physiology of digestion - copy

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    Introduction

    The digestive system is a portal for nutrients from the

    environment to gain access to the circulatory system. Before

    such transfer can occur, foodstuffs first have to be reduced to

    very simple molecules by a combination of physical and

    mechanical digestion. The resulting sugars, amino acids,

    fatty acids and the like are then transported across the

    epithelium lining the intestine into blood.

    Physical digestion refers to the grinding of large pieces of

    food into tiny particles while chemical digestion describes

    use of enzymes released into the digestive system to break

    down large biopolymers into monomers or simple forms.

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    A. Physical Digestion of Macromolecules

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    Methodology

    1. Stared and imagined how it tastes like

    2. Smelled the aroma and imagined its

    flavor

    3. Took a bite and observed specific parts

    of the mouth that ground the food.

    Mouth should be as dry as possible before the experimentObservations from start to swallowing were taken note of

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    Results and Discussion

    - Salivate (brought by sight, smell,

    taste)- Incisors, Canine, Pre-molar, Molar

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    B. Chemical Digestion of Carbohydrates

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    Methodology

    C

    1

    C

    2

    C

    3

    C

    4

    C1: 3.0 ml distilled H2O

    C2: 3.0 ml salivary amylase

    C3: 3.0 ml salivary amylase with 10

    drops HCl

    C4: 3.0 ml salivary amylase

    solution & place tube in boilingwater for 5 minutes

    Added 5.0 ml of starch solution to each tube

    and

    incubated at 370C water bath for1 hour.

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    Methodology

    C

    1

    C

    2

    C

    3

    C

    4

    C

    1

    C

    2

    C

    3

    C

    4

    Check for the presence ofstarch.

    (Lugols Test)

    -Lugols iodine solution

    -Blue to black: Starch is

    present(+)

    -Amber coloration (-)

    Check for the presence of

    maltose.

    -(Benedicts test)

    -5.0 ml Benedicts reagent

    *place in boiling H2O for10 mins

    -Green (small amts), Yellow

    (moderate amts), Orange to Red

    (large amts)

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    Lugols Iodine (Lugols solution, 1829)

    a solution of elemental iodine and potassium

    iodide in water

    consists of 5 g iodine (I2) and 10 g potassium

    iodide (KI) mixed with 85 ml distilled water, to

    make a brown solution with a total iodine content

    of150 mg/mL.

    Uses:

    As an indicator test for the presence of starch in

    organic compounds, with which it reacts byturning a dark blue/black. iodine interacts with

    the coil structure of the polysaccharide.

    An antiseptic and disinfectant

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    Results and Discussion

    LUGOLS TEST

    C1: ++++

    C2: +

    C3: ++

    C4: +++

    *presence of starch in all test tubes; they only varied

    with the amount of starch present.

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    Benedicts Reagent

    (Benedicts solution orBenedicts Test)

    C1: + (remained blue)

    C2: ++++

    C3: ++

    C4: +++

    used as a test for the presence of reducing sugars, presence of

    aldehyde, and alpha-hydroxy-ketones (e.g. fructose)

    used to determine how much reducing sugar is present. contains blue copper(II) ions (Cu2+) which are reduced to copper(I)

    (Cu+). These are precipitated as red copper(I) oxide which is

    insoluble in water.

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    EXPERIMENT OBSERVATION INTERFERENCE

    Substance in water + 3ml

    Benedicts solution, then boil for

    few minutes and allow to cool

    Red ppt or green ppt or yellow ppt

    obtained

    Reducing sugar e.g. Glucose is

    present

    Substance in water + 3ml

    Benedicts solution, then boil for

    few minutes and allow to cool

    Solution remains clear Non-reducing sugar e.g. Sucrose is

    present

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    C. Chemical Digestion of Protein

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    Methodology

    P

    1

    P

    2

    P

    3

    P

    4

    P

    5

    Added 5 ml of pepsin toeach tube except P4

    P1:10 drops of distilled

    water

    P2:10 drops of HCl

    P3:10 drops of HCl and

    put in ice bath

    P4: 5 ml of distilled water

    and 10 drops of HCl

    P5:10 drops of NaOHIncubate all except P3 in 37oC

    water bath for 90 mins

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    Methodology

    Examined egg whites slices in incubation.

    Took note:

    if any digestion occurred

    any color change to the solution

    * (+) digested with or without color change

    * (-) not digested

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    Results

    Set-up Number Observation

    P1 (pepsin and water) + fast (second)

    P2 (pepsin and HCl) + fastest

    P3 (pepsin and HCl on ice) + fast (third)

    P4 (water and HCl) + slowest

    P5 (pepsin and NaOH) - no digestion

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    Discussion

    Just like our stomach, test tube 2 is very acidic.

    Therefore, its acidity caused the fastest

    breakdown of protein in the egg white. HCl

    somehow speeded up the digestive function ofpepsin.

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    Temperature also affected the activity of theenzymes as test tube 3 (the one placed in an ice

    bath) digested the egg white slower. Too high and

    too low temperatures could disrupt an enzymes

    function; a moderate temperature is required for

    them to work efficiently.

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    Test tube 1 followed because it does not contain

    HCl that would catalyze pepsin. Test tube 4 ranks

    fourth because HCl alone cannot breakdown

    covalent bonds. Finally, the basic substance in testtube 5 adversely affected pepsin, completely

    stopping its digestive function.

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    D. Chemical Digestion of Triglycerides

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    Methodology

    F

    1

    F

    2

    F

    3 3.0 ml of cream in each tube

    F1: 5.0 distilled H2O + few grains of bile salt

    F2: Pancreatin solution

    F3: Pancreatin solution + few grains of bile salt

    Shook.

    Measured INITIAL PHIncubated tubes in 37o C water

    bath for1 hour

    Measured pH every 20, 40, and 60 minutes

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    Results

    EXPERIMENTAL

    F1 F2 F3

    START BASIC BASIC ACIDIC

    20 minutes BASIC BASIC ACIDIC

    40 minutes BASIC SLIGHTLY ACIDIC ACIDIC

    60 minutes BASIC SLIGHTLY ACIDIC ACIDIC

    THEORETICAL

    F1 F2 F3

    START BASIC BAS

    IC AC

    IDIC

    20 minutes BASIC BASIC ACIDIC

    40 minutes BASIC SLIGHTLY ACIDIC ACIDIC

    60 minutes BASIC SLIGHTLY ACIDIC ACIDIC

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    Discussion

    Pancreatin

    :mixture of digesting enzymes produced by the

    pancreas, including amylase, lipase, and trypsin.

    Bile salts

    :negatively charged cholesterol derivatives

    :amphipathic - both hydrophobic (lipid soluble) and

    hydrophilic

    :emulsification agents

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    Lipids aggregate into large droplets minimizingthe surface area of contact between fat and

    water.

    Digestive enzymes are hydrophilic, only able to

    digest molecules on the surface. Amphiphatic molecules break down fats droplets

    to tiny emulsification droplets.

    Lipases can come contact with the triglycerides

    and hydrolyze them into amphiphatic free fattyacids and monoglycerides.

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    Conclusion

    For food to be utilized by the body, it must

    first undergo a series of processes which we

    call digestion. After we perform the only

    really voluntary actions involved in theprocess of nutritionputting the food into our

    mouths, chewing and swallowingthe

    balance of the digestive process is the

    function of the autonomic or involuntarynervous system.

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    THE END.

    February 15, 2010