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Nutrition and Metabolism: Macronutrients, Micronutrients, and Cellular Energy Pathways

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Nutrition and Metabolism

Introduction to Nutrients

Nutrients are substances in food essential for growth, maintenance, and repair of the body. They are classified as macronutrients (carbohydrates, lipids, proteins), micronutrients (vitamins, minerals), and water. Essential nutrients must be obtained from the diet because the body cannot synthesize them.

  • Macronutrients: Carbohydrates, lipids, and proteins; provide energy and structural materials.

  • Micronutrients: Vitamins and minerals; required in small amounts for specific physiological functions.

  • Water: Vital for all biochemical reactions and considered a nutrient.

Energy value is measured in kilocalories (kcal), where one dietary "Calorie" equals 1 kcal.

Dietary Guidelines

The USDA's MyPlate provides a visual guide for balanced eating, emphasizing appropriate portions of fruits, vegetables, grains, protein, and dairy.

USDA MyPlate food guide

  • Eat a variety of foods from all groups.

  • Prioritize whole grains, fruits, and vegetables.

  • Limit intake of processed foods and added sugars.

Macronutrients

Carbohydrates

Carbohydrates are the primary energy source for most cells, especially neurons and red blood cells. They are classified as complex (starches, fibers) or simple (sugars).

  • Sources: Grains, vegetables, fruits, sugars, milk.

  • Uses: Glucose is used to produce ATP; excess is stored as glycogen or fat.

  • Dietary Recommendation: 45–65% of total calories, mainly from complex carbohydrates.

  • Health: Excess simple sugars can lead to obesity and metabolic disorders.

Food Sources

Recommended Daily Allowance

Excesses

Deficits

Complex carbs: bread, cereal, pasta, rice, potatoes; Simple carbs: sugar, fruit, honey

130 g; 45–65% of total caloric intake

Obesity, diabetes, nutritional deficits

Tissue wasting, metabolic acidosis

Summary of Carbohydrate Nutrients

Lipids

Lipids provide energy, insulation, and are essential for cell membranes and hormone synthesis. They include triglycerides, phospholipids, and cholesterol.

  • Sources: Animal fats, dairy, oils, nuts, seeds.

  • Essential Fatty Acids: Linoleic (omega-6) and linolenic (omega-3) acids must be obtained from the diet.

  • Uses: Energy storage, cell membrane structure, precursor for hormones.

  • Dietary Recommendation: 20–35% of total caloric intake; saturated fats <10%.

  • Health: Excess leads to obesity, cardiovascular disease; deficiency affects growth and skin health.

Food Sources

Recommended Daily Allowance

Excesses

Deficits

Animal/plant oils, nuts, seeds

65 g; 20–35% of total caloric intake

Obesity, cardiovascular risk

Weight loss, poor growth

Summary of Lipid Nutrients

Proteins

Proteins are required for tissue structure, enzymes, and hormones. Complete proteins contain all essential amino acids; incomplete proteins lack one or more.

  • Sources: Animal products (meat, eggs, dairy), soybeans, legumes, nuts, grains.

  • Uses: Structural (muscle, collagen), functional (enzymes, hormones).

  • Dietary Recommendation: 0.8 g/kg body weight; 12–20% of total caloric intake.

  • Health: Excess can strain kidneys; deficiency leads to tissue wasting and impaired growth.

Essential amino acids and protein sources

Food Sources

Recommended Daily Allowance

Excesses

Deficits

Meat, eggs, dairy, legumes, grains

0.8 g/kg body weight; 12–20% of total caloric intake

Obesity, kidney stones

Weight loss, edema, impaired growth

Summary of Protein Nutrients

Micronutrients

Vitamins

Vitamins are organic compounds that function mainly as coenzymes. They are classified as water-soluble (B complex, C) or fat-soluble (A, D, E, K).

  • Water-soluble: Not stored; excess excreted (e.g., B vitamins, vitamin C).

  • Fat-soluble: Stored in body (except K); excess can be toxic (e.g., vitamins A, D, E, K).

  • Sources: Fruits, vegetables, dairy, meats, grains.

  • Functions: Antioxidants, vision, bone health, blood clotting, metabolism.

Table of vitamins, sources, functions, and deficiencies

Minerals

Minerals are inorganic elements required for various physiological processes, including bone formation, nerve function, and fluid balance.

  • Major minerals: Calcium, phosphorus, potassium, sulfur, sodium, chlorine, magnesium.

  • Trace minerals: Iron, iodine, zinc, etc.

  • Sources: Vegetables, dairy, meats, grains.

  • Functions: Bone structure, oxygen transport, enzyme function, electrolyte balance.

Table of minerals, sources, functions, and deficiencies

Metabolism

Overview of Metabolism

Metabolism is the sum of all biochemical reactions in the body. It includes anabolism (building molecules) and catabolism (breaking down molecules for energy).

  • Anabolism: Synthesis of large molecules from smaller ones (e.g., protein synthesis).

  • Catabolism: Breakdown of complex molecules into simpler ones (e.g., glycolysis).

Stages of Metabolism

Metabolism of nutrients occurs in three stages:

  1. Digestion, absorption, and transport to tissues.

  2. Cellular processing (synthesis or breakdown in cytoplasm).

  3. Oxidative breakdown in mitochondria to produce ATP.

Three stages of metabolism of energy-containing nutrients

Oxidation-Reduction and Coenzymes

Oxidation-reduction (redox) reactions transfer energy via electrons. Coenzymes such as NAD+ and FAD are essential for these reactions.

  • Oxidation: Loss of electrons or hydrogen.

  • Reduction: Gain of electrons or hydrogen.

  • Key enzymes: Dehydrogenases (remove H), oxidases (transfer O).

Oxidation of succinic acid to fumaric acid

ATP Synthesis Mechanisms

ATP is synthesized by two main mechanisms:

  1. Substrate-level phosphorylation: Direct transfer of phosphate to ADP from a substrate.

  2. Oxidative phosphorylation: Indirect formation of ATP via electron transport chain and chemiosmosis.

Substrate-level phosphorylationOxidative phosphorylation

Carbohydrate Metabolism

Glucose Catabolism

Glucose is the primary fuel for ATP production. Its complete oxidation involves glycolysis, the citric acid (Krebs) cycle, and the electron transport chain (ETC).

  • Overall reaction:

  • Pathways: Glycolysis (cytosol), Krebs cycle (mitochondria), ETC (mitochondria).

ATP formation in cytosol and mitochondria

Glycolysis

Glycolysis is a 10-step anaerobic pathway in the cytosol that breaks glucose into two pyruvic acid molecules. It consists of three phases:

  1. Sugar activation: Glucose is phosphorylated twice, using 2 ATP.

  2. Sugar cleavage: Fructose-1,6-bisphosphate splits into two 3-carbon fragments.

  3. Sugar oxidation and ATP formation: Fragments are oxidized, producing NADH and ATP.

Phase 1 of glycolysis: sugar activationPhase 2 of glycolysis: sugar cleavagePhase 3 of glycolysis: sugar oxidation and ATP formationSummary of glycolysis phases

  • Net products: 2 pyruvic acid, 2 NADH, 2 ATP (net gain).

  • Fate of pyruvic acid: With O2, enters mitochondria; without O2, converted to lactic acid.

Complete glycolysis pathway

Krebs (Citric Acid) Cycle

The Krebs cycle occurs in the mitochondrial matrix and completes the oxidation of glucose derivatives. Each turn produces CO2, NADH, FADH2, and ATP.

  • Transitional phase: Pyruvic acid is converted to acetyl CoA.

  • Cycle products (per glucose): 6 CO2, 8 NADH, 2 FADH2, 2 ATP.

Krebs cycle overviewKrebs cycle details

Electron Transport Chain and Oxidative Phosphorylation

The ETC uses electrons from NADH and FADH2 to create a proton gradient, driving ATP synthesis via chemiosmosis. Oxygen is the final electron acceptor, forming water.

  • ETC: Series of protein complexes in the inner mitochondrial membrane.

  • ATP synthase: Enzyme that synthesizes ATP as protons flow back into the matrix.

Oxidative phosphorylation overviewEnergy harvesting in the electron transport chainChemiosmosis and ATP synthesisStructure and function of ATP synthaseATP synthase mechanismATP synthase mechanism details

Summary of ATP Yield

  • Substrate-level phosphorylation: 4 ATP (2 from glycolysis, 2 from Krebs cycle).

  • Oxidative phosphorylation: 28 ATP (from NADH and FADH2).

  • Total: ~30 ATP per glucose (after accounting for transport costs).

Glycogenesis, Glycogenolysis, and Gluconeogenesis

  • Glycogenesis: Formation of glycogen from excess glucose (mainly in liver and muscle).

  • Glycogenolysis: Breakdown of glycogen to glucose when blood sugar is low.

  • Gluconeogenesis: Synthesis of glucose from non-carbohydrate sources (e.g., amino acids, glycerol) in the liver.

Lipid Metabolism

Lipid Catabolism and Anabolism

Lipids yield more energy per gram than carbohydrates or proteins. Triglycerides are broken down into fatty acids and glycerol, which are oxidized for energy or used in gluconeogenesis.

  • Beta oxidation: Fatty acids are broken into acetyl CoA units, which enter the Krebs cycle.

  • Lipogenesis: Synthesis of triglycerides from excess acetyl CoA.

  • Lipolysis: Breakdown of stored fats for energy.

  • Keton bodies: Produced from excess acetyl CoA during prolonged fasting or diabetes; can lead to ketoacidosis.

Lipid oxidation pathwayLipid metabolism overviewSummary of lipid reactions

Conclusion

Understanding the roles of nutrients and the metabolic pathways that process them is essential for maintaining health and supporting cellular function. Proper nutrition and efficient metabolism are foundational to all physiological processes in the human body.

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