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Keshav Raj Bhusal
University of Oslo
Faculty of mathematics and natural science
Department of bioscience
Biological process catalysed by FAS
FATTY ACID SYNTHESIS
Fatty acid synthesis - overview
Functional /Catalytic domains of
FAS complex
ACP = acyl carrier protein
AT = acetyl transferase
KS = ketoacyl synthase
MPT = malonyl/ palmitoyl
transferase
KR = ketoreductase
DH = dehydratase
ER = enoyl reductase
Class of Fatty acid synthase
Fatty acid synthase
Type I Type II
● huge multifunctional
protein
● fungi and mammals
● mono functional
proteins(dissociated)
● Bacteria and plants
Type I FAS -Fungal
Catalytic domains are distributed over two non-identical polypeptide
chains
Overall architecture of the fungal FAS
height =260A ° width = 230A °
●barrel shaped with
equatorial ring
(wheel), and dome
shaped apical rings
●KS and KR domain
found in equatorial
ring
●MPT departs
directly from the
wheel and lead to ER.
● AT, DH, along with
ER form apical ring
The central wheel
●Equatorial region of a
complex resembles a
wheel like structure
●Two domains KS and KR
forms outer circular frame(3
each domains arranged in
alternating fashion)
●central hub is built from
tightly packed 6 alpha
helices
● spoke radiates from hub
and connects KS and KR
domains
Distribution of the  and chains
●alpha subunit which
contains KS and KR
domains forms central
wheel
●beta subunit that contains
AT, DH, ER forms apical
rings
The reaction chamber
●Central wheel divides
complex into two reaction
chambers.
●Each reaction chamber has
3 full set of catalytic
domains.
●ACP is attached to two
ancher points A1, and A2.
● Domains of each sets are
arranged around the anchor
point A1 in the reaction
order.
Summary
 Fungal FAS is barrel shaped(central wheel and two arms).
 Central wheel divides complex into two reaction chamber.
 Catalytic domains are distributed over two polypeptide
chains.
  chain forms central wheel
  chains form arms.
Fungal FAS Vs mammalian FAS
(A short comparison)
Fungal FAS Mammalian FAS
66-heterododecamer
2.6 megadalton
2homodimer
0.54 megadalton
Mammalian
Malonyl-CoA/Acetyl CoA trasacylase
(MAT)
Transfer of both substrates
Fungal
●Acetyl transferase (AT)
transfer of Acetyl CoA
●Malonyl/palmitoyl trasferase(MPT)
transfer of Malonyl CoA
Fungal
Mammalian
All catalytic domains are distributed over single polypeptide chain.
Fungal Mammalian
Conclusion
 FAS catalyses synthesis of fatty acids .
 Two types- type I and II
 Animals and fungi posses Type I FAS that integrate all
steps of fatty acid biosynthesis into complex assemblies
 Bacteria and plant posses Type II FAS with dissociated
enzymes.
 Architectural structure differs within type I FAS.
References
Jenni, Simon, et al. "Architecture of a fungal fatty acid synthase at 5 Å
resolution." Science 311.5765 (2006): 1263-1267.
Leibundgut, Marc, et al. "The multienzyme architecture of eukaryotic fatty
acid synthases." Current opinion in structural biology 18.6 (2008): 714-725.
Maier, Timm, Marc Leibundgut, and Nenad Ban. "The crystal structure of a
mammalian fatty acid synthase." Science 321.5894 (2008): 1315-1322.
Maier, Timm, Simon Jenni, and Nenad Ban. "Architecture of mammalian
fatty acid synthase at 4.5 Å resolution." Science 311.5765 (2006): 1258-1262.

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Fatty acid synthase

  • 1. Keshav Raj Bhusal University of Oslo Faculty of mathematics and natural science Department of bioscience
  • 2. Biological process catalysed by FAS FATTY ACID SYNTHESIS
  • 3. Fatty acid synthesis - overview Functional /Catalytic domains of FAS complex ACP = acyl carrier protein AT = acetyl transferase KS = ketoacyl synthase MPT = malonyl/ palmitoyl transferase KR = ketoreductase DH = dehydratase ER = enoyl reductase
  • 4. Class of Fatty acid synthase Fatty acid synthase Type I Type II ● huge multifunctional protein ● fungi and mammals ● mono functional proteins(dissociated) ● Bacteria and plants
  • 5. Type I FAS -Fungal Catalytic domains are distributed over two non-identical polypeptide chains
  • 6. Overall architecture of the fungal FAS height =260A ° width = 230A ° ●barrel shaped with equatorial ring (wheel), and dome shaped apical rings ●KS and KR domain found in equatorial ring ●MPT departs directly from the wheel and lead to ER. ● AT, DH, along with ER form apical ring
  • 7. The central wheel ●Equatorial region of a complex resembles a wheel like structure ●Two domains KS and KR forms outer circular frame(3 each domains arranged in alternating fashion) ●central hub is built from tightly packed 6 alpha helices ● spoke radiates from hub and connects KS and KR domains
  • 8. Distribution of the  and chains ●alpha subunit which contains KS and KR domains forms central wheel ●beta subunit that contains AT, DH, ER forms apical rings
  • 9. The reaction chamber ●Central wheel divides complex into two reaction chambers. ●Each reaction chamber has 3 full set of catalytic domains. ●ACP is attached to two ancher points A1, and A2. ● Domains of each sets are arranged around the anchor point A1 in the reaction order.
  • 10. Summary  Fungal FAS is barrel shaped(central wheel and two arms).  Central wheel divides complex into two reaction chamber.  Catalytic domains are distributed over two polypeptide chains.   chain forms central wheel   chains form arms.
  • 11. Fungal FAS Vs mammalian FAS (A short comparison) Fungal FAS Mammalian FAS 66-heterododecamer 2.6 megadalton 2homodimer 0.54 megadalton
  • 12. Mammalian Malonyl-CoA/Acetyl CoA trasacylase (MAT) Transfer of both substrates Fungal ●Acetyl transferase (AT) transfer of Acetyl CoA ●Malonyl/palmitoyl trasferase(MPT) transfer of Malonyl CoA
  • 13. Fungal Mammalian All catalytic domains are distributed over single polypeptide chain.
  • 15. Conclusion  FAS catalyses synthesis of fatty acids .  Two types- type I and II  Animals and fungi posses Type I FAS that integrate all steps of fatty acid biosynthesis into complex assemblies  Bacteria and plant posses Type II FAS with dissociated enzymes.  Architectural structure differs within type I FAS.
  • 16. References Jenni, Simon, et al. "Architecture of a fungal fatty acid synthase at 5 Å resolution." Science 311.5765 (2006): 1263-1267. Leibundgut, Marc, et al. "The multienzyme architecture of eukaryotic fatty acid synthases." Current opinion in structural biology 18.6 (2008): 714-725. Maier, Timm, Marc Leibundgut, and Nenad Ban. "The crystal structure of a mammalian fatty acid synthase." Science 321.5894 (2008): 1315-1322. Maier, Timm, Simon Jenni, and Nenad Ban. "Architecture of mammalian fatty acid synthase at 4.5 Å resolution." Science 311.5765 (2006): 1258-1262.