Citric acid cycle

Citric acid cycle

Term 1

Term 1

Glycolysis
Electron transport chain and oxidative phosphorylation
Glycogen metabolism
Citric acid cycle
Gluconeogenesis
Pentose phosphate pathway
Fatty acid oxidation
Fatty acid synthesis
Cholesterol metabolism
Ketone body metabolism
Amino acids and protein folding
Enzyme function
Amino acid metabolism
Nitrogen and urea cycle
Protein structure and synthesis
Cellular structure and function
Cell membrane
Selective permeability of the cell membrane
Extracellular matrix
Cell-cell junctions
Endocytosis and exocytosis
Osmosis
Resting membrane potential
Cell signaling pathways
Nuclear structure
Cytoskeleton and intracellular motility
Inflammation
Ischemia
Free radicals and cellular injury
Atrophy, aplasia, and hypoplasia
Metaplasia and dysplasia
Hyperplasia and hypertrophy
Oncogenes and tumor suppressor genes
DNA structure
Transcription of DNA
Translation of mRNA
DNA replication
DNA damage and repair
Cell cycle
Mitosis and meiosis
DNA mutations
Mendelian genetics and punnett squares
Inheritance patterns
Gene regulation
Epigenetics
Independent assortment of genes and linkage
Polymerase chain reaction (PCR) and reverse-transcriptase PCR (RT-PCR)
Gel electrophoresis and genetic testing
DNA cloning
Galactosemia
Homocystinuria
Phenylketonuria (NORD)
Tay-Sachs disease (NORD)
Pyruvate dehydrogenase deficiency
Kwashiorkor
Marasmus
Folate (Vitamin B9) deficiency
Vitamin B12 deficiency
Down syndrome (Trisomy 21)
Patau syndrome (Trisomy 13)
Edwards syndrome (Trisomy 18)
Turner syndrome
Klinefelter syndrome
Ehlers-Danlos syndrome
Marfan syndrome
Myocardial infarction
Iron deficiency anemia
Alpha-thalassemia
Beta-thalassemia
Sickle cell disease (NORD)
Glucose-6-phosphate dehydrogenase (G6PD) deficiency
Autoimmune hemolytic anemia
Introduction to pharmacology
Pharmacokinetics: Drug metabolism
Cystic fibrosis
Osteomalacia and rickets
Septic arthritis
Rheumatoid arthritis
Juvenile idiopathic arthritis
Gout
Osteoarthritis
Osteoporosis
Diabetes mellitus
Gestational diabetes
Lower urinary tract infection
Insomnia
Major depressive disorder
Selective serotonin reuptake inhibitors
Serotonin and norepinephrine reuptake inhibitors
Suicide
Generalized anxiety disorder
Anxiety disorders: Clinical
Social anxiety disorder
Panic disorder
Obsessive-compulsive disorder
Endocrine system anatomy and physiology
Acromegaly
Insulin
Glucagon
Growth hormone deficiency
Hunger and satiety
Wound healing
Anticoagulants: Direct factor inhibitors
Platelet plug formation (primary hemostasis)
Cartilage structure and growth
Oxygen-hemoglobin dissociation curve
Karyotyping
Fluorescence in situ hybridization
Bone histology
Nasal cavity and larynx histology
Adrenal gland histology
Bronchioles and alveoli histology
Cartilage histology
Thyroid and parathyroid gland histology
Pancreas histology
Skeletal muscle histology
Trachea and bronchi histology
Arteriole, venule and capillary histology
Sympathetic nervous system
Parasympathetic nervous system
Nervous system anatomy and physiology
Cholinergic receptors
Muscle contraction
Muscle weakness: Clinical
Skin anatomy and physiology
Psoriasis
Epidermolysis bullosa
Albinism
Vitiligo
Acne vulgaris
Skin cancer
Alopecia areata
Sunburn
Actinic keratosis
Burns
Cell-mediated immunity of CD4 cells
Cell-mediated immunity of natural killer and CD8 cells
Pneumonia
Vaccinations
Introduction to the immune system
Monoclonal antibodies
Antibody classes
B-cell activation, differentiation, and contraction
B-cell development
Body temperature regulation (thermoregulation)
Cluster headache
Tension headache
Migraine
Meningitis
Brain abscess
Hashimoto thyroiditis
Thyroid hormones
Euthyroid sick syndrome
Human development week 2
Human development days 4-7
Human development week 3
Ectoderm
Mesoderm
Endoderm
Adrenal cortical carcinoma
Primary adrenal insufficiency
Congenital adrenal hyperplasia
Adrenocorticotropic hormone
Synthesis of adrenocortical hormones
Ornithine transcarbamylase deficiency
Neuron action potential
Fats and lipids
Innate immune system
T-cell development
Cytokines
T-cell activation
MHC class I and MHC class II molecules
B- and T-cell memory
Graves disease
Asthma
Polymerase chain reaction (PCR) and reverse-transcriptase PCR (RT-PCR)
Williams syndrome
Calcium pyrophosphate deposition disease (pseudogout)
Osteomalacia
Lipid-lowering medications: Statins
Hyperlipidemia
Blood brain barrier
Cerebrospinal fluid
Guillain-Barre syndrome
Raynaud phenomenon
Myasthenia gravis
Muscular dystrophy
Subarachnoid hemorrhage
Diabetic retinopathy
Hypopituitarism
Hyperpituitarism
Kallmann syndrome
Phosphate, calcium and magnesium homeostasis
Parathyroid hormone
Calcitonin
Vitamin D
Hypercalcemia
Hypocalcemia
Hyperparathyroidism
Hypothyroidism
Hyperthyroidism
Cushing syndrome

Transcript

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For cells to perform any function, any work, they must have energy.

You can’t go jogging or lifting weights if you’re tired, because a cell won’t work without the help of chemical energy.

The main energy currency in the cells is adenosine triphosphate, or ATP, but any nucleoside triphosphate, like guanosine triphosphate, GTP, will do.

For cells to make ATP, a process generating electricity has to take place in our mitochondria.

Electricity is power!

And thanks to this electricity, ATP is made.

Now to create electricity, electron rich molecules must deliver electrons to a chain of complexes, the electron transport chain, which move them to a final acceptor, a molecule of oxygen.

And there are two electron donor molecules: nicotinamide adenine dinucleotide, or NADH, and flavin adenine dinucleotide, or FADH2.

But of course, the cell has to produce NADH and FADH2 in the first place, and they’re produced by critical enzymes called dehydrogenases.

Dehydrogenases are the main enzymes found in the citric acid cycle or Kreb’s cycle.

In fact, the citric acid cycle is a set of 8 enzymatic reactions that start with a molecule called acetyl-CoA, and four of the enzymes, half of them, are dehydrogenases.

And in this process, AcetylCoA gets converted into carbon dioxide.

Acetyl-CoA comes from various sources depending on whether you’ve just eaten or are starving.

Let’s say that you’re hungry and a bit angry - so you’re feeling hangry.

That’s when stress hormones like glucagon, epinephrine, and cortisol start to rise.

In this hangry state, fatty acids from triglycerides become the primary source of acetyl-CoA.

Now, let’s say you have a bowl of delicious French onion soup, everything changes - insulin is plentiful and you have plenty of acetyl-CoA from breaking down glucose, fructose, and galactose -with glucose playing the biggest role.

Now, alcohol is also a source of Acetyl-CoA in the liver where it’s metabolized.

In addition, proteins can also help contribute to acetyl-CoA production.

But in the case of glucose, after a meal, one glucose, a 6-carbon molecule, splits into two 3 carbon pyruvate molecules through glycolysis, which occurs in the cytoplasm of the cell.

Each of the pyruvate molecules then enter the mitochondria.

In the mitochondria, an enzyme called pyruvate dehydrogenase snatches a carbon and two oxygens, from pyruvate, and adds coenzyme A, making acetyl-CoA.

In the process two electrons are also transferred to a nearby NAD+, in the form of a hydride ion, making NADH, while the carbon and two oxygens are released to form carbon dioxide or CO2.

This step links glycolysis to the citric acid cycle, but really isn’t considered part of either process.

Yet, it is a source of NADH and CO2 and shares some similarity with enzymes of the citric acid cycle.

As we go through the citric acid cycle, we’ll keep track of our total GTP, NADH, FADH2, and CO2 count with these energy counters.

And remember that this cycle has many dehydrogenases.

Okay, citric acid cycle starts when acetyl-CoA is joined to a 4-carbon molecule called oxaloacetate by an enzyme called citrate synthase, making a 6-carbon molecule - citrate.

This process also releases coenzyme A.

Next, another enzyme, aconitase, rearranges the chemical shape of citrate to make its isomer, isocitrate, without adding or removing any carbon molecules.

So far we haven’t made anything related to energy.

But here comes the first dehydrogenase, called isocitrate dehydrogenase, which removes a carbon and two oxygens from isocitrate.

In the process two electrons are also transferred to a nearby NAD+, in the form of a hydride ion, making our first NADH, and the carbon and oxygens give us our first CO2, leaving us with a 5-carbon molecule called alpha ketoglutarate.

High levels of ATP and NADH in the cell can inhibit isocitrate dehydrogenase, signaling the cycle to slow down since the cell has plenty of energy.

Key Takeaways

The citric acid cycle, also known as the tricarboxylic acid (TCA) cycle or the Krebs cycle, is a series of chemical reactions in aerobic organisms' cells. The TCA cycle generates energy in the form of ATP from nutrients able to give acetyl-CoA molecules. These include carbohydrates, lipids, alcohol, and ketogenic amino acids. Molecules.

The citric acid cycle begins with pyruvate oxidation to acetyl-CoA by the enzyme pyruvate dehydrogenase. Acetyl-CoA is then transported into the mitochondrial matrix and enters the TCA cycle, where it is oxidized by succinyl-CoA synthase to succinyl-CoA, which is then oxidized by Succinate dehydrogenase to fumarate. Fumarate is then hydrated by fumarase to malate, and malate is oxidized by malate dehydrogenase to oxaloacetate. Oxaloacetate is then reduced by phosphoenolpyruvate carboxykinase to phosphoenolpyruvate. Phosphoenolpyruvate is then dehydrogenated by pyruvate kinase to pyruvate.