Analysis of Carbs Flashcards

1
Q

Carbs importance

A

Source of NRG
Textural properties
Physiological properties
A large % of the diet

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2
Q

Carbohydrates by difference

A

Easiest way to measure carbs

(100 - protein - fat - water - ash) / 100 g of food

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3
Q

Qualitative methods

A

Color reaction in strong acids
Yields furan derivatives (furfurals)

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4
Q

Alpha naphthol

A

For all carbs (mono, di, and polysaccharides)
Purple color

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5
Q

Resorcinol

A

Test for ketoses
Fructose, allulose
Red color

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6
Q

Orcinol

A

Test for pentoses
Aribonse, xylose, ribose
Yellow –> blue

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7
Q

Tollens

A

Test for aldoses
React with silver
Create a precipitate

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8
Q

Reducing sugar tests

A

Somogyi Nelson
DNS
Tollens
Fehling’s

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9
Q

Somogyi Nelson

A

Reduction of Cu ions
Cu ions reduce an arsenomolybdate complex
Create a blue color

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10
Q

Quantative analysis

A

Cuprous oxide measured gravimetrically

Titration

Calibration curves

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11
Q

DNS test

A

3,5-dinitrosalycilate is reduced to 3 amino 5 nitrosalicylic acid

Absorbs in UV range

Reducing sugar test

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12
Q

Analysis of mono and oligosaccharides

A

Chromatography (paper, thin layer, GC, HPLC)

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13
Q

Paper + thin layer chromatogrphy

A

Polar solvents
Develop with heat, acid, chromogen

TLC densitometry

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14
Q

Specific analysis of mono and oligosaccharides

A

Electrophoresis

Capillary electrophoresis

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15
Q

HPLC

A

Quantative and qualitative
Analyze complex mixtures
Anion/cation exchange colums

Sugars might hydrolyze, be careful with temp and pH

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16
Q

GC

A

Sugars converted into volatile derivatives

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17
Q

Fehling’s

A

Copper sulfate, potassium tartrate

Distinguish between functional groups of ketones and carbohydrates that are water-soluble

18
Q

Enzymatic pros

A

Cheap
Simple to use
Any sugar
Convenient
Specific to substrate

19
Q

Enzymatic reaction types

A

Measuring reaction

Indicating reaction

20
Q

Measuring reaction

A

Molecule we want to quantify is used by the specific enzyme to create products

Useless on its own

21
Q

Indicating reaction

A

One of the products from the 1st reaction is used as the substrate

Reduce Nad+

Need a dehydrogenase enzyme

Measure NADH with an absorbance change

22
Q

Only reliable starch method

A

Complete conversion of starch into D glucose w/ a specfic enzyme

23
Q

Dietary fiber

A

Sum of non digestable components of food

24
Q

Soluble fiber

A

Pectin
Hydrocolloids
Gums

25
Insoluble fiber
Cellulose Lignin Hemicellulose
26
Crude fiber method
Fat extracted with a solvent Digestion w/ H2SO4 and NaOH Insoluble residue collected, dried, weighed, ashed
27
Crude fiber cons
Hemicellulose and pectin are solubilized
28
Crude fiber foods
Grains, soybeans, pet food
29
Detergent methods measure
Lignin Cellulose (Acid detergent fiber) Hemicellulose (Natural detergent fiber)
30
Detergent methods cons
Doesn't include pectin and gums
31
Fiber methods
Often measured gravimetrically Gelatinization and hydrolysis of starch Inulin and oligosaccharides can be lost in extract Best when samples are low fat, dry, ground
32
Microscopy
Examine starchy fooods Granule size, shape, form Polarized light microscope Can see biofringence
33
Microscopy uses
Eval gelatinzation Look at mechanical damage Extent of starch hydolysis
34
Specific gravity
Ratio of density of a substance compared to refernece substance (water)
35
Refractive index varies with
Concentration Temp Wavelength
36
Polarimetry
A way to measure the optical activity of compounds Optically active = rotates polarized light Different sign/values based on the direction of light rotation
37
Rotating capacity/angle is proportional to
concentration and length of column
38
Polarimetry pros
Nondestructive and fast
39
Polarimetry cons
Need a clean and colorless solution Make standards to calculate unknown concentration
40
Polarimetry uses
analysis of invert sugar, purity of sucrose
41
Optical rotation
Sample rotates the plane of a polarized light beam
42
How does polarimetry work
Polarized light oscillating in 1 plane --> tube with solution --> plane of light rotates