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Dehydrated culture media

Modified Nocive Brewers Bacteria Agar Base

Selective medium for the detection of contaminating, spoilage microorganisms in brewery.

Cat. No.
LC-1438
Format
500 g
Storage
2 to 25 °C
Minimum guaranteed shelf life
15 months

Modified Nocive Brewers Bacteria Agar Base is a medium used for the detection of beer spoilage bacteria.

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Cat. No.FormatPrice
LC-1438500 g

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Key features

Applications

Detection and selective enrichment of microorganisms of the brewing industry.

Industry

Alcoholic beverages.

Preparation

66.3 g in 500 mL of distilled water and 500 mL of beer without gas; boil for one minute, sterilize in autoclave at 121 °C for 15 minutes.

Principles and uses

This medium contains a wide variety of nutrients including pancreatic digest of casein, yeast extract, beef extract, dextrose and maltose. These nutrients favour the growth of spoilage microorganisms in beer and other samples. Potassium acetate (instead of sodium acetate) makes the medium less inhibitory for the growth of spoilage bacteria that deteriorate beer and other samples. Polysorbate 80 is incorporated to neutralize phenols, hexachlorophene and formalin. L-Cysteine hydrochloride is the reducing agent. Disodium phosphate acts as a buffer system. Bacteriological agar is the solidifying agent.

Technical specifications

SolubilityWithout residues
AppearanceFine powder
Color of the dehydrated mediumBeige
Color of the prepared mediumPink-red
Final pH (25 °C)5.8 ± 0.2
Amount66.3 g in 500 mL of distilled water and 500 mL of beer without gas
Storage2 to 25 °C

Formula

Ingredientg/L
Bacteriological agar15
Beef extract2
Dextrose15
Disodium phosphate2
Maltose15
Pancreatic digest of casein5
Polysorbate 800.5
Yeast extract5
L-Malic acid0.5
L-Cysteine HCl0.2
Chlorophenol red0.07
Potassium acetate6

Typical formula in g/L, adjusted and/or supplemented as required to meet performance criteria.

Preparation and use

Preparation

Suspend 66.3 grams of the medium in 500 mL of distilled water and 500 mL of beer without gas. Mix well and dissolve by heating with frequent agitation. Boil for one minute until complete dissolution. Sterilize in autoclave at 121 °C for 15 minutes. Cool to 45-50 °C, mix well and dispense into plates.

Instructions for use

Pour plate method:

  1. Deposit 1 mL of the initial suspension and/or diluted sample in an empty Petri dish.
  2. Add 12-15 mL of agar cooled to 44-47 °C in each Petri dish and mix gently moving the plate.
  3. Allow the plates to solidify and incubate in an inverted position at a temperature of 30-35 °C for 4 days.
  4. Take the acid-producing colonies and carry out the catalase and Gram stain tests.

Quality control

Microbiological test

Incubation conditions: 30-35 °C / 4 days.

MicroorganismSpecificationCharacteristic reaction
Pediococcus damnosusATCC 29358Good growthAcid production (trace yellow-yellow)
Pediococcus acidilacticiATCC 8042Good growthAcid production (trace yellow-yellow)
Lactobacillus brevisATCC 8287Good growthAcid production (trace yellow-yellow)

Bibliography

  • Back, 1980 Brauwelt 1562
  • Dacha, 1981, Brauwelt 1778

What you receive

The product

Shipped under controlled temperature when the product requires it.

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Frequently asked questions

Can I ask for formats other than those listed?

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