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BIOL 2460 Microbiology Exam 3 Review 2026/2027 | Study Guide, Practice Questions & Answers

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BIOL 2460 Microbiology Exam 3 Review 2026/2027 | Study Guide, Practice Questions & Answers

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2460 - EXAM 3 REVIEW - PARKS - MICROBIOLOGY.pdf10/20/2026, 4:09:33 AM
2460 - EXA




BIOL 2460 - EXAM 3 REVIEW - PARKS -
MICROBIOLOGY
✅
Binary Fission Steps- G - growth and increase in cell size R - replication
of DNA D - cytoplasmic division; cytokinesis S - septum formation and
daughter cell divisions

Z-ring- formed during cytokinesis with the FtsZ protein to form a divisome
Divisome-promotes the formation of peptidoglycan and septum

Generation Time-time takes to double population

E. coli-20 min.

S. aureus-30 min.

B. subtilis-120 min.

M. tuberculosis-15-20hrs

Nn-number of cells at generation n

n-number of generations

N0-initial number of cells

Growth curve-closed system with finite nutrients

Lag Phase-cells grow larger and metabotically active (inoculum cells)

Log Phase-exponential; binary fission; cell replication > cell death




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Stationary Phase- cells enter survival mode and < less susceptible to
antibiotics; cell replication = cell death

Death Phase- cell replication < cell death; endospores; persisters
surviving cells with slow metabolism (tuberculosis)
Persisters-

Sustainable Growth-Open system cultures have infinite resources

Chemostat-used to maintain a continuous culture in which nutrients are
supplied at a steady rate


Direct microscopic cc- cells are counted under a microscope; CANNOT
distinguish between live or dead cells; Known volume is transferred to a
calibrated slide (Petroff-Hausser chamber) and cells are manually counted


Fluorescence Staining- cells are counted under a microscope or flow
cytometer; Red stain binds to damaged cells to indicate DEAD cells


Coulter counter- detects electrical resistance change due to cell density;
CANNOT differentiate live/dead


Viable plate counts- count of live cells; samples are diluted and grown on
solid media;
300 - TNTC; Limited only to easily cultured species; serial dilution is plated
and counted via pour plate or spread plate technique


Pour Plate Method- bacterial sample mixed with warm agar - > sample
poured onto sterile plate -> sample swirled to mix, allowed to solidify ->
plate incubated until bacterial colonies grow


Spread Plate Method- sample poured onto solid medium -> spread
sample evenly over the surface -> plate incubated until bacterial colonies
grow on the surface of the medium




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✅
Optical Density (turbidity)- Measured w/ spectrophotometer; light is
passed through culture and is measured on other side


Alternate Patterns of Growth- fragmentation in cyanobacteria and
budding in planctomycetes: Gemmata obscuriglobus


Biofilm Formation- Attachment of planktonic cells to a substrate
Attachment becomes irreversible; cells become sessile
Growth & division on substrate
Production of extracellular polymeric substance (EPS)
Attachment of secondary colonizers & dispersion of microbes to new
locations


Extracellular polymeric substances (EPS)- Hydrated polysaccharide gel
with other macromolecules and channels (sugar-gel) EX: (rivers, pipelines,
oral cavity) (cuts and wounds, lungs, intestines)

Quorum Sensing- cell to cell communication

Autoinducer- small molecules are produced to induce various actions
(positive-feedback)


Biofilm and Human Health- Cells in deep layers may
be metabolically inactive
EPS may slow diffusion of
biocidal agents
Provide optimal environment
for sharing of plasmids

Optimal oxygen concentration- ideal concentration of O2 (best for
growth)

Minimum permissive oxygen concentration- lowest O2 concentration
allowing growth




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