2.4: Microbial Locomotion Flashcards

(36 cards)

1
Q

what is the most common device bacteria use to move

A

flagellum

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2
Q

what are flagellum

A
  • hollow protein filaments
  • allow motility
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3
Q

flagellum are not visible with brightfield microscope, what are some special techniques needed to view it?

A
  • flagella stain
  • dark-field
  • TEM (transmission electron microscope)
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4
Q

what are the 4 different flagellum types, used for identification

A
  • Monotrichous -single flagellum
  • Amphitrichous - flagella at opposite sides
  • Lophotrichous -Multiple flagella in a single tuft
  • Peritrichous -Flagella distributed around the cell
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5
Q

Describe the 3 parts of flagellar structure

A
  1. Filament -Rigid helical protein ~20 um long, composed of identical protein subunits -flagellin
  2. Hook-Flexible coupling between filament and basal body
  3. Basal Body (motor) -consists of central rod that passes through a series of rings:
    * L-Ring- LPS layer
    * P ring -Peptidoglycan
    * MS ring -Membrane
    * C-ring-cytoplasm (associated with cytoplasmic membrane)
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6
Q

what are the 4 rings the basal body passes through (and what layer of envelope they’re found)

A
  • L ring -found in LPS layer (in outer leaflet of outer membrane in gram negatives)
  • P ring -Peptidoglycan -middle of periplasm
  • MS ring -Membrane (embedded in-integral protein)
  • C-ring-cytoplasm (peripheral proteins) associated with membrane by the MS ring of cytoplasm)

they’re rougly named for layer of envelope they’re found in

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7
Q

where does the energy to turn the flagella come from

A

* the proton motive force -gradient of protons (H+) across the cytoplasmic membrane
-high [H+] outside (periplasm is considered outside for gram negative bc of outer membrane presence. outer membrane not a permeability barrier)
-low [H+] inside
* Mot proteins form a channel that allows H+ to move into the cytoplasm, providing the energy needed to turn the flagellum

(mot proteins > think motor)

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8
Q

what’s the difference between the movement of eukaryotic flagella and prokaryotic

A
  • eukaryotic flagella moves back and forth like a whip to pull the cell forward
  • prokaryotic flagella turns like a propellor to push the cell forward
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9
Q

describe the steps of flagellar synthesis

A
  1. The basal body is made first and assembled into the cytoplasmic membrane and periplasm with rod and rings.
  2. The hook is added to the basal body
  3. flagellin proteins are synthesized in the cytoplasm (to build filament)
    -fed through a 3 nm channel in the flagellum
    -a cap protein adds new flagellin unit to the growing filament, flagellum grows from its tip (as flagellin is added capping protein moves further out)
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10
Q
A
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11
Q

what do all filaments of prokaryotes (fimbriae, flagella etc) have in common?

A
  • grow from the tip
  • hollow
  • anchored in the cytoplasmic membrane (cuz filaments are protein)
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12
Q

what does flagellar rotation and speed depend on the …

A

depends on the PMF

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13
Q

how many times can a flagella rotate per second

A

up to 300 times per second

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14
Q

how many cell lengths does the flagella propel the cell per second

A

60 cell lengths per second

compared to cell length move very fast

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15
Q

describe the pattern of movement by flagella (peritrichous)

A
  • forward motion occurs when all flagella rotate counter-clockwise in a bundle -Run -occurs for a pretty constant period of time
  • periodically, the flagella will reverse direction and rotate clockwise-called a tumble.
  • this causes the flagella bundle to open, and the cell to reorient in a random new direction
  • after a short time, a return to counter-clockwise rotation begins a new run and leads the cell off in its new direction (this run will approx be equivalent to previous run)

random changes in run usually ends with no net movement of population just individual cells moving in like circles

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16
Q

what’s different about archaea flagella compared to bacteria flagella

A
  • the rigid filament is thinner than that of bacteria
  • there are fewer protein types that form the basal body (and they’re different)
  • rotation of the filament is driven by ATP
  • while they look similar and have same function, they are NOT related!
17
Q

Archaea flagella are not related to bacteria’s. What is archaea flagella actually related to?

A

Type IV pilus (used for twitching motility)

18
Q

what is taxis

A

directed movement in reponse to chemical or physical gradients

19
Q

Chemotaxis

A

directed movement in response to chemicals, toward an attractant or away from a repellent

20
Q

phototaxis

A

directed movement in response to light

21
Q

what is aerotaxis

A

directed movement in response to oxygen

22
Q

osmotaxis

A

directed movement in reponse to ionic strength

(like osmolarity has to do with concentration of ions in solvent)

23
Q

Hydrotaxis

A

directed movement in response to water

24
Q

for chemotaxis what are attractants and repellants sensed by

A

chemoreceptors

25
what happens in the absence of a chemical attractant (in e. coli ex.)? what is this called?
* E. coli will move in a series of runs and tumbles * individual cells will all seem to move in random directions but there will be no net movement of population * called **random walk**
26
when does chemotaxis occur
when there is a concentration gradient
27
explain chemotaxis example of what happens when attractant Glucose is present
* The cell still exhibits series of runs and tumbles * If it senses that the concentration of glucose in an area is increasing: -the tumble is delayed -and the run lasts longer * there is a net movement of cells toward the attractant (even thought some individual cells will be headed in the wrong direction) * this is called biased random walk
28
what happens in chemotaxis when a cell tumbles in wrong direction away from attractant ex: glucose and it senses glucose is conc. decreasing
it will run for the normal amount of time (and not longer but not shorter than normal time).
29
what happens if the cell senses that the concentration of a repellent like hydrogen sulfide is increasing?
If the cell senses the repellent increasing (is going towards the repellent) it will run for the normal amount of time.
30
how is chemotaxis measured? (to find whether bacteria are attracted to or repelled by chemical)
* a capillary tube containing a chemical is inserted into a medium containing motile bacteria (overtime chemical will diffuse through capillary and some bacteria will swim in. -chemical gradient forms surrounding the tip of the capillary -after short time, count the number of bacteria in the capillary and in the medium -if bacteria number is higher in the capillary, the chemical is attractant -if number is lower in capillary, chemical is repellent, but would not be 0 in capillary bc of random walk
31
how does surface motility contrast to flagellar motility
It's considerably slower than flagellar motility and requires surface contact, while flagellar motility allows for movement in liquid.
32
what are the 3 different mechanisms of surface motility? describe them
* **excretion of slime** -loosely bound polysaccharide creates slime layers and some excrete enough slime to move. *** twitching motility** -requires type IV pili, which extent from one pole of the cell, and attach to a surface -ATP hydrolysis causes the pilus to retract dragging the cell forward * **Gliding** -smooth movement across the long axis of the cell without help from external propelling structures
33
what are the 3 sets of proteins are involved in gliding motility? and where they located?
* stationary "gliding motors" -anchored in CM * Helical protein track -in peptidoglycan layer * Extracellular adhesion proteins -on surface of outer membrane
34
how does gliding motility work
* Gliding motors use energy from PMF to rotate, causing displacement of the helical track, moving the adhesion proteins. * causes cell to rotate on its axis and it is propelled forward
35
which domain does gliding motility
Several bacteria (but not archaea)
36
which domains do twitching motility?
* many bacteria and some archaea