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exponential growth
N= N 0 x 2 n
- N= final cell number
- N0 = initial cell number
- n = number of generations
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generation time (doubling time)
g = t/n
t = time elapsed during exponential growth
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batch culture
- closed system of a fixed volume where bacterial growth alter environment
- 1) lag phase
- 2) log phase
- 3) stationary phase
- 4) death phase
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Lag phase
- when a stationary phase culture is diluted into fresh medium or when cells transferred from rich to minimal medium
- must synthesize proteins for rapid growth or specific proteins needed to produce nutrients not in culture medium
-
stationary phase
- growth is limited
- run out of essential nutrient or accumulate toxic waste product
- no net change in cell number
- some processes can continue
- sigma s protein controls response to stresses
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chemostat
open system maintained in chemically constant environment
- dilution rate = fraction of volume replaced per time
- too fast - culture washes out, cell division can't keep up
- too slow - nutrient isn't supplied fast enough
- increase nutrient concentration - growth rate and yield affected, then only yield affected
- total yield determined by most limiting nutrient
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rich/complex medium
contains complex organic molecules
-
defined or minimal medium
contains precise amounts of known chemicals
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autotrophs
- can get all of the C they need to build structures from CO2
- can gain energy from photons or by oxidizing inorganic compounds
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heterotrophs
- require an organic C source
- most use NH3- or NO3- as nitrogen source
- only nitrogen-fixing bacteria can use N2
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obligate aerobes
must use O2 as an electron receptor in respiration
-
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facultative anaerobe
can use O2 in respiration or use other metabolic strategies
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microaerophile
require low O2 concentration
-
-
reactive oxygen species
- cause cell damage
- superoxide radical union
- hydrogen peroxide
- hydroxyl radical
- enzymes remove toxic oxygen species
- superoxide dismutase
- catalase
- peroxidase
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problems of high temperature thermophiles
- critical enzymes are denatured
- membranes too fluid and cannot maintain barrier
-
solutions to problems of high temperature thermophiles
- proteins are more stable because contain fewer glycine residues and N-termini H-bonded to rest of protein
- synthesize chaperones to refold
- synthesize phospholipids with saturated fatty acids, pack tightly to form membrane
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problems of low temperature psychrophiles
- not much thermal motion, perform reactions slow
- membrane fluidity decreases, inhibits function of critical proteins
-
solutions to problems of low temperature psychrophiles
- proteins are more flexible
- phospholipids with highly unsaturated fatty acids, remain mobile
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hypotonic medium (solute concentration less than in cytoplasm)
- water enters the cell
- bacteria have rigid cell walls, prevent lysis
- mechanosensitive channels can leak specific solutes out
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hypertonic medium (solute concentration greater than cytoplasm)
- water exits the cell
- can synthesize/import compatible solutes
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compatible solutes
small molecules or ions that do not disrupt cell metabolism, increase internal osmolarity, help retain water
-
halophiles
- bacteria that require high NaCl concentration for growth
- proteins adapted because use K+ as compatible solute
-
acidophiles/alkaliphiles
- membranes are more impermeant to protons
- ether-linked lipids are less leaky and more resistant to acid hydrolysis
-
acidophiles
expend energy to scavenge protons from environment using Na+/H+ antiporters, use membrane gradient of Na+ to drive flagellar rotation, nutrient uptake because H+ is limiting
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