Glycolysis

Last updated: January 15, 2025

Glycolysis

Bea :)

Bea :)

Introduction to the cardiovascular system
Bones and joints of the thoracic wall
Anatomy of the pleura
Anatomy of the superior mediastinum
Muscles of the thoracic wall
Anatomy of the lungs and tracheobronchial tree
Anatomy of the coronary circulation
Anatomy of the inferior mediastinum
Anatomy clinical correlates: Thoracic wall
Anatomy clinical correlates: Pleura and lungs
Anatomy clinical correlates: Mediastinum
Electron transport chain and oxidative phosphorylation
Glycogen metabolism
Physiological changes during exercise
Citric acid cycle
Gluconeogenesis
Pentose phosphate pathway
Fatty acid synthesis
Fatty acid oxidation
Amino acid metabolism
Development of the cardiovascular system
Fetal circulation
Development of the respiratory system
Cardiac muscle histology
Arteriole, venule and capillary histology
Artery and vein histology
Blood histology
Bronchioles and alveoli histology
Trachea and bronchi histology
Deep vein thrombosis
Cyanotic congenital heart defects: Pathology review
Iron deficiency anemia
Pneumothorax
Pulmonary edema
Apnea of prematurity
Deep vein thrombosis and pulmonary embolism: Pathology review
Apnea, hypoventilation and pulmonary hypertension: Pathology review
Pleural effusion, pneumothorax, hemothorax and atelectasis: Pathology review
Cholinergic receptors
Muscarinic antagonists
Adrenergic receptors
Adrenergic antagonists: Presynaptic
Antihistamines for allergies
Bronchodilators: Beta 2-agonists and muscarinic antagonists
Cyanide poisoning
Cardiovascular system anatomy and physiology
Coronary circulation
Laminar flow and Reynolds number
Compliance of blood vessels
Pressures in the cardiovascular system
Resistance to blood flow
Control of blood flow circulation
Microcirculation and Starling forces
Measuring cardiac output (Fick principle)
Cardiac contractility
Cardiac preload
Law of Laplace
Stroke volume, ejection fraction, and cardiac output
Frank-Starling relationship
Cardiac afterload
Cardiac and vascular function curves
Altering cardiac and vascular function curves
Cardiac cycle
Cardiac work
Changes in pressure-volume loops
Pressure-volume loops
Normal heart sounds
Abnormal heart sounds
Action potentials in myocytes
Action potentials in pacemaker cells
Cardiac excitation-contraction coupling
Excitability and refractory periods
Cardiac conduction system
Cardiac conduction velocity
ECG axis
ECG cardiac infarction and ischemia
ECG QRS transition
ECG rate and rhythm
Baroreceptors
Chemoreceptors
Blood components
Erythropoietin
Platelet plug formation (primary hemostasis)
Coagulation (secondary hemostasis)
Role of Vitamin K in coagulation
Clot retraction and fibrinolysis
Parasympathetic nervous system
Sympathetic nervous system
Respiratory acidosis
Metabolic acidosis
Metabolic alkalosis
Respiratory alkalosis
Respiratory system anatomy and physiology
Reading a chest X-ray
Lung volumes and capacities
Alveolar surface tension and surfactant
Combined pressure-volume curves for the lung and chest wall
Compliance of lungs and chest wall
Ventilation
Ventilation-perfusion ratios and V/Q mismatch
Regulation of pulmonary blood flow
Breathing cycle
Diffusion-limited and perfusion-limited gas exchange
Airflow, pressure, and resistance
Boyle's law
Henry's law
Alveolar gas equation
Gas exchange in the lungs, blood and tissues
Oxygen binding capacity and oxygen content
Carbon dioxide transport in blood
Oxygen-hemoglobin dissociation curve
Breathing control
Pulmonary chemoreceptors and mechanoreceptors
Pulmonary changes during exercise
Pulmonary changes at high altitude and altitude sickness
Anatomy of the larynx and trachea
Glycolysis
Hypertension
Hypotension
Obstructive lung diseases: Pathology review
Adrenergic antagonists: Alpha blockers
Adrenergic antagonists: Beta blockers
Arsenic poisoning
ECG intervals
ECG cardiac hypertrophy and enlargement
Ketone body metabolism

Transcript

Watch video only

Let’s say that you just ate a big slice of pizza with onions, mushrooms, bell peppers, and jalapenos. To pull energy out of the glucose in that pizza or really any food, requires glycolysis.

Glycolysis is a series of enzymatic reactions in which glucose, a 6 carbon sugar molecule, is broken down into two 3 carbon pyruvate molecules.

And as glucose gets processed, energy is produced in the form of adenosine triphosphate, or ATP.

Now, glycolysis happens in the cytoplasm of cells, and no special organelles or even oxygen are needed to turn glucose into ATP.

Therefore, all cells can use glucose to make energy; and it’s possible to do glycolysis even when oxygen levels are low.

Glycolysis can be divided into two phases: an energy-consuming phase, and an energy-producing phase.

It’s like a business investment - the cell needs to spend some energy before it can start making energy, and like any good investment the cell gets more energy back than it puts in.

The energy-consuming phase requires ATP, and the energy-producing phase generates ATP, as well as other molecules like reduced nicotinamide adenine dinucleotide, or NADH, which can be used to make ATP.

We can keep track of all of this using an energy counter.

Going back to that delicious pizza, first, glucose from those ingredients has to first get from the small intestine into the bloodstream.

In response to high blood glucose, the pancreatic beta-cells secrete insulin.

Now, to get inside the cells, glucose utilizes glucose transporters, or GLUT, which are on the cell membrane.

In fact, some GLUTs like GLUT2 in the liver and pancreatic beta-cells are particularly responsive to glucose in the presence of insulin.

Once glucose gets inside the cell, it’s prevented from diffusing across the cell membrane back into the circulation by enzymes called kinases which phosphorylate the glucose.

Adding a phosphate group changes the shape of the glucose molecule, which means it can’t easily diffuse out of the cell, a bit like a criminal that’s handcuffed to the table in an interrogation room.

The phosphate comes from the breakdown of ATP into ADP and phosphate - so this initial phosphorylation step drops us to -1 on that energy counter.

Specifically, there are two enzymes called hexokinase and glucokinase, and they both add a phosphate group to the 6th carbon in the glucose molecule, turning it into glucose-6-phosphate.

Both enzymes pretty much do the same thing, but hexokinase is found in all cells, whereas glucokinase, like GLUT2, is induced by the presence of insulin, and is found in the liver cells and the beta-cells of the pancreas.

This first step is irreversible, meaning that the reaction can only go in the glucose to glucose-6-phosphate direction, and not vice versa.

Glucose-6-phosphate is converted to its isomer, fructose-6-phosphate by an enzyme called phosphoglucoisomerase.

So at this point, it’s still a 6 carbon molecule.

Fructose-6-phosphate is then phosphorylated by the enzyme phosphofructokinase-1, or PFK1, which adds a phosphate group to the 1st carbon on the fructose molecule, making fructose-1,6-bisphosphate.

This is the second irreversible reaction in glycolysis and it also uses ATP as a phosphate source - so we’re at -2 on that counter now.

This reaction is considered the rate-limiting step of glycolysis - meaning that how fast PFK1 converts fructose-6-phosphate to fructose-1,6-bisphosphate determines the speed at which all of glycolysis happens.

In other words, it’s the rate limiting step of glycolysis. It’s a bit like an assembly line in a factory, if the slowest step is putting tires on a car, then that’s the step that determines how many cars get built in a day.

Because of this, cells closely regulate PFK1 activity by using another enzyme, called phosphofructokinase 2 - or PFK2.

You see - PFK2 can also phosphorylate fructose-6-phosphate - but it adds phosphate to the 2nd carbon instead, making fructose 2,6-bisphosphate. PFK2 activity varies depending on the level of glucose in the blood.

When the body is well-fed, like right after eating that slice of pizza, blood glucose levels go up, and the pancreas secretes insulin, which activates PFK2 - resulting in more fructose-2,6 bisphosphate.

Now, here’s the key - increased levels of fructose-2,6 bisphosphate activates PFK1, which means it increases the rate of available PFK1 enzymes.

So more PFK1 means that the slowest step in glycolysis speeds up, and more glucose is turned into energy. More tires, more cars.

Now, when the body is in a fasting state, like a few hours after a meal, blood glucose goes back down, and the pancreas secretes glucagon instead of insulin.

Glucagon inhibits PFK2, resulting in less fructose-2,6-bisphosphate, which inhibits PFK1, decreasing the rate of PFK1 enzymes, and that slows down glycolysis. Fewer tires, fewer cars.

PFK1 is also inhibited in other ways. For example, when cells are in high energy states, there is a lot of ATP floating around as well as citrate, because that’s a by product of fatty acid synthesis.

Key Takeaways

Glycolysis is a process that breaks down glucose into two molecules of pyruvate. Pyruvate is then used in the citric acid cycle to produce energy in the form of ATP. Glycolysis occurs in the cytoplasm of cells and does not require oxygen.