Lecture 5-processing and physiochemical properties Flashcards

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1
Q

what is the purpose of extraction and isolation of food protiens, like what is it used for?

A
  • to prepare comerical products like lactase
  • to make nutritional protiens like soy protien isolate
  • for certain biopharmaceuticals like insulin
  • research/anylatic purposes like protien
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2
Q

What is done to a sample in order to prepare it

A
  1. drying
  2. reducition of particle size
  3. defatting
  4. lipid oxidation protection (if working with fat in sample)
  5. enzymatic inactivation
  6. microbrial growth and contamination
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3
Q

what are the three methods of drying to remove moisture content?

A
  1. heating
  2. drying reagents
  3. freeze drying: this is used in products that have thermosenstiative compounds. First the product is froze, then ice is removed by sublimnation under low pressure. This plays off the idea that as vacum pressure increases boiling point will decrease
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4
Q

What is the purpose of reducing the particle size of sample and what are some important notes

A

This is done to achieve homgenization. The sample should be dry before as a wet sample can result in lots of moisture loss and chemical changes. It is important that when grinding the sample should not be heated so make sure not overload and to cool with liquid nitrogen and then store at low temperatures

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5
Q

Explain the importance of defatting and how it is done

A

If a protien is surrounded by fat which is hydrophobic, the extraction of a protien by any buffer is prevented. So therefore it is important to defat to allow for a homogenoous sample that can be easily accessed. This is done by a fat soluble solvent (non-polar) like hexane

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6
Q

If you want to work with fat in sample it is important to protect from lipid oxidation, how is rhat done?

A
  1. store sample under nitrogen or vaccum (no oxygen avaiable)
  2. add antioxdiants if it does not interfere with anaylsis
  3. control storage conditions→ dark as to avoid light initiated photooxidation
  4. store in low temperatures
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7
Q

Since enzymes can degrade food components it is important to inactive/eliminate them, how is this done?

A
  1. heat treatmeant to inactivate enzymes in nonheat senstive foods
  2. freezer storage
  3. change pH
  4. salting out
  5. addition of reducing agents for oxidative enzymes
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8
Q

how can you decrease/prevent microbrial growth/contamination

A
  1. freezing
  2. driving
  3. chemical perservatives (benzoates, nitrites, sulphites)
  4. a combo of methods above
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9
Q

why is protien extraction done and what are the products?

A

this is done to get a higher protien content than the raw material \

products:

  1. flour= less than 30% protien
  2. concentraate=30-85%
  3. isolate= more than 85%
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10
Q

distinguish between wet and dry processing methods of protien extractions

A

wet processing methods are done to get a higher purity, as dry methods cannot give you an isolate. Dry and wet are used to obtain concentrates. Wet methods extract protiens based on 2 properties→ solubility and size and then have coressponding techinques

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11
Q

what are the drawbacks of using wet extraction methods?’

A
  • use of chemicals, water and energy have a high cost and negative impact on enviroment
  • loss of functional protien properties because of harsh conditixtions
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12
Q

what is the flowchart of wet extraction?

A
  1. raw material goes through milling and defating to result in flour
  2. the flour is defatted and then the first seperation step happens which is done by alkaline/acid/salt/alchohol extraction
  3. this results in a soluble protien the extract and the residue which is insoluble materials and is discarded
  4. the extract goes through precipitation/ultrafiltration to result in percipitate wich is non soluble and then the supernatant which is soluble
  5. the supernatant goes through ultrafitltration, diafiltration, spray/freeze dry and results in protien isolate 2
    1. the percipitate is wash, neutralized and spray/freeze dried to result in protien isolate/concentrate 1
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13
Q

what are the steps of alkaline extraction?

A

whole pulse→milling→ alkali extraction (protien is very soluble in alkaline conditions)→centrifugation (seperates soluble protiens from insoluble)→isolectric precipitation (pH is adjusted to isolectric point, there is no repulsion because no charge which will cause soluble protien to percipitate)→centrifugation (seperates percipated protiens from other soluble compounds)→drying→milling

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14
Q

what is the process of salting in/out (micellization)?

A
  1. Salting In: At low salt concentrations, proteins become more soluble in water. This happens because the salt helps reduce electrostatic interactions between protein molecules, which would normally cause them to stick together. By breaking up these interactions, the proteins remain dissolved in the solution. This is called the “salting-in” effect.
  2. Salting Out:As the salt concentration increases beyond a certain point, the opposite happens: proteins start to precipitate (come out of solution). This is because the salt binds to water molecules, leaving less water available to hydrate the proteins. Without enough water, the proteins clump together and precipitate out of the solution. This process is called “salting out.”
  • Salting in occurs at low salt concentrations and increases protein solubility.
  • Salting out occurs at high salt concentrations and causes proteins to precipitate out.
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15
Q

what is a common salt used in micellization and why?

A

ammonium sulfate (NH4)2SO4 because it has a high water solubilitgy

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16
Q

what is the problem with the salting in and out techinque?

A

large concentrations of salt that are needed contaminate the solution and need to be removed before the protien is resolubilized

17
Q

what is the isolectric point of a protien?

A

the pH where the net charge on the protien is zero

18
Q

what is the principle of isolectric percipitation?

A

protiens tend to percipitate/aggregate at their pI since there is no electrostatic repulsion from charges keeping them apart. The pI differs from protien to protien, so when one pI is reached that protien will be percipitated and the protiens with different pIs will remain in solution. The percipitated protien can be resolubilized in another solution at a different pH

19
Q

what is the process of acid wash extraction

A

this is used for soybean protien which is insoluble in water at a pH of 4.2. The acid will change the pH, reaching the isolectric point of soybean protien. This allows for the dissolving of sugars with no special solvents and is a lot safer because of that

20
Q

what are the common steps of preparing soyprotien isolate?

A

processes is done to seperate fibers of carbohydrates from soy protien concentrate. 1. use alkaline water at pH 8-9 and then 2. isolectric focussing at pH 4.2-4.5 by hydrochloric/phosphoric acid to adjust pH. 3. Then remove insoluble protiens from soluble carbs by centrifugation

21
Q

what is the idea behind solevent fractionation and how is it done?

A

The idea here is that the solubility of a protien depends on the dielectric constant of the solution surrounded the protien. If there are charges your protien will be stable and soluble→ but remove those charges and the protien will percipitate as it is less soluble. in other words as the dielectric constant of a solution decreases there is an increase in interactions between protien molecules as there is decreased repulsion→ resulting in percipitation.

This is done by adding water soluble ogranic solvents like acetone or ethanol as they decrease the dielectric constant of aqeuous solutions

22
Q

why is solvent fractionation done at 0 degrees or below??

A

because organic solvent+ water= heat so need to ensure the solution is cool to prevent denaturation by heat

23
Q

what is the amount of organic solvent required in solvent fractionation dependent on?

A

depends on the protien, normally varies from 5-60%

24
Q

what is aqueos alcohol extraction used for and what is the process?

A

it is used for soy protien isolate. defatted soy flakes are used as the raw material→ aqueos alchohol is added and sugars are disolved and protien percipitates→alchohol is recovered by evaporation→ protien flakes are dried with hot air and milled

25
Q

explain how heat is used for soy protien extraction

A

if protien is heat stable like in the case of soy protien, seperation from protiens and other things can be done by heat. By heating the protien the protien is unfolded and coagulated which causes percipitation. Sugars are removed by using hot water

26
Q

what is dialysis

A

it is a process used to seperate molecules in solution by the use of semipermeable membranes that allow for smaller molecules to pass but prevent larger molecules from passing

27
Q

what is the process of diaylisis?

A

protien solution is placed in a diaylsis tubing which sealed and placed in a large volume of water or buffer and is slowly stired. This process can take up to 12 hours to be completed. The solutes with low molecular weights will flow through the bag and the large ones will stay in the bag (the protiens).This is often used after salting out to remove salt

28
Q

what is ultrafiltration

A

a dyalsis process with the addition of pressure, making this a much faster techinque. It is important to note that the semipermeable membranes have a cutoff point, anything larger than that number cannot get out

29
Q

what is the result of ultrafiltration

A

Retenate and ultrafiltrate

retenate is the portion retained by the cell→ the large molecules

ultrafiltrate is the the parts that pass through the membrane→ small molecules

30
Q

what is diafiltration?

A

a speciliazed ultrafiltration process where the retenate is diluted with water and ultrafiltered again to enhance purity and yield

31
Q

explain what gel permeation is

A

Molecules pass through a hydrophilic polymer and will be seperated by size. The polymer beads are made of cross linked dextran which is very porous so small protiens will enter these beads as they get stuck in the pores and will get out slower, but larger protiens will come out first as they cant fit in the pores.

32
Q

explain what polyacrylamide gel electrophersis is

A

the electrophersis seperates protiens based on size using an electrical current, the small ones move faster in porous gel than the large ones

33
Q

what is the process of dry extraction (air classification)?

A
  1. material is milled to get a flour (milling mechanically detaches protien from other cellular compounds)→ samples that contain oil must be defatted
  2. air stream is applied to the flour
34
Q

what 2 fractions are obtained from dry extraction

A
  1. light or fine fractions (protiens)
  2. heavy/coarse fraction (starch)
35
Q

what can be done to get higher purity of protien concentrates?

A

milling and air classification can be reapeated

36
Q

what are the advantages of dry extraction?

A
  • no solvent used (prep doesnt count)
  • reduced water consumption and energy
  • protiens have better functionality since they keep their native properties since there is no heating because no drying step and no exposure to chemicals
37
Q

what are the disadvantages of dry extraction?

A
  • less efficient in seperating protiens compared to wet methods
  • higher amounts of ANF, oils, fibers
  • if starch is present and it has similar properties to protien this method may not be abke to serparate strach
  • moisture and lipid content in flour can affect fractitionation efficiency