MICR221 Lecture 10 - Bacterial ATP Synthesis and How It Becomes The Newest Target-Space For Antibiotics Flashcards

1
Q

what 2 processes are tightly coupled in bacteria?

A

cellular respiration and ATP synthesis

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2
Q

what governs all steps of central carbon metabolism, ETC activity and ATP synthesis?

A

the balance of anabolism:catabolism and proton back pressure

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3
Q

what is an uncoupled cell?

A

a cell that has broken links between central carbon metabolism, ATP synthesis and ETC activity therefore the cell will exhaust energy currencies to try and restore the PMF

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4
Q

what is the soluble fraction in the F1Fo-ATPsynthase?

A

F1 unit

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5
Q

what is the F1Fo-ATPsynthase composed of?

A

composed of 2 major components –> the F1 unit and the Fo unit

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6
Q

what is the F1 unit of F1Fo-ATPsynthase?

A

the unit located in the cytoplasm that binds to ADP+Pi and converts to ATP

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7
Q

what is the Fo unit of F1Fo-ATPsynthase?

A

this unit is the motor and is able to rotate

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8
Q

what is the turbine of the F1Fo-ATPsynthase?

A

the turbine is driven by H+ flow and rotates the central stalk in the F1 unit. This unit is the fraction sensitive to oligomycin

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9
Q

what is the relationship of the F1 unit and the Fo unit in the F1Fo-ATPsynthase?

A

both the F1 and the Fo unit are chemomechanically coupled

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10
Q

what are the 2 key subunits of the F1Fo-ATPsynthase?

A

catalytic subunits and ion-binding subunits

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11
Q

what are the 2 catalytic subunits of the F1Fo-ATPsynthase?

A

beta catalytic subunit

gamma catalytic subunit

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12
Q

what is the function of the beta catalytic subunit?

A

binds ADP + Phosphate –> ATP

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13
Q

what is the function of the gamma catalytic subunit?

A

rotates and induces conformational changes

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14
Q

what are the 2 ion-binding subunits of the F1Fo-ATPsynthase?

A

alpha ion-binding subunit

c ion-binding subunit

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15
Q

what is the function of the alpha ion-binding subunit?

A

takes H+ and passes it to the c subunit

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16
Q

what is the function of the c ion-binding subunit?

A

rotates and releases H+ into the cytoplasm

17
Q

what do the other subunits in general terms have roles in from the F1Fo-ATPsynthase?

A

other subunits have roles in regulation and complex stability

18
Q

what are the 3 major conformations of the binding change mechanism?

A

open
loose
tight

19
Q

what is the open conformation of the binding change mechanism?

A

when nothing is bound

20
Q

what is the loose conformation of the binding change mechanism?

A

when ADP + Pi is bound

21
Q

what is the tight conformation of the binding change mechanism?

A

when its closed and forms ATP

22
Q

what are the 3 major steps in rotation?

A

open –> loose –> tight –> open etc they are 3x 120 degree steps

23
Q

how many substeps may be in the major conformations of the binding change mechanism?

A

may be 6 or more substeps and this varies between organisms

24
Q

how many H+ protons are used for every 1 ATP made?

A

3.3 H+ protons are used for every 1 ATP made

25
Q

why are 3.3 H+ protons used for every 1 ATP made?

A

because the mitochondrial enzyme has 10 c-subunits and this equals 10 H+ protons for a full rotation therefore 3 ATP are produced from 10 H+ protons. However different organisms have different amounts of c subunits varying from anywhere between 2.7-5 H+ protons per ATP

26
Q

when is a sodium-motive force an advantage?

A

a sodium motive force is an advantage when passive proton leak/loss is high in some anaerobes which occurs in high temps or pH used by some pathogens

27
Q

what is a sodium motive force?

A

a Na+ coordinated c-ring pocket by glutamate and others

28
Q

what is the difference between a sodium motive force and a proton motive force?

A

a sodium motive force is an Na+ coordinated c-ring pocket by glutamate and others and a proton motive force is a c-ring of glutamate that binds H+

29
Q

what is a proton motive force?

A

c-ring of glutamate that binds H+

30
Q

what is fermentation?

A

the synthesis of ATP exclusively by substrate level phosphorylation that has a lower ATP yield and is used when oxidative phosphorylation is not possible

31
Q

what do most pathogens use?

A

oxidative phosphorylation

32
Q

why is fermentation a last resort strategy?

A

because the end products are toxic and must be secreted and is not viable in the long term

33
Q

what is lactic acid fermentation?

A

the metabolic process by which glucose or other 6 carbon sugars are converted into cellular energy and lactic acid

34
Q

what is homolactic lactic acid fermentation?

A

only lactate is produced eg yoghurt

35
Q

what is heterolactic acid fermentation?

A

lactate, ethanol and acetate are produced e.g sauerkraut

36
Q

what is mixed acid fermentation?

A

end products vary according to environmental conditions but still undergoes the same oxidative phosphorylation linked steps

37
Q

what is alcohol fermentation?

A

an interest in the production of bioethanol