Lecture 5 Flashcards

(29 cards)

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
Life in the heat
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
Polymerase chain reaction
cyclical heating of DNA to 94C and requires a heat-resistant polymerase
27
Taq polymerase
Thermus aquaticus and hot spring bacterium
28
Acidophiles
optimal growth < pH 5.5
29
Alkaliphiles
optimal growth > pH 8