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Violet red bile glucose agar vrbg

Manufactured by ITW Reagents
Sourced in Germany

Violet Red Bile Glucose Agar (VRBG) is a selective and differential culture medium used for the detection and enumeration of Enterobacteriaceae in food, water, and other samples. It is formulated to support the growth of Gram-negative, lactose-fermenting bacteria while inhibiting the growth of Gram-positive and non-lactose-fermenting organisms.

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3 protocols using violet red bile glucose agar vrbg

1

Microbial Analysis of Raw Beef Patties

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Each raw beef patty sample was collected under aseptic conditions and mixed with buffered peptone water (Panreac, Darmstadt, Germany). To determine the TVC, Plate Count Agar (PCA; Panreac) was employed and incubated at 37 °C for 48 h. Enumeration of the LAB was performed using De Man, Rogosa, and Sharpe agar (MRS; Merck, Darmstadt, Germany), with an incubation period of 48 h at 37 °C. For Enterobacteriaceae enumeration, Violet Red Bile Glucose Agar (VRBG; Panreac) with a double layer was used and incubated at 37 °C for 24 h. Microbiological analyses were conducted in duplicate, and microbial counts were expressed as logarithms of colony-forming units per gram (log CFU/g). Additionally, the presence of Salmonella sp. was assessed in 25 g of the beef patties. For this purpose, a 25 g sample was mixed with 225 mL of sterile buffered peptone water solution (0.1%, Panreac) for bacterial prepropagation. Selective proliferation of bacteria was carried out using Rappaport-Vassiliadis Soy Broth medium (Merck) and bacterial isolation was performed using Hektoen (Merck KGaA, Darmstadt, Germany) and Xylose Lysine Deoxycholate (XLD; Merck) agars. Previously, the microbiological characterization of CF was conducted, and the results are as follows: TVC: 6.83 log CFU/g; Enterobacteriaceae: <1.6 log CFU/g; LAB: 2.71 log CFU; Salmonella sp.: absence; and Listeria monocytogenes: absence.
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2

Microbiological Analysis of Raw Burgers

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Microbiological analyses were carried out in a vertical laminar-flow cabinet (model AV 30/70 Telsar, Spain). 10 g of each raw burger were aseptically taken and mixed with 90 mL of buffered peptone water (Panreac, Germany) to give 1/10 dilution. After 2 min in a stomacher blender (Stomacher Colworth 400, Seward, London, UK), appropriate decimal dilutions were plated in duplicate on Violet Red Bile Glucose Agar (VRBG) (Panreac, Germany) with a double layer for Enterobacteriaceae (37 ºC for 24 h) and on Plate Count Agar (PCA) (Panreac, Germany) for the total viable counts (TVC) (30 ºC for 72 h). All microbial counts were converted to logarithms of colony-forming units per gram (log cfu/g).
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3

Microbiological Analysis of Raw Burgers

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Microbiological analyses were carried out in a vertical laminar-flow cabinet (model AV 30/70 Telsar, Spain). 10 g of each raw burger were aseptically taken and mixed with 90 mL of buffered peptone water (Panreac, Germany) to give 1/10 dilution. After 2 min in a stomacher blender (Stomacher Colworth 400, Seward, London, UK), appropriate decimal dilutions were plated in duplicate on Violet Red Bile Glucose Agar (VRBG) (Panreac, Germany) with a double layer for Enterobacteriaceae (37 ºC for 24 h) and on Plate Count Agar (PCA) (Panreac, Germany) for the total viable counts (TVC) (30 ºC for 72 h). All microbial counts were converted to logarithms of colony-forming units per gram (log cfu/g).
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