Humboldt State University ® Department of Chemistry

Richard A. Paselk

Chem 431

Biochemistry

Fall 2008

Lecture Notes: 21 November

© R. Paselk 2008
 
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Kreb's TCA Cycle, cont.

Note that because all catalysts (oxaloacetate, enzymes etc.) must be regenerated in looking at the overall operation of the cycle, only the acetyl group of acetyl-CoA can be oxidized completely. Some intermediates, such as citrate, can be partially oxidized, but Kreb's cycle intermediate catabolism requires leaving the cycle at oxaloacetate and then returning as acetyl-CoA. Note that this requires leaving the mitochondria for some reactions, and since the extremely low concentrations of oxaloacetate don't allow its efficient transport across the mitochondrial membrane (the Km of the carrier is much higher than [oxaloacetate]), malate is the species which actually leaves the mitochondria.

Glucose Catabolism Control

Regulation and Control of glucose metabolism is summarized on the aerobic catabolism of glucose diagram.

Interconversion of metabolic intermediates

The TCA cycle has a central place in metabolism (even in anaerobic organisms) via its use to interconvert metabolites as summarized in Figure 16.15 in your text. We will look further at these interactions as the course proceeds. These reactions, and in particular the making of oxaloacetate from pyruvate and/or PEP are used to fill the Cycle, are referred to as anapleurosis.

Glycogen Metabolism

Phosphoglucomutase

Start with G-6-P, again note that this molecule is at a metabolic crossroads. First convert to G-1-P using Phosphoglucomutase:

structural diagram of the reaction catalyzed by phophoglucomutase

This reaction is very much like PGA Mutase, requiring the bis phosphorylated intermediate to form and to regenerate the phosphorylated enzyme intermediate. Note that this reaction is easily reversible, though it favors G-6-P.

Again a separate "support" enzyme, Phosphoglucokinase, is required to form the intermediate, this time using ATP as the energy source:

daigram of the reaction catalyzed by Phosphoglucokinase to form the intermediate G-1,6-bisP from glucose

UDP-glucose pyrophosphorylase

This enzyme, which catalyzes the next reaction to give UDP-glucose, has a near zero DeltaG° ':

structural diagram of the reaction catalyzed by UDP-glucose pyrophosphorylase

It is driven to completion by the hydrolysis of the PPi to 2 Pi by Pyrophosphatase with a DeltaG° ' of about -32 kJ (approx. one ATP's worth of energy).

Glycogen Synthase

Finally glycogen is synthesized with Glycogen Synthase:

UDPGlucose + (glucose)n UDP + (glucose)n+1

This reaction is favored by a DeltaG° ' of about 12 kJ, thus the overall synthesis of glycogen from G-1-P is favored by a standard free energy of about 40 kJ. Note that the glucose is added to the non-reducing end of a glycogen strand, and that there is a net investment of 2 ATP equivalents per glucose (ATP to ADP and UTP to UDP, regenerated with ATP to ADP). Note also that glycogen synthase requires a 'primer.' That is it needs to have a glycogen chain to add on to. What happens then in new cells to make new glycogen granules? Can use a special primer protein (glycogenin). Thus glycogen granules have a protein core.

Branching enzyme

The preceding reactions will give linear glycogen strands, additional reactions are required to produce branching. Branching enzyme [amylo-alpha-(1,4) to alpha-(1,6)-transglycosylase] transfers a block of residues from the end of one chain to another chain making a 1,6-linkage (cannot be closer than 4 residues to a previous branch). [FYI: For efficient release of glucose residues it has been determined that the optimum branching pattern is a new branch every 13 residues, with two branchs per strand.]

Glycogen Breakdown

Glycogen is broken down using Phosphorylase to phosphorylize off glucose residues:

(glucose)n + Pi (glucose)n-1 + G-1-P

Note that no ATP is required to recover Glucose phosphate from glycogen. This is a major advantage in anaerobic tissues, get one more ATP/glucose (3 instead of 2!). [FYI: Phosphorylase was originally thought to be the synthetic as well as breakdown enzyme since the reaction is readily reversible in vitro. However it was found that folks lacking this enzyme - McArdle's disease - can still make glycogen, though they can't break it down.]

Phosphorylase can only cleave 1,4-linkages, so now need Debranching enzyme. Debranching enzyme has two activities: a) amylo-alpha-1,4-transferase moves the terminal three residues of a chain onto another branch; whereas alpha-1,6-glucosidase hydrolyzes the 1,6-linkage to give free glucose. Thus muscle can release a small quantity of glucose into the blood without actually doing gluconeogenesis.


Pathway Diagrams

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Last modified 21 November 2008