Semisolid RV HiVeg™ Medium Base

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MV1428
For isolation of Salmonella species from food stuffs and other materials based on selective motility.


Semisolid RV HiVeg™ Medium Base is used for the isolation of Salmonella from food stuffs and other materials based on selective motility.

Product Profile

Vegetable based (Code MV) Animal based (Code M)
MV1428 M1428
HiVeg hydrolysate No. 1 Tryptose
HiVeg hydrolysate Casein enzymic hydrolysate

Recommended for: Isolation of Salmonella from food stuffs and other materials based on selective motility.

Composition

Ingredients Grams/Litre
HiVeg hydrolysate No. 1 4.60
HiVeg hydrolysate 4.60
Sodium chloride 7.34
Magnesium chloride, anhydrous 10.93
Malachite green 0.037
Agar 2.70

Final pH (at 25°C) 5.4 ± 0.2

Formula adjusted, standardized to suit performance parameters.

Reconstitution

Reconstitution: 30.20 g/l

Quantity on preparation (500g): 16.55 L

pH (25°C): 5.4 ± 0.2

Supplement: IMRV / RV Selective Supplement (FD193)

Sterilization

Boiling (DO NOT AUTOCLAVE)

Storage

Dry Medium - Below 30°C, Prepared Medium 2 - 8°C.

Directions

Suspend 15.10 grams in 500 ml distilled water. Heat to boiling to dissolve the medium completely. DO NOT AUTOCLAVE. Cool to 45°C and aseptically add 1 vial of IMRV/RV Selective Supplement (FD193). Mix well and pour into sterile petri plates.

Note: The motility of Salmonellas can be drastically reduced when the agar surface becomes too dry. Hence the plates should be well dried before use. If visible moisture occurs on the lid of the plates or the surface of agar, it must be removed. While incubation, incubate the plates aerobically in an upright position for no longer than 24 hours at 42°C.

Principle and Interpretation

Semisolid RV HiVeg Medium Base is prepared by using HiVeg hydrolysates which makes the medium free from BSE/TSE risks. Semisolid RV HiVeg Medium Base is the modification of Semisolid RV Medium Base based on the formulation described by DeSmedt et al (1) for the detection of motile Salmonella species from food and environmental specimens. This medium like the conventional medium detects more Salmonella positive samples than the routinely used enrichment procedures (2, 3, 4). HiVeg hydrolysate No.1, HiVeg hydrolysate provides the nitrogenous and carbonaceous substances and other essential growth nutrients. Novobiocin and malachite green in the medium inhibits most gram positive organisms. Salmonella survives at slight high osmotic pressure owing to presence of magnesium chloride in the medium, grows at slightly low pH and is comparatively resistant to malachite green.

The working of medium is based on the ability of Salmonella species to migrate in the selective medium competing with other motile organisms, thus producing opaque halos of growth. The motile bacteria will show a halo or zone of growth originating from inoculation spot.

Quality Control

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

Gelling: Firm, comparable with 0.27% Agar gel.

Colour and Clarity: Blue coloured clear to slightly opalescent semisolid medium forms in petri plates.

Reaction: Reaction of 3.02% w/v aqueous solution is pH 5.4 ± 0.2 at 25°C.

Cultural Response

Cultural characteristics observed after an incubation at 42°C for 18-24 hours. when one drop of culture is inoculated in the centre of the medium plate.

Organisms (ATCC)

Organisms (ATCC) Inoculum (CFU) Growth Motility
Citrobacter freundii (8090) 102-103 inhibited -
Pseudomonas aeruginosa (27853) 102-103 inhibited -
Salmonella serotype Enteritidis (13076) 102-103 luxuriant + #
Salmonella serotype Typhimurium (14028) 102-103 luxuriant + #

Key: # = opaque halos of growth originating from the inoculation spot

More Information
Product Name Semisolid RV HiVeg™ Medium Base
SKU MV1428
Product Type HiVeg™
Physical Form Powder
Origin Animal Free (Veg)
Packaging type HDPE
References 1. De Smedt J.M., Balderdijk R., Rappold H. and Lautenschlaeger D., 1986, J. Food Prot., 49:510.2.De Smedt J.M., Balderdijk R., 1987, J. Food Prot., 50:658.3.De Zutter L. et al, 1991, Int. J. Food Microbiol., 13:11.4.De Smedt J.M. et al, 1991, Int. J. Food Microbiol., 13:301.
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