Milk is the secretion of mammary glands in humans and animals after childbirth. It provides complete nutrition for newborns as it contains carbohydrates, lipids, proteins, minerals, and vitamins. Milk's composition varies between species, with human milk containing less protein and minerals than cow's milk. Milk is made up of water, organic constituents like proteins (casein, lactalbumin, lactoglobulin), lipids, and carbohydrates (lactose), and inorganic constituents including minerals and vitamins. Its physical properties include white color, slightly acidic pH, specific gravity, taste, odor, and freezing/boiling points. Milk undergoes changes through processing like pasteurization, sterilization, and cheese/
2. Def:
It is the secretion of mammary glands in human and animals
after labour.
It is the only food for newborn for a long period till weaning
time.
Before birth the fetus receives its nutrition through the
placenta.
2
3. Milk secretion is stimulated by Prolactin.
Milk flow is decreased by Estrogen and
Progesterone while increased by
Thyroxin.
Also Squalene present in HELBA
increase milk flow.
Initiation of lactation may result from
sudden removal of the placenta and other
factors.
Oxytocin (posterior pituitary hormone)
responsible for milk ejection
3
4. Milk is considered as a complete diet as:-
It contains all of the components necessary for growth,
maintenance of life and reproduction.
e.g:
Carbohydrates, Lipid, Protein, Minerals and Vitamins.
But, it is deficient in:
Vitamin C, Vitamin D, Vitamin K, Iron, Copper
4
6. Property 1- Color
White color → due to presence of:
Fat globules in emulsion form.
Protein in colloidal form.
Ca. phosphate and Ca. Casinate.
Yellowish (creamy) color → due to presence of
Carotene and
Xanthophyll pigments (specially in cow's milk) and
colostrums (1st fresh milk in pregnancy).
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7. Property 2 - Reaction
Fresh milk is amphoteric in reaction as it contains acid & base.
Milk is an excellent buffer as it contain:
Protein.
Phosphate.
Bicarbonate.
Citrate.
pH of fresh milk:
6.6 – 6.8 Cow's milk.
6.8 – 7.4 Human's milk
Milk pH is changed to alkaline in case of:
Mastitis
Late period of lactation.
If the milk left to stand for a long period specially in warm
temperature, lactose is fermented to lactic acid by bacteria present
normally in milk as:
Streptococcus Lactis
Lactobacillus Lactis
7
8. Property 3 – Specific Gravity
It is the ratio between weight of a given volume of milk
compared with the same volume of water at a specific
temperature. Measured by Lactometer
It measure total solids of milk, and determine if any
constituent added or removed from milk..
Normal specific gravity:
1020 – 1030 Cow's milk.
1030 – 1035 Human's milk.
Fat is the only constituent in milk with specific gravity
lower than 1000, so, when fat present in milk in high
amount, specific gravity decrease than normal values.
8
9. Property 4 – Taste
Normal characteristic milky taste.
Milk taste changed in case of :
Souring: due to increased acidity.
Boiling: due to certain biochemical changes and
evaporation of volatile fatty acids.
Late stage of lactation: due to increase chloride
percent.
Mastitis: inflammation of udder.
Property 5 - Odor
Characteristic milky odor
9
10. Property 6 – Freezing point of milk
It is the temperature at which the liquid milk freeze or
crystallize.
The freezing point of cow or buffalo milk ranges from (-
0.53) to (-0.57) °C with average (-0.55) °C
Milk freezes at a temperature slightly lower than that of
water due to the soluble constituents in milk such as
lactose, minerals which lower the freezing point.
This test is important for detection of the amount of water
added to pure milk
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11. Addition of Water to Milk
The addition of 9% water to milk will raise the
freezing point by 0.05 °C.
i.e., if milk freezing point is -0.45 °C, it means addition
of 18% water.
-0.45 – (-0.55) = -0.45 + 0.55 = +0.10
0.05 → 9 %
0.10 → X
X = = 18 %
9x0.1
0.05
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12. Property 7 – Boiling Point
Milk boiling point is 100.5 °C , more than water due to
presence of dissolving substances
Property 8 – Cream Line Formation
When milk left at room temperature the fat globules
coalesce, clumped at surface of the container and form
cream line.
12
16. 1- Protein:
Milk protein less in human than in cow's milk.
All milk protein synthesized in the mammary gland.
Milk protein of high coefficient digestibility (85 – 95%)
X 100
Amount of N2 absorbed
Total N2 in the protein
Total amount of protein differ according to species and affect
rate of growth
Young rabbit reach double weight in 5 days as milk protein 10 gm/dl.
Young calf reaches double weight in 50 days as milk protein 3.7 gm/dl.
Young child reach double weight in 5 - 8 months as milk protein 1.5 gm/dl.
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18. (i) Casein
It is the main and most dominant milk protein.
Casein is the only milk protein that not coagulated on
boiling.
It represents 25% in human's milk and 83% in cow's
milk.
It is a compound protein (Phospho-protein) of high
biological value.
The high phosphate content of casein allows it to
associate with calcium and form calcium phosphate
salts.
So, at normal PH of fresh milk (6.6 PH)
casein present as insoluble Ca. caseinate
phosphate complex.
18
19. Casein is deficient in cystiene and cystin so give negative
result with sulpher test.
Casein : (Lactalbumin - Lactglobulin) ratio is 1:3 which
facilitate its digestion.
According to molecular weight and electrophoresis
process, casein is separated in to 3 fractions, each one of
them has its own amino acid composition :
α Casein → 75%.
β Casein → 22%.
γ Casein → 3%.
1
=
Casein
3
Lactalbumin + Lactglobulin
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22. Milk Souring (Milk Curdling – Zabadi)
The principle of coagulation, or curd formation, at acidic
pH is the basis for Yoghurt (Zabadi) formation. How?
Fermentation of lactose to lactic acid by:
Lactic acid producing bacteria present normally in milk.
Addition of acid (acetic acid).
Addition of starter culture (yoghurt).
Lactose + lactic acid bacteria Lactic acid ↓ pH
Worm temp.
Fermentation
22
23. Milk Clotting (Cheese Manufacturing)
During digestion (in new born):
Rennin enzyme acts on casein, converting it to soluble
Paracaseinate which is bounded to Ca and form insoluble
Ca. paracaseinate (milk clot).
Rennin enzyme:
Derived from 4th stomach of calves and used externally in
cheese manufacture.
It is secreted inactive as pro-rennin.
Its optimum PH 4.
It is absent in adult stomach.
Formation of milk clot: prevents rapid passage of milk from
stomach to intestine so give the sense of fullness to
newborn.
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25. (ii) Lactalbumin
Represent 87% of whey protein.
PPT by full saturation with ammonium sulphate.
Rich in cystein and cystin so give +ve result with sulpher test.
Simple, soluble and easily digested protein.
Consists of two fractions:
α Lactalbumin 32% of whey protein.
β lactglobulin 55% of whey protein.
Where,
β lactglobulin called globulin because it need small amount of
NaCl to be dissolved but it is not PPT by half saturation as
albumin.
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26. (iii) Lactglobulin
Represent 13% of whey protein.
PPT by half saturation with ammonium sulphate solution.
Rich in cystein and cystin so give +ve result with sulpher test.
Simple, soluble and easily digested protein.
Consists of two fractions:
True globulin (Euglobulin) 50%.
False globulin (Pseudoglobulin) 50%.
They carry antibodies causing immunity so called
immunoglobulins.
They present in higher concentration in colostrum.
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28. 1- Catalase:
Carried by fat globules.
Act on hydrogen peroxide (H2O2) producing water and
oxygen.
Increased in case of mastitis.
2- Xanthin oxidase:
Carried by fat globules.
Act on hypoxanthin and xanthin to produce uric acid.
Milk enzymes
28
29. 3- Peroxidase:
Carried by lactalbumin.
Act on hydrogen peroxide (H2O2).
It is heat stable enzyme (resist destruction by heat).
It is destroyed by milk sterilization.
Milk sterilization:
Heating of milk to 116◦C for 15 minutes which destroy all
harmful and non harmful microorganisms.
Milk sterilization leads to alteration in milk taste and
destruction of vitamin C and vitamin B2.
N.B:
Absence of peroxidase enzyme indicates milk sterilization.
Milk enzymes
29
30. 4 - Alkaline phophatase:
Carried by fat globules.
Catalyze hydrolysis of phosphate ester.
Destroyed by the same temperature that destroys the
harmful bacteria.
e.g:
Tubercle bacilli.
Absence of Alkaline phophatase enzyme indicates milk
pasteurization.
Milk pasteurization:
Heating of milk to 60◦C for 30 minutes or 70◦C for 15 minutes
followed by sudden cooling which destroy the harmful
microorganisms only.
Milk enzymes
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31. 5- Amylase:
Carried by lactalbumin.
Catalyze hydrolysis of α 1, 4 glycosidic linkage of starch and glycogen.
Increased in case of mastitis.
Milk enzymes
6- Lipase:
Carried by casein.
Catalyze hydrolysis of primary ester linkage in triacylglycerol.
Act on milk fat producing free fatty acids and undesirable taste
(Rancidity).
7- Aldehyde oxidase (Schardinger's enzyme):
Its absence indicates milk boiling.
Schardinger's test:
Milk + Methyl blue + Formaldehyde
Blue color appeared in case of boiled milk.
Colorless in case of unboiled milk.
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32. Beside milk proteins milk also contains:
A) Lactoferrin binding protein:
It contains iron which is bounded to a glycoprotein.
It facilitates iron transport and storage.
Found in high concentration in human colostrums and milk.
B) Vitamin B12 binding protein:
It carries vitamin B12.
Lactoferrin and vitamin B12 binding protein deprive
pathogenic intestinal bacteria from iron and vitamin B12 so
they have bacteriostatic action.
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34. C) Carbohydrates:
Lactose (milk sugar) is the only carbohydrate of milk.
It is a reducing disaccharide consists of glucose and
galactose.
Human's milk contains 7% lactose while cow's milk contains
5% lactose.
Lactose may be excreted in urine during last third of
pregnancy physiologically so it should be differentiated from
glucose by osazon test.
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36. 1- Minerals:
Human milk contain less mineral elements (0.4%) than cow's milk (0.8%).
Milk rich in Ca and P which are present in their proper ratio for
absorption (2:1) in human milk while in cow's milk (1:2) which is not
suitable for their maximum absorption .
Ca and P are essential for:
1. Growth of bone and teeth.
2. Stability of casein.
Milk is deficient in Fe and Cu which are supplied by their storage in
liver during prenatal life (this store is sufficient till weaning time).
N.B:
Milk is deficient in Iron but it is more in human milk than cow's milk
Thus anaemia in breast feeding is less common.
Milk contain adequate amount of Na, K, Mg.
Human milk contains Na:K (1:2) which is suitable for the optimal
growth of newborn.
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37. 2- Vitamins:
Milk is deficient in: Vitamin C, Vitamin D, Vitamin K.
Milk contain adequate amount of vitamin B complex which are sufficient
for first week of life. e.g: Pantothenic acid
Although milk is deficient in Fe, Cu, vitamin C, vitamin D, and vitamin K it
is complete natural food for the following reasons:
1. Easily digested absorbed and metabolized.
2. Contain all the nutrients required for the newborn at early stage of
life.
3. Balanced ratio between carbohydrates, lipid and protein.
4. Milk Protein of high biological value as:
It contains all essential amino acids.
Easily digested.
Easily absorbed.
Easily metabolized.
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39. Definition:
It is a process by which cow's milk is made to be as near as
human's milk.
Aim:
Protein of human's milk (casein) form 25% of milk protein
while casein in cow's milk form 5/6 of milk protein so it
form dense clot in newborn stomach which can't be
digested leading to vomition.
Lactose in human's milk higher than that in cow's milk
(7:5).
39
40. Steps:
1. Pasteurization of milk:
Heating of milk to 60 ◦C for 30 minutes followed by sudden
cooling then the pasteurized milk left in cool place for 4 hours
to allow separation of cream.
2. Separate the cream and the residual milk called
Skimmed milk.
3. Skimmed milk is divided to two halves.
To one half add:
Separated cream.
Equal amount of water.
Complete lactose to 7%.
Iron, vitamin C, vitamin D may be added.
4. Mix well then sterilize the milk:
Heating of milk to 116 ◦C for 15 minutes.
40
41. Advantages of human milk (Breast Feeding)
1. Psychological effect on both child and mother.
2. Breast milk is supplied in suitable temperature.
3. Sterile and not liable to be contaminated.
4. Cheaper than animal milk.
5. Not liable to adulteration.
6. Lactation may act as a contraceptive measure.
7. Lactation minimize the risk of breast tumors.
8. Lactation help involution of the uterus.
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43. Defn: Lactose in milk is estimated in the clear filtrate after
precipitating proteins. Tungestic acid, and
Trichloroacetic acid can be used to precipitate milk
proteins.
Useful Instruments:
1. Estimated pipette.
2. Volumetric flask.
3. Funnel.
4. Beaker.
5. Burette.
6. Burette holder.
7. Porcelain dish.
43
44. Procedures:
a) PPT of casein:
In a clean dry volumetric flask add:
5ml of milk
5ml of 10% sodium tungstate solution
5ml of 2/3 N sulphuric acid drop by drop.
Shake gently after each addition .
Complete to the 100-ml mark by distilled water.
Left for sometime (1/4 – 1/2 hr) until the precipitate of
casein settles down.
b) Filtration:
Filter into a dry clean beaker.
The filtrate must be clear, if not refilter again
44
45. c) Reduction:
When about half the volume is filtered, wash the burette
with little of the filtrate.
Then fill the burette with the filtrate.
In a porcelain dish place:
10 ml of Fehling’s solution.
20 ml of distilled water.
Heat the Fehling’s solution until it gently boils and
Begin the reduction adding the filtrate slowly and regularly
in order to keep Fehling’s solution boiling all the time.
Continue the reduction until the last trace of blue color is
just discharged.
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46. d) Calculation:
R = number of mls of the filterate used for complete
reduction of fehling’s solution.
10 ml Fehling’s solution are completely reduced by
0.0678 gm lactose.
Total dilution of milk (T.D):
Lactose in milk (g%):
0.0678 x 20 x 100
Lactose in milk =
R
100
20 =
5
46
48. Principle of the test:
The quantitative determination of glucose or lactose in
gm/dl in the solution depends upon their reducing
property to Fehling’s solution.
Instruments used in the estimation:
Pipette 5 and 10-ml capacity.
Conical flask of 100 cc capacity.
Burette 50 ml capacity
Burette holder.
Porcelain dish.
Beaker.
48
49. Reagents and solutions required:
Glucose or lactose, solution under estimation.
Fehling quantitative reagent.
Potassium ferrocyanide acidified with glacial acetic acid
(external indicator).
Significance of the test:
This test considered the bases of tests used for the
determination of blood glucose.
Used for estimation of lactose in milk, for detection of
adulteration of milk by the addition of water.
49
50. procedures:
(A) Rough estimation:
Fill the burette with glucose or lactose solution after its careful
rinsing with water.
Put in the porcelain dish
10-ml of Fehling quantitative reagent.
20 ml of distilled.
Heat until the Fehling boils in the dish.
Begin the reduction by slow addition of solution in order to
keep the Fehling boiling all the time.
Continue reduction till the last trace of the blue color of the
Fehling’s reagent turn to red brown PPT of Cu2O.
Record the rough reading R (number of mls of glucose or
lactose descended from the burette).
If the (R) rough reading is below 5ml make dilution to the
glucose or the lactose solution under the estimation.
If the (R) rough reading is above 5ml calculate the percentage of
glucose or the lactose solution under the estimation.
50
51. (B) Preparation of diluted sugar solution:
Mutiply the (R) by 4.
The result is equaled to 5, 10 or 20.
In 100 ml volumetric flask add:
? ml of the glucose or lactose sugar solution.
Completed with distilled water to 100 ml mark and well
mixed.
In this case the sugar solution is diluted 5, 10 or 20 times.
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52. (C) Accurate estimation:
Wash the burette with distilled water and rinse it with little of
diluted sugar,
fill it again with the diluted sugar.
In the porcelain dish add:
10 ml of Fehling’s quantitative solution.
20 ml of distilled water.
Heat till gentile boiling.
Begin the reduction by slow addition of the diluted sugar
solution drop by drop in order to keep the Fehling’s solution
boiling all the time.
Continue reduction till the last trace of the blue color
disappeared and changed to red brown PPT of Cu2O
52
53. Using an external indicator near the end point (Potassium
Ferrocyanide solution acidified with Glacial Acetic acid) to
ensure the complete reduction of Fehling's solution:
If no brown color or PPT is formed on the addition of one
drop of the solution to the external indicator it indicates:
complete reduction of Fehling's solution.
If brown color or PPT appeared it indicates:
Incomplete reduction of Fehling's solution.
Complete reduction till the yellow color of the indicator
doesn’t change.
Record the number of mls used for reduction of 10 ml Fehling’s
quantitative solution and give it symbol (V) ml.
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54. (D) Calculation:
10 ml Fehling’s solution are completely reduced by 0.0678 gm
lactose.
g/dl
0.0678 x T.D x 100
Lactose in solution =
V
g/dl
0.0678 x 100
Lactose in solution =
R
10 ml Fehling’s solution are completely reduced by 0.05 gm
glucose.
g/dl
0.05 x 100
Glucose in solution =
R
g/dl
0.05 x T.D x 100
Glucose in solution =
V
54