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21 Cards in this Set

  • Front
  • Back
4 Phases of the Bacterial Growth Curve?
-Where is the bacteria most sensitive to antibiotics? Where does transformation occur?
-lag phase
-log (exponential) phase (most sensitive to antibiotics) (late log phase - transformation occurs)
-stationary phase
-death phase
Groups Based on Optimum Temperature for Max. Growth
-mesophiles
-thermophiles
-psychrophiles (cold)
Groups Based on Optimum Temperature for Max. Growth
-neutrophiles
-acidophiles
-alkalinophiles
Groups Based on Growth in Presence of O2
-obligate aerobe: O2 req.
-microaerophile: required in low amts
-obligate anaerobe: O2 is toxic
-facultative: not needed for growth, but used when present
-aerotolerant anaerrobe: not required nor utilized
Enzymes that Detoxify Radicals
-superoxide dismutase (converts radicals into H2O2 and O2; not found in obligate anaerobes)
-peroxidase (further converts H2O2; found in aerotolerant anaerobes)
-catalase (further converts H2O2; found in obligate aerobes and facultative)
Chemoheterotrops:
-Energy Source?
-organic compounds
Catabolism:
-Degrade/synthesize complex molecules?
-Use/produce energy storage molecules?
-degrade complex molecules
-produce energy storing molecules
Secondary Energy Storage Molecules:
-Names?
-How much ATP made?
-NADH = 3 ATP from ETC
-FADH2 = 2 ATP from ETC
Glucose Catabolism:
Aerobic Conditions:
-Processes?
-End Result?
-glycolysis (makes 2 pyruvates) -> krebs cycle -> ETC
-end result: 38 ATP
Glucose Catabolism:
Anaerobic Conditions:
-Processes?
-End Result?
-glycolysis (makes 2 pyruvates) -> fermentation
-end result: 2 ATP (from glycolysis)
Glucose Catabolism:
Entner-Duodoroff Pathway
only occurs in prokarotic cells
Frederick Griffith Experiment
-R strain = mouse lives
-S strain = mouse dies
-heat-killed S strain = mouse lives
-heat-killed S strain + R strain = mouse dies
-demonstrates transformation
Transformation
-Mechanism?
-Natural Transformation?
-competent bacterial cells pick up naked ss DNA fragments from dead cells (facilitated by DNA binding prots) and incorporate them into its genome (facilitated by Rec A protein)
-nat. transfrmtn.: in adverse conditions, bact develop ability to pick up DNA from environment
Conjugation:
-Mechanism
-F+ extends pilus to create cell-cell contact with F- and genetic transfer occurs

*note: can transfer entire chromosome
Conjugation:
-F Plasmid?
-High Frequency Recombination cell?
-F plasmid has gene for sex pilus; R plasmid has a drug resistance gene
-Hfr cells have F plasmid incorporated into chromosome
Transduction:
-Mechanism?
-Generalized vs. Specialized?
-mediated by bacteriophages
-generalized: any host gene can be trnsfred; results from lytic cycle
-specialized: only specific host genes are trnsfred; results from lytic and lysogenic cycle
Transposition:
-Mechanism?
-Transposon structure
-transfer of genetic material within a cell; transposons (jumping genes) can change position on a genome or be transferred b/w different DNA molecules
-structure: palindromic sequences at ends; insertion sequence with transposase gene and/or antibiotic resistance gene
Common Targets of Antibiotics (4 differences b/w eukaryotic and prokaryotic cells)
-cell wall (only in bact)
-DNA condensation mech (DNA gyrase in bact)
-txn (RNA pol II in euk. vs RNA pol in bact)
-trnslation (50S, 30S in bact)
Steps of Peptidoglycan Synthesis
1. 4 AAs (tetrapeptide) attached ot NAM in cytosol
2. ^ attached to bactoprenol
3. NAG is attached
4. monomer is transported to periplasmic spc thru bactoprenol
5. autolysis break glycosidic bonds b/w peptidoglycan monomers and pentaglycine peptide x-bridges linking rows of sugars in existing peptidoglycan
5. transglycosylase forms bonds b/w new monomer and NAG/NAMs of existing peptidoglycan
6. transpeptidase reforms pentaclycine peptide x-links b/w rows
DNA Condensation:
-Condensation Enzyme?
-Decondensation Enzyme?
-condensation: DNA gryrase
-decondensation: topoisomerase IV
Bacterial RNA Polymerase Subunits:
-Number?
-Vs. Eukaryotic RNA Pol?
-4 subunits (2 alpha, 2 beta)
-euk RNA Pol has 12 subunits