Digestion & Absorption

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Digestion: An Overview

  • Digestion is the hydrolysis of large biological molecules into smaller molecules that can be absorbed across cell membranes.
  • Proteins are hydrolysed into amino acids.
  • Carbohydrates are hydrolysed into simple sugars.
  • Lipids are hydrolysed into glycerol and fatty acids.
  • The small molecules produced are used by cells to release energy via respiration and to build new molecules for growth, repair and function.
  • The human digestive system is an organ system containing a series of organs that work together to digest and absorb food.

Organs of the Digestive System

  • Mouth and salivary glands: teeth break food into smaller pieces; saliva is secreted; amylase begins starch digestion into maltose.
  • Stomach: protease enzymes begin protein digestion; hydrochloric acid provides a suitable pH for enzymes and destroys pathogens.
  • Liver: produces bile salts, which aid lipid digestion and neutralise stomach acid as it exits the stomach.
  • Pancreas: produces amylase, protease and lipase, which are released into the duodenum.
  • Small intestine (duodenum): acidic stomach contents are neutralised by bile and become slightly alkaline; enzymes complete chemical digestion.
  • Small intestine (ileum): food and water are absorbed into the blood via villi in the lining.

Enzymes in Digestion

  • Digestive enzymes are extracellular, meaning they function outside body cells.
  • The three main types of digestive enzymes are carbohydrases, lipases and proteases.
  • Carbohydrases include amylase, maltase and lactase.
  • Amylase hydrolyses starch into the disaccharide maltose; it is made in the salivary glands, pancreas and small intestine.
  • Maltase hydrolyses maltose into the monosaccharide glucose; it is a membrane-bound disaccharidase attached to the cell-surface membranes of epithelial cells lining the small intestine.
  • Lipase enzymes in the lumen of the small intestine break down lipids to glycerol, monoglycerides and fatty acids.
  • Bile salts emulsify lipids by binding to large lipid droplets and breaking them into smaller droplets, increasing surface area for lipase action.
  • Bile is not an enzyme and does not carry out chemical breakdown of lipids.

Protein Digestion

  • Protein digestion involves endopeptidases, exopeptidases and dipeptidases.
  • Endopeptidases hydrolyse peptide bonds within polypeptides, creating shorter polypeptide chains.
  • Exopeptidases hydrolyse peptide bonds at the ends of polypeptide chains, producing single amino acids.
  • Dipeptidases are a type of exopeptidase that break down dipeptides into individual amino acids.
  • Membrane-bound dipeptidases are attached to the cell-surface membrane of epithelial cells in the small intestine.
  • Remember: endo = within, exo = outside.

Investigating Digestive Enzymes

  • The effect of pH on amylase activity can be investigated using the iodine test.
  • A strong positive iodine test (blue-black) means starch is present at high concentration, so amylase activity is absent or very low.
  • A weak positive iodine test means starch is present at low concentration, so amylase activity is high.
  • A negative iodine test (orange-brown) means no starch remains, so amylase has converted all starch to maltose.
  • Control variables include: equal volume and concentration of enzyme solution, equal volume and concentration of substrate solution, equal volumes of buffer solution, and the same stirring method.
  • The point at which iodine no longer changes colour can be subjective; a colorimeter can measure the reaction objectively.
  • The effect of bile salts on lipase activity can be investigated using milk, phenolphthalein indicator and sodium carbonate solution.
  • Phenolphthalein is pink in alkaline conditions and colourless in acidic conditions; as lipase breaks down lipids, fatty acids lower the pH and the pink colour disappears.

Mechanisms of Absorption: Co-transport

  • Amino acids and monosaccharides are absorbed via co-transport.
  • Co-transporter proteins are found in the cell-surface membranes of epithelial cells in the small intestine.
  • Step 1: Sodium ions are actively transported from the epithelial cell into the blood via a sodium-potassium pump, decreasing sodium ion concentration in the epithelial cell.
  • Step 2: Sodium ions move down their concentration gradient from the intestine into the epithelial cell, carrying an amino acid or glucose at the same time via the co-transporter protein (a form of facilitated diffusion).
  • Step 3: The concentration of amino acids or glucose in the epithelial cell increases, and they diffuse down their concentration gradient into the blood.
  • While the co-transporter protein action is passive, energy is required to create the sodium ion gradient, so co-transport is considered overall active transport.

Mechanisms of Absorption: Lipids

  • The products of lipid digestion are fatty acids and monoglycerides.
  • Monoglycerides and fatty acids associate with bile salts to form micelles, which transport insoluble molecules to the cell-surface membranes of epithelial cells.
  • Micelles constantly break up and reform; when they break apart, their lipid-soluble contents can cross the membrane by diffusion.
  • The contents of micelles are non-polar and can diffuse through the phospholipid bilayer of the cell membrane.
  • Short fatty acid chains can move directly into the blood via diffusion.
  • Longer fatty acid chains recombine with monoglycerides and glycerol to form triglycerides in the endoplasmic reticulum.
  • Triglycerides are packaged into chylomicrons, which eventually enter the bloodstream.

Modelling Absorption with Visking Tubing

  • Visking tubing (dialysis tubing) is a non-living, partially permeable membrane made from cellulose.
  • Pores in the tubing prevent passage of large molecules (e.g. starch) but allow smaller molecules (e.g. glucose) to pass through by diffusion.
  • Method: tie one end of tubing, fill with starch and amylase mixture, suspend in a beaker of water, and test the outside liquid at intervals for starch and glucose.
  • Results show glucose is present outside the tubing while starch is absent; starch molecules are too large to pass through the pores, but amylase digests starch into glucose, which diffuses out.
  • The rate of absorption/diffusion can be measured quantitatively using colorimetry to determine glucose concentration.
  • The model can investigate the effect of pH (using buffer solutions) and temperature (using water baths).

Limitations of the Visking Tubing Model

  • Visking tubing does not contain biological membranes or membrane features such as channel proteins.
  • Active transport cannot occur across Visking tubing due to a lack of carrier proteins and energy from respiration.
  • The surface area of Visking tubing is less than that of intestinal epithelium due to the absence of villi.
  • The distilled water does not flow like blood, so it does not maintain the concentration gradient.

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Übungsfragen

Gratis-Vorschau — 8 von 59 Fragen. Registriere dich, um alle zu sehen.
  1. 1.Which of the following is the correct definition of a gland in the context of digestion?

    Medium
    • AA group of cells that secretes substances such as enzymes or bile
    • BA muscular organ that churns food
    • CA membrane that absorbs nutrients
    • DA type of enzyme that breaks down food
  2. 2.Which statement correctly describes why the stomach is classified as part of the alimentary canal whereas the liver is not?

    Medium
    • AThe stomach is a hollow tube through which food passes, while the liver is an accessory organ that secretes bile.
    • BThe stomach produces enzymes, while the liver does not.
    • CThe stomach absorbs nutrients, while the liver stores them.
    • DThe stomach is connected to the mouth, while the liver is connected to the pancreas.
  3. 3.Which row correctly completes the table for the digestion of the named molecules?

    Medium
    • AK = amino acids; L = lipids; M = sucrase
    • BK = amino acids; L = fatty acids and glycerol; M = maltase
    • CK = peptides; L = lipids; M = sucrase
    • DK = amino acids; L = lipids; M = maltase
  4. 4.Which of the following are features of the environment inside the stomach that enable chemical and physical digestion? (select all that apply)

    Medium
    • APresence of hydrochloric acid
    • BPresence of protease enzymes
    • CPresence of bile salts
    • DMuscular contractions
    • EPresence of amylase
  5. 5.In an experiment examining the rate of reaction of an amylase-catalysed reaction, what would be the final colour observed from the iodine test in a test tube containing denatured amylase?

    Medium
    • ABlue-black
    • BOrange-brown
    • CBrick red
    • DPurple
  6. 6.Which of the following is a suitable control variable in an experiment measuring the effect of temperature on the rate of a lipase-catalysed reaction?

    Medium
    • AVolume and concentration of lipase solution
    • BThe temperature of the water bath
    • CThe time taken for the pH to change
    • DThe final pH of the solution
  7. 7.Which of the following correctly describes the role of structures 0.5–1.0 mm in length present on the epithelial lining of the small intestine?

    Medium
    • AThey increase surface area for absorption of digested food.
    • BThey secrete digestive enzymes into the lumen.
    • CThey produce bile salts to emulsify fats.
    • DThey store faeces before egestion.
  8. 8.Which of the following is a property of Visking tubing that makes it a good choice for experiments that model the action of enzymes in the gut?

    Medium
    • AIt is partially permeable, allowing small molecules to pass through but not large ones.
    • BIt contains carrier proteins for active transport.
    • CIt has villi to increase surface area.
    • DIt contains biological membranes that mimic epithelial cells.

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