Use LEFT and RIGHT arrow keys to navigate between flashcards;
Use UP and DOWN arrow keys to flip the card;
H to show hint;
A reads text to speech;
99 Cards in this Set
- Front
- Back
endospores
define |
specialized resting cells
|
|
Genera that form endospores
|
Bacillus
Clostridium |
|
spore stain
define |
differential stain
used to detect endospores |
|
spore stain
primary stain |
malachite green
|
|
spore stain
secondary stain |
safranin
|
|
organism used in the endospore lab
|
Bacillus megaterium
|
|
acid fast stain
define |
differential stain
used to detect "acid fast" organisms |
|
examples of acid fast organisms
|
Mycobacterium tuberculosis
Mycobacterium leprae Mycobacterium smegmatis |
|
organism used in acid fast lab
|
Mycobacterium smegmatis
|
|
acid fast stain
primary stain |
carbolfuchsin
|
|
acid fast stain
counter stain |
methylene blue
|
|
psychrophile
optimum temperatures |
-5*C - 20*C
refrigeration temperature |
|
mesophile
optimum temperatures |
20*C - 50*C
|
|
thermophiles
optimum temperatures |
50*C - 80*C
|
|
hyperthermophiles
optimum temperaturs |
above 80*C
|
|
effects of temperature on growth lab
organisms used |
Bacillus stearothermophilus
Escherichia coli |
|
effects of temperature on growth lab
temperatures used |
4*C
25*C 37*C 55*C |
|
thermal death point
define |
lowest temperature in which organisms in a liquid suspension are killed in 10 minutes
|
|
thermal death time
define |
minimal length of time required to kill a bacterial suspension at a given temperature
|
|
lethal effects of temperature lab
organisms used |
Escherichia coli
Bacillus megaterium |
|
lethal effects of temperature lab
temperatures used |
40*C
80*C 100*C |
|
lethal effects of temperature lab
times used |
0 Control
10 20 40 |
|
P-1000 micropipette
|
.2ml - 1ml
blue tips |
|
P-200 micropipette
|
.02ml - .2ml
yellow tips |
|
non ionizing short wavelength radiation
|
4 - 400 nm
|
|
what wavelength is most harmful to bacteria?
why? |
260nm
it is the site of pyrimidine dimer formation; there are too many dimers and repair mechanism is overwhelmed |
|
what are the disadvantages to the use of UV light in hospitals, restaurants, labs
|
not very penetrating
damaging to eyes & skin |
|
UV light lab
organisms used |
Staphylococcus epidermidis
Bacillus megaterium |
|
UV light lab
swab method used |
three way swab
|
|
UV light lab
times used for each organism |
S. epi - 1 min, 5 min, 10 min
B. meg - 1 min, 10 min, 1 hour |
|
hypotonic solution
|
solute concentration is LOWER on the external environment
water moves into the cell, causing the cell to burst |
|
isotonic solution
|
equilibrium
|
|
hypertonic solution
|
solute concentration is HIGHER on the external environment
water moves OUT of the cell, causing shrinkage/plasmolysis |
|
halophile
|
organism that thrives in environments with very high concentrations of salt
|
|
halotolerance
|
adaptation of living organisms to conditions of high salinity
|
|
osmophile
|
an organism with an affinity for solutions of high osmotic pressure
|
|
pH
|
the measurement of the hydrogen ion concentration
|
|
acidophiles
optimum pH |
0 - 5.5
|
|
basophiles
optimum pH |
8.5 - 11.5
|
|
neutrophiles
optimum pH |
6.5 - 7.5
|
|
pH lab
organisms used |
Staphylococcus epidermidis
Saccharomyces cerevisieae |
|
pH lab
method used |
inoculate one broth tube
|
|
pH lab
pHs used |
4.5
7 11 |
|
pH lab
type of broth used for Staphylococcus epidermidis |
nutrient broth
|
|
pH lab
type of broth used for Saccharomyces cerevisiae |
nutrient broth + glucose
|
|
osmolarity lab
organisms used |
Escherichia coli
Staphylococcus epidermidis Halobacterium salinarium |
|
osmolarity lab
%s NaCl used |
.5%
7.5% 15% 25% |
|
examples of toxic by-products of oxygen metabolism
|
superoxide radicals
singlet oxgen peroxides |
|
examples of enzymes that get rid of toxic oxygen by-products
|
superoxide dismutases
catalases peroxidases |
|
classifications of organisms based on effect of oxygen on growth
|
obligate anaerobes
obligate aerobes facultative anaerobes aerotolerant anaerobes microaerophiles |
|
oxygen tolerance lab
organisms used |
Escherichia coli
Pseudomonas fluorescens Clostridium sporogenes Enterococcus faecium |
|
oxygen tolerance lab
method |
inoculate FTM tubes (stab with needle)
incubate with lids lose at 37*C |
|
oxygen tolerance lab
medium used |
fluid thioglycollate medium
|
|
oxygen indicator in fluid thioglycollate medium
|
resazurin
|
|
growth of anaerobes - bio bag
function of palladium |
catalist
|
|
growth of anaerobes - bio bag
indicator |
resazurin
|
|
bacterial growth
define |
increase of number of cells
|
|
bacterial division
|
binary fission
budding |
|
generation time
define |
time required for the cell to divide and double its population
|
|
generation time
for E. coli |
20 minutes
|
|
generation time
for Mycobacterium leprae |
16 days
|
|
lag phase
|
number of cells does not change much, period of little cell division
period of bacterial adaptation |
|
log phase
|
cellular reproduction is most active
period of exponential growth |
|
stationary phase
|
growth rate slows, number of microbial deaths balances the number of new cells
phase of equilibrium |
|
death phase
|
number of deaths exceeds the number of new cells
|
|
measurement of microbial growth
direct methods |
direct microscopes count
filtration most probable number plate count (only live cells are counted) |
|
measurement of microbial growth
indirect methods |
turbidity
metabolic activity dry weight |
|
serial dilutions
purpose |
to dilute original inoculum to be able to get a countable number of organisms (30-300)
|
|
serial dilutions
advantages |
measures number of viable cells only
|
|
serial dilutions
disadvantages |
takes 24 hours or more for results to be read
|
|
The waxy outer layer found in acid-fast organisms is composed of
|
glycolic acid
|
|
what method was used to stain the endospores
|
Shaeffer-Fulton
|
|
example of a mesophile
|
E. coli
|
|
example of a thermophile
|
B. stearothermophilus
|
|
effect of temperature on growth
which organism was more heat resistant? |
B. stearothermophilus
because of its endospores |
|
what is the structure formed in DNA by UV exposure?
|
pyrimidine dimer formation
|
|
UV lab
which genera tested was the most resistant to UV exposure? |
Bacillus megaterium
|
|
what is one method by which bacteria can repair DNA damage caused by UV radiation?
|
non ionizing radiation
|
|
100-900 nm
|
non ionizing radiation
|
|
facultative anaerobe
|
an organism which can grow without oxygen, but which grows better in the presence of oxygen
|
|
microaerophilic
|
requires oxygen for growth, but is killed by high concentrations of oxygen
|
|
catalse
|
an enzyme which detoxifies hydrogen peroxide to water and oxygen gas
|
|
cytochrome c
|
an oxidizing agent
|
|
pH =
|
-log [H+]
|
|
pH lab
S. epi and S. cervisiae are both.. |
neutrophiles
|
|
an organism which prefers to grow at a low pH is called an
|
acidophile
|
|
what is the normal range of pHs within which most bacteria grow?
|
5 - 9
|
|
pH lab
which organism would be expected to grow best at pH 5.0? why? |
Saccharomyces cerevisiae
it is an acidophile |
|
osmolarity lab
Halobacterium is a.. |
halophile
|
|
osmolarity lab
E. coli is a.. |
halotolerant
|
|
osmolarity lab
S. epi is a.. |
halotolerant
|
|
halophile
|
organisms that thrive in environments with very high concentrations of salt
|
|
an organism which requires high solute concentration is an..
|
osmophile
|
|
does Staphylococcus aureus require high solute concentration for growth?
|
no; it is halotolerant
|
|
5. In which direction will water move across the cell membrane of a bacterial cell placed into distilled water?
|
into the cell
|
|
how do you determine which plate will give you the most accurate count?
|
the most accurate plate is the one with 30-300 organisms
|
|
is viable cell number an indirect or direct counting method?
|
direct
|
|
the spectrophotometer measures what? of a sample to determine the amount of bacteria present
|
turbidity
|
|
what chamber is used for direct microscopic counts?
|
Peteroff-Hauser
|