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BIOL 200: Chapter 12

Associations w/ other species
Symbiotic: organisms live in close nutritional relationships, required by on or both members Mutualism Commensalism Parasitism Non symbiotic: organisms are free-living, relationships not required for survival Synergism Antagonism
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Mutualism
obligatory dependent both members benefit termites & protozoa/bacteria deep sea worms & chemoautotrophic bacteria
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Commensalism
the commensal benefits other member not harmed staphylococcus aureus haemophilus satellite colonies
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Synergism
members cooperate and share nutrients ex: soil bacteria azotobacter: Nitrogen fixer Cellulomonas: cellulose degrader
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Antagonism
some members are inhibited or destroyed by others bacteria inhibiting growth of another or anything = antibiosis
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Gas requirements
Chemical composition of atmosphere 78% N 20% O .04% CO2 Oxygen processing is importante! some microbes need others = toxic
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Oxygen Metabolism
Molecular Oxygen = somewhat toxic can be partially reduced to form reactive oxygen species (ROS) Love --> hate aerobe facultative aerobe microaerophile anaerobe
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Aerobe
can use oxygen in metabolism Obligate aerobe: requires oxygen ex: people Ex: pseudomonas aeruginosa
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Facultative aerobe
doesn't require oxygen but can use it staphylococcus aureus escherichia coli
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microaerophile
metabolic processes with low levels of oxygen (1-15%) doesn't grow well in air b/c there's too much oxygen
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anaerobe
can't use oxygen to perform metabolic processes obligate anaerobe: can't survive in presence of oxygen ex: clostridium butyricum
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Defenses against toxic effects of Oxygen Metabolism
Aerobes generally have defenses against toxic effects Antioxidants absorb oxygen radicals so they can't damage other molecules Glutathione, vitamin C, A, E (ROS use O2 to live) Ex: enzymes - superoxide dismutase, catalase Convert ROS to less toxic forms converts into molecular O2, water, hydrogen peroxide - catalase turns into water & oxygen
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Carbon Dioxide Metabolism
all organisms generally require some amount of CO2 some prefer more amounts than normal (3-10%) Capnophiles: several different types of pathogens Candle Jars Gas Pad
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Environmental factors influence microbial growth rates
every species has optimal conditions where it grows best every species has tolerances minimum required maximum tolerated temperature = large contributing factor: controls molecular motion, bacteria can't regulate temp only environment can can't grow effectively @ all temps
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Measuring Growth
Growth takes place on 2 levels individually: cell synthesizes new cell components and increases in size metabolism population growth: # of cells in the population increases based on binary fission * not always growing as fast as can: nutrients available = huge influence
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Exponential growth
replication to produce new bacteria after n generations: 2^n cells 5 generations: 1 - 2 - 4 - 8 - 16 - 32 = 2^5
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Generation time
how long it takes to divide doubling time find from growth curves
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Logarithmic Scale
straight line relationship between growth and time makes it easier to read
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Phase 1: lag phase
Bacteria are preparing to grow not exponentially growing fresh food or new environment = takes awhile adjusting to the new influx of nutrients
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Phase 2: Log Phase
bacteria grow exponentially let the good times roll
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Stationary Phase
nutrients run out and waste products build up everyone dying waste building no replication over extended time will die PARTY'S OVER!
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Death Phase
bacteria death occurs @ an exponential rate most bacteria die off
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Long Term Stationary Phase
The # of bacteria begins to decline very slowly dormant/survival state not a lot of nutrients needed dead bacteria release nutrients some adapt/survive low nutrient conditions
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Growth Curves
account for different stages of infections takes time to adjust replicate like crazy immune response fight we win they die off some infections = persistant
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Indirect Growth Measurements
As bacteria grow turbidity increases Measure how 'cloudy' a liquid is OD 600
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OD 600
Indirect measure use a spectrophotometer to read how much light is blocked @ 600 nm light source thru sample into detector, light measured no bacteria = clear, light more bacteria = light blocked
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Direct Measurements
Viable plate counts CFUs Hemocytometer Cell counters Coulter Counter Flow Cytometer
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Viable Plate Count - CFUs
CFU = colony forming units bacteria formed colony on plate of auger seeing # of CFUs on plate detects living cells
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Hemocytometers
a bit of culture on a glass slide etched w/ grid look under microscope & count how many there are
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Cell Counters
Coulter Counters when light is blocked counts bacteria Flow cytometer detectors, lasers looking @ fluorescent molecules suspend in liquid detector counts & tells about size/shape/gram type!
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Characteristics of microbial Populations
Biofilm formation Quorum sensing Human body is a rich habitat for symbiotic bacteria, fungi, and some protozoa = normal microbial flora Biofilms form when organisms attach to a substrate by some form of extracellular matrix that binds them together in complex organized layers
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Biofilms
almost all species of microorganisms can make them not only bacteria but archaea, algae, etc. will form on basically every stable moist surface on earth cover structure of most natural environments many medical implants
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Biofilms & Quorum Sensing
Bacteria have way to sense/communicate w/ other bacteria way to coordinate expression of genes based on population density communicate and cooperate in the formation & function of biofilms Quorum sensing the release or sensing of molecules correlated to population density signaling molecules = inducers
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Biofilms & Quorum sensing cont.
find unoccupied substrate stick together replicate to threshold inducers sensed by bacteria & cause changes in transcription/translation of chromosomes control proteins being made
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