ch 11 Flashcards

1
Q

why is coordination needed

A

constantly chaining conditions
regulation for good energy use!!!!

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2
Q

biosynthesis coronation evidence

A

radiolabeled glycerol, coordination of fueling

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3
Q

richness of medium effects

A

growth rate, richer = faster

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4
Q

modes of regulation (for macromolecule making?)

A
  1. changing enzyme activity
  2. changing about of enzyme
  3. changing amount of substrate
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5
Q

enzyme control by

A

substrate amount, couple transcription and translation, mRNA are short lived. operons

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6
Q

control enzyme activity with what modifacations

A

less common
covalent modification
allostery- sRNA interaction w protien

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7
Q

covalent mod

A

not as common
important in chemotaxis
ex phosphorylation, adenylation, methylation

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8
Q

chemotaxis

A

move to or away from chemical

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9
Q

allostery

A

smthing binds to active site to alter it

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10
Q

feedback inhibition

A

if too much product is made, it will block the first steps to prevent more from being made
allosteric

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11
Q

sRNA can - a reaction

A

inhibit, modify, activate, tether

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12
Q

allosteric examples

A

feedback inhibition (biosyn), regulating RNA, inhibition or activation dependent allosteric effects (feuling)

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13
Q

reg mech of protein synthesis

A

1) DNA topology
2) promotor rec
3) trancrip repression
4) transcription activation
5) transcription enhancement
6) attenuation
7)sRNA
8) mRNA stability
9) translation control
10) proteolysis

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14
Q

DNA topology

A

supercoiling/ packaging prevent sigma from binding

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15
Q

transcription repression involve

A

regulatory proteins/ DNA control regions

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16
Q

promoter recognition

A

alternate sigma factor expressed under certain conditions (for recognizing the promotor)

17
Q

operon

A

histrionic genes that are trans together

18
Q

lac operon consist of

A

prokaryotic
promoter, genes, transcription terminator, operator, reg genes

19
Q

enhancers

A

long distance control DNA sequence, bending of DNA,
enhancer binding proteins

20
Q

activators

A

positive regulator protein to increase trxn

21
Q

repressor

A

negative protien

22
Q

what has lac taught us

A

1) transcription initiation from promoter of operon regulation
2) trancrip initiation can be allosterically controlled
3) increased expression can be use to relief of negative control (off unless on)

23
Q

attenuation (me thinks)

A

stopping of transcription bc translation can occur

24
Q

sRNA

A

regulatory RNA, allosteric
blocks promoter DNA, form termination loop on mRNA to degrade

25
Q

mRNA stability

A

shit is unstable
lifespan
sRNA, to regulate

26
Q

translational control

A

too much protein, Binding to mRNA – sRNA, metabolites, or r-
proteins

27
Q

proteolysis

A

degrading protiens after translation
usually for regulatory proteins
regulated process

28
Q

regulons

A

multi operons simultaneously regulated by this

29
Q

modulons

A

group of regulons (hella operons)

30
Q

modulon examples

A

catabolite repression system
stringent response system

31
Q

catabolite repression

A

glucose used first
when gone, increases of cAMP production os it can bind to CAP

32
Q

stringent responce system

A

respons eto starvation

33
Q

Fueling inhibition or activation is dependent

A

on allosteric effectors