Overview of Carbohydrate Metabolism Flashcards
5 portions of carbohydrate metabolism
- Glycolysis
- TCA cycle
- Gluconeogenesis
- Glycogen synthesis and breakdown
- The Pentose Phosphate Pathway
An Ox Red Cat & OIL RIG
Anion - oxidation
Cation - reduction
Oxidation Is Loss, Reduction Is Gain
What is the final electron acceptor in mitochondria?
Oxygen
Km and Vmax
Km = concentration (of substrate) at which the reaction is half maximal
Vmax = Maximal rate of a reaction catalyzed by an enzyme
3 ways to identify key steps
- Important molecule changes its location (enter/exit cell)
- Investing energy in transition of a molecule to another state
- Rate limiting step (bottleneck, often use energy to activate
Glycolysis
Purpose: generation of energy and useful chemical intermediates from the breakdown of glucose.
Key steps:
- Glucose to G6P: this involves investment of ATP, G6P becomes “trapped” within the cell because of the charge associated with the P group
- Fructose 6-P to Fructose 1,6 BP: this is the RLS, regulated by the enzyme PFK-1.
- PEP to pyruvate: mediated by pyruvate kinase
2 fates of pyruvate
- Presence of oxygen & mitochondria: enters TCA cycle to be oxidized to CO2 and water via Acetyl CoA & ETC. End result is ATP and water.
- Hypoxia/exercise/no mitochondria: converted to lactate and exported out of the cell. Regenerates NAD from NADH, which allows glycolysis to continue.
Explain how the TCA cycle is “flexible”
In the presence of oxygen and mitochondria, the TCA cycle enables the complete oxidation of acetyl-CoA to produce GTP, NADH, and FADH2.
In energy surplus the acetyl-CoA can leave TCA without being oxidized
In energy deficit, acetyl-CoA can continue around and release energy from the conversion of NAD and FAD to NADH and FADH2.
Alternatively, pyruvate from lactate or AA metabolism can enter as oxaloacetate and leave to join gluconeogenesis
Describe the pathway from lactate to PEP in gluconeogenesis
Lactate –> Pyruvate –> TCA cycle as OAA –(PEPCK)–> PEP
Gluconeogenesis
Purpose: glycolysis in reverse - get moar glucose.
Key steps:
- Pyruvate –(PEPCK)–> PEP
- Fructose 1,6 BP –(fructose 1,6 bisphosphatase)–> Fructose-6-P
- Glucose-6-P –(glucose-6-phosphatase)–> free glucose (ONLY in liver and kidney)
Glycogen
Purpose: rapidly available source of glucose for acute energy needs
Key steps:
- Glucose-1-P –> UDP-glucose; committed step
- UDP-glucose to growing glycogen molecule via glycogen synthase + branching enzyme
(note that the reverse enzyme is glycogen phosphorylase + debranching enzyme to go from glycogen to glucose-1-P)
HMP Shunt
Purpose:
- Make NADPH for FA biosynthesis and defense against oxidative stress
- Generation of riboses for nucleotide synthesis
4 ways to regulate flux through a pathway
- Amount of substrate available
- Levels/amount of key enzymes available
- Allosteric regulation - another molecule alters the activity of a key enzyme in a pathway
- Covalent modification of a key enzyme - mostly ends up modifying its activity; this is a common way that hormones modify flux. Can also be through changes in Km or Vmax.
Counter-regulatory hormones
glucagon, catecholamines, growth hormone, cortisol
Action of catecholamines and glucagon
Bind to membrane associated receptors to change levels of cAMP and protein kinases, which in turn alter key enzyme activities.
Fed state: insulin high; counter regulatory hormones low