Lecture 5 Flashcards

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1
Q

Growth

A

Increase in cell number
Growth = reproduction

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2
Q

Population

A

Total cells from one microbe

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3
Q

Applications of cell division

A

Infectious diseases and food preservation

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4
Q

Binary fission

A

Division of one fell into two
Elongation to septum formation
Generation time typically 30 min to 6 hours

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5
Q

Generation time is affected by

A

Environmental factors (nutrient availability and temperature) and genetic factors (particular to different microbial species)

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6
Q

Divisome

A

Directs cell division in prokaryotes
Embedded in cytoplasmic membrane
Comprises of Fts (filamenting temperature-sensitive) proteins

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7
Q

FtsZ

A

Forms a ring around the center of the dividing cell
In bacteria and archaea
Relates to tubulin

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8
Q

ZipA

A

Connects to FtsZ ring to the cytoplasmic membrane
The anchor

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9
Q

FtsA

A

Attracts other Fts protein to the divisome
The recruiter

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10
Q

FtsI

A

Peptidoglycan synthesis
- implications for drug design (new antibiotics)

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11
Q

MreB protein

A

Form cellular cytoskeleton
Absent in coccoid bacteria
Present in rod-shapes bacteria (if it’s inactive they become coccoid)

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12
Q

Exponential growth

A

Cells double each generation
Rate of cell production increases each generation
Healthiest state of cells for study
App. Standards for bacterial counts in food

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13
Q

Microbial growth cycle

A

Lag phase, exponential phase, stationary phase, and death phase

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14
Q

Lag phase

A

Growth rate= positive (low)
Recovery phase from previous conditions

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15
Q

Stationary phase

A

Growth rate = zero
Nutrient depletion and waste accumulation

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16
Q

Cryptic growth

A

Few cells still dividing
Few cells dying
Average of two makes stationary phase

17
Q

Death phase

A

Growth rate = negative (cell death)

18
Q

Continuous culture

A

Chemostat- constant conditions over time
Controls- dilution rate and nutrient concentration
Applications- ecology and physiology

19
Q

Microscopic counts

A

Cell counts
Adv: simple method
Dis: counts live and dead cells & difficulties with low cell numbers and motile cells

20
Q

Viable counts

A

Plate counts
Adv: high sensitivity and counts viable cells
Dis: possible errors (plating consistencies, incubation length, cell “clumps”

21
Q

Turbidimetric methods

A

Cell mass -> cell number
Adv: simple method & non-destructive
Dis: possible errors, cell clumps and films

22
Q

Cardinal temperatures

A

Minimum (no growth), optimal (fastest growth), maximum (cell death)

23
Q

Extremophiles

A

Live in very cold or very hot environments
- deep ocean, glaciers, polar regions
- hot springs, surface soils, and water

24
Q

Psychrophiles

A

Optimal temperature <15C
Typical slow growing
“Pockets” of water
Ex. Snow algae and seaice diatoms
Molecular adaptations:
- cytoplasmic membrane (high in unsaturated/short-chain FAs and fluidity at low temperature)
- cyroprotectants (“cold-shock” proteins, like anti-freeze for the cell)

25
Q

Life in the heat

A

Optimal temperature:
- >45C thermophiles
- > 80C hyperthermophiles
Ex. Boiling springs bacteria, hot spring Cyanobacteria, and hydrothermal vent microbes
Molecular adaptations:
- cytoplasmic membrane (high saturated FAs and stability at high temps)
Heat protectants (heat shock proteins through more ionic bonds)

26
Q

Polymerase chain reaction

A

cyclical heating of DNA to 94C and requires a heat-resistant polymerase

27
Q

Taq polymerase

A

Thermus aquaticus and hot spring bacterium

28
Q

Acidophiles

A

optimal growth < pH 5.5

29
Q

Alkaliphiles

A

optimal growth > pH 8