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Stages of bacterial growth curve
Lag phase, exponential (log) phase, stationary phase, death phase, and long-term stationary phase
What happens during lag phase
Cell synthesizes new components to replenish spent materials or adapt to a new medium/conditions; length varies, sometimes very short or absent
What happens during exponential (log) phase
Rate of growth and division is constant and maximal; population is most uniform in chemical and physical properties
What happens during stationary phase
Population growth ceases and total viable cell number remains constant; active cells stop reproducing or reproduction is balanced by death rate; caused by nutrient limitation, limited oxygen, toxic waste accumulation, or reaching critical population density
What happens during death phase
Number of viable cells declines exponentially at a constant rate due to detrimental environmental changes like nutrient deprivation and toxic waste buildup
What happens during long-term stationary phase
Population continually evolves through successive waves of genetically distinct variants; natural selection occurs
Growth rate constant (k)
The number of generations per unit time; k = (log Nt - log N0)/0.301t
Generation (doubling) time
The time required for a population to double in size; g = 1/k
Steps of binary fission
Chromosome replication and partitioning, followed by cytokinesis (septation)
Where does bacterial DNA replication take place
At the origin of replication, proceeding in both directions around the chromosome until reaching the terminus (located opposite the origin)
Origin of replication
The single starting point on a bacterial chromosome where DNA replication begins; origins move to opposite ends of the cell during replication
End result of binary fission
Two genetically identical daughter cells
What happens during cytokinesis in bacteria
Septation - formation of a cross wall between two daughter cells - via site selection, assembly of the Z ring (FtsZ), assembly of cell wall-synthesizing machinery, and constriction/septum formation
Role of FtsZ
Tubulin homologue that polymerizes to form the Z ring (a contractile ring) at the division site, driving septum formation during cytokinesis
Role of the MinCDE system
Oscillates from pole to pole in E. coli; high MinC concentration at the poles prevents Z ring formation there, limiting Z ring formation to the cell center
Bacterial ribosome composition
70S ribosomes composed of a 30S and 50S subunit
Proteins involved in bacterial cell shape and elongation
MreB (actin homologue, positions peptidoglycan synthesis machinery for rod shape/elongation), FtsZ (division ring), CreS/crescentin (curved shape)
Bacterial chromosome partitioning proteins
ParA, ParB, and the parS region on the chromosome
Difference between bacterial and archaeal cell cycles
Bacterial cycles have three phases (growth, chromosome replication/partitioning, cytokinesis); archaeal cycles (e.g., Sulfolobus) resemble a eukaryotic mitotic cycle with G1, S phase (DNA replication), G2, chromosome segregation, and cytokinesis
Archaeal chromosome segregation proteins
SegA and SegB, similar in function to bacterial ParA/ParB (SegA is structurally similar to ParA; SegB is structurally unique but functionally similar to ParB)
Bacterial and archaeal species used as cell cycle examples
E. coli (bacteria) and Sulfolobus (archaea)
Extremophiles
Microorganisms that grow under harsh conditions that would kill most other organisms
Types of extremophiles
Halophiles/extreme halophiles, psychrophiles/psychrotrophs, mesophiles, thermophiles/hyperthermophiles, acidophiles, alkaliphiles, barotolerant/barophilic organisms
Psychrophile temperature range and environment
Grow between 0°C and 20°C; found in cold environments like polar regions and the deep sea
Adaptations of psychrophiles
Enzymes/transport systems/protein synthesis machinery function well at low temp; membranes have high unsaturated fatty acid content to stay semifluid when cold; accumulate compatible solutes and synthesize antifreeze proteins to lower cytosol freezing point
Adaptations of thermophiles
Proteins stabilized by more H-bonds, more proline, and chaperones; DNA stabilized by nucleoid-associated proteins and reverse DNA gyrase; membranes stabilized by more saturated/branched/higher molecular weight lipids or ether linkages (in archaea)
How non-extremophiles adapt to unfavorable conditions
Morphological changes like endospore formation, entering the stationary phase, using cellular components as nutrients, activating stress response genes/proteins, entering a viable-but-nonculturable state, or forming persister cells
Biofilms
Complex, slime-enclosed communities of attached (sessile) microorganisms
What biofilms do
Protect microbes from harmful agents like UV light and antibiotics; allow metabolic exchange, DNA uptake, and communication among attached organisms
What biofilms are comprised of
A slimy extracellular matrix (EPS) made of various polymers, released by microbes after reversible attachment to a conditioned surface
How biofilms function
Microbes reversibly attach to a conditioned surface, release the EPS matrix, and form a heterogeneous community with differences in metabolic activity and location; cells communicate via quorum sensing and can slough off to spread
Quorum sensing
A density-dependent form of cell-cell communication in bacterial populations using small diffusible signaling molecules (autoinducers)
Why bacteria use quorum sensing
To coordinate population-wide behaviors once a critical population density is reached, such as converting to a competent state, bioluminescence, virulence factor production, and DNA uptake for antibiotic resistance genes
Autoinducer
A small signaling molecule (peptide or other) that increases in concentration as a microbial population grows and, once at high enough levels, diffuses into cells to induce expression of target genes
Autoinducers used in quorum sensing
Autoinducing peptides (AIPs), first observed in Gram-positive bacteria; N-acylhomoserine lactone (AHL), which diffuses across the plasma membrane and is cell-density dependent