BS EN ISO 6785:2007 2008
$167.15
Milk and milk products. Detection of Salmonella spp.
Published By | Publication Date | Number of Pages |
BSI | 2008 | 34 |
PDF Catalog
PDF Pages | PDF Title |
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7 | Contents Page |
8 | Foreword |
9 | Milk and milk products�— Detection of |
11 | Milk and milk products�— Detection of 1��� Scope 2��� Normative reference 3��� Terms and definitions 4��� Principle 4.1��� General 4.2��� Pre-enrichment in non-selective liquid medium 4.3��� Enrichment in selective liquid media |
12 | 4.4��� Streaking out and recognition 4.5��� Confirmation 5��� Culture media, reagents and sera 5.1��� Water |
13 | 5.2��� Culture media 5.2.1��� Pre-enrichment medium: Buffered peptone water 5.2.1.1��� Composition 5.2.1.2��� Preparation 5.2.2��� First selective enrichment medium: Rappaport-Vassiliadis modified, magnesium chloride/ma… 5.2.2.1��� Solution�A 5.2.2.1.1��� Composition 5.2.2.1.2��� Preparation 5.2.2.2��� Solution�B 5.2.2.2.1��� Composition 5.2.2.2.2��� Preparation |
14 | 5.2.2.3��� Solution�C 5.2.2.3.1��� Composition 5.2.2.3.2��� Preparation 5.2.2.4��� Complete medium 5.2.2.4.1��� Composition 5.2.2.4.2��� Preparation 5.2.3��� Second selective enrichment medium: Selenite/cystine medium 5.2.3.1��� Base 5.2.3.1.1��� Composition 5.2.3.1.2��� Preparation |
15 | 5.2.3.2��� l 5.2.3.2.1��� Composition 5.2.3.2.2��� Preparation 5.2.3.3��� Complete medium 5.2.3.3.1��� Composition 5.2.3.3.2��� Preparation 5.2.4��� First selective solid medium: Brilliant green/phenol red agar (Edel and Kampelmacher) 5.2.4.1��� Base 5.2.4.1.1��� Composition 5.2.4.1.2��� Preparation |
16 | 5.2.4.2��� Sugar/phenol red solution 5.2.4.2.1��� Composition 5.2.4.2.2��� Preparation 5.2.4.3��� Brilliant green solution 5.2.4.3.1��� Composition 5.2.4.3.2��� Preparation 5.2.4.4��� Complete medium 5.2.4.4.1��� Composition 5.2.4.4.2��� Preparation 5.2.4.4.3��� Preparation of the agar plates |
17 | 5.2.5��� Second selective solid medium 5.2.6��� Nutrient agar 5.2.6.1��� Composition 5.2.6.2��� Preparation 5.2.6.3��� Preparation of agar plates 5.2.7��� Triple sugar/iron agar (TSI agar) 5.2.7.1��� Composition 5.2.7.2��� Preparation |
18 | 5.2.8��� Urea agar (Christensen) 5.2.8.1��� Base 5.2.8.1.1��� Composition 5.2.8.1.2��� Preparation 5.2.8.2��� Urea solution 5.2.8.2.1��� Composition 5.2.8.2.2��� Preparation 5.2.8.3��� Complete medium 5.2.8.3.1��� Composition 5.2.8.3.2��� Preparation |
19 | 5.2.9��� l 5.2.9.1��� Composition 5.2.9.2��� Preparation 5.3��� Reagents 5.3.1��� Saline solution 5.3.1.1��� Composition 5.3.1.2��� Preparation 5.3.2��� Reagents for 5.3.2.1��� Toluene 5.3.2.2��� Buffer solution 5.3.2.2.1��� Composition 5.3.2.2.2��� Preparation |
20 | 5.3.2.3��� ONPG solution 5.3.2.3.1��� Composition 5.3.2.3.2��� Preparation 5.3.2.4��� Complete reagent 5.3.2.4.1��� Composition 5.3.2.4.2��� Preparation 5.3.3��� Reagents for Voges-Proskauer (VP) reaction 5.3.3.1��� VP medium 5.3.3.1.1��� Composition 5.3.3.1.2��� Preparation 5.3.3.2��� Creatine solution ( 5.3.3.2.1��� Composition 5.3.3.2.2��� Preparation |
21 | 5.3.3.3��� 1-Naphthol, ethanolic solution 5.3.3.3.1��� Composition 5.3.3.3.2��� Preparation 5.3.3.4��� Potassium hydroxide solution 5.3.3.4.1��� Composition 5.3.3.4.2��� Preparation 5.3.4��� Reagents for indole reaction 5.3.4.1��� Tryptone/tryptophan medium 5.3.4.1.1��� Composition 5.3.4.1.2��� Preparation 5.3.4.2��� Kovac’s reagent 5.3.4.2.1��� Composition 5.3.4.2.2��� Preparation |
22 | 5.3.5��� Semi-solid nutrient agar 5.3.5.1��� Composition 5.3.5.2��� Preparation 5.3.5.3��� Preparation of agar plates 5.4��� Sera 6��� Apparatus and glassware 6.1��� Apparatus for wet sterilization (autoclave) 6.2��� Oven 6.3��� Incubator 6.4��� Water bath 6.5��� Water baths 6.6��� Loops 6.7��� pH-meter 6.8��� Culture bottles 6.9��� Culture tubes 6.10��� Measuring cylinders |
23 | 6.11��� Graduated pipettes 6.12��� Petri dishes 7��� Sampling 8��� Preparation of test sample 9��� Procedure 9.1��� Safety precautions 9.2��� Test portion and pre-enrichment 9.2.1��� General 9.2.2��� Raw milk, heat-treated milk and liquid milk products 9.2.3��� Dried milk products 9.2.4��� Lactose |
24 | 9.2.5��� Casein, caseinates, cheese 9.2.6��� Butter 9.2.7��� Frozen milk products (including edible ices) 9.2.8��� Fermented milks, yoghurt, custards, desserts 9.3��� Enrichment 9.3.1��� Non-selective pre-enrichment 9.3.2��� Selective enrichment 9.3.2.1��� Transfer 9.3.2.2��� Incubate the inoculated RVS medium ( 9.4��� Streaking out and recognition 9.4.1��� Using the culture obtained in the RVS medium ( |
25 | 9.4.2��� Using the culture obtained in the selenite/cystine medium ( 9.4.3��� Incubate the plates (bottom uppermost) in the incubator ( 9.4.4��� After incubating the RVS medium and the selenite/cystine medium for a further 9.4.5��� After each incubation ( 9.4.6��� On brilliant green/phenol red agar ( 9.5��� Confirmation 9.5.1��� Selection of colonies for confirmation 9.5.2��� Incubation 9.5.3��� Biochemical confirmation 9.5.3.1��� General 9.5.3.2��� Triple sugar/iron agar ( |
26 | 9.5.3.3��� Urea agar ( 9.5.3.4��� l 9.5.3.6��� Voges-Proskauer reaction ( |
27 | 9.5.3.8��� Interpretation of the biochemical tests 9.5.4��� Commercially diagnostic systems 9.5.5��� Serological confirmation 9.5.5.1��� General 9.5.5.2��� Elimination of auto-agglutinable strains 9.5.5.3��� Examination for O-antigens 9.5.5.4��� Examination for Vi-antigens |
28 | 9.5.5.5��� Examination for H-antigens 9.5.5.6��� Interpretation of serological reactions 9.5.6��� Interpretation of biochemical and serological reactions 9.5.7��� Definitive confirmation 10��� Control cultures 11��� Expression of results 12��� Safety precautions 12.1��� The procedure specified in this International Standard shall only be carried out in labor… 12.2��� These procedures shall not be performed in quality control laboratories, or in food manuf… 12.3��� Full bacteriological precautions shall be taken at all times whilst carrying out the proc… |
29 | 12.4��� Special care should be taken with the laboratory use of selenite solutions because of the… 13��� Test report |
30 | Diagram of procedure |
31 | Specification for brilliant green B.1��� Bacteriological performance B.2��� Test method B.2.1��� Medium B.2.2��� Procedure |
32 | Standard method for streaking agar plates |
33 | Bibliography |