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A set of vocabulary-style flashcards covering the definitions, methods, and conditions used for the physical control of microbial growth as presented in the lecture notes.
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Sterilization
The absolute destruction of all life forms on an object.
Disinfection
The destruction of vegetative pathogens but not necessarily endospores or viruses; intended to reduce or inhibit growth.
Antisepsis
Chemical disinfection of skin, mucous membranes, or other living tissue.
-cide
A suffix for a chemical agent that rapidly kills microbes but not endospores.
-stasis
A suffix indicating that microbial growth and multiplication are inhibited.
Asepsis
The absence of pathogens from an object or area.
Degerming
The removal of transient microbes from the skin by mechanical cleansing or the use of an antiseptic.
Sanitization
The reduction of pathogens on eating utensils to safe public health levels by mechanical cleansing or chemicals.
Decontamination
The treatment of an object or surface to make it safe to handle.
Standard Autoclave Conditions
Sterilization at 121∘C and 15PSI for 15minutes.
Geobacillus stearothermophilus
The biological indicator (formerly called Bacillus stearothermophilus) used to test for sterility by using its spores.
High-temperature short-term (HTST) pasteurization
Also known as flash pasteurization; involves heating at 72∘C for 15seconds followed by rapid cooling.
Ultrahigh-temperature (UHT) sterilization
Heating at 140 to 150∘C for 1 to 3seconds.
Tyndallization
Fractional steam sterilization involving heating at 90–100∘C for three consecutive days with incubation at 37∘C in between.
Hot-air sterilization
A dry heat method involving an oven at 160 to 170∘C for 2 to 3hours.
Incineration
The physical destruction of microorganisms by burning at 500∘C, used for solid wastes.
Moist Heat Effects
Mechanism of action including the degradation of nucleic acids, denaturation of enzymes and essential proteins, and disruption of cell membranes.
Dry Heat Effects
Mechanism of action involving the oxidation of cell constituents and denaturation of proteins.
Deep freezing
Rapid cooling of a pure culture in suspension liquid to −50∘C to −95∘C, effective for several years of preservation.
Lyophilization (freeze drying)
A preservation method where material is frozen at −54∘C to −72∘C and dehydrated in a vacuum.
Depth filters
Filters made of fibrous or granular materials (like diatomaceous earth or unglazed porcelain) bonded into a thick layer with small diameter twisting channels.
Membrane filters
Porous membranes made of synthetic materials such as cellulose acetate, cellulose nitrate, polycarbonate, or polyvinylidene fluoride.
HEPA filters
High-efficiency particulate air filters used for air filtration in environments like biosafety cabinets.
Ionizing radiation
Very short wavelength, high energy radiation (X-rays, Gamma rays) that causes death by destroying DNA, disrupting hydrogen bonds, and oxidizing double bonds.
Non-ionizing radiation
Short wavelength UV rays (220–300nm) that cause mutation or death through the formation of thymine dimers; most absorbed by DNA at 260nm.
High intensity pulsed electric field treatment
A non-thermal control method involving exposure to an electric field of 15–20kV/cm for milliseconds, leading to electroporation.