Microbial competition Flashcards

1
Q

What is the difference between a contact independent & dependent system?

A
independent = bacteria produce molecule that diffuses through medium & affects other bacteria
dependent = requires cell-cell contact
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2
Q

what kind of system are bacteriocins?

what is it for?

why does it have a narrow target range?

what is the structure & what do these domains do?

in what e.coli are they found?

A

contact independent

toxic proteins - kill of competing bacteria (but often not killed by them as develop immunity)

must bind to surface & become internalised by bacteria which required protein-protein/cell surface receptors so it’s very species specific- often of same species

T = translocation domain = facilitates colicins entering cell
R = receptor binding = binds to surface of target cell
A = activity = enzyme that degrades part of the cell
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3
Q

What system is bacteriophage?

What does it do?

when the cells lyse, how does this look on a lawn of bacteria?

describe:
capsid head
tail
end of tail
tail fibres

what are the 4 steps for how the phage injects DNA?

A

Contant independent

Attaches to target cell & hijacks cell machinery with genome in head - once enough lyses

clear hole

holds genetic info in protein capsule
made of central tube surrounded by sheaths
end of tail = baseplate from which tail fibres extend
bind to surface bacteria & cell surface receptors

  1. fibres attach receptors on surface bacteria
  2. position phage so tail is perpendicular to surface
  3. tail sheath contracts which drives central tube into membrane
  4. opening created so DNA translocated through
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4
Q

what is the phage lytic life cycle?

how is the cell lysed?

what is a lysogenic life cycle?

how is it reactivated?

what life cycle to virulent phages have?

temperature phages?

A

phage infects bacteria & codes for production of more phages to then lyse the cell & release phages

endolytic enzymes

phage infects bacteria & introduces genome into cell which is integrated into the bacterial genome & lays dormant

trigger signals from stress- phage activates & produce more phage particles leading to lysis

lytic only

lytic & lysogenic

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5
Q

what are pyocins?

what is the difference between an S-pyrocin & R-pyrocin?

how do R-pyrocins work then?

how can you alter its specificity?

what system is this?

A

bacteriocins produced by Pseudomonas aeruginosa

S = colicins with R, T, A domains
R = like phage without NA in capsid head

sheath on tail contracts driving it into membrane- makes holes/channels so cell components flow out

specificity through tail fibres- can takes tail fibres from 1 pyocin and put it onto another

contact independent

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6
Q

What does the T6SS secretion system do?

how can you label the T6SS to monitor how quickly it polymerises the structure?

the proteins that are shot out, what are they?

what is the maximum target range of attack?

what does it require?

A

forms inside of a cell, so when sheaths contract protein spike is shout out of cell & stab nearby cells

label it with GFP

can be toxic at same time- can embed in structure with protein fusion/protein-protein interactions

half its own width (of the predator)- short distance

requires target to be adjacent to predator & stably associated (doesn’t need receptor)

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7
Q

what is contact dependent inhibition?

what are the 4 domains of the CDI protein?

what are the genes in them?

what do they do?

what happens if you grow unrelated bacteria with CDI+ in cell?

grow CDI- with CDI+ of same species?

grow CDI+ with CDI+ of same species?

A

when 1 bacterial strain inhibits the growth of another

core = with toxic domain
immunity protein & membrane protein

core = cdiA
membrane = cdiB
immunity = cdiI

cdiI prevents the bacteria producing the protein being targeted by it
cdiB enables cdiA to be displayed on the surface of the cell

because they require target receptors- no inhibition as they are unrelated

is inhibition- related so CDI- lacks cdiI protein so when CDI+ binds, toxin is taken up & growth is inhibited

both express the same immunity protein- so toxin is taken up but neutralised

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