01c: Oxidative Phosphorylation Flashcards
Ox Phos: respiration depends on and is coupled to (X).
X = ATP phosphorylation
Experimentally adding mitochondria with succinate and P. What should be added to initiate oxygen consumption?
ADP
List the P/O ratios for NADH and FADH2.
NADH: 3 (new is 2.5)
FADH2: 2 (new is 1.5)
Experimentally adding mitochondria with succinate and P. Adding DNP will cause (stimulation/inhibition) of oxygen consumption.
Stimulation (without ADP) and rapid oxygen consumption;
DNP is an “uncoupler”
Experimentally adding mitochondria with succinate and P. After adding an inhibitor of ETC, what do you have to add to initiate oxygen consumption?
You can’t.. if the entire ETC is inhibited, oxygen consumption won’t occur
Experimentally adding mitochondria with succinate and P. After adding an inhibitor of phosphorylation, what do you have to add to initiate oxygen consumption?
DNP (uncoupler); even if phosphorylation inhibited, respiration can then proceed on its own
List the flavin carriers in ETC. How many hydrogens/electrons does each transport?
FAD and FMN;
2 hydrogens and electrons (FADH2, FMNH2)
The non-heme iron, aka (X), proteins are ETC carriers that transport (Y) number of hydrogens/electrons.
X = FeS; Y = 1 electron
The heme iron, aka (X), proteins are ETC carriers that transport (Y) number of hydrogens/electrons.
X = cytochromes; Y = 1 electron
CoQ, aka (X), is an ETC carrier that transport (Y) number of hydrogens/electrons.
X = Ubiquinone Y = 2 hydrogens and electrons (QH2)
NADH gets oxidized by ETC complex (1/2/3/4), formally called (X), which passes the electrons to (Y).
Complex I
X = NADH-Q Reductase
Y = CoQ
CoQ receives electrons from which complex(es)?
- Complex I (NADH-Q reductase)
- Complex II (succinate dehydrogenase)
- ACD (acyl-CoA dehydrogenase)
- GPDHm (mito G3P dehydrogenase)
CoQ in ETC passes its electrons to (X).
X = Complex III (QH2-cytochrome c reductase)
Complex III passes electrons to (X) and then they’re passed to (Y).
X = cytochrome c Y = Complex IV (cytochrome oxidase)
(X), the final electron acceptor in ETC, takes the electrons from (Y) carrier.
X = O2 Y = Complex IV (cytochrome oxidase)
T/F: All ETC complex pump H out of mitochondria matrix.
False - only complex I, III, IV
Which complex is the ATP synthase?
Complex V
Rotenone amytal inhibits (X) complex of ETC. Can electrons still get to CoQ?
X = Complex I (NADH-Q reductase)
Yes, via FAD dehydrogenases
Antimycin A inhibits (X) complex of ETC. Can electrons still get to CoQ?
X = Complex III (QH2-cytochrome c reductase)
Yes, but ETC won’t work since can’t get past complex III
CO is dangerous partly due to its inhibition of (X) ETC carrier.
X = Complex IV (cytochrome oxidase)
Oligomycin is dangerous due to its inhibition of (X) ETC carrier.
X = Complex V (ATPase)
ETC: The function of the (X) and (Y) shuttles is to shuttle what to where?
X = glycerol-P Y = malate-asp
Reducing equivalents from cytosol into mitochondria (to ETC)
Which enzyme is key for the glycerol-P shuttle? Its product, (X), is capable of passing (Y).
G3P dehydrogenase
X = G3P or Dihydroacyteone-P (depending on direction of reaction)
Y = mito membranes
In glycerol-P shuttle, the electrons are taken from (X) and given eventually to (Y).
X = NADH Y = FAD (to become FADH2)
In malate-asp shuttle, (X) takes electrons from (NADH/FADH2) and becomes (Y). Which enzyme catalyzes this?
X = oxaloacetate;
NADH;
Y = malate
Malate dehydrogenase
T/F: Malate can cross mito membranes.
True
In malate-asp shuttle, the electrons are taken from (X) and given eventually to (Y).
X = Y = NADH
Aspartate aminotransferase (AST) is important enzyme in (X) because it converts (Y) to (Z).
X = Malate-asp shuttle Y = oxaloacetate and Glu Z = aspartate and alpha-ketoglutarate
(which can cross mito membrane)
One of the first tests for liver damage is measuring (X) enzyme levels in blood, which would be (increased/decreased).
X = AST (Aspartate aminotransferase);
Increased (leak out of cells)
All else equal, there is a difference of (X) ATP yield per glucose depending on if glycerol-P or Malays-asp shuttle used.
X = 2
Theoretically, GP shuttle gives 36 and M-A shuttle 38
ETC: Membrane potential exists due to (X) process, which drives ATP (into/out of) mito.
X = H pumping (membrane more positive on outside);
Out via ANT (Adenosine NT Translocase) since ATP more negative than ADP
What’s the mechanism of ETC uncoupling by poisons?
Carry protons across membrane to collapse H gradient
T/F: In cases of ETC uncoupling, the ETC keeps pumping, despite lack of ATP synthesis.
True
Actual ATP yield is (more/less) than the theoretical yield per glucose. Why?
Less (30 ATP);
Some E from proton needed to maintain membrane potential and drive ANT (Adenine NT translocase)
ANT (Adenosine NT translocase) is important because it provides (X) with (Y). Explain.
X = ATP synthase Y = ADP
Exchanges ATP (out) for ADP (into mito)
Oligomycin inhibits (electron transport/mito phosphorylation).
Mito phosphorylation