Brilliant Green Agar

Brilliant Green Agar

KM0038 Brilliant Green Agar is used for the selective isolation of Salmonella species from clinical specimens and food samples.

Brilliant Green Agar was first cited by Kristensen et al. and later modified to improve selectivity. The medium is highly selective and may not be suitable for the isolation of Salmonella spp. from samples where numbers of salmonellae are low. If this is suspected to be the case, or if the sample is suspected to contain Salmonella typhi, other selective media such as Xylose Lysine Deoxycholate (XLD) Agar (E&O KM0013), Hektoen Enteric Agar (E&O KM0032) or Deoxycholate Citrate Agar (E&O KM0050) may be inoculated with the specimen in parallel. The United States Pharmacopeia indicates that the medium may be used to confirm the absence of salmonellae in nutritional and dietary supplements. The medium may also be used as a secondary plating medium for subculture from selective enrichment media during food and environmental testing, and as a primary isolation medium in the identification of Salmonella species from clinical specimens according to Public Health England’s UK Standards for Microbiology Investigations.

Additional Information

Shelf Life (days)

Storage Temp (°C)

Dehydrated Medium Appearance

Prepared Medium Appearance

Dehydrated Medium Colour

Prepared Medium Colour

Dehydrated pH

Prepared pH

Product Description

Organisms Ref. No Result
Salmonella typhimurium NCTC 12023 Growth: Red colonies
Salmonella enteritidis ATCC 13076 Growth: Red colonies
Escherichia coli NCTC 12241 Inhibited
Enterococcus faecalis NCTC 12697 Inhibited

Formula*

g/L
Beef extract 5.0
Peptone 10.0
Yeast extract 3.0
Di-sodium hydrogen phosphate 1.0
Sodium di-hydrogen phosphate 0.6
Lactose 10.0
Sucrose 10.0
Phenol red 0.09
Brilliant green 0.0047
Agar 12.0
Total 52.0
*Adjusted/supplemented as required to meet performance requirements

Preparation

Suspend 52g of the medium in one litre of deionised / purified water. Allow the medium to soak whilst mixing for 10 minutes. Heat with frequent agitation and boil for one minute to completely dissolve the medium. DO NOT AUTOCLAVE this medium. Cool to 45-50°C and aseptically dispense into appropriate sterile containers.