Burning fuel to power living organisms since before mitochondria moved into eukaryotes No it does not take place in the lungs of cells.

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Presentation transcript:

Burning fuel to power living organisms since before mitochondria moved into eukaryotes No it does not take place in the lungs of cells

C 6 H 12 O 6 + 6O 2 → 6 CO H 2 O + energy Type of oxidation-reduction (redox) reaction

MITOCHONDRION STRUCTURE Double membrane- allows compartmentalization OUTER MEMBRANE INNER MEMBRANE (CRISTAE) –contains Electron transport proteins MATRIX- contains enzymes for KREBS CYCLE INTERMEMBRANE SPACE- between cristae and outer membrane Place where H + ions accumulate during ETC

GLYCOLYSIS “Glykos”= sweet; “lysis”=split apart GLUCOSE → 2 PYRUVATE Occurs in cytosol Requires 2 ATP to get started Produces 4 ATP (net gain 2 ATP) Produces 2 NADH

GLYCOLYSIS PATHWAY Regulated by phosphofructokinase ALLOSTERIC enzyme near beginning of pathway AMP turns pathway on (AMP is high when ATP is needed) ATP turns pathway off (don’t waste energy making ATP when not needed)

EVOLUTIONARY LINKS Glycolysis = Most widespread metabolic pathway Earliest fossil bacteria (3.5 billion years ago) but large amounts of oxygen not present until 2.7 BYA Works without oxygen ~suggests ancient prokaryotes probably used glycolysis to make ATP before oxygen was present happens in cytoplasm without mitochondria ~ suggests it was in early prokaryotic cells before eukaryotes appeared eukaryotes appeared 1 billion years after prokaryotes (Endosymbiotic theory)

WITHOUT OXYGEN (anaerobic) Pyruvate → FERMENTATION Regenerates NAD+ carriers to allow glycolysis to continue ALCOHOLIC FERMENTATION Pyruvate → CO 2 + alcohol + NAD + Used by microorganisms to make beer/wine Used by yeast to make bread LACTIC ACID FERMENTATION Pyruvate → lactic acid + NAD + Human muscle cells when oxygen is low during exercise

WITH OXYGEN GLYCOLYSIS → KREBS CYCLE → ETC HIGH ENERGY ELECTRON CARRIERS: (B-vitamin coenzymes) NAD + → NADH FAD → FADH 2 FACULTATIVE ANAROBES (Ex: yeast/some bacteria) can switch back and forth between fermentation/respiration depending on O 2 availability

Pyruvate transported into mitochondrial matrix Uses 1 ATP/pyruvate for active transport ACETYL CO-A CHARGING (B-vitamin coenzyme) Co enzyme A receives carbons from pyruvate feeds them into Krebs cycle Enzyme removes CO 2 from pyruvate producing Acetyl CoA Each glucose produces 2 C NADH

KREBS (CITRIC ACID) CYCLE Releases 6 original carbons in glucose as 6 CO 2 Stores energy in NADH/FADH 2 Occurs in Mitochondrial MATRIX OAA (oxaloacetic acid) receives 2 carbons from Acetyl CoA to make CITRIC ACID Each glucose requires TWO turns of cycle 1 GLUCOSE produces: 6 CO 2, 2 FADH 2, 2 ATP, 8 NADH

ELECTRON TRANSPORT- stage that produces the MOST ATP Attached to CRISTAE inner membrane Uses energy from NADH & FADH 2 to create proton gradient and make ATP Includes: THREE transmembrane PROTON PUMPS; Carrier molecules between pumps = UBIQUINONE (Q); and CYTOCHROMES

Each NADH makes 3 ATP (drops its electrons at top of ETC; hits all 3 proton pumps) Each FADH 2 makes 2 ATP (drops its electrons at Q; skips 1 st proton pump; so makes less ATP) Electrons passing down ETC provide energy for pumping H + ions into INTERMEMBRANE SPACE Final electron acceptor at end of ETC = O 2 (O 2 + 2e- +2H + → H 2 O) 1 glucose yields 36 net ATP

Proton gradient powers ATP SYNTHASE to ADP + P i → ATP PROTON MOTIVE FORCE = potential energy of hydrogen ion gradient CHEMIOSMOSIS = Generation of ATP from a proton gradient (It occurs in all living things)

OXIDATIVE PHOSPHORYLATION using proton gradient created by electron transport chain in cristae membrane to make ATP ETC + CHEMIOSMOSIS = OXIDATIVE PHOSPHORYLATION SUBSTRATE LEVEL PHOSPHORYLATION (found in glycolysis & Krebs cycle) Addition of phosphate group directly WITHOUT proton gradient and ATP synthase

OTHER FUEL MOLECULES Fats, proteins, carbohydrates can be broken down to release energy 1 g of fat → twice as much ATP as 1 g of carbohydrate BETA OXIDATION = breakdown of fatty acids into 2 carbon fragments can enter Krebs cycle as acetyl CoA