Title: Chapter 7 Control of Microorganisms
1Chapter 7Control of Microorganisms
- Definitions
- Conditions Influencing Antimicrobial Activity
- Physical Methods
- Chemical Agents
- Preservation of Microbial Cultures
2Definitions
- Sterilization A treatment that kills or removes
all living cells, including viruses and spores,
from a substance or object - Disinfection A treatment that reduces the total
number of microbes on an object or surface, but
does not necessarily remove or kill all of the
microbes - Antiseptic A mild disinfectant agent suitable
for use on skin surfaces
3Definitions
- Sanitation Reduction of the microbial population
to levels considered safe by public health
standards - -cidal A suffix meaning that the agent kills.
For example, a bacteriocidal agent kills bacteria - -static A suffix that means the agent inhibits
growth. For example, a fungistatic agent
inhibits the growth of fungi, but doesnt
necessarily kill it.
4Conditions Influencing Antimicrobial Activity
- Under most circumstances, a microbial population
is not killed instantly by an agent but instead
over a period of time - The death of the population over time is
exponential, similar to the growth during log
phase
5Conditions Influencing Antimicrobial Activity
- Several critical factors play key roles in
determining the effectiveness of an antimicrobial
agent, including - Population size
- Types of organisms
- Concentration of the antimicrobial agent
- Duration of exposure
- Temperature
- pH
- Organic matter
- Biofilm formation
6Physical Methods
- Moist Heat
- Dry Heat
- Low Temperatures
- Filtration
- Radiation
7Physical Methods Moist Heat
- Mechanism of killing is a combinantion of
protein/nucleic acid denaturation and membrane
disruption - Bacterial spores much more difficult to kill than
vegetative cells
8Physical Methods Moist Heat
- Methods of Moist Heat
- Boiling at 100C
- Effective against most vegetative cells
ineffective against spores unsuitable for heat
sensitive chemicals many foods - Autoclaving/pressure canning
- Temperatures above 100C achieved by steam
pressure - Most procedures use 121.1C, achieved at approx.
15 psi pressure, with 15 - 30 min autoclave time
to ensure sterilization - Sterilization in autoclave in biomedical or
clinical laboratory must be periodically
validated by testing with spores of Clostridium
or Bacillus stearothermophilus
9Physical Methods Moist Heat
- Methods of Moist Heat
- Pasteurization
- Used to reduce microbial numbers in milk and
other beverages while retaining flavor and food
quality of the beverage - Retards spoilage but does not sterilize
- Traditional treatment of milk, 63C for 30 min
- Flash pasteurization (high-temperature short term
pasteurization) quick heating to about 72C for
15 sec, then rapid cooling
10Physical Methods Moist Heat
- Methods of Moist Heat
- Ultrahigh-temperature (UHT) sterilization
- Milk and similar products heated to 140 - 150C
for 1 - 3 sec - Very quickly sterilizes the milk while keeping
its flavor quality - Used to produce the packaged shelf milk that
does not require refrigeration
11Physical Methods Dry Heat
- Incineration
- Burner flames
- Electric loop incinerators
- Air incinerators used with fermenters generally
operated at 500C - Oven sterilization
- Used for dry glassware heat-resistant metal
equipment - Typically 2 hr at 160C is required to kill
bacterial spores by dry heat this does not
include the time for the glass to reach the
required temp (penetration time) nor does it
include the cooling time
12Physical MethodsLow Temperatures
- Refrigerator
- around 4C
- inhibits growth of mesophiles or thermophiles
psychrophiles will grow - Freezer
- ordinary freezer around -10 to -20C
- ultracold laboratory freezer typically -80C
- Generally inhibits all growth many bacteria and
other microbes may survive freezing temperatures
13Physical Methods Filtration
- Used for physically removing microbes and dust
particles from solutions and gasses often used
to sterilize heat-sensitive solutions or to
provide a sterilized air flow - Depth filters eg. Diatomaceous earth, unglazed
porcelean - Membrane filters eg. Nitrocellulose, nylon,
polyvinylidene difluoride - HEPA filters High efficiency particulate air
filters used in laminar flow biological safety
cabinets
14Physical Methods Radiation
- Ionizing Radiation
- Gamma radiation produced by Cobalt-60 source
- Powerful sterilizing agent penetrates and
damages both DNA and protein effective against
both vegetative cells and spores - Often used for sterilizing disposable plastic
labware, e.g. petri dishes as well as
antibiotics, hormones, sutures, and other
heat-sensitive materials - Also can be used for sterilization of food has
been approved but has not been widely adopted by
the food industry
15Physical Methods Radiation
- Non-Ionizing Radiation
- Ultraviolet Radiation
- DNA absorbs ultraviolet radiation at 260 nm
wavelength - This causes damage to DNA in the form of thymine
dimer mutations - Useful for continuous disinfection of work
surfaces, e.g. in biological safety cabinets
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17Chemical Agents
- Phenolics
- Alcohols
- Halogens
- Heavy metals
- Quaternary Ammonium Compounds
- Aldehydes
- Sterilizing Gases
- Evaluating Effectiveness of Chemical Agents
18Chemical Agents Phenolics
- Aromatic organic compounds with attached -OH
- Denature protein disrupt membranes
- Phenol, orthocresol, orthophenylphenol,
hexachlorophene - Commonly used as disinfectants (e.g. Lysol)
effective in presence of organic matter, remain
on surfaces long after application - Disagreeable odor skin irritation
hexachlorophene once used as an antiseptic but
its use is limited as it causes brain damage
19Chemical Agents Alcohols
- Ethanol isopropanol used at concentrations
between 70 95 - Denature proteins disrupt membranes
- Kills vegetative cells of bacteria fungi but
not spores - Used in disinfecting surfaces thermometers
ethanol-flaming technique used to sterilize
glass plate spreaders or dissecting instruments
at the lab bench
20Chemical Agents Halogens
- Act as oxidizing agents oxidize proteins other
cellular components - Chlorine compounds
- Used in disinfecting municiple water supplies (as
sodium hypochlorite, calcium hypochlorite, or
chlorine gas) - Sodium Hypochlorite (Chlorine Bleach) used at 10
- 20 dilution as benchtop disinfectant - Halazone tablets (parasulfone dichloroamidobenzoic
acid) used by campers to disinfect water for
drinking
21Chemical Agents Halogens
- Iodine Compounds
- Tincture of iodine (iodine solution in alcohol)
- Potassium iodide in aqueous solution
- Iodophors Iodine complexed to an organic
carrier e.g. Wescodyne, Betadyne - Used as antiseptics for cleansing skin surfaces
and wounds
22Chemical Agents Heavy Metals
- Mercury, silver, zinc, arsenic, copper ions
- Form precipitates with cell proteins
- At one time were frequently used medically as
antiseptics but much of their use has been
replaced by less toxic alternatives - Examples 1 silver nitrate was used as opthalmic
drops in newborn infants to prevent gonorrhea
has been replaced by erythromycin or other
antibiotics copper sulfate used as algicide in
swimming pools
23Chemical Agents QuaternaryAmmonium Compounds
- Quaternary ammonium compounds are cationic
detergents - Amphipathic molecules that act as emulsifying
agents - Denature proteins and disrupt membranes
- Used as disinfectants and skin antiseptics
- Examples cetylpyridinium chloride, benzalkonium
chloride
24Chemical Agents Aldehydes
- Formaldehyde and gluteraldehyde
- React chemically with nucleic acid and protein,
inactivating them - Aqueous solutions can be used as disinfectants
25Chemical Agents Sterilizing Gases
- Ethylene oxide (EtO)
- Used to sterilize heat-sensitive equipment and
plasticware - Explosive supplied as a 10 20 mixture with
either CO2 or dichlorofluoromethane - Its use requires a special EtO sterilizer to
carefully control sterilization conditions as
well as extensive ventilation after sterilization
because of toxicity of EtO - Much of the commercial use of EtO (for example,
plastic petri dishes) has in recent years been
replaced by gamma irradiation
26Chemical Agents Sterilizing Gases
- Betapropiolactone (BPL)
- In its liquid form has been used to sterilize
vaccines and sera - Decomposes after several hours and is not as
difficult to eliminate as EtO, but it doesnt
penetrate as well as EtO and may also be
carcinogenic - Has not been used as extensively as EtO
- Vapor-phase hydrogen peroxide
- Has been used recently to decontaminate
biological safety cabinets
27Chemical AgentsEvaluating the Effectiveness
- Phenol Coefficient Test
- A series of dilutions of phenol and the
experimental disinfectant are inoculated with
Salmonella typhi and Staphylococcus aureus and
incubated at either 20C or 37C - Samples are removed at 5 min intervals and
inoculated into fresh broth - The cultures are incubated at 37C for 2 days
- The highest dilution that kills the bacteria
after a 10 min exposure, but not after 5 min, is
used to calculate the phenol coefficient
28Chemical AgentsEvaluating the Effectiveness
- Phenol Coefficient Test (cont.)
- The reciprocal of the maximum effective dilution
for the test disinfectant is divided by the
reciprocal of the maximum effective dilution for
phenol to get the phenol coefficient - For exampleSuppose that, on the test with
Salmonella typhiThe maximum effective dilution
for phenol is 1/90The maximum effective dilution
for Disinfectant X is 1/450The phenol
coefficient for Disinfectant X with S. typhi
450/90 5
29Chemical AgentsEvaluating the Effectiveness
- Phenol Coefficient Test (cont.)
- Phenol coefficients are useful as an initial
screening and comparison, but can be misleading
because they only compare two pure strains under
specific controlled conditions - Use dilution tests and simulated in-use tests
- Are tests designed to more closely approximate
actual normal in-use conditions of a disinfectant
30Preservation of Microbial Cultures
- Periodic Transfer and Refrigeration
- Mineral Oil Slant
- Freezing in Growth Medium
- Drying
- Lyophilization
- Ultracold Freezing
31Preservation of Microbial CulturesPeriodic
Transfer and Refrigeration
- Stock cultures are aseptically transferred at
appropriate intervals to fresh medium and
incubated, then stored at 4C until they are
transferred again - Many labs use agar slants care has to be taken
to avoid contamination - Major problem with possible genetic changes in
strains most labs need a way to keep long term
storage of original genetic stocks
32Preservation of Microbial CulturesMineral Oil
Slant
- Sterile mineral oil placed over growth on agar
slants to preserve cultures for longer period of
time in the refrigerator - Contamination problems messy many organisms are
sensitive to this generally it is a poor
technique and doesnt work well
33Preservation of Microbial CulturesFreezing in
Growth Medium
- Used as a long term storage strategy
- Broth cultures of the organisms are frozen at
-20C - Often, sterile glycerin (glycerol) is added at a
25 50 final concentration this helps to
prevent ice crystal formation and increases
viability of many organisms
34Preservation of Microbial CulturesDrying
- Suitable for some bacterial species
- Samples are grown on sterile paper disks
saturated with nutrient, then the disks are
allowed to air dry and stored aseptically - Reconstituted by dropping disk into nutrient
broth medium
35Preservation of Microbial CulturesLyophilization
- Suitable for many bacterial species as well as
fungi and viruses - Broth cultures are placed in special ampules and
attached to a vacuum pump the vacuum removes all
of the water from the cells leaving a
freeze-dried powder - The culture is reconstituted by adding broth to
the lyophilized powder and incubating it - Considered the best method of long-term storage
for most bacterial species
36Preservation of Microbial CulturesUltracold
Freezing
- Similar to freezing, but at very cold temperature
- At about -70 to -80C, in liquid nitrogen or in
an ultracold freezer unit