces and live in polysaccharide-encased communities.

The Dutch scientist Anton van Leeuwenhoek first noticed biofilms back in 1683. When placing a

scraping of plaque from his own teeth under one of his first-generation microscopes, he spotted a

host of “very little living animalcules, very prettily a-moving.” For most of the next 300

years, however, biofilms were largely ignored, as microbiology focused on individual organisms in

their free-floating, or planktonic, state.

BIOFILMS

65% of human bacterial infections

involve biofilms .

INTERACTION OF MIXED MICROBIAL COMMUNITIES

• Prokaryotes in the environment grow in close associations with many different species.

• Following are some examples:

1. bacteria that cannot grow in presence of O2 can grow in the mouth because some bacteria in the mouth consume O2 during their metabolism creaing a microenvironments that lack O2.

2. Some metabolic wastes of one species of bacteria may serve as a nutrient for another.

3. Some bacteria can synthesize toxic compounds that inhibit other bacterial competitors.

4. Diifrent bacterial species in such communities usually compete for hytrients.

OBTAINING A PURE CULTURE IN THE LAB

• Only an estimated 1% of all bacteria can currently be cultivated successfully.

• Fortunately most of the known medically significant bacteria can be grown in pure culture.

• Understandably the associations of the bacteria in a natural environment cannot be reproduced in the lab.

OBTAINING A PURE CULTURE IN THE LAB

• To obtain a pure culture we need:

The the glassware, media, and instruments to be sterile before using it.

We should work using aseptic techniques.

OBTAINING A PURE CULTURE IN THE LAB

• Colony when supplied with the right nutrients and conditions a single bacterium will multiply on a solid medium in a limited area to form a colony.

• Around 1 million cells are required for a colony to be visible to the naked eye.

• Agar polysaccharide extracted from marine algae.

• 95°C or above liquid• 45°C solidify.

BACTERIAL GROWTH IN LABORATORY

• In the laboratory, bacteria are typically grown in broth contained in a tube or on an agar plate.

• These are considered closed systems because nutrients are not renewed, nor are waste products removed.

BACTERIAL GROWTH CURVE

• In any closed system the cell population increases in number in a predictable fashion and then eventually declines.

• Bacteria in a closed system fallow a pattern of stages that is called growth curve.

• This growth pattern is most distinct in a broth

culture rather than a plate culture.

5 PHASES IN A BACTERIAL GROWTH CURVE

1. Lag Phase: where the bacteria absorb nutrients, synthesize enzymes, and prepare for division. There is no increase in bacterial number in this phase.

During this time they synthesize macromolecules required for multiplication, including enzymes, ribosomes, and

nucleic acids, and they generate energy in the form of ATP.

If cells are transferred from a nutrient-rich medium to one containing fewer nutrients, the lag time tends to be longer.

5 PHASES IN A BACTERIAL GROWTH CURVE

2. Log Phase (logarithmic growth phase): where rapid multiplication occur causing very high increase in the number of bacteria.

The cells divide at a constant rate and their numbers increase by the same percentage during each time interval.

Doubling time (generation time) is measured during this period.

At this stage bacteria are most susceptible to antibiotics and other chemicals.

At this stage bacteria also produce metabolites that are commercially valuable (e.g. flavoring agents, food supplements antibiotics)

5 PHASES IN A BACTERIAL GROWTH CURVE

3. Stationary Phase: where the nutrients in the media decrease and the toxic waste resulting from bacterial metabolism increase. As a result, the multiplication is slowing down. The number of dividing bacteria equals the number of dead bacteria.

Length of time cells remain in this stage varies depending on the species and on environmental

conditions.

5 PHASES IN A BACTERIAL GROWTH CURVE

4. Death Phase: where overcrowding occurs and the bacteria are dying very rapidly because of lack of nutrients and accumulation of toxic waste. Very few bacteria will remain alive in this stage.

Once bout 99% of the cells have died off, the remaining members of the population enter a

different phase.

5 PHASES IN A BACTERIAL GROWTH CURVE

5. Phase of Prolonged Decline very gradual decrease in the number of viable cells in the population, lasting for days to years.

Many members of the population are dying and releasing their nutrients, while a few “fitter” cells more

able to cope with the deteriorating environmental conditions are multiplying.

This dynamic process generates successive waves of slightly modified populations, each more fit to survive

than the pervious ones.

Phase of Prolonged

decline

FACTORS AFFECTING MICROBIAL GROWTH

There are some factors that affect and control the growth of microorganisms around us, in hospitals, in the

laboratory, and in industrial settings. These factors are:

1. Availability of Nutrients2. Moisture3. Temperature4. pH5. Osmotic pressure6. Atmospheric Pressure7. Gaseous Atmosphere

1. AVAILABILITY OF NUTRIENTS

• Nutrients are crucial for microorganisms to survive in the environment.

• Type of nutrient needed vary based on type of microorganism.

• Bacteria should synthesize its cell components from these nutrients.

Chemical FunctionCarbon, oxygen, and hydrogen Components of cellular

constituents including amino acids, lipids, nucleic acids, and sugars.

Nitrogen Component of amino acids and nucleic acids.

Sulfur Component of some amino acids

Phosphorus Component of nucleic acids, membrane lipids, and ATP

Pottassium, magnesium, and calcium

Required for the functioning of certain enzymes; additional functions as well.

Iron Part of certain enzymes.

1. AVAILABILITY OF NUTRIENTS

Prokaryotes in general have a remarkable ability to use diverse sources of these elements. For

example, prokaryotes are the only organisms able to use atmospheric nitrogen as a nitrogen source.

2. MOISTURE

• All organisms on planet need water for their metabolic processes and most will die if moisture is too little.

• Some bacteria and parasites can stay dormant in endospores and cysts until moisture is available for their growth.

Dissolved substances such as salt & sugars interact with water

molecules and make the water unavailable

to the cell .

3. OSMOTIC PRESSURE

Halophilic organisms (salt lovers):

Are organisms that require high levels of sodium

chloride. e.g. microorganisms living in

the Dead Sea.

Prokaryotes that can grow in high solute solutions maintain the

availability of water in the cell by increasing their internal solute

concentrations .Halotolerant organisms: Are organisms that can grow

in relatively high salt solutions, up to

approximately 10% NaCl

3. OSMOTIC PRESSURE• Isotonic solutions : solutions where the concentration of the solute is equal to that of normal cells found in it; thus no osmotic pressure is exerted. Most organisms prefer isotonic solutions.

• Hypotonic solutions: Solutions where solute concentration outside the cell is less than that inside the cell. This cause microbial cells to swell then burst (die).

• Hypertonic solutions :Solutions where solute concentration outside the cell is more than that inside the cell. This cause microbial cells to shrink (inhibiting growth).

4. ATMOSPHERIC PRESSURE

• Most bacteria live at normal atmospheric pressure (14.7 psi ) and are not affected by minor changes in it.

Barophiles:Organisms that like very

high atmospheric pressure e.g. organisms living in oil

wells and deep oceans.

5. TEMPERATURE

• Microorganisms have optimum temperature required for their growth, this temperature depends on their enzymes.

• Each species of microorganism has a well-defined upper and lower temperature limit within which it grows. Within this range lies the optimum growth temperature (the temperature at which the organism multiplies most rapidly.)

5. TEMPERATURE

Microorganisms can be classified according to their preferred temp. into:

1 Thermophiles (heat lover): Microorganisms that grow best at high temp. 45-80°C e.g. organisms living in hot springs, archaea.

2 Mesophiles: Microorganisms that grow best at moderate temp. 15-40°C e.g. Normal Flora, most disease-causing bacteria.

3 Psychrophiles (cold lover): Microorganisms that grow best at low temp. -5 and 15°C e.g Bread Mold.

5. TEMPERATURE & FOOD STORAGE• Refrigeration temperatures retards food spoilage

because it limits the growth of otherwise fast-growing mesophiles. However psychrophiles can grow and multiply and consequently spoilage will still occur.

Long term storage freezing is better. Freezing is NOT an effective mean to destroy

microbes.

6. PH

• Most microorganisms prefer a neutral or slightly alkaline growth medium pH 7-7.4.

• Some microorganisms like acidic or alkaline environments:

1. Acidophiles: microorganisms that grow best in acidic media pH 2-5 e.g. Fungi & Helicobacter pylori.

2. Alkaliphiles: microorganisms that grow best in alkaline media pH 8.5-11 e.g. Vibrio cholera (the only alkaliphilic human pathogen).

3. Neutrophiles: bacteria that can live an multiply within the range of pH5 -8. most bacteria are neutrophiles.

6. PH

• Despite the pH of the external environment, cells maintain a constant internal pH, typically near

neutral .

7. GASEOUS ATMOSPHERE

Microorganisms can be classified according to their requirement for oxygen

GASEOUS ATMOSPHERE

Obligate Aerobes require 20-22% O2. get energy by aerobic respiration

Obligate Anaerobes will die in the presence of O2. get energy by anaerobic respiration or fermentation

Facultative Anaerobes Grow better if O2 is present, but can grow without it.

Microaerophiles require 5% only of O2 higher concentrations will inhibit their growth.

Aerotolerant Indifferent to O2

7. GASEOUS ATMOSPHERE

• O2 can be converted into a number of compounds that are highly toxic such as:

Superoxide O2-

Hydrogen peroxide H2O2

To survive this the bacteria must have enzymes that can convert these toxic derivatives to non-toxic forms, these enzymes include:

Superoxide dismutase catalase

BACTERIAL GROWTH IN VITRO• In order for bacteria to grow in the laboratory it need

appropriate growth medium and special environmental conditions like temperature, pH, O2,.. to multiply.

• Bacteria can be cultured on many different culture media according to its nutritional needs such as Nutrient Agar, Blood Agar, Mac Conkey Agar, CLED,..

• After inoculation of media, they should be incubated in chambers to maintain appropriate environment.

• Temperature and time of incubation differ for each type of bacteria to grow.

GENERAL CATEGORIES OF CULTURE MEDIA

• Chemically Defined Media: Composed of precise amounts of pure chemicals.

Usually used in research to study the nutritional requirements of bacteria.

• Complex Media: Contains a variety of ingredients such as meat

juices and digested proteins. Many ingredients can be added to this media according to our need.

GENERAL CATEGORIES OF CULTURE MEDIA

• Selective Media: Inhibit the growth of organisms other than the one

being studied.

• Differential Media: Contain a substance that certain bacteria change

in a recognizable way.

DIFFERENTIAL MEDIA

SELECTIVE MEDIA

SELECTIVE AND DIFFERENTIAL MEDIA

BACTERIAL COUNT

Microbiologists tend to measure the number of bacteria present in a liquid for quality control purposes in FDA

(Food and Drug Administration) monitored fields e.g. dairy farms, drinking water supply, drug industry...

METHODS OF MEASURING BACTERIAL GROWTH

• Direct Cell Count: used to determine total number of cells, it count both dead

and living cells Direct microscopic count:

Done using counting chamber. cheap and rapid but at least 107cells /ml must be present to be effective.

Cell-counting instrument:

Use machines such as coulter counters and flow-cytometers. Both count cells in a suspension as they pass as single line through small tube.

COUNTING CHAMBER

METHODS OF MEASURING BACTERIAL GROWTH

• Viable Cell Count: This method is used to quantify the number of cells capable of

multiplying. Plate Count: We use the fact an isolated bacterial cell on a culture plate will give rise

to one colony. A simple count of the colonies determines how many cells were in the initial sample.

Membrane Filtration: Used when number of organism in a sample is relatively low, concentrate

the bacteria in a filter then place the filter in appropriate media and incubate then count.

THE VIABLE PLATE COUNT METHOD

1. Serial dilutions of the sample are prepared.

2. From each dilution, 1ml or 0.1ml is inoculated on Nutrient Agar media.

3. All the plates are incubated for 24hours at 37°C.

4. After incubation, the bacterial colonies are counted from the plates. Then the number is multiplied by the dilution factor to get the number of bacteria in the original sample.

METHODS OF MEASURING BACTERIAL GROWTH

• Measuring Biomass: Turbidity: needs one-time correlation with plate counts to use

turbidity for determining cell number.