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1. Introduction to biochemistry
- Prof. Gerald W. Feigenson
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2. Amino acids and peptides
- Prof. Gerald W. Feigenson
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3. Protein structure principles
- Prof. Gerald W. Feigenson
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4. Observed protein structures
- Prof. Gerald W. Feigenson
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5. Protein folds and IV structure
- Prof. Gerald W. Feigenson
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6. Protein stability and folding
- Prof. Gerald W. Feigenson
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7. Haemoglobin structure and stability
- Prof. Gerald W. Feigenson
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8. Enzyme specificity and catalysis
- Prof. Gerald W. Feigenson
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9. Enzyme kinetics (Michaelis-Menten)
- Prof. Gerald W. Feigenson
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10. Enzyme inhibition; chymotrypsin
- Prof. Gerald W. Feigenson
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11. Enzyme regulation and coenzymes
- Prof. Gerald W. Feigenson
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12. Lipids, biomembranes and membrane proteins
- Prof. Gerald W. Feigenson
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13. Structure and function of carbohydrates
- Prof. Gerald W. Feigenson
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14. Metabolism principles
- Prof. Gerald W. Feigenson
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15. Glycolysis - energy and useful cell chemicals
- Prof. Gerald W. Feigenson
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16. Glycolysis control
- Prof. Gerald W. Feigenson
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17. Metabolism of pyruvate and fat
- Prof. Gerald W. Feigenson
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18. Urea cycle; oxidative phosphorylation 1
- Prof. Gerald W. Feigenson
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19. Urea cycle; oxidative phosphorylation 2
- Prof. Gerald W. Feigenson
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20. Light-driven reactions in photosynthesis
- Prof. Gerald W. Feigenson
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21. Gluconeogenesis and the Calvin cycle
- Prof. Gerald W. Feigenson
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22. Synthesis of lipids and N-containing molecules 1
- Prof. Gerald W. Feigenson
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23. Synthesis of lipids and N-containing molecules 2
- Prof. Gerald W. Feigenson
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24. Hormone mechanisms
- Prof. Gerald W. Feigenson
Printable Handouts
Navigable Slide Index
- Introduction
- Lecture outline
- Let's get oriented
- Overview of what happens during 'e- transport'
- The mitochondrial electron transport chain (1)
- Complex I: NADH dehydrogenase
- Complex II: succinate dehydrogenase
- The mitochondrial electron transport chain (2)
- Complex III: cytochrome bc1 complex
- Zooming in on complex III
- Complex IV: cytochrome c oxidase
- NADH in cytosol and H+ gradient in mitochondria
- Chemiosmotic mechanism's thermodynamics
- ATP synthase enzyme
- ATP synthesis: binding site change model
- ATP synthesis
- Lecture summary
Topics Covered
- Electronic transport in Mitochondria (Complexes I to IV)
- H+ gradient in mitochondria and Chemiosmotic mechanism
- ATP synthase
Links
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Talk Citation
Feigenson, G.W. (2022, November 27). Urea cycle; oxidative phosphorylation 2 [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved November 21, 2024, from https://doi.org/10.69645/XOIJ4488.Export Citation (RIS)
Publication History
Financial Disclosures
- Gerald Feigenson has no commercial/financial relationships to disclose.
Urea cycle; oxidative phosphorylation 2
Request access to the Principles of Biochemistry lecture series, an extensive introductory to the field of biochemistry. An HSTalks representative will contact you with more information about this series and getting unrestricted access to it.
A selection of talks on Biochemistry
Transcript
Please wait while the transcript is being prepared...
0:00
Greetings. My name is Jerry Feigenson.
I am a professor at Cornell University in the USA.
Welcome to Part 2 of lecture 18.
We ended Part 1 with a brief discussion of
Peter Mitchell's breakthrough chemiosmotic theory
that energy is stored as a gradient of
protons and voltage across the inner mitochondrial membrane.
0:26
In this Part 2,
you will see four different protein complexes that make up
the mitochondrial electron transport chain. And finally,
we will look at the ATP synthase enzyme,
which uses this gradient to catalyze ATP synthesis.
0:46
We're going to look at reactions that happen in
liver mitochondria and especially with the inner membrane of the mitochondria.
So let me orient you.
The outer membrane of mitochondria is very permeable.
We'll show this as dashed lines schematically
indicating lots of holes in the outer mitochondrial membrane.
Then there's an inner mitochondrial membrane which is
extremely tight, extremely impermeable.
It's the tightest of all known biological membranes.
Then we'll notice that the cytosol has
a higher proton concentration and a more positive electrical potential than the matrix.
What about the enzymes that are involved?
Well, early on it was realized that there are
four protein complexes that are involved in ATP synthesis.
They are indicated as complex 1,
complex 2, complex 3,
and complex 4, and we're going to look at reactions in each one of these.
Now it's realized that complexes 1, 3,
and 4 seem to be loosely bound together into what could be called a super complex.
Actually, each complex by itself
can work to generate the proton and voltage gradient.
But now, complexes 1, 3,
and 4 are known to be associated and there's
further research going on to understand the importance of that finding.
It's these four complexes that get and give
electrons by means of mobile electron carriers.
So let's see how that works.