Microorganisms are commonly found suspended in air, including bacteria, fungi, algae, viruses, and protozoa. The most important factors affecting the types and numbers of airborne microorganisms are temperature, humidity, and air currents. While air is not suitable for microbial growth, it acts as a transport medium for microbes picked up from environmental sources like soil, water, and human activities like coughing and sneezing. Methods to isolate microorganisms from air samples include impingement onto solid or into liquid collection media, followed by incubation and counting of colonies.
An introduction to microorganisms found in the atmosphere, including algae, bacteria, fungi, and viruses.
Discussion on methods of isolating microorganisms from air, environmental factors affecting their survival, and sources of air microflora.
Explanation of air as a non-conducive environment for organism growth due to low moisture and nutrient levels, and various sources of airborne microorganisms.
Overview of solid and liquid impingement methods for isolating and counting airborne microorganisms.
Materials and procedural steps for isolating airborne microorganisms using agar plates and incubation.
Data collection and calculation of colony counts for fungi and bacteria isolated from air samples.
Isolation of microorganismfrom air
•Atmosphere(The layer nearest to the
earth) contains all major groups of
microbes ranging from algae to the
viruses.
•Microbes Found in Air- In addition to gases, dust
particles and water vapour, air also contains
microorganisms.
•There are vegetative cells and spores of bacteria, fungi
and algae, viruses and protozoan cysts.
3.
•Since air isoften exposed to sunlight, it has a higher
temperature and less
•moisture. So,, most of these microbial forms will die
4.
•Environmental factors thataffect air
microflora include atmospheric
temperature(There is a progressive
increase in the death rate with an increase
in temperature from -18°C to 49°C ),
humidity(Low and high relative humidity
cause the death of most
microorganisms) , air current.
5.
•Air current isalso important in the
dispersal of microorganisms as it carries
them over a long distance.
•
In still air the particles with microorganisms
tend to settle down. But a gentle air can
keep them in suspension for long periods.
6.
•Air is nota medium in which organism
grow but is a carrier of particulate
matter ,dust particles,spores ect
•Air is mainly transport medium for
microorganisms. They occur in small numbers in
air when compared with soil or water.
•The microflora of air can be studied under two
headings outdoor and indoor microflora.
7.
•Air is nota natural environment for
microorganisms as it doesn't contain enough
moisture and nutrients to support their growth
and reproduction.
•1-One of the most common sources of air
microflora is the soil.
•2-microorganisms found in water may also be
released into the air in the form of water droplets
•from plant or animal surfaces 3-
•4-The main soures of airborne microorganism is
human beings. by activities like coughing,
sneezing, talking and laughing
8.
•They are differentmethods to isolate microorganism
1-solid impingement
2-liquid impingement
•There are several methods designed for the enumeration
of microorganisms in air. The most important ones are
solid and liquid impingement
•It is not collects and counts all the microorganisms in the
air sample tested. Some microbial cells are destroyed
and some entirely pass through in all the processes.
9.
•Impingement in liquids:
•Inthis method, the air drawn is through a
very small opening tube and bubbled
through the liquid. The organisms get
trapped in the liquid medium. Aliquots of
the liquid
•then plated to determine microbial content
10.
•Impingement on solids:
•Inthis method, the microorganisms are
collected on the solid surface of agar
medium. Colonies develop on the medium
where the organism impinges.
11.
•Aim…….to isolate microoganismfrom air
Materials:
Petri dishes
Slides
Cover slips
Czapek dox agar
Nutrient agar
Distil water
Gram stain
Aniline blue
Glycerol
Microscope
Incubator
Colony counter
12.
procedure
•1-pour melted ,cooledCzapek dox agar
With steptomycen and nutrient agar in petri
dishes.
2-allow them to solidify.
3-remove cover and expose the petri dishe
for 5-10minute at differnet location.
4-cover the lid and incubate the plate.
13.
•5-Czapek dox agarin25°c for7days,and
nutrient agar in 35°c for 24-48 hours
14.
observation
•1-observe the platesand count the distribution of
fungal and bacterial colonies on Czapek dox
agar
and nutrient agar.
2-record your result for the total number of
colonies using colony counter and fungi each
plate.
•Bacterial count
Percentage occurrence=number of colonies of indivdiual species
__________________________________
Total number of colonies of all species