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Glycolysis, Krebs, and ETC

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Glucose gains 2Ps from 2 ATP molecules-become fructose, 1-6 diphosphate ... facultative anaerobe-can do ferm or aerobic respiration ... – PowerPoint PPT presentation

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Title: Glycolysis, Krebs, and ETC


1
Glycolysis, Krebs, and ETC!
2
Things to know
  • Making ATP ultimately base on food source
    breakdown (usually sugar)
  • Begins with GLYCOLYSIS
  • If no oxygen present continues to-anaerobic
    fermentation
  • Lactic acid fermentation
  • Alcohol fermentation
  • If oxygen present-continues to KREBS cycle (AKA
    Citric Acid Cycle or TCA cycle) then ETC

3
Glycolysis
  • In cytoplasm
  • Glucose is OXIDIZED (leo) to pyruvate
  • Major steps
  • Glucose gains 2Ps from 2 ATP molecules-become
    fructose, 1-6 diphosphate
  • F1-6 split into (2)3 carbon G3P-FIRST ½ DONE
  • NAD takes an H off each G3P (so another P can be
    attached) 2 Ps on each 3Carbon molecule
  • Both Ps ripped off both 3 carbon molecules (ADP-gt
    ATP)-
  • (2) 3 carbon molecules (pyruvate) left

4
Summary of Glycolysis
  • 2 ATPs used-4 made per glucose
  • Net?
  • 4 ATPs are made from substrate level
    phosphorylation (get P from substrate)
  • NAD-gt NADH

5
What Happens NEXT?
  • Depends on organism and availability of oxygen
  • If none presentfermentation
  • Fermentation itself produces no energy.
  • Whats its point?

LA fermentation
alcohol fermetation
6
LA vs Alcohol ferm
  • In animals, some microbes
  • Pyruvate accepts H from 2 NADH molecules?lactic
    acid (3 carbon)
  • Lactic acidsore
  • Microbes like bacteria, yeast
  • Pyruvate loses CO2 and accepts H from 2 NADH?
    ethanol (2 carbon)

Some microbes are ANAEROBIC-can't tolerate oxygen
facultative anaerobe-can do ferm or aerobic
respiration
7
IF oxygen present after GlycolysisKREBS!
  • In mitochondria
  • It IS a cycle
  • Pyruvate loses CO2-becomes 2C Acetyl CoA
  • Acetyl CoA joined w/4 Carbon cmpd
  • 6 C compoud loses CO2 and H to become a 5C cmpd,
    the 4 C again
  • 4C cmpd recycled again
  • Released Hs-carried by NADH and FADH to ETS!

ATP
8
Krebs summary
  • NAD and FAD pick up released Hs
  • ADP P make ATP- substrate level phosphorylation
  • CO2 released
  • Where do they go?
  • NADH H and FADH2 bring their H to ETC
  • CO2exhale!

9
ETC-Electron Transport Chain
  • Sometimes called oxidative phosphorylation (P is
    not coming from a substrate)
  • Intermembrane space of mitochodria

10
ETC
  • NADH FADH2 drop their H and electrons off at
    protein carriers w/in membrane
  • Electrons flow thru chain-reaching higher energy
    levels as they travel
  • Hpumped outside membrane
  • Haccumulates outside

electron carriers
protein complexes
11
ETC continued
  • Oxygen accepts 2 electrons from chain and 2 H
    from surroundings
  • What does this make?
  • H now in higher conc. Outside membrane-moves
    back in via ATP synthase (Like an H water
    wheel-makes energy)-called chemiosmosis
  • Energy make joins ADP PATP

overall equation-glycolysis ETC
glucose oxygencarbon dioxide water 36 ATP
12
Poisons can stop respiration
  • Block ETC
  • Rotenoneblocks e- from traveling past 1st
    carrier
  • Cyanide and Carbon Monoxideblock electrons in
    3rd carrier from binding to oxygen
  • Block ATP synthase
  • -oligomycin-blocks H from entering

13
Poisons contd
  • Uncoupling Agents-destroys chemiosmotic
    gradient-moves H BACK into mito thru membrane,
    not synthase
  • - 2,4-Dinitrophenol-former diet pill!
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