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Bio — 6.1

digestion

QuestionAnswer
Alimentary Canal organs through which foods actually passes (esophagus, stomach, small intestine, large intestine)
Accessory Organs aids in digestion but do not actually transfer food (salivary glands, pancreas, liver, gall bladder)
Mouth - mechanical digestion of food by chewing and mixing with saliva - saliva contains lubricants and enzymes such as salivary amylase that starts starch digestion
Esophagus - hollow tube connecting oral cavity to stomach (separated from trachea by epiglottis) - food is mixed with saliva and then is moved in bolus via action of peristalsis - secretes mucus - sphincters to prevent acid from coming up
Stomach - temporary storage tank where food is mixed by churning and protein digestion begins - lined by gastric pits that release digestive juices, which create acidic environment (pH~2)
Small Intestine - long, highly folded tube where usable food substances (nutrients --> lipids, carbs, proteins, nucleic acids) are absorbed - three sections --> duodenum, jejunum, ileum - neutralizes stomach acids
Large Intestine - final section of alimentary canal, where water and dissolved minerals (i.e. ions) are absorbed - further digestion --> carbs by symbiotic bacteria - formation and storage of feces
Salivary Glands release saliva to moisten food and contains enzyme (e.g. amylase) to initiate starch breakdown
Pancreas - production and secretion of lipase, endopeptidase, amylase - released into small intestine via duodenum - secretes certain hormones (insulin, glucagon) to regulate blood sugar concentrations
Liver - takes raw materials absorbed by small intestine and uses them to make key chemicals - role includes secretion of surfactants in bile to break up liquid droplets
Gall Bladder - storages bile produced by liver (bile salts are used to emulsify fats) - bile stored in gall bladder is released into small intestine via common bile duct
Mechanical Digestion food is physically broken down into smaller fragments via acts of chewing (mouth), churning (stomach), and segmentation (small intestine)
Mechanical Digestion — Mouth (Chewing) - food is broken down by grinding action of teeth (chewing or mastication) - tongue pushes food towards back of throat, where it travels down esophagus as bolus - epiglottis prevents bolus from entering trachea; uvula prevents it from nasal cavity
Mechanical Digestion — Churning (Stomach) - stomach lining has muscles which physically squeeze and mix food with strong digestive juices - digested for several hours and turned into creamy paste called chyme - chyme enters duodenum where absorption will occur
Movement of Food — Peristalsis - principal mechanism of movement in esophagus (in stomach and gut as well) - continuous segments of longitudinal smooth muscle rhythmically contract and relax - moved unidirectionally along alimentary canal in caudal direction (mouth to anus)
Movement of Food — Segmentation - contraction and relaxation of non-adjacent segments of circular smooth muscle in intestines - move chyme in both directions, allowing for greater mixing of food with digestive juices - bidirectional propulsion can slow overall movement
Chemical Digestion food is broken down by action of chemical agents (such as enzymes, acids, and bile)
Chemical Digestion — Stomach Acids - contains gastric glands which release digestive acids to create pH 2 - denature proteins and other macromolecules - stomach epithelium has mucous membrane which prevents acids from damaging gastric lining
Chemical Digestion — Bile - liver produces bile and is stored within gall bladder prior to release in small intestine - bile salts interact with fat globules to divide them into smaller droplets (emulsification) - increase total SA for lipase
Chemical Digestion — Enzymes - biological catalysts speed up chem reaction by lowering activation energy - occur at body temps at sufficient speeds for survival requirements - substrate specific and can allow digestion of certain molecules to occur in distinct locations
Digestive Enzymes — Proteases/Endopeptidases - digest proteins/polypeptides - proteins --> peptides --> amino acids
Digestive Enzymes — Amylase - digest sugars - starch --> maltose
Digestive Enzymes — Nuclease - digest DNA/RNA - nucleic acid --> nucleosides
Digestive Enzymes — Lipase (+ Bile Salts from Liver) - lipase (digest fats) and bile salts (emulsify fats) - dietary fat/triglycerides --> monoglycerides/fatty acids
Carbohydrate Digestion - mouth with release of amylase from salivary glands (amylase = starch digestion) - amylase is also secreted by pancreas in order to continue carb digestion within small intestine - enzymes for hydrolysis are on small intestine's epithelium
Protein Digestion - stomach with release of proteases that function in acidic pH - smaller polypeptide chains enter small intestine where they are broken down by endopeptidases by pancreas - work in neutral environments (pH~7) as pancreas neutralizes acids in intestine
Lipid Digestion - intestines with emulsification of fat globules by bile released from gall bladder - smaller fat droplets are then digested by lipases released from pancreas
Nucleic Acid Digestion pancreas also releases nucleases which digest acids (DNA, RNA) into smaller nucleosides
Ingestion food is taken into body via act of eating
Absorption digested food products are absorbed into bloodstream
Assimilation digested food products are moved from bloodstream into cells
Elimination undigested food residues are egested from body as semi-solid feces
Structure of Small Intestine — Serosa protective outer covering composed of layer of cells reinforced by fibrous connective tissue
Structure of Small Intestine — Muscle layer outer layer of longitudinal muscle (peristalsis) and inner layer of circular muscle (segmentation)
Structure of Small Intestine — Submucosa composed of connective tissue separating muscle layer from innermost mucosa
Structure of Small Intestine — Mucosa highly folded inner layer which absorbs material through its surface epithelium from internal lumen
Structure of Small Intestine — Epithelial Cells absorbs digested materials in small intestine
Structure of Small Intestine — Villi - increase SA for absorption - highly folded into finger-like projections - protrude into intestinal lumen
Features of Villi — Microvilli ruffling of epithelial membrane further increases SA
Features of Villi — Rich blood supply dense capillary network rapidly transports absorbed products
Features of Villi — Single layer epithelium minimizes diffusion distance between lumen and blood
Features of Villi — Lacteals absorbs lipids from intestine into lymphatic system
Features of Villi — Intestinal glands exocrine pits release digestive juices
features of Villi — Membrane proteins facilitates transport of digested materials into epithelial cells
Starch Digestion — Process - digestion of starch is initiated by salivary amylase in mouth and continued by pancreatic amylase in intestines - maltose and dextrin are digested by maltase and dextrinase which is fixed into epithelial lining of small intestine --> forms glucose
Starch Digestion — Formats of Starch - can exist in one of two forms — linear chains (amylose) or branched chains (amylopectin) - amylase digests amylose into maltose - amylase digests amylopectin into branched chains called dextrins
Modelling Digestion - core function of digestive system is to break down large molecules into smaller subunits that can absorbed by cells - cell membranes are impermeable to large molecules (polypeptides, polysaccharides) unless transport is facilitated by proteins
Dialysis Tubing (size-specific permeability of cell membranes) - contains pores typically ranging from 1-10 nm in diameter and is semi-permeable according to molecular size - large molecules such as starch cannot pass through tubing, however smaller molecules (such as maltose) can cross
Dialysis Tubing (permeability) unlike membranes of living cells, dialysis tubing is not selectively permeable based on charge (ions can freely cross)
Dialysis Tubing to Model Digestive Processes (Starch Breakdown and Maltose Absorption) — Prediciton - water will enter via osmosis - amylase will digest starch into maltose - maltose will leave via diffusion - meniscus level will drop (less solute = less osmosis)
Dialysis Tubing to Model Digestive Processes (Starch Breakdown and Maltose Absorption) — Control and Experiment - control: dialysis tube with starch solution only - experiment: dialysis tube with starch and amylase
Dialysis Tubing to Model Digestive Processes (Starch Breakdown and Maltose Absorption) — Expected Results - amylase will digest starch into maltose - maltose will leave tubing via diffusion - benedict's reagent will detect maltose in beaker (leading to color change)
Created by: soguzman
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