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15 Cards in this Set

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Chemotaxis

The mvmt of a cell toward or away from a chemical signal, AA, sugars, oxygen, e- acceptors


****Moves toward attractants and away from repellents****

What is a run?

CCW




Multiple flagella form a bundle and work together to propel the cell forward

What is a tumble?

CW


- Individual filaments go "haywire" and stop working together


- Tumbling reorients cell randomly!

What are 2 mechs bacteria with a single flagella use to change direction?

1. CCW to move forward // CW to move backward on same line




2. CW rotation to move forward // cell stops, reorients then goes CW to move forward again

2 Assays for testing chemotaxis to a variety of compounds

1. soft agar + compound that a. attracts bacteria & b. can be metabolized


- cells inoculated @ center and swim around in circle up the gradient (6-48 hrs)


2. Agarose plug containing attractant placed in center of liquid and eats toward the bottom then outwards (takes minutes)

What does it mean to say chemotaxis is biased?

cells in homogenous environment have a baseline behavior.


--> If its getting closer to attractant, it will have a longer run.


--> Further attractant results in more tumbles to reorient itself

Why study chemotaxis?

1. chemotaxis= not essential for life; therfore, can mutate a lot w/o killing the cell


2. chemotaxis signaling is very sensitive--> can respond to very small changes


3. its effective over a wide range of attractant concen.

What parts make up MCPs?

1. Periplasmic sensing domain-> binds attractant


2. HAMP domain transmits info of ligand binding to rest of protein


3. methylation region functions in adaptation


4. signaling region-> binds CheW & CheA (relays info to downstream proteins)

What do MCPs do?

influence activiy of 2-component signaling proteins


CheA= histidine kinase


CheY= response regulator


increase attractant binding= decrease in CheA-P

Mech behind more tumbles/ shorter runs

decreased attractant binding to MCPs--> increased CheA activity (more CheA-P)--> more phototransfer to cheY (more cheY-P)--> more cheY-P binding to FliM--> CheZ deactivates CheY

Mech behind longer runs/ few tumbles

increased attractant binding to MCPs--> decreased cheA activity (less CheA-P)--> Less phosphotransfer to cheY (Less CheY-P)--> Less cheY binding to FliM--> CheZ deactivates CheY

How does a bacterium know if it is swimming up a gradient?

Temporal sensing mech


Reset their signaling system rapidly to "feel" whether there is more attractant now than there was a sec ago

How does adaptation work?

cell responds to changes in the amount of attractant in the environment.




Continuously resets Baseline




Dip= low->high concen.


Spike= high-> low concen.



What causes more/ less ability to stimulate CheA?

buildup of methyl groups on MCP = more ability to stimulate cheA




fewer methyl groups on MCP= less ability to stimulate cheA



Fun Fact about Chemotaxis receptors

* Chemotaxis receptors cluster at bacterial cell poles




* Trimer clusters can influence each others signaling just because they're touching