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54 Cards in this Set

  • Front
  • Back
Who proposed chemiosmotic theory?
Peter Mitchell
What is required for respiration?
ADP must be present
What is an example of uncoupler?>
DNP -dinitrophenol

--oxidation rxn w/o conservation of energy -- o2 consumeed w/o ADP
What are uncoupler?
lipid soluble weak acids
mitchell;s postulates for chemiosmotic theory?
1. inner membrane impermeable to H
2. ETC generates H gradient
3. ATP synthase creates ATP by H gradient
Protonmotive force --
energy of the H concentration gradient --- both chemical and electrical -delta G/ nF
Cofactors wiht ETC
flavins (FAD and FMN) Fe-S heme like structures
How does e- travel in ETC?
direction of increasing reduction potentials
strong reducing agent #
strong oxidizing agent #
reducing agents negative -- NADH best reducing agent

oxidizing # Positive O2 best oxidizing agent
Complex 1
NADH ubiquinone oxidoreductasa
NADH transfers 2 e- as hydride ion to FMN and then to Q
complex 2
succinate -Q oxidioreductase
forms qh2
Complex 3 - for each e- pair
1. 2 cyto c reduced
2. 4H transfered
3. 1 Qh2 oxidized
What is Fo sensitive to?
oligomycin
adenine nucleotide translocase--

phosphate transpoter -
unidirectional exchange of atp for adp -antiport

symporter H and Po3
2 shuttles for moving nadh into matrix
1. glycerol P shuttle
2. malate aspartate shuttle
What is made substrate for FA synthesis?
Malonyl CoA
Acetly CoA carboxylase-
Acetyl CoA into Malonyl CoA
What does the breakdown of 1 glucose yield?
6 CO2, 4 ATP, 10NADH, 2 QH2
What direction does e- travel through the ETC?
increasing reduction potentials
NADH-strong red agent
O - strong ox agent
Complex I-
largest one - NADH-ubiquinone oxidoreductase -transfers 4e-
Complex II-
does not contribute to gradient succinate to ubiquinone - but still supplies e- to give to III
Complex III
Ubiquinol-cytochrome C -moves 4Hs across 4 from QH2 -- Q cycle - 2 QH2 are oxidized but I regenerated
Complex IV
Cytochrome c oxidase- final e- acceptor =O2 - catalyzes a 4e- reduction of O2 from e- from complex III - 2H+ across for 2e-
F1 knob of ATP synthase
contains the catalytic subunits - which makes the ATP - its a hexamer - 3 active sites
F0 knob of ATP synthase
the stalk- 3H/ATP synthesized - sensitive to oligomycin
What are the 3 sites in the ATP synthase?
Open, Loose and closed
Where does FA synthesis mainly occur?
Liver and fat cells
How does FA synthesis occur?
Where does it occur?
by addition of 2C repetitively to the end of a hydrocarbon while its attached to a ACP -- happens in cytoplasm
What does citrate divide into?
OAA and Acetyl CoA
What are the steps for initiation of FA synthsis
1. Send citrate outside cell
2. convert Acetyl CoA into malonyl CoA 3. hook them both to proteins 4. then connect them to form acetoacetyl ACP
What needs to be done after initiation to get the molecule ready for elongation?
2 NADPH need to be consumed for each 2C added, need to release a CO2
How many ATPs are needed for synthesis of TG from fatty acids.
2 ATP equivalents
What is the building block for triacylglycerol synthesis?
Glycerol 3 P
What is the last double bond mammals can make in FA chains?
cant make one after 9
Where is cholesterol made?
Liver or intestine
HMG-CoA reductase-
catalyzes the first committed step and is the key point for regulation
What is the starting point of cholesterol?
2 Acetyl CoA
HMG-CoA reductase-
HMG-CoA to Mevalonate
What are the most common 2 bile salts
taurocholate and glycocholate
What helps lipase bind to the emulsified fats? what does lipase do?
colipase -- convert fatty acids to acyl coA molecules
What is the largest lipoprotein?
a chylomicron - delivers triacylglyerols and cholesterol from intestine to tissues
What is cholesterol mainly carried by?
LDL
What are the 3 stages for beta oxidation of fatty acids/
1. Activation of fatty acid in cytosol
2. transport - into mito or peroxisomes through shuttle
3. degradation as 2C fragments as acetyl CoA in the matrix
Carnitine shuttle system-
way to move long fatty acyl CoA into the matrix -- changes Fatty acyl CoA into Acylcarnitine to leave cytoplasm and then forms back into fatty acyl coA in matrix
Ketone bodies when catabolizes form what? where are they formed/
acetoacetate and beta hydroxy butyrate mito of liver cells
nitrogenase -
converts N2 to 2NH3 uses a ton of energy 16 ATP to do 1 reaction
PLP-
takes the amino group and transfers it usually from glutamate to another molecule
How are ubiquitins added to a protein?
through a lysine residue
p53-
a tumor repressor protein normally regulated by mdm2
What is the first step in aa break down?
removal of alpha amino group
glucogenic aa with examples
ketogenic-
glucogenic - degraded to pyruvate or CAC intermediates --arginine
ketogenic - acetyl CoA acetoacetate and others in the formation of FA or ketone bodies - lysine
PKU -
defect in tyrosine formation from phenylalanine by PAH
Maple Syrup -
Cant break down all 3 branched chain amino acids - leucine, valine, and isoleucine
Where is urea produced?
liver