chap 4 Flashcards
how microbes grow
bacterial growth refers to
increase in population (not size)
direct counting and examples
count cells
with microscope, flow cytometer, spread plate, pour plate, filtration
viable direct counting methods
Spread plate and pour plate
indirect counting (mass or density)
weighing, spectrophotometry, genome amount
flow cytometer
fast, automated, living and dead cell sorter, total particle count,
analyzes: size, shape, topography, complexity, and sorts
serial dilution
used to create a plate with countable colonies, 30
and 300 colonies per plate, for viable direct counting
weighting cells reserved for
mold and filamentous bacteria
spectrophotometry
bacteria scatter light (more scattering, more bacteria)
measured in OD (optical density)
Spectrophotometry is used on - amounts of bacteria
large
4 bacteria phases of growth
lag, log/exponential, stationary, death
lag phase
bacteria get used to new environment, population undergoes metabolic activity
exponential phase
divides a shit ton
stationary
slowed growth rate, nutrients exhausted, death rate and growth rate balanced
death phase
deaths exceed growth
endospores
resting cells, stationary, highly resistant, made when nutrients are low, not reproduction
sporulation
endospore formation
Germination
spore returns to vegetative state
endospores produced by
bacteria
bacillus (yea idk) , clostridium (diff and botulism)
balanced growth
cell increases by the same proportion over any interval of time
chemostat
allows for log growth, used for long experiments, growth rate dependent of medium amount, cell density is constant
large scale industrial fermentation is done in
chemostat
the faster the cell grows,
the bigger the cell, more ribosomes, RNA, Protein, and DNA
Extremophiles condition examples
temperature, hydrostatic pressure, osmotic pressure, pH, oxygen, radiation
temperatures impact of microbial growth
membrane permeability and enzyme stability
max growth temp
highest temp microbe will grow
protein stability (thermophiles)
charged amino acid on surface to be stable, has mechanisms to correct (chaperons and heat shock proteins)
DNA stability adaptions (thermophiles)
positive supercoiled DNA, high mg, more DNA binding proteins
membrane stability adaptions (thermo)
special lip membranes, isoprenoids, ether bonds, bi/monolayer
decimal reduction time/ d value
time that 90% of population is killed
low temperature shift effect on microbe
may be lethal