Bile Aesculin Azide Agar, 500g

R6,100.89

Available on backorder

For the detection and enumeration of intestinal enterococci (faecal streptococci) acc. to ISO 7899-2

For items in stock, allow 3-5 working days delivery period within South Africa

and 7-10 working days for orders within Southern Africa

Description

Mode of Action
The presence of intestinal enterococci, also termed faecal streptococci, serves as an indicator for faecal contamination, particularly when the contamination took place a long time ago and the less resistant coliform bacteria, including Escherichia coli, may be already dead when the analysis is carried out.


Bile salt aesculin azide agar is employed acc. to ISO 7899-2 as a confirmation and enumeration medium for typical isolate on the primary isolation Membrane Enterococcus Selective Agar acc. to Slanetz and Bartley.
Enterococci and some species of the genus Streptococcus namely S. bovis and S. equines can reproduce normally in this medium.
Esculin hydrolysis and bile tolerances are regarded as reliable characteristics of enterococci (FACKLAM 1971,1973).
Intestinal Enterococci hydrolyse the glycoside esculin to give dextrose and esculetin. Esculetin forms an olive green to black complex with iron(III) ions.
Enterococci are bile tolerant. Bile salts inhibit the growth of numerous accompanying bacteria. The concentration of sodium azide present in this medium largely inhibits the growth of the accompanying Gram-negative microbial flora, while sparing the enterococci.
The use of sodium azide as a selective inhibitor for Gramnegative bacteria was reported in the studies of EDWARDS
(1933, 1938) and HARTMANN (1936) on the isolation of Str.agalactiae. MALLMANN (1940) and SNYDER and LICHSTEIN(1940) later showed that sodium azide can also be used for the isolation of enterococci from water.


Typical Composition (g/litre)
Peptone from Casein 17.0; peptone 3.0; yeast extract 5.0; sodium chloride 5.5; aesculin 1.0; ammonium iron(III) citrate 0.5; ox bile 10.0; sodium azide 0.15; agar-agar 13.0:


Preparation
Suspend 54.65 g in 1 litre water and dissolve by boiling. Sterilise for 15 min. at 121 °C. After cooling to 45-50 °C pour into Petridishes to a depth of 3 mm to 5 mm and allow to solidify.
pH: 7.1 ± 0.2 at 25 °C.
The plates are clear and yellow.
Poured plates can be stored at +2 – +8°C for up to 2 weeks.


Experimental Procedure and Evaluation
For the confirmation typical red, maroon or pink coloured colonies on membrane filter Enterococcus selective agar acc. to Slanetz and Bartley  are transferred, with sterile forceps without inverting the filter onto
a plate of bile salt aesculin azide agar which has been pre-heated at 44°C. After the inoculation plates are incubated at 44 ± 0.5°C for 2h.
Regard all typical colonies showing a tan to black colouration in the surrounding medium as giving a positive reaction and count as intestinal enterococci.

Additional information

Weight 0.5 kg

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