SN/T 4546-2017 in English
VALIDCommercial kit method-Staphylococcus aureus-Test method Ⅰ
- Issued on:2017-05-12
- Implemented on:2017-12-01
- File Format:PDF
- Delivery:Via email within 1~3 business days
$194.00
Introduction
Analysis of the Standard's Core Content
This standard replaces SN/T 1895-2007. Major technical changes include: revision of the standard title, addition of calculation formulas and Appendix B, and deletion of Method 2. Testing is performed using the Petrifilm™ Staphylococcus aureus Test Plate and is applicable to the microbiological safety control of food raw materials and finished products.
Key Technical Points
| Technical Parameters | Standard Requirements | Implementation Points |
|---|---|---|
| Culture Conditions | 36℃±1℃/24h±2h | Stacking should not exceed 20 plates. Denaturation resistance test confirms that 35-37℃/22-26h is acceptable. |
| Result Interpretation | Direct counting of purple-red colonies | When confirmation of the reaction is required, a pink halo indicates a positive characteristic (DNase reaction) |
| Counting Range | 15-150CFU | Exceeding the range requires special handling according to Clause 9.2 |
Method Validation Data
Validation in 15 types of food matrices shows:
- Linear equation slope 0.9767-1.1332, R²≥0.9696
- T test values compared with GB 4789.10 reference method are both <2.131 (P>0.05)
- Inter-batch variation RSD≤3.12%, showing good repeatability
Implementation Suggestions
- Sample processing: Homogenization time should be controlled within 1-2 minutes, and pH should be adjusted to 6.5-7.5
- Inoculation technique: Use a pressure plate to ensure even coverage of the sample solution, and let it stand for 1 minute to allow the gel to solidify
- Quality control: Each batch should include a blank control and a positive control (ATCC 25923)
- Data recording: Pay attention to the distinction between direct counting and confirmation counting results
Technology evolution analysis
Compared with the 2007 version of the standard, this version has the following major improvements:
- Introduction of Confirmation reaction plate to improve specificity (detection of DNase activity)
- Addition of calculation formula to standardize the processing of multiple dilution results
- Delete the Petrifilm™ MPN method and focus on the plate count method

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