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Wikipedia / Eagle's minimal essential medium

Minimal essential medium (MEM) is a synthetic cell culture medium developed by Harry Eagle first published in 1959 in Science that can be used to maintain cells in tissue culture. It is based on six salts and glucose described in Earle's salts in 1943: calcium chloride, potassium chloride, magnesium sulfate, sodium chloride, sodium phosphate and sodium bicarbonate. The medium is further supplemented with thirteen essential amino acids, and eight vitamins: thiamine (vitamin B1), riboflavin (vitamin B2), nicotinamide (vitamin B3), pantothenic acid (vitamin B5), pyrodoxine (vitamin B6), folic acid (vitamin B9), choline, and myo-inositol (originally known as vitamin B8). Many variations of this medium have been developed, mostly adding additional vitamins, amino acids, and/or other nutrients.

Eagle developed his earlier "Basal Medium Eagle" (BME) in 1955–1957 on mouse L cells and human HeLa cells, with 13 essential amino acids and 9 vitamins added. BME contains biotin (vitamin B7), which Eagle later found to be superfluous. His 1959 "minimal essential medium" doubles the amount of many amino acids to "conform more closely to the protein composition of cultured human cells. This permits the cultures to be kept for somewhat longer periods without refeeding".

DMEM (Dulbecco's modified Eagle's medium) was originally suggested as Eagle's medium with a 'fourfold concentration of amino acids and vitamins' by Renato Dulbecco and G. Freeman published in 1959. The commercial versions of this medium have additional modifications, see an example in the table below.

α-MEM (minimal essential medium Eagle – alpha modification) is a medium based on MEM published in 1971 by Clifford P. Stanners and colleagues. It contains more non-essential amino acids, sodium pyruvate, and vitamins (ascorbic acid (vitamin C), biotin, and cyanocobalamin) compared with MEM. It can also come with lipoic acid and nucleosides.

Glasgow's MEM (Glasgow minimal essential medium) is yet another modification, prepared by Ian MacPherson and Michael Stoker.

Composition

One liter of each medium contains (in milligrams):

Medium

BME

MEM

α-MEMa

DMEM

Glycine

50

30

L-alanine

25

L-arginine hydrochloride

21

126

126

84

L-asparagine-H2O

50

L-aspartic acid

30

L-cysteine hydrochloride-H2O

100

L-cystine 2HCl

16

31

31

63

L-glutamic acid

75

L-glutamine

292

292

292

584

L-histidine

8

31

42

L-histidine hydrochloride-H2O

42

42

L-isoleucine

26

52

52

105

L-leucine

26

52

52

105

L-lysine hydrochloride

36.47

73

73

146

L-methionine

7.5

15

15

30

L-phenylalanine

16.5

32

32

66

L-proline

40

L-serine

25

42

L-threonine

24

48

48

95

L-tryptophan

4

10

10

16

L-tyrosine disodium salt dihydrate

26

52

52

104

L-valine

23.5

46

46

94

Ascorbic acid

50

Biotin

1

0.1

Choline chloride

1

1

1

4

D-calcium pantothenate

1

1

1

4

Folic acid

1

1

1

4

Niacinamide

1

1

1

4

Pyridoxal hydrochloride

1

1

1

4

Riboflavin

0.1

0.1

0.1

0.4

Thiamine hydrochloride

1

1

1

4

Vitamin B12

1.36

i-Inositol

2

2

2

7.2

Calcium chloride (CaCl2, anhyd.)

200

200

200

200

Ferric nitrate (Fe(NO3)3·9H2O)

0.1

Magnesium sulfate (MgSO4, anhyd.)

97.67

97.67

97.67

97.67

Potassium chloride (KCl)

400

400

400

400

Sodium bicarbonate (NaHCO3)

2200

2200

2200

3700

Sodium chloride (NaCl)

6800

6800

6800

6400

Sodium phosphate monobasic (NaH2PO4-H2O)

140

140

140

125

D-Glucose (dextrose)

1000

1000

1000

1000

Lipoic acid

0.2

Phenol red

10

10

10

15

Sodium pyruvate

110

110

See also

  • RPMI 1640 (Roswell Park Memorial Institute medium), for lymph cells

References