* Occurs in **inner membrane / cristae** of mitochondria
\ * Aerobic process
\ * Removes e- from glucose, pyruvate and Acetyl CoA
\ * ==**Oxidative phosphorylation**== occurs here
\ * ==**Carrier proteins (I, II, III, IV)**== **in inner membrane (electron acceptors):** receive electrons from electron transporters (NADH, FADH2) → pump protons against \[ \] gradient into intermembrane space to supply energy to ATP synthase * Highly acidic environment in intermembrane space * ==CoQ (Ubiquinon):== can be fully oxidized and reduced during passing of electrons b/w protein complexes * Soluble carrier * ==Cyt C (Cytochrome C):== bound to Iron atom which transfers electrons b/w **Complex III and Complex IV** for redox rxns * Protein carrier * Used for genetic relations
\ * Final electron acceptor (after electrons have passed though all proteins): ==**Oxygen**== → combines w/ H+ to form H2O
\ * ==**ATP Synthase:**== drives protons down the gradient towards matrix (high \[ \] → low \[ \]) to catalyze ADP + Pi → ATP * pH + Electrical Gradient: **Proton Motive Force** * If pH of intermembrane space is higher than normal → less H+ → less cellular respiration occurring
\ * NADH creates more ATP (3x) than FADH2 (2x) * NADH pumps more protons to carrier proteins than FADH2 because NADH enters the protein complex earlier than FADH2 and it enters Complex I (FADH2 enters Complex II)
\ * Total glucose produced = 36 ATP in eukaryotes and 38 in prokaryotes (no mitochondria so don’t need to pump NADH into matrix → saving 2 ATP during glycolysis)
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Oxidative phosphorylation
Process of ADP → ATP from NADH and FADH2 via passing of e- through various carrier proteins in the electron transport chain
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Electron carriers
NADH and FADH2
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What are the products of 1 Glucose molecule that has __**only**__ undergone the Krebs cycle?
\ * ==**Cori Cycle:**== lactate from muscle cells transported into blood stream → liver → converted to glucose → blood stream → used to generate ATP through glycolysis
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Catabolic rxns
Releases energy by breaking down large molecules into smaller molecules
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Anabolic rxns
Requires energy to build molecules from smaller molecules
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Cellular metabolism
Anabolic & Catabolic rxns
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What happens if a cell does not have glucose?
1. Uses other carbohydrates 2. Lipids 3. Proteins (last resort)
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Carbohydrates as a source of energy
* Glycogen (polysacc.): storage for glucose * found mainly in muscle and liver cells
\ * ==**Glycogenesis:**== formation of glycogen (glucose → glycogen)
\ * ==**Glycogenolysis**==: break down of glycogen (glycogen→glucose)
\ * Glucose-6-phosphate main molecule for rxn
\ * Regulated by Insulin and glucagon
\ * First broken down in mouth → stomach → duodenum → small intestine
\ * Disaccharides hydrolyzed into monosaccharides → converted to glucose or glycolytic intermediates
\ * All cells can store glycogen but only skeletal muscle and liver cells can store large amounts
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Gluconeogenesis
* Forming glucose from non-carbs * Occurs in liver and kidney
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Why is phosphate added to a glucose molecule?
To keep the molecule w/n the cell and prevent it from diffusing out of the cell
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Insulin
* Endocrine hormone * Released by pancreas when glucose ↑ * Triggers cells to: * make glycogen from glucose for storage * undergo glycolysis to form ATP → activates ==**Phosphofructokinase**== (R.D.S)
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Glucagon
* Released by pancreas when glucose ↓ * Similar to epinephrine (triggers formation of glucose) * Triggers cells to: * ==**Glycogenolysis**== to form glucose * Inhibit ==**glycogenesis**== to inhibit glycogen production
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Lipids as a source of energy
* Long hydrocarbon chains that are highly reduced → have more energy than carbs
\ * ==**Lipases**== in adipose tissue are hormone sensitive (e.g., to glucagon)
\ * ==**Lipolysis:**== break down of lipids into glycerol and the fatty acids by **lipase enzymes** * Glycerol → ==**Glyceraldehyde 3 Phosphate**== (DAP/G3P/PGAL) → enters glycolysis * Fatty acid chains activated by 2 ATP → ==**β-oxidation of** __**saturated**__ **FA in mitochondrial matrix**== (breaks 2 carbons at the β position) → 1 NADH + 1 FADH2 and 1 Acetyl CoA → citrate in Krebs cycle → 120 ATP generated * ==**β-oxidation of** __**unsaturated**__ **FA**== → 1 less FADH2 for each double bond
\ * Lipids combine w/ soluble proteins → ==**lipoproteins (contain Apoproteins)**== * Classified by density (fat : protein ratio) * B/w meals, most lipids in plasma are in the form of lipoproteins
\ * Lipoproteins large and less dense when ratio is also large * ==**Chylomicrons:**== first fat transporters to leave enterocyte and enter lacteals (small lymphatic vessels)
\ * ==**LDL (low protein density):**== unhealthy due to high fat content * ==**HDL (high protein density):**== healthy cuz transport fat away from tissues → liver → cholesterol for bile → expelled during digestion
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What carries fatty acids in blood?
Albumin
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Lipid digestion
* Stored as ==**adipose tissue**==
\ * Only broken down in duodenum:
1. ==Bile== released from gall bladder to emulsify fats & ==pancreatic lipase== to break down lipids into FA chains and monoacylglycerides
\ 2. Absorbed into enterocytes of small intestine
\ 3. Reassembled into triglycerides, and then, along with cholesterol, proteins or phospholipids → packaged into ==**chylomicrons**==
\ 4. Chylomicrons move to lymph capillary → circulatory system
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Proteins as a source of energy
* Excess amino acids used for energy
\ * ==**Oxidative deamination:**== removal of amino group to form metabolic intermediates (Acetyl CoA, pyruvate, Oxaloacetate) * Directly removes ammonia from AA * Deamination in liver * **By-product:** NH3 (ammonia) → ==**urea**== → excreted as urine in mammals * Uric acid in insects, birds, reptiles
\ * Digestion occurs in stomach: ==**pepsin**== breaks down proteins into polypeptides
\ * In the small intestine: ==**trypsin**== breaks down specific polypeptides into amino acids