Humboldt State University ® Department of Chemistry

Richard A. Paselk

Chemistry 431 - Fall 2008

BIOCHEMISTRY REVIEW

Pentose Phosphate Shunt (aka Hexose Monophosphate Shunt)

  • What are the two portions of this pathway?
    • Oxidative
      • Know oxidation steps.
      • What is the net result of this portion?
      • Is this portion reversible?
        • Why or why not?
    • Sugar interconversions
      • Why are these reactions needed?
        • Is it always necessary to run the two parts are the same rate? (i.e. do three G-6-P's always give two F-6-P's and a Ga-3-P?)
      • Know flow diagram.
      • What is the net result of this portion?
        • When might these reactions be run backwards?
    • In which tissues are the different portions elaborated?
  • Which intermediates are common to glycolysis and pentose-P?
  • How can this pathway be used to completely oxidize glucose?
    • Does it?
    • Always?
  • How is pentose-P controlled?
    • How does control integrate it to biosynthesis?
      • Example: Assume that 40% of the reducing equivalents used in fatty acid biosynthesis come from the HMP Shunt:
        • If a cell makes fatty acid requiring a total of 550 reduction reactions, how many glucose molecules will be run through G-6-P DH? KEY
      • Example: Assume that 50% of the reducing equivalents used in fatty acid biosynthesis come from the HMP Shunt and that each acetyl-CoA from glycolysis provides two C's for fatty acid biosynthesis:
        • How many glucose molecules are needed to add 12 carbons to a fatty acid, assuming maximum incorporation into fatty acids? KEY
  • Be familiar with detailed mechanisms for:
    • Transketolase
      • Given the substrates and catalysts,
        • What cofactor is needed?
        • be able to explain their mechanisms in catalytic terms,
        • be able to show reasonable electron movements for bond making/breaking, including the structure of the chemically active ring of the catalyst. KEY
      • Be able to correlate the chemical mechanism with kinetic mechanism.
    • Transaldolase (Note that the mechanism is the same as for aldolase, so you don't need to learn a new mechanism, just insert new substrates and follow to new products!)
      • Given the substrates and catalysts,
        • be able to explain their mechanisms in catalytic terms,
        • be able to show reasonable electron movements for bond making/breaking. KEY

Schedule

 

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©R A Paselk

Last modified 9 December 2008