CH. 7: The Control of Microbial Growth Flashcards
ignaz semmelweis/joseph lister
first efforts on microbial control (~100 years ago)
methods of control (2)
physical
chemical
sepsis:
refers to microbial contamination
asepsis:
the absence of significant contamination
sterilization:
removing ALL microbial life
via heating and filtration
sterilant:
sterilizing agent
commercial sterilization (and procedure):
killing C. botulinum endospores (via heating)
disinfection:
removing/destroying pathogens (vegetative cells, NOT endospores)
antisepsis:
removing pathogens from (disinfection of) LIVING TISSUE
degerming:
removing microbes from a limited area
- *mechanical removal**
e. g. alcohol swabs
sanitization:
lowering microbial counts to levels safe for public health and to minimize disease transmission
biocide/germicide:
killing microbes (NOT endospores)
bacteriostasis:
INHIBITING, not killing, microbes
i.e. stops growth temporarily
rate of microbial death?
bacterial populations tend to die at a constant rate
effectiveness of antimicrobial treatment depends on:
- number of microbes
- environment
- time of exposure
- microbial characteristics
[# of microbes] larger populations…
take longer to eliminate
[environment] organic matter…
inhibits antimicrobial chemicals
[environment] temperature:
disinfectants work better in warmer environments
[environment]
biofilms
fat/proteins protect microbes when heat treated
acidic conditions are favourable for disinfectants
[time of exposure]
extended exposure time is more effective against resistant microbes or endospores
[microbial characteristics] gram positive…
gram + bacteria more susceptible than gram negative (due to lipopolysaccharide in gram negative cell wall)
actions of microbial control agents (3)
- alteration of membrane permeability
- damage to proteins
- damage to nucleic acids
[actions of microbial control agents]
alteration of membrane permeability
–> target phospholipids and proteins to cause leaks in plasma membrane
[actions of microbial control agents]
damage to proteins
–> heat and chemicals can denature enzymes (hydrogen bonds are more easily destroyed than covalent bonds)
[actions of microbial control agents]
damage to nucleic acids
- -> heat, chemicals, radiation can damage DNA/RNA thus interfering with vital functions (replications, metabolic enzymes)
- -> often lethal to microbial cells
Heat
- used to sterilize (lab media, glassware, hospital instruments, preserve canned food)
- DENATURES & INACTIVATE PROTEINS
resistance of microbes to heat treatment is assessed by:
thermal death point (TDP) and thermal death time (TDT) (these give an idea of severity of treatment to kill a population of bacteria)
thermal death point (TDP):
lowest temperature at which cells in a culture are killed IN TEN MINUTES.
thermal death time (TDT):
minimal time during which ALL CELLS in a culture are killed at a given temperature.
decimal reduction time (DRT):
minutes required to kill 90% of a population at a given temperature
moist heat sterilization
DENATURES proteins
boiling for 10 mins = kills vegetative forms of bacteria, fungi, and their spores, and most viruses
(not perfect for sterilization - some viruses, endospres can resist boiling for a long time)
(moist heat sterilization) autoclave
steam under pressure
@ 15 psi & 121C: all organisms AND endospores in contact will die within 15 minutes
steam sterilization, steam must…
contact item’s surface
pasteurization
reduces spoilage organisms and pathogens
equivalent tx to pasteurization
30 mins at 63C
high-temperature short-time pasteurization:
72C for 15 seconds for milk
- thermoduric organisms survive
- unlikely to cause disease
ultra-high-temperature sterilization:
140C for <1 sec for milk
dry heat sterilization
kills by OXIDATION
- dry heat
- flaming
- incineration
- hot-air sterilization = longer time than moist heat because it takes longer for heat in air to be transferred to a cold body (ie. hot air needs 170C for 2 HRS; autoclave needs 121C for 15 mins)