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Flussdiagramm

Lipid Degradation Prep

Chinazor Okeke Biology Biology Englisch

Flowchart on Lipid Degradation and Fatty Acid Processing: hormone mobilization, FA activation and beta oxidation

Flowchart: Lipid Degradation and Fatty Acid Processing

Inhalt des Flussdiagramms

  1. Three stages of FA processing from lipids

  2. 1. Mobilization via hormones

  3. 2. Activation of FAs

  4. 3. Beta oxidation of FAs

  5. Epinephrine and glucagon = THE hormones

  6. Step 1: Bind hormone to 7TM receptor to induce conformational change

  7. Step 2: GTP activates adenylate cyclase

  8. Step 3: Adenylate cyclase catalyzes conversion of ATP into cAMP

  9. Step 4: cAMP activates PKA

  10. Step 5: PKA phosphorylates peripellin

  11. Step 5: PKA phosphorylates HS-lipase

  12. Step 6: Activated Peripellin induces fat droplet rearrangement

  13. Step 7: Release of cofactor for ATGL (lipase)

  14. Step 8: Degrade TAG into DAG

  15. Step 9: DAG degraded into MAG via phosphorylated HS-lipase

  16. Step 6: Degrade DAG into MAG

  17. Step 7: Degrade MAG into glycerol and FA using MAG lipase

  18. Step 8: Transport FA to other fuel deprived tissues using blood-derived albumin protein

  19. Step 10: Degrade MAG into glycerol and FA using MAG lipase

  20. Step 11: Transport FA to other fuel deprived tissues using blood-derived albumin protein

  21. Step 8: Glycerol absorbed by liver and phosphorylated

  22. Glycerol --> L-glycerol-3P

  23. Step 9: L-glycerol-3P ---> DHAP

  24. Step 10: DHAP ---> D-GAP via TPI (Triose Phosphate Isomerase)

  25. Produces one NADH and one H+ as a result of G-3P dehydrogenase activity

  26. D-GAP = GAP = equivalent of intermed. in glycolysis and gluconeogenesis

  27. Can be used to make glucoses or pyruvates

  28. Step 1. ATP hydrolyzes to AMP and PPi via Nu: attk by -COOH end of FA

  29. Requires Acyl CoA synthase (the enzyme resp. for catalyzing FA activation), FA, ATP, and CoA (with -SH group)

  30. Step 2: AMP binds its PO4-3 group to COO- of FA

  31. Step 3: FA-AMP undergoes Nu: attk by deprotonated -SH of CoA-SH at carbonyl

  32. Recall from an earlier chapter that PPi does not exist normally in cells, and is irreversibly hydrolyzed by pyrophosphatase

  33. Step 4: Likely tetrahedral intermediate formed

  34. Step 5: AMP kicked off as good LG to create FA-S-CoA, an activated FA w/ a thioester

  35. ATP-->AMP +PPi is the equivalent of hydrolyzing two ATP mlcs.

  36. FA-AMP is an acyl adenylate, found in pathways that need activated carboxyl groups (ex. amino acid synthesis)

  37. Occurs on outer mitochondrial membrane

  38. Occurs in mitochondrion matrix

  39. Requires specialized transport of activated acyl CoA (if longer than 10C) from inner membrane to matrix

  40. Step 1: Transfer acyl from CoA to zwitterion alcohol carnithine via carnitine acyltransferase 1 (CA1)

  41. Step 2: Use translocase to shuttle acyl carnitine across mitochondrial membrane into mitochondrial matrix

  42. If the acyl-CoA is less than 10C long, then no carnitine transferase, translocase enzymes needed b/c it can pass thru. membr into matrix directly

  43. Step 3: Use CA2 to transfer acyl from carnitine to CoA

  44. Step 4: One carnitine transferred out of matrix for every acyl carnitine transferred into matrix

  45. FADH2, NADH, and ATP prod. during FA Beta oxidation

  46. Step 1: Oxidation of acyl-CoA into trans-Δ²-enoyl CoA via...

  47. Isozymes exist for acyl CoA dehydrogenase depending on FA length

  48. Contains Flavin (as FAD) in AS

  49. Acyl-CoA dehydrogenase

  50. Isozymes = enzymes with diff a.a structure but same specificity for catalyzing certain reactions

  51. E2 mechanism to remove Beta H+ using a general base

  52. Steps of aβ unsaturation

  53. 1. General base takes away α H+ to form enolate (enolate formation)

  54. 2. Carbonyl of thioester reforms again and α Carbon is a carboanion

  55. 3. Radical rxn. initiation has FAD take an e- from the 2x bond of acyl-CoA and abstract a H+ from an acid (HA).

  56. 4. Used to form an FA radical and semiquinone

  57. 5. Abstraction of β H+ from acyl CoA by FAD derived semiquinone (Termination)

  58. 5. FADH2 transferred to high-E flavoprotein

  59. 6. That flavoprotein transfers the e- to the new ETF: ubiquinone reductase

  60. 7. Ubiquinone reductase reduces ubiquinone to ubiquinol

  61. 8. Ubiquinol transfers e- to second H+ pumping ETC protein site

  62. Ubiquinone reductase = an Fe-S protein

  63. Step 2: Hydration of trans-Δ²-enoyl CoA into L-3-hydroxyacyl CoA via...

  64. Its FAD in its active site is reduced by E2 elimination @ β, and which then reduces the FAD of an ETF, which reduces an ETF with an Fe-S component, which reduces ubiquinone to ubiquinol

  65. enoyl CoA hydratase

  66. Only hydrolyzes into the L isomer of 3-hydroxyacyl CoA with the trans-Δ²-enoyl CoA

  67. Only hydrolyzes into the D isomer of 3-hydroxyacyl CoA with the cis-Δ²-enoyl CoA

Informationen

Beschreibung
Biology Biology Flussdiagramm am Lipid Degradation Prep, erstellt von Chinazor Okeke am 18/04/2017.
Erstellt von
Chinazor Okeke
Aufrufe
5
Tags
lipid degradationepinephrineglucagon7tmrperipellinacyl-coacoappibeta-oxidation
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