Overview of Carbohydrate Metabolism Flashcards
Main metabolic pathways of carbohydrates
- Glycolysis
- The TCA cycle
- Gluconeogenesis
- Glycogen synthesis and breakdown
- The Pentose Phosphate Pathway
Oxidation definiction
- transfer of electrons from a reduced molecule to an acceptor
- reduced molecule = contains lots of potential chemical energy (electrons)
- e.g. glucose
Fxn of “linked enzyme pathways”
- facilitate the stepwise modification of the parent molecule in an energy-efficient manner
- e.g. glycolysis
Km definition
- concentration of substrate @ which the rxn proceeds at half maximal rate
- low Km = substrates have strong affinity for enzyme; rxn will proceed @ low substrate concentrations
Vmax definition
- Vmax = maximal rate of rxn
- high Vmax = rxn will produce a lot of product over a short period of time
Characteristics of/clues to “key steps” in biochemical pathways
- step in which important molecule changes location
- e.g. enters/leaves cell, mitochondria,etc
- step in which energy is used to transition from one molecular state to another
- e.g. addition of phosphate group
- rate limiting step
Key steps in glycolysis
- Glucose ==> cytoplasm via glucose transporter
- Glucose + ATP ==> Glucose-6-P
- G6P is now trapped in cell
- G6P + Phospho-fructo-kinase (PFK) + ATP ==> Fructose 1,6-biphosphate
- activating step
- Fructose 1,6-bis-P ======> Pyruvate + ATP + NADH
- pyruvate = 3 Carbon compound
Pyruvate destination: oxygen vs. no oxygen
- if O2 + mitochondria present:
- pyruvate ==> mitochondria
- pyruvate ==> acetyl CoA ==> TCA cycle
- ==> complete oxidation to CO2 & generation of NADH & FADH2
- energy of NADH & FADH2 ==> electron transport chain @ wall of mitochondria ==> O2 ==> production of ATP & H2O
- if NO O2 or mitochondria:
- pyruvate ==> lactate ==> exported from cell
Steps of TCA cycle
- pyruvate ==> mitochondria ==> acetyl-CoA
- acetyl-CoA ==> TCA cycle = circle of linked enzymatic reaction
- ==> CO2 production + NADH + FADH2 + GTP (“energy carrier” molecules)
- NADH & FADH2 ==> electron transport chain
Primary fxn of glycolysis
The purpose of glycolysis is the generation of energy and useful chemical intermediates from the breakdown of glucose
Primary fxn of gluconeogenesis
- @ negative energy balance, the liver and to a lesser extent the kidney produce glucose.
- Lactate, or glycerol, or AA → liver → glucose
- The process of gluconeogenesis is essentially glycolysis in reverse except that it uses different enzymes and is regulated in an opposite manner.
Primary fxn of glycogen synthesis/breakdown
- Glycogen synthesis: A rapidly available source of glucose for oxidative needs when the body needed energy is glucose stored within tissues as glycogen. This polymer of glucose is synthesized from glucose-6-P.
- Glycogen breakdown: glycogen is a highly branched polymer. This allows the rapid release of many glucose molecules when needed.
Primary fxn of TCA cycle
- TCA cycle is at the heart of oxidative metabolism
- circle of linked enzymatic reactions
- TCA cycle provides a flexible circuit (like a roundabout at an intersection) into which a variety of carbon skeletons can enter and be modified while always replenishing substrates within the cycle.
Primary fxn of electron transport system
- linked reactions of the electron transport system are separate from the TCA cycle
- occur @ inner mitochondrial membrane and the space between the inner and outer mitochondrial membranes
- ==> conversion of O2 to H2O and ADP to ATP in a process known as oxidative phosphorylation
Glucose levels impact on metabolic pathways
- When glucose is abundant, glycolysis predominates.
- When glucose is in short supply, gluconeogenesis predominates.
- When more glucose is available, glycogen storage becomes a site for glucose disposal.
- When glucose is particularly abundant, it is directed to the pentose phosphate pathway
Positive vs. negative energy balance impact on carbohydrate metabolic
- Glycogen synthesis is stimulated when the liver/skeletal muscle is in positive energy balance
- glycogen breakdown is activated when the body is in negative energy balance
General factos that impact fluctuation of metabolic pathways (enzymatic factors)
- More substrate → more product
- More enzymes for a given pathway → more flux down this pathway
- Allosteric regulation
- Covalent modification of a key enzyme
- Hormones can regulate flux through these pathways as well
Major forms of enzyme modification
- Allosteric regulation: a molecule/product can alter activity of a key enzyme in a pathway
- Covalent modification of a key enzyme: enzyme activity can be changed if phosphorylated or otherwise modified