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binary fission
prok: 1 → 2
mitosis
euk: 1 → 2
discrete colony
cell aggr.
autotrophs
use inorganic source of carbon (co2)he
heterotrophs
catabolize reduced org. molcs
chemotrophs
energy from redox rxns w/ in/organics molcs
phototrophs
light
effect of temp on membs (w/ lipids)
low: rigid & fragile. high: fluid, oozy
neutrophiles
bact + protozoa, 6.5-7.5 ph
acidophiles
bact + fungi, acidic env
alkalinophiles
alk soils & water, up to 11.5 ph
hypertonic
plasmolysis → shrink
hypotonic
lysis → bursts
halophiles
9%+ nacl concen for cell wall support
extreme halophile
35% nacl
facultative halophiles
dont need high salt can tolerate
singlet oxy *O2
higher state electrons
superoxide rads O2. -
anaerobes die if not detox, form during incomplete reduction of oxy in resp. anaerobes make SOD to detox
peroxide anion (o22-)
formed during SOD rxns. aerobes have catalse/peroxidate to detox. obligate anerobes have insuff enzymes to treat.
hydorxyl radical (.OH-)
from ionizing radiation/incomplete hydrogen peroxide rxn. most reactive. doesn’t harm aerobes bc of catalase/peroxidase
superoxide dismutase (sod)
2 superoxide + 2 H+ → h2o2 (hyd peroxide) & o2
catalse
2 h2o2 → 2 h2o + o2
peroxidase
h2o2 + 2H+ → 2 h2o
aerobe response to oxy
aero resp
anaerobe response to oxy
dont use aerobic metab
facultative anaerobes
ferment, an/aerobic resp
aerotolerant anaerobe
dont aero metab, but its enzymes detox oxy
microaerophile
aerobes that need 2-10% oxy lvl, limited ability to detox h2o2 and superoxide rads
growth time
20-30 min for pop to double
growth phases
lag, stationary, death
measuring bact methods
direct count, viable count, biomass, indirect
counting chambers (direct count)
overcount bc cant distinguish dead/alive
viable count methods
plate count, filtration, most prob number (mpn)
plate count
ideally use 20-200 colonies
filtration
for extremely diluted, need large vol
indirect count
metab activity, dry weight, turbidity (cloudiness)
typ diff media
blood agar
typ selective + differential
MacConkey agar: inhibits gram pos, detects lactose ferm
bacterial control methods
sterilization, commercial sterilization, disinfection, antisepsis, sanitization, biocide, bacteriostasis, antimicrobial
sterilization
destroys everything
commercial botulism
kills botulism
disinfection
destroys harmfuls
antisepsis
destroys harmfuls from live tissue
sanitization
reduces microrganisms on utensils for safe lvls
bacteriostasis
inhibits microbes
antimicrobial modes
memb perm, dmg to proteins/nucleic acids
therm death pt (tdp)
lowest temp to kill all in 10 min
thermal death time (Tdt)
lowest time to kill all at specific temp
decimal reduction time (drt)
minutes to kill 90% of population
moist heat
pasteurization, autoclave
pasteurization
reduces spoilable organisms/pathogens. 63 C for 30 min. high temp short time (htst): 72 C for 15s. ultra high temp (uht): 140 c for 4s
autoclave
flowing steam, 121 C at 15 psi for 25 min, kills all organisms/endospores, touch surface
dry heat
kills thru oxidation: flame, incinerate, hot air sterilization
filtration
HEPA for >0.3 micrometers, memb filters > 0.22 micrometers
bacteriostatic - low tmp
fridge, deep freeze, lyophilization (freeze dry)
DESSICATION
no water → no metab
ionizing radiation (x ray, gamma ray, e beams)
ionize water → reactive oxy, mutate DNA
nonionizing radiation
UV rays dmg dna
microwaves
kill heat, but not microbes
phenol/phenolics
dmg & leak membs
halgens - iodine
alters protein synthesis & memb. tincture: alc solution. iodophore: combined with org molcs
halgens - chlorine
oxidizing that shuts down enzyme. bleach, chloramine
alcohol
denature protein, dissolve lipids, dont effect endospores/viruses, need water
heavy metals
oligodynamic action (tiny amt → antimicrobial), denature. ag, hg, cu, zn
surface active agents
soap - degerm, emuls. sanitizers - anions react with memb. quats (quat ammonium compounds) - kill bact, denature protein, disrupt memb