Thacker Introduction Flashcards

Lipids, Proteins, Carbohydrates

1
Q

5 pillars of animal health

A

Nutrition, breeding, disease, environment, management

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2
Q

5 functional components of plant/animals tissue

A

Fats, CHOs, Protein, Ash, Water

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3
Q

Absorption

A

Passage of the end-products of digestion from the GI into the body via the blood and lymph

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4
Q

Digestion

A

Taking big particles and making them small by a series of chemical reactions and hydrolysis

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5
Q

Metabolism

A

changes which nutrients undergo between the absorption and excretion as waste products

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6
Q

Anabolism

A

making molecules bigger. uses energy

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7
Q

Catabolism

A

making molecules smaller, gives off energy

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8
Q

purpose of nutrition

A

meet requirements at the lowest cost

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9
Q

(5) What makes a good diet?

A
  1. Contains all the ingredients
  2. All the essential nutrients in the right proportions
  3. Palatable
  4. Economical
  5. No toxic substances
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10
Q

Nutrient

A

a chemical element or compound in the diet of an animal that supports normal life processes (essential nutrients are key)

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11
Q

6 Classes of nutrients

A
  1. Vitamins,
    1. Minerals
    2. Water
    3. CHOs
    4. Protein
    5. Lipids
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12
Q

5 reasons for doing a feed analysis

A
  1. Give a balanced diet
  2. For use in estimating TDN or Net energy
  3. Solve a production problem
  4. Give a market value for feed
  5. Verify a commercial guarantee??
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13
Q

Nutrition

A

Science of how nutrients in the feed are utilized and converted into animal products

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14
Q

Cautions with NRC tables (3)

A
  1. minimum requirements
  2. don’t consider stress, disease or parasite load
  3. sensitive to environmental conditions
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15
Q

6 parts to the Proximate Analysis

A
  1. Moisture content
  2. Ash (minerals)
  3. Crude protein
  4. ether extract (lipid measure)
  5. crude fiber (CHOs)
  6. nitrogen free extract (NFE - for CHOs)
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16
Q

Steps to measure moisture (4)

A

Weigh –> go to 100C in oven —> weigh –> calc (weight after/ beginning weight)

17
Q

Ash - characteristics (5)

A
  • not individual measurement
  • 600C burning
  • P and Se are destroyed
  • measuring is the same procedure as water
18
Q

Wet ashing

A

using HClO (perchloric acid) to burn for P and Se

19
Q

Kjeldahl Process (6)

A

weigh –> Boil in H2SO4 (to get ammonia sulfate) –> Add NaOH (ammonia OH) –> Add water in a known amount of HB (boric) –> Titrate in HCl (measures ammonia) –> multiply by 6.25

20
Q

Flaws in Kjeldahl (2)

A
  1. all nitrogen comes from protein

2. all protein contains 16% N

21
Q

Soxhlet process (4)

A

Weigh —> dehydrate –> extract with petroleum ether (or soxhlet extractor) –> evaporate (whats left is lipid)
High extract = high energy feed

22
Q

Inaccuracies in Soxhlet (2)

A
  1. Accounts for undigestible lipids

2. does not get the individual vitamins (so we expect the in the feeds anyway)

23
Q

Process of measuring CF (4)

A

Weigh –> Boil in H2SO4 (30 min) –> Boil in NaOH (30 min) —> dry and weigh –> residue/beginning weight. This process simply mimicks the stomachs process

24
Q

Van Soest method

A

partitions fiber into soluble and insoluble

25
Q

NDF =

A

Hemicellulose, Cellulose, and Lignin (hemicellulose is the most indigestible)

26
Q

ADF =

A

Lignin and Cellulose

27
Q

NFE calculation

A

NFE = 100 - (H2O, ASH, CF, CP, EE)

28
Q

Advantages of Proximate Analysis (3)

A

cheap, decently accurate, basis of TDN

29
Q

Amino Acid Analysis Steps (4)

A

Hydrolysis —> Separation —> Detection —> ID and quantify

30
Q

3 methods of hydrolysis

A
  1. Acid (6 Normals HCl for a day)
  2. Basic Hydrolysis (4 Normals NaOH) - doesn’t get Trp
  3. Performic Acid Hydr. (for Cysteine and Serine)

This is just to liberate the AA

31
Q

Acid Hydrolysis doesn’t account for

A

Met, Cys, Trp

32
Q

Basic Hydrolysis doesn’t account for

A

most except Trp

33
Q

Performic acid does account for

A

Cys, Ser

34
Q

How do you separate after Hydrolysis?

A

Ion exchange chromotography - in an AA chromatogram

35
Q

Quantifying AA content

A

take the area under the curve of the Chromatogram

36
Q

What chemicals are used to identify AA?

A

Ninhydrin, and OPA

37
Q

Steps in Atomic Absoprtion (5)

A

Ash –> solubilize them (HCl) —> suck sample into flame (to be in ground state) –> use energy from a hollow cathode lamp (for specific emittance) –> amount of light will reflect concentration

38
Q

Which element is not measured by Atomic Absoprtion and how is it measured?

A

P, by colorimetric method

39
Q

What does GLC do (gas-liquid chromatography)?

A

measures individual fatty acids. Shorter ones come off first. Also, double bonds fall off later.