(3.3) Digestion & Absoprtion
Digestion
process in which large molecules are hydrolysed by enzymes into small molecules which can be absorbed & assimilated
Physical Breakdown
if food is large, broken into smaller pieces via teeth - makes it possible to ingest & increases surface area for chemical digestion
muscles in stomach wall contract to churn it, physically breaking it up
Chemical Digestion
hydrolyses large insoluble molecules -> small soluble molecules
carbohydrases = carbohydrates -> monosaccharides
via enzymes
lipases = lipids -> glycerol & fatty acids
proteases = proteins -> amino acids
Carbohydrate Digestion
amylase produced in mouth & pancreas
hydrolyses alternate glycosidic bonds -> maltose
maltase produced in ileum lining
hydrolyses maltose -> alpha glucose
saliva contains salivary amylase hydrolyses starch in mouth -> maltose. contains mineral salts (maintains pH neutral) food enters stomach & acid denatures amylase. food enters small intestine mixes with pancreatic juice. contains pancreatic amylase hydrolyse remaining starch -> maltose. food pushed along ileum, maltase on CSM of epithelial cells, hydrolyses maltose -> alpha glucose
sucrase hydrolyses single glycosidic bond in sucrose -> glucose & fructose
lactase hydrolyses single glycosidic bond in lactose -> glucose & galactose
Lipid Digestion
lipases produced in pancreas & hydrolyse ester bonds
triglycerides -> glycerol & fatty acids
emulsification = lipids split up into micelle droplets by bile salts (produced by liver)
increases lipids SA to speed up lapses
Protein Digestion
peptidases hydrolyse large, complex molecules
endopeptidases = hydrolyse peptide bonds between amino acids in central region of protein -> peptide molecules
exopeptidases = hydrolyse peptide bonds on terminal amino acids of peptide molecules formed by endopeptidases -> dipeptides & amino acids
dipeptidases = hydrolyse bond between 2 amino acids (membrane bound to CSM of ileum's epithelial cells)
Structure of the Ileum
villi = foldings of ileum wall, thin walls & network of blood capillaries (increase SA of ileum & increase absorption rate)
Adaptations of villi
situated between lumen of intestines & blood/tissues of body
increase SA for diffusion
thin walls = reduce diffusion distance
contain muscle & can move = as products are absorbed, new material replaces it (increases efficiency)
well supplied with blood vessels = blood carries away absorbed molecules, maintains diffusion gradient
maintains diffusion gradients
microvilli = finger like projections on CSM of epithelial cells (further increase SA)
Absorption
Amino acids & Carbohydrates
- Na+ out of epithelial cells (active transport) by NaK Pump into blood. takes place in protein carrier molecule in CSM of epithelial cells
- maintains higher conc Na+ in lumen of intestine than inside epithelial cells
- Na+ diffuse into epithelial cells down this conc gradient by co-transport protein in CSM. Na+ carry either amino acid/glucose into cell with them
- amino acid/glucose pass into blood plasma by facilitated diffusion using another carrier
amino acids/glucose move against their own conc gradient using Na+ conc gradient = indirect form of active transport
Triglycerides
- monoglycerides & FA still associated with bile salts from digestion = micelles form
- micelles come into contact with epithelial cells of villi, break down & release monoglycerides & FA, they're non-polar & diffuse across CSM -> epithelial cells
- monoglycerides & FA epithelial cells -> endoplasmic reticulum (form triglycerides)
- triglycerides endoplasmic reticulum -> Golgi apparatus, associate with cholesterol & lipoproteins -> form chylomicrons
chylomicrons = particles adapted for lipid transport
- chylomicrons mover epithelial cells -> lymphatic capillaries (lacteals) via exocytosis -> bloodstream -> cells