DA34232543 | Coliform Chromogenic Agar CCA ISO | SICAP.ai

DA34232543

12 Octombrie 2023

1.450 RON

Oferta acceptata

4301073 - DIRECTIA DE SANATATE PUBLICA JUDETEANA CONSTANTA

Constanta, Constanta

17788699 - S.C. ALL LAB SYSTEMS S.R.L. S.R.L.

Furnizare

24931250-6 - Medii de cultura (Rev.2)

E.COLI COLIFORMS CHROMOGENIC AGAR (CCA) ISO 9308-1 CAT Nº: 2080 Selective medium for the simultaneous detection of E.coli and other coliforms in water samples FORMULA IN g/l Sodium Chloride 5.00 Tryptophan 1.00 Di-sodium hydrogen phosphate 2.70 Salmon-beta-D-galactoside 0.20 Sodium dihydrogen phosphate x 2H2O 2.20 Tergitol® 15-S-7 surfactant 0.15 Yeast Extract 2.00 X-beta-G-glucuronide CHX salt 0.10 Enzymatic Digest of Casein 1.00 IPTG 0.10 Sodium Pyruvate 1.00 Agar 10.00 Sorbitol 1.00 Final pH 6.8 ± 0.2 at 25ºC PREPARATION Suspend 26.45 grams of the medium in one liter of distilled water. Mix well and dissolve by heating with frequent agitation. Boil for one minute until complete dissolution. AVOID OVERHEATING. DO NOT AUTOCLAVE. Cool to 45-50ºC and pour into petri plates. Homogenize gently and dispense into Petri dishes. The prepared medium should be stored at 8-15°C, protected from light. The color of the prepared medium is amber. The standard recommends not using freshly prepared plates but to store them at 5±3°C, away from light, during at least one month. Dry off moisture before use. The dehydrated medium should be homogeneous, free-flowing and beige in color. If there are any physical changes, discard the medium. USES E.COLI-COLIFORMS CHROMOGENIC AGAR (CCA) is a selective medium for the detection of E.coli and other coliforms in water and foods. The interaction of ingredients in the medium, such as peptone, sorbitol, etc., allows a quick colony growth, including in

1.450 RON

Cantitate: 1

Unitate masura: bucata

Coliform Chromogenic Agar CCA ISO

E.COLI COLIFORMS CHROMOGENIC AGAR (CCA) ISO 9308-1 CAT Nº: 2080 Selective medium for the simultaneous detection of E.coli and other coliforms in water samples FORMULA IN g/l Sodium Chloride 5.00 Tryptophan 1.00 Di-sodium hydrogen phosphate 2.70 Salmon-beta-D-galactoside 0.20 Sodium dihydrogen phosphate x 2H2O 2.20 Tergitol® 15-S-7 surfactant 0.15 Yeast Extract 2.00 X-beta-G-glucuronide CHX salt 0.10 Enzymatic Digest of Casein 1.00 IPTG 0.10 Sodium Pyruvate 1.00 Agar 10.00 Sorbitol 1.00 Final pH 6.8 ± 0.2 at 25ºC PREPARATION Suspend 26.45 grams of the medium in one liter of distilled water. Mix well and dissolve by heating with frequent agitation. Boil for one minute until complete dissolution. AVOID OVERHEATING. DO NOT AUTOCLAVE. Cool to 45-50ºC and pour into petri plates. Homogenize gently and dispense into Petri dishes. The prepared medium should be stored at 8-15°C, protected from light. The color of the prepared medium is amber. The standard recommends not using freshly prepared plates but to store them at 5±3°C, away from light, during at least one month. Dry off moisture before use. The dehydrated medium should be homogeneous, free-flowing and beige in color. If there are any physical changes, discard the medium. USES E.COLI-COLIFORMS CHROMOGENIC AGAR (CCA) is a selective medium for the detection of E.coli and other coliforms in water and foods. The interaction of ingredients in the medium, such as peptone, sorbitol, etc., allows a quick colony growth, including infectious Coliforms. Tergitol inhibits Gram-positive bacteria. Sodium chloride maintains the osmotic balance and Phosphate salts act as a buffer system. Bacteriological agar is the solidifying agent. The chromogenic mixture contains chromogenic substrates such as Salmon-GAL and X-glucuronide. Coliform enzymes produced, such as galactosidase and glucuronidase, cleave these substrates, resulting in the different coloration of certain bacteria colonies. The ß-D-galactosidase cleaves Salmon-GAL substrate, and gives a salmon to red color to the coliform colonies. E.coli cleaves both substrates Salmon-Gal and X-glucuronide, giving a dark blue to violet color to the colonies, easily distinguishable from other coliform colonies that have a salmon to red color. The addition of tryptophan to the medium allows the performance of the Indole test for further E. coli confirmation. Process 1.- Filter sample through a membrane 2.- Place the membrane filter over a coliforms chromogenic agar plate. 3.- Incubate the membrane filter at (36±2)°C during (21±3) hrs. 4.- Count the ß-D-galactosidase colonies (pink to red in color) as presumptive coliform bacterias that are not E. coli 5.-To avoid false positive results, caused by oxidase-positive bacteria, for example Aeromonas spp, confirm bacterial colonies through an oxidase-negative reaction. The positive colonies β-D-galactosidase and β-D-glucuronidase (dark blue to violet) are counted as E. coli. LABORATORIOS CONDA, S.A. www.condalab.com 2 The total coliform bacteria count is the sum of oxidase-negative colonies, β-D-galactosidase-positive colonies (pink to red) and all colonies which dark blue to violet. Note: Some Shigella strains contain the enzyme ß-D-glucuronidase and can grow as light blue colonies. The negative E. coli ß-glucuronidase colonies are colorless, e.g. E. coli O157:H7. MICROBIOLOGICAL TEST The following results were obtained in the performance of the medium from type cultures after incubation at a temperature of 36 ± 2°C and observed after 21±3 hours. Microorganisms Quantitative Productivity Qualitative Selectivity Qualitative Specificity Colony Color Escherichia coli ATCC 25922 ≥0,7 Blue-dark violet Escherichia coli ATCC 8739 ≥0,7 Blue-dark violet Enterobacter aerogenes ATCC 13048 ≥0,7 Red- rose Enterococcus faecalis ATCC 19433 Total inhibition Pseudomonas aeruginosa ATCC 10145 Growth Colorless Colorless BIBLIOGRAPHY ISO 9308-1/2014 Water quality — Enumeration of Escherichia coli and coliform bacteria —Part 1: Membrane filtration method for waters with low bacterial background flora. ISO 7218:2007, Microbiology of food and animal feeding stuffs — General requirements and guidance for microbiological examinations Byamukama D., Kansiime F., Mach R.L., Farnleitner A.H. Determination of Escherichia coli. (2) Contamination with Chromocult Coliform Agar Showed a High Level of Discrimination Efficiency for Differing Fecal Pollution Levels in Tropical Waters of Kampala, Uganda. Appl. Environ. Microbiol. 2000, 66 pp. 864–868 [3] Geissler K ., M anafi M ., A moros I ., A lonso J.L. Quantitative determination of total coliforms and Escherichia coli in marine waters with chromogenic and fluorogenic media. J. Appl. Microbiol. 2000, 88 pp. 280–285 [4] Ossmer R ., Schmidt W., Mende U. Chromocult Coliform Agar — Influence of Membrane Filter Quality on Performance. Poster presentation, 1999. Congreso de la Sociedad Española de Microbiologia, Granada, Spain (http://www.univie.ac.at/chromogenic/OSSMER.PDF) [5] USEPA: 40 CFR Part 141 (sec. 141.21) Federal Register/Vol. 67, No. 209, Tuesday October 29, 2002/Rules and Regulations [6] Lange B ., S trathmann M ., O ssmer R. Performance validation of chromogenic coliform agar for the enumeration of Escherichia coli and coliform bacteria. Lett. Appl. Microbiol. 2 013, 57 pp. 547–553 (http://onlinelibrary.wiley.com/doi/10.1111/lam.12147/suppinfo) [7] http://www.wfcc.info/pdf/WDCM_Reference_Strain_Catalogue.pdf (viewed 03-01-2014)