Microbial Growth at a Cellular Level Flashcards

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1
Q

What is generation time

A

doubling time

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2
Q

What are the 5 steps of septation

A

selection of site where septum will be formed
assembly of the FtsZ ring
linkage of the FtsZ ring to plasma membrane
assembly of the cell wall synthesizing machinery
constriction of the cell and septum formation

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3
Q

Where will the septum form in rod shaped organisms

A

the exact midpoint of the cell

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4
Q

The smallest concentration of MinC and minD is at the ___________

A

exact mid point

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5
Q

FtsZ is inhibited by large concentrations of ___________

A

minC and minD

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6
Q

What is the function of minE

A

forms an intracellular track

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7
Q

What does minD do?

A

rotates along the track made my minE

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8
Q

What are the four steps of cell wall synthesis?

A

autolysin activity
Bactoprenol
glycolase actvity
transpeptidation

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9
Q

What is the function of autolysin activity

A

cleaves beta 1,4 glycosidic linkages between NAM and NAG

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10
Q

what is the function of glycosylase activity?

A

helps bind new sugars to existing sugars

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11
Q

What happens during transpeptidation?

A

forms new crosslink

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12
Q

where does transpeptidation get the energy from to form new crosslinks?

A

uses the removal of extra D-alanine to get the energy to form the crosslinks

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13
Q

What system do caulobacter use for chromosome replication

A

partioning system, par system

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13
Q

what are caulobacter?

A

stalked bacteria, commonly soil organisms, not pathogenic

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14
Q

In the par system, at replication initiation, we see the anchoring of psrent chromosomes to _______ pole of the cell

A

one

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15
Q

popz proteins are localized to the ________ pole in caulobacter

A

stalked

16
Q

in the par system, parB binds to a _________ sequence within the original chromosome

A

parS

17
Q

what happens when parB binds to a specific parS sequence in a chromosome

A

once bound causes a conformational change that allows parB to bind to popZ

18
Q

popZ=_________

A

anchor

19
Q

ParB = ______________

A

seeking sequence to bind

20
Q

after binding popZ, replication goes on, and parB will find another _____ sequence, popZ will already be taken up, ______ (ATPase, motor protein) will bind to parB then energy will be used to move parB to other pole

A

parS, parA

21
Q

In E.Coli (pathogenic), sepration occurs at the ______ of replication

A

end

22
Q

____________ cuts/unlinks the chromosomes in E.coli

A

topioisomerase IV

23
Q

__________ proteins grab the chromosomes as they gravitate to poles in E. Coli

A

MukBEF

24
Q

___________ oscillate on an intracellular track, and have their highest concentration at the poles, with the lowest at the exact midpoint, why is this important?

A

MinC+D, allows the cell to know where the middle is

25
Q

where are ftsZ molecules inserted? what is formed

A

at the exact midpoint, ftS ring

26
Q

What is the function of FtsA and ZipA

A

cell membrane anchors

27
Q

what is the function of FtsK

A

chromosome segregation (binds to chromosomes holding them in place)

28
Q

what is the function of Ftsi

A

peptidoglycan synthesis (septum is forming while elongation is happening)

29
Q

T/F there are multiple sites of elongation

A

T

30
Q

What are the proteins involved in the divisome

A

FtsA, zipA, FtsK, Ftsi

31
Q

the midpoint and other sites go through _____________ for cell wall elongation

A

cell wall synthesis

32
Q

MreB sites = _____________

A

elongasomes

33
Q

What are the functions of elongasomes

A

associated with plasma membrane
holds cell in the right shape, additional sites of peptidoglycan synthesis

34
Q

MreB is homolgous to ________

A

actin

35
Q
A