Rippey-Cabelli HiVeg™ Agar Base

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MV859
Used for differential and selective isolation of Aeromonas hydrophila species from water samples using membrane filtration technique.


Intended Use

Rippey-Cabelli HiVeg Agar Base is recommended for differential and selective cultivation of Aeromonas hydrophila from water samples using membrane filter technique.

Composition

Ingredients Grams/Litre
HiVeg hydrolysate No. 1 5.0
Trehalose 5.0
Yeast extract 2.0
Sodium chloride 3.0
Potassium chloride 2.0
Magnesium sulphate 0.2
Iron (III) Chloride 0.1
Bromo thymol blue 0.04
Agar 15.0
Final pH (at 25°C) 8.0 ± 0.2

Formula adjusted, standardized to suit performance parameters.

Product Profile

Vegetable based (Code MV) Animal based (Code M)
MV859 HiVeg hydrolysate No. 1 M859 Tryptose
Recommended for Differential and selective cultivation of Aeromonas species from water samples using membrane filter technique.
Reconstitution 32.34 g/l
Quantity on preparation (100g) 3.09 L
pH (25°C) 8.0 ± 0.2
Supplement Rippey-Cabelli Supplement (FD107), Ethanol.
Sterilization 121°C / 15 minutes.
Storage Dry Medium - Below 30°C, Prepared Medium 2-8°C.

Directions

Suspend 16.17 grams in 500 ml distilled water. Heat to boiling to dissolve the medium completely. Sterilize by autoclaving at 15 lbs pressure (121°C) for 15 minutes. Cool to 50°C and aseptically add 10 ml ethanol and rehydrated contents of 1 vial of Rippey-Cabelli Supplement (FD107). Mix well before pouring into sterile petriplates.

Principle and Interpretation

This medium is prepared by replacing Tryptose with HiVeg hydrolysate No 1 which makes the medium free of BSE/ TSE risks. Rippey-Cabelli HiVeg Agar Base is the modification of Rippey-Cabelli (RC) Agar formulated by Rippey and Cabelli (1). The medium is differential as it depends on ability of organisms to ferment trehalose. HiVeg hydrolysate and yeast extract support the growth of Aeromonas species. Ampicillin, and ethanol are the selective agents inhibiting gram positive bacteria, coliforms, Shigella species, Proteus mirabilis and Actinomyces. Ethanol inhibits overgrowth of Klebsiella species on the filter. Ampicillin is unsuitable as a selective agent with Plesiomonas (2). The limitation of medium is that it fails to recognize lysine-positive Aeromonas strains. As most enteric organisms ferment trehalose, specificity of this medium is insufficient due to clear characteristics to distinguish Aeromonas colonies from the Enterobacteriaceae (3). Sensitivity and specificity are higher when pure cultures are used (4).

Quality Control

Appearance of powder: Light green coloured, homogeneous, free flowing powder.

Gelling

Firm, comparable with 1.5% Agar gel.

Colour and Clarity

Dark green coloured, clear to slightly opalescent gel forms in petri plates.

Reaction

Reaction of 3.23% w/v aqueous solution is pH 8.0 ± 0.2 at 25°C

Cultural Response

Cultural characteristics observed after an incubation at 35-37°C for 24 hours on addition of Rippey-Cabelli Suplement (FD107).

Organisms (ATCC) Inoculum (CFU) Growth Recovery Trehalose fermentation
Aeromonas hydrophila (7966) 102-103 luxuriant >50% +
Escherichia coli (25922) 102-103 none-poor <20% -
Shigella flexneri (12022) 102-103 inhibited 0% -
Staphylococcus aureus (25923) 102-103 inhibited 0% -

Key: + = acid production, yellow colour

- = no colour change (blue-green colour)

References

  1. Rippey S.R. and Cabelli V.J., 1979, Appl. Environ. Microbiol. 38 (1):108.
  2. Von Graevenitz A. and Bucher C., 1983, J. Clin. Microbiol, 17 (1):16.
  3. Roland, F.P., 1977, Med. Microbiol. Immunol., 163:241.
  4. MacFaddin J.F., 1985, Media for Isolation Identification Cultivation and Maintenance of Medical bacteria, Vol. I Williams and Wilkins, Baltimore.
More Information
Product Name Rippey-Cabelli HiVeg™ Agar Base
SKU MV859
Product Type HiVeg™
Physical Form Powder
Origin Animal Free (Veg)
Packaging type HDPE
References 1. Eaton A. D., Clesceri L. S. and Greenberg A. E., (Eds.), 1995, Standard Methods for the Examination of Water andWastewater, 19th Ed., American Public Health Association, Washington, D.C.2.Austin B., Altwegg M., Gosling P. and Joseph S. W., (Eds.), 1996, The Genus Aeromonas, John Wiley and Sons, Chichester ,U.K.3.Rippey S. R. and Cabelli V. J., 1979, Appl. Environ. Microbiol., 38(1): 108.4.MacFaddin J. F., 1985, Media for Isolation-Identification-Cultivation-Maintenance of Medical Bacteria, Vol. I Williamsand Wilkins, Baltimore.5.Roland, F. P., 1977, Med. Microbiol. Immunol., 163:241.6.Von Graevenitz A. and Bucher C., 1983, J. Clin. Microbiol., 17(1):16.
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