This site is a B2B information site for professional use - clinical diagnostics products listed are for
Research Use Only unless otherwise stated.
MMGA - Merck 's New Complete Medium for the Resuscitation of Sublethally Injured E. coli
Mineral Modified Glutamate Agar, MMGA Merck's new complete medium for the resuscitation of sublethally injured E. coli according to ISO 16649 Part 1
Resuscitation, a mandatory method for sublethally injured E. coli in food and foodstuff.
During food processing, such as heating, drying, chemical preservation, freeze-drying or acidification, organisms like E. coli can be injured. Consequently, they do not growth reliably on strongly selective media, e.g. TBX agar, which can cause false negative results.
To minimize the risk, ISO 16649 Part 1 recommended a resuscitation step to allow the E. coli to recover; MMGA is the medium used for this recovery step.
In the past, food business operators preparing MMGA used e.g. DEV glutamate broth to which the agar had to be added. As other media used did not even contain glutamate, they also had to add a glutamate solution.
For convenience, this new medium Mineral Modified Glutamate Agar (Cat. No. 1.09045) from Merck includes both glutamate and agar and, of course, is granulated for safety reasons. With its unique combination of glutamate, selected minerals and agar, the use of Merck's MMGA results in a very rapid and effective recovery of injured E. coli.
After incubation at 37°C for only 4 hours, most of the bacteria are sufficiently repaired - guaranteeing reliable growth on ChromoCult® TBX agar at 44°C.
Your benefits:
Safe - All E. coli can be detected, both injured and non-injured.
Fast - Only 4 hours resuscitation
Easy - MMGA from Merck is a complete medium - nothing needs to be added.
Available products:
Merck Catalogue Number
MMGA
1.09045.0500
ChromoCult® TBX
1.16122.0500
For further information about the wide range of products available from Merck Millipore please contact Merck Millipore (see details above) or EMD Chemicals in the USA or click the link below.
NOTE: This item is from our 'historic' database and may contain information which is not up to date.