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TSC Agar, Fluorocult (Fluorocult TSC Agar) (Fluorocult Tryptose Sulfite Cycloserine Agar) (Tryptose Sulfite Cycloserine Agar, Fluorocult)

[所屬分類:培養基配方] [發布時間:2021-12-24] [發布人:網站管理員2] [閱讀次數:] [返回]

TSC Agar, Fluorocult
(Fluorocult TSC Agar)
(Fluorocult Tryptose Sulfite
Cycloserine Agar)
(Tryptose Sulfite Cycloserine
Agar, Fluorocult)

山東拓普生物工程有限公司 培養基配方 //ljxinglong.com

Composition per liter:

Agar ..................................................................15.0g
Tryptose ............................................................15.0g
Peptone from soymeal ........................................5.0g
Yeast extract........................................................5.0g
Na2S2O5 ..............................................................1.0g
Ammonium ferric citrate ....................................1.0g
D-Cycloserine......................................................0.2g
4-Methylumbelliferyl-phosphate
disodium salt ...........................................50.0mg
Source: This medium is available from Merck.
Preparation of Medium: Add components to
distilled/deionized water and bring volume to 1.0L.
Mix thoroughly. Autoclave for 15 min at 15 psi pres
sure–121°C. Cool to 45°–50°C. Pour into sterile Petri
dishes.
Use: For the isolation and enumeration of the vege
tative and spore forms of Clostridium perfringens in
foodstuffs. The culture medium complies with the
recommendations of the International Organization
for Standardization (ISO) (1978) and the DIN Norm
10165 for the examination of meat and meat prod
ucts. It also conforms with the APHA recommenda
tions for the examination of foods (1992). D-Cyclo
serine inhibits the accompanying bacterial flora and
causes the colonies which develop to remain smaller.
4-Methylumbelliferyl-phosphate (MUP) is a fluoro
genic substrate for the alkaline and acid phosphatase.
The acid phosphatase is a highly specific indicator
for C. perfringens. The acid phosphatase splits the
fluorogenic substrate MUP forming 4-methylumbel
liferone which can be identified by its fluorescence in
long wave UV light. Thus a strong suggestion for the
presence of C. perfringens can be obtained.

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