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54 Cards in this Set
- Front
- Back
Who proposed chemiosmotic theory?
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Peter Mitchell
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What is required for respiration?
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ADP must be present
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What is an example of uncoupler?>
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DNP -dinitrophenol
--oxidation rxn w/o conservation of energy -- o2 consumeed w/o ADP |
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What are uncoupler?
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lipid soluble weak acids
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mitchell;s postulates for chemiosmotic theory?
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1. inner membrane impermeable to H
2. ETC generates H gradient 3. ATP synthase creates ATP by H gradient |
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Protonmotive force --
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energy of the H concentration gradient --- both chemical and electrical -delta G/ nF
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Cofactors wiht ETC
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flavins (FAD and FMN) Fe-S heme like structures
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How does e- travel in ETC?
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direction of increasing reduction potentials
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strong reducing agent #
strong oxidizing agent # |
reducing agents negative -- NADH best reducing agent
oxidizing # Positive O2 best oxidizing agent |
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Complex 1
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NADH ubiquinone oxidoreductasa
NADH transfers 2 e- as hydride ion to FMN and then to Q |
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complex 2
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succinate -Q oxidioreductase
forms qh2 |
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Complex 3 - for each e- pair
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1. 2 cyto c reduced
2. 4H transfered 3. 1 Qh2 oxidized |
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What is Fo sensitive to?
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oligomycin
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adenine nucleotide translocase--
phosphate transpoter - |
unidirectional exchange of atp for adp -antiport
symporter H and Po3 |
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2 shuttles for moving nadh into matrix
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1. glycerol P shuttle
2. malate aspartate shuttle |
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What is made substrate for FA synthesis?
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Malonyl CoA
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Acetly CoA carboxylase-
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Acetyl CoA into Malonyl CoA
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What does the breakdown of 1 glucose yield?
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6 CO2, 4 ATP, 10NADH, 2 QH2
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What direction does e- travel through the ETC?
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increasing reduction potentials
NADH-strong red agent O - strong ox agent |
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Complex I-
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largest one - NADH-ubiquinone oxidoreductase -transfers 4e-
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Complex II-
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does not contribute to gradient succinate to ubiquinone - but still supplies e- to give to III
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Complex III
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Ubiquinol-cytochrome C -moves 4Hs across 4 from QH2 -- Q cycle - 2 QH2 are oxidized but I regenerated
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Complex IV
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Cytochrome c oxidase- final e- acceptor =O2 - catalyzes a 4e- reduction of O2 from e- from complex III - 2H+ across for 2e-
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F1 knob of ATP synthase
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contains the catalytic subunits - which makes the ATP - its a hexamer - 3 active sites
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F0 knob of ATP synthase
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the stalk- 3H/ATP synthesized - sensitive to oligomycin
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What are the 3 sites in the ATP synthase?
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Open, Loose and closed
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Where does FA synthesis mainly occur?
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Liver and fat cells
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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
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What does citrate divide into?
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OAA and Acetyl CoA
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What are the steps for initiation of FA synthsis
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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 |
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What needs to be done after initiation to get the molecule ready for elongation?
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2 NADPH need to be consumed for each 2C added, need to release a CO2
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How many ATPs are needed for synthesis of TG from fatty acids.
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2 ATP equivalents
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What is the building block for triacylglycerol synthesis?
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Glycerol 3 P
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What is the last double bond mammals can make in FA chains?
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cant make one after 9
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Where is cholesterol made?
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Liver or intestine
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HMG-CoA reductase-
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catalyzes the first committed step and is the key point for regulation
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What is the starting point of cholesterol?
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2 Acetyl CoA
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HMG-CoA reductase-
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HMG-CoA to Mevalonate
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What are the most common 2 bile salts
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taurocholate and glycocholate
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What helps lipase bind to the emulsified fats? what does lipase do?
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colipase -- convert fatty acids to acyl coA molecules
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What is the largest lipoprotein?
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a chylomicron - delivers triacylglyerols and cholesterol from intestine to tissues
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What is cholesterol mainly carried by?
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LDL
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What are the 3 stages for beta oxidation of fatty acids/
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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 |
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Carnitine shuttle system-
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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
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Ketone bodies when catabolizes form what? where are they formed/
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acetoacetate and beta hydroxy butyrate mito of liver cells
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nitrogenase -
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converts N2 to 2NH3 uses a ton of energy 16 ATP to do 1 reaction
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PLP-
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takes the amino group and transfers it usually from glutamate to another molecule
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How are ubiquitins added to a protein?
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through a lysine residue
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p53-
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a tumor repressor protein normally regulated by mdm2
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What is the first step in aa break down?
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removal of alpha amino group
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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 |
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PKU -
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defect in tyrosine formation from phenylalanine by PAH
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Maple Syrup -
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Cant break down all 3 branched chain amino acids - leucine, valine, and isoleucine
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Where is urea produced?
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liver
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