Enzymes, Digestion And Excretion Flashcards

1
Q

What are enzymes?

A

Enzymes are biological catalysts, globular proteins, and can catalyze intracellular or extracellular reactions. They have specificity, with an active site complementary to a specific substrate to form enzyme-substrate complexes. Enzymes are sensitive to denaturation due to temperature and pH.

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2
Q

What is a metabolic pathway?

A

A metabolic pathway is an enzyme-catalyzed cascade of reactions.

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3
Q

How do enzymes lower activation energy?

A

Enzymes destabilize bonds in reactants to make them more reactive, thereby lowering the activation energy.

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4
Q

What is the induced fit hypothesis?

A

The induced fit hypothesis suggests that the enzyme’s active site can change shape slightly after substrate binding, undergoing conformational changes. This replaces the earlier ‘lock and key’ hypothesis.

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5
Q

How is enzyme activity investigated?

A

Enzyme activity is investigated by measuring the rate at which product is formed or reactants are used up.

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6
Q

What factors affect enzyme activity?

A
  • Temperature: Enzymes have an optimum temperature. At too low a temperature, the rate of reaction (RoR) is too slow due to fewer collisions and lower energy collisions. At too high a temperature, denaturation occurs, breaking the bonds holding the tertiary structure together and permanently damaging the active site.
  • pH: Enzymes have an optimum pH. Extreme pH levels can cause denaturation by weakening hydrogen and ionic bonds.
  • Enzyme concentration: As enzyme concentration increases, the RoR increases. However, if substrate concentration is low, enzyme concentration can become a limiting factor.
  • Substrate concentration: Similar to enzyme concentration, substrate concentration increases RoR, but once all active sites are saturated, a plateau occurs, and enzyme concentration becomes the limiting factor.
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7
Q

What are reversible inhibitors?

A

Regulatory in metabolic pathways. Non-competitive inhibitors bind to a separate active site on regulatory enzymes (e.g., end-product inhibition of PFK in respiration). 2 types:
- Competitive inhibitors: Similar in shape to the substrate and bind to active sites, forming an enzyme-inhibitor complex. Increasing substrate concentration reduces their effect.
- Non-competitive inhibitors: Bind to a separate site on the enzyme, changing the shape of the active site or deforming the enzyme-substrate complex.

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8
Q

What are irreversible inhibitors?

A

Irreversible inhibitors form permanent covalent bonds with one of the groups vital for catalysis to occur. Examples include arsenic, cyanide, and mercury. These inhibit neurotransmitter, requiring the production of new enzymes for translation and transcription, which is a slow process.

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9
Q

What are cofactors?

A

Cofactors are inorganic ions that stabilize enzymes or may participate in reactions at the active site. An example is chlorine in amylase.

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10
Q

What are coenzymes?

A

Coenzymes are organic cofactors that can be either permanent or temporary. They carry electrons and chemical groups to aid in catalysis.

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11
Q

Which vitamins are part of the B group and what do they do?

A
  • Pantothenic acid: Forms coenzyme A.
  • Nicotinic acid: Forms NAD.
  • B1 (Thiamine): Forms FAD.
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12
Q

What is the process of digestion and absorption?

A

Large, insoluble molecules are broken down into smaller molecules that can pass through the cell membrane. These smaller molecules are used to release energy or build other molecules for growth and repair.

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13
Q

What are the main parts of the human digestive system?

A
  • Mouth: Teeth chew food to increase surface area for enzyme action; carbohydrate digestion occurs here, and salivary glands release amylase enzymes to form a bolus.
  • Oesophagus: Food passes into the stomach by peristalsis of muscular walls.
  • Stomach: Protein digestion occurs here, and hydrochloric acid lowers the pH to provide optimum conditions for proteases and to unravel proteins. It can also kill microbes.
  • Small intestine:
    • Duodenum: Carbohydrate, lipid, and protein digestion occurs using enzymes secreted by the pancreas and small intestine.
    • Jejunum + Ileum: Absorption of digested molecules into the bloodstream and absorption of water. The walls are lined with villi. Smooth muscular walls contract in peristalsis.
  • Large intestine: Absorbs water, vitamins, and minerals.
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14
Q

How are carbohydrates digested?

A
  • In the mouth and small intestine: Amylase made in the pancreas, salivary glands, and small intestine hydrolyzes starch into maltose. Membrane-bound disaccharidases, such as maltase and lactase, embedded in the microvilli membrane of epithelial cells in the small intestine, further break down carbohydrates into monosaccharides.
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15
Q

How are proteins digested?

A
  • In the stomach: Endopeptidases hydrolyze peptide bonds between protein molecules to form smaller protein chunks.
  • In the small intestine: Pancreatic fluid, containing endopeptidases and exopeptidases, breaks bonds at the end of polypeptide chains to form dipeptides. Dipeptidases in the small intestine hydrolyze peptide bonds between dipeptides to form amino acids by hydrolysing peptide bonds, which can be absorbed.
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16
Q

How are lipids digested?

A
  • Fatty liquids in droplets from the stomach enter the small intestine.
  • Bile, made in the liver and secreted by the gallbladder, emulsifies fats into smaller droplets by bile salts binding to lipids to increase surface area.
  • Lipase produced in the pancreas digests lipids in the small intestine with the help of coenzyme colipase.
17
Q

How are amino acids absorbed in the small intestine?

A

Amino acids are co-transported through specific membrane proteins in epithelial cells with sodium ions via facilitated diffusion. The sodium ion concentration gradient is maintained by active transport through the sodium-potassium pump, moving sodium ions out of the cell and into the blood.

18
Q

How is glucose absorbed in the small intestine?

A

Glucose is absorbed similarly to amino acids, using specific carrier proteins for glucose and co-transport with sodium ions via facilitated diffusion.

19
Q

How are fatty acids and glycerol absorbed in the small intestine?

A
  • Fatty acids and glycerol associate with phospholipids and bile salts to form micelles, which are not soluble.
  • Micelles are transported to the epithelial membrane, where they break down and form a pool of fatty acids.
  • Smaller fatty acid chains pass through the membrane by simple diffusion and enter the bloodstream.
  • Long-chain fatty acids combine with glycerol to form triglycerides in the smooth endoplasmic reticulum (SER). These triglycerides are packaged into lipoproteins, forming chylomicrons, which pass through the lacteal lymph vessel and enter the blood via exocytosis.
20
Q

What is excretion?

A

Excretion is the removal of toxic waste products and excess molecules from the body. Undigested food material is passed into the rectum and excreted through the anus.

21
Q

What are examples of metabolic waste products?

A
  • Carbon dioxide: Can cause acidosis if the blood pH falls below normal. It is excreted through the lungs.
  • Nitrogenous waste: Includes ammonia (from deamination of amino acids), urea (from the ornithine cycle), and uric acid (from the breakdown of adenine and guanine).
    • Ammonia can increase cell pH and interfere with NMDA neurotransmitter receptors, leading to overactivity and motor impairment and can also cause aromatic amino acids to pass through the blood brain barrier which are precursors to dopamine.
    • Urea can cause cells to take up water by osmosis, leading to cell lysis.
    • Uric acid can form crystals in joints, causing gout arthritis.
  • Bile pigments: From the breakdown of hemoglobin in red blood cells (RBCs), which can build up in the skin, causing jaundice.
22
Q

What is the structure of the liver?

A
  • External structure:
    • Oxygenated blood flows to the liver from the hepatic artery to provide metabolites for respiration in metabolically active liver cells.
    • Blood from the digestive system passes through the hepatic portal vein to absorb and metabolize nutrients.
    • Deoxygenated blood flows back to the heart through the hepatic vein.
    • The liver is connected to the gallbladder, which stores bile made of bile salts and bile pigments, including bilirubin. Bile passes into the duodenum through the bile duct.
  • Internal structure:
    • The liver is made up of hepatocytes arranged into lobules, supplied by branches of the hepatic artery and hepatic portal vein.
    • Blood from the hepatic artery and portal vein mix in large capillaries called sinusoids, which exchange substances with nearby hepatocytes.
    • A branch of the hepatic vein carries blood away from the lobules to the heart.
23
Q

What are the functions of the liver?o

A
  • Storage of glycogen: Insulin triggers glycogenesis when blood glucose levels rise, converting glucose into glycogen for storage in hepatocytes. Glycogen is metabolized by phosphorylase into glucose when needed.
  • Formation of urea:
    • Deamination: The amino group and hydrogen are removed from amino acids, forming ammonia. The remaining keto acid can be converted into glucose for respiration or stored as glycogen.
    • Ornithine cycle: Ammonia reacts with carbon dioxide to form urea and water, preventing toxicity. Urea diffuses out of hepatocytes into the kidneys via plasma.
  • Detoxification:
    • Lactate: Oxidized back to pyruvate and converted into glucose.
    • Alcohol (ethanol): Transported to hepatocytes, metabolized by alcohol dehydrogenase to ethanal, which enters respiration. Continuous detoxification of alcohol generates ATP, reducing fat metabolism and causing fatty liver and cirrhosis due to stored fats impairing hepatocytes and causing scarring.
    • Hydrogen peroxide: Broken down by catalase.
    • Medications: Detoxified by the liver.
24
Q

How does the liver break down hemoglobin?

A

The liver breaks down hemoglobin from dead red blood cells into bilirubin, which is a bile pigment.