A) inoculation.
B) incubation.
C) infection.
D) isolation.
E) identification.
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A) The microbiologist used too much inoculum.
B) The culture is contaminated.
C) The incubation temperature was incorrect.
D) The culture medium must be selective.
E) The culture medium must be differential.
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A) Salmonella
B) Streptococcus
C) Neisseria
D) Staphylococcus
E) Escherichia
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A) uses electron's to produce a specimen image.
B) is a type of compound microscope.
C) requires the use of dyes like acridine and fluorescein.
D) is commonly used to diagnose certain infections.
E) requires an ultraviolet radiation source.
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A) 0.2 µm.
B) 0.2 mm.
C) 0.1 µm.
D) 0.3 µm.
E) 2.0 µm.
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A) to stain the cells blue
B) to prevent the smear from drying out
C) to slow bacterial movement so you can see cells better
D) to increase the resolution
E) to reduce the amount of heat reaching the slide from the light source
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A) Sterile swab, loop dilution, TSB
B) Hockey stick, spread plate technique, and 4 degree Celsius incubation temperature
C) Loop dilution, TSA, hockey stick, 37 degree Celsius incubator
D) Inoculating loop, incinerator, streak plate method, 37 degree Celsius incubator
E) Sterile swab, streak plate method, 37 degree Celsius incubator
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A) are used on a wet mount of the specimen
B) use heat to force the dye into cell structures
C) have outcomes based on cell wall differences
D) use a negative stain technique
E) are differential stains
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A) TSA plate
B) TSB tube
C) Transport media
D) Pour plate
E) Quadrant streak plate
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True/False
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A) bright-field.
B) dark-field.
C) phase-contrast.
D) fluorescence.
E) electron.
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A) synthetic.
B) complex.
C) reducing.
D) enriched.
E) All of the choices are correct.
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