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Food Testing · Mikrobiyoloji

Bacillus

TS EN ISO 7932 (Bacillus cereus count, 30 °C)TS EN ISO 21871 (detection and counting of low numbers of B. cereus)TS EN ISO 6887 series (sample preparation)
Food Testing laboratory work

What Is Bacillus?

Bacillus cereus analysis is the determination of the number of this bacteria that forms spores and causes food poisoning with two different types of toxins. Spores survive cooking and germinate and reproduce rapidly when cooked food is kept at inappropriate temperatures.

Purpose of Bacillus

The aim is to evaluate the risk posed by disruptions in the cooling and warming chain, especially in rice, pasta and starch-based baked goods.

Which Products Is Bacillus Applied To?

  • Cooked rice and pasta products
  • Ready meals and mass consumption products
  • Spices and dry herbal products
  • Milk powder and baby food
  • Starch based products

In Which Sectors Is Bacillus Used?

FoodAgricultureRetail

Standards Related to Bacillus

  • TS EN ISO 7932 (Bacillus cereus count, 30 °C)
  • TS EN ISO 21871 (detection and counting of low numbers of B. cereus)
  • TS EN ISO 6887 series (sample preparation)

Bacillus Conditions

Culture medium
Selective medium defined in the standard
Incubation
At standard defined temperature and time
Verification
Confirmation tests on typical colonies

Equipment for Bacillus

  • Sterile cabinet and incubators
  • Autoclave and medium preparation
  • Stomacher
  • Colony counter

Sample Requirements for Bacillus

  • The sample must be sent unopened and in its original packaging, maintaining the cold chain. Whether the sampling method is representative of the batch determines the validity of the result; The result from a single unit is not enough to make a decision about the party.
  • Cooling time and temperature records must be reported for baked products
  • Sample quantity is determined according to the sampling plan
  • Temperature recording contributes to analysis interpretation in products kept warm

Duration of Bacillus

Counting lasts as long as the incubation period; Additional time is added when confirmatory tests are required.

Bacillus Procedure

  1. 1The sample is prepared and diluted aseptically.
  2. 2Broadcast planting is done on selective media.
  3. 3It is incubated at defined temperature and time.
  4. 4They are considered typical colonies.
  5. 5Confirmation tests are applied.
  6. 6The result is calculated as cfu/g.

Bacillus Acceptance Criteria

(EC) 2073/2005 defines criteria for preceptive B. cereus for certain food categories (especially baby and young children's products). In other categories, the acceptance criterion is the level determined and justified by the enterprise in the hazard analysis. Acceptance criteria are microbiological criteria defined on a food category basis in (EU) 2073/2005. The regulation distinguishes two types of criteria: the food safety criterion (can the product be placed on the market) and the process hygiene criterion (is the production process under control). Which one applies depends on the product category and is confirmed by the text of the applicable regulation.

Evaluation of Results

The result should be read together with the temperature history of the product: cooking does not kill spores, so the low number comes from rapid cooling, not good cooking. A high number usually indicates slow cooling or insufficient keep-warm temperature.

Bacillus Report

  • Specimen identification and batch information
  • Applied standard and medium
  • Counting result and measurement uncertainty
  • Verification results
  • Temperature history information, if available

Accreditation

EUROLAB holds internationally recognised accreditation obtained from accreditation bodies party to the IAF and ILAC multilateral recognition arrangements, under ISO/IEC 17025 for laboratory testing, ISO/IEC 17020 for inspection and surveillance, and ISO/IEC 17021-1 and ISO/IEC 17065 for system and product certification. This chain ensures the reports and certificates issued are accepted worldwide.

Whether this test can be offered within accredited scope depends on your product and the standard applied; since accreditation is method-based, the scope is confirmed in writing at the quotation stage.

Scope and authorisations

Related Regulations

  • (EC) 2073/2005 Microbiological Criteria Regulation
  • Food Hygiene Regulation (EC) 852/2004

Food Testing — What Does This Testing Field Cover?

The section below describes the field that the Bacillus test belongs to; the conditions and acceptance criteria of this particular test are given in the sections above. The scope specific to your product is confirmed in writing at the quotation stage.

Food testing shows that a product is safe for consumption and contains what its label states. The family works along three axes: microbiological safety, chemical safety and nutritional composition. All three require different laboratory infrastructure, a different body of methods and a different turnaround time.

The most distinctive feature of the field is TIME PRESSURE. A steel specimen can wait on a shelf; a raw milk or fresh meat sample cannot. The time the sample was taken, the transport temperature and how long it takes to reach the laboratory directly determine the validity of the result. In food microbiology the cold chain record is therefore an inseparable part of the test report.

On the microbiological side there are two different questions and they must not be confused. DETECTION of a pathogen is a qualitative question: is Salmonella present in the sample or not? ENUMERATION of indicator organisms is a quantitative question and an indicator of production hygiene. The absence of a pathogen in a product does not show that hygiene is good; if the total mesophilic aerobic count is high, there is a problem in the process.

On the chemical side, pesticide residues, mycotoxins, heavy metals, additives, veterinary drug residues and process contaminants (acrylamide, furan, PAH) are measured. Multi-residue methods in this area (QuEChERS-based LC-MS/MS and GC-MS/MS) can screen hundreds of active substances in a single analysis; limits are defined separately for each product–substance pair.

On the composition side, protein, fat, moisture, ash, fibre, sugar profile, fatty acid composition, vitamin and mineral content are determined. These values are the basis of the nutrition declaration on the label and the tolerance ranges are defined in legislation — the difference between the declared value and the measured value must stay within that tolerance.

There is NO CE marking on food, and this shapes how the field works. Conformity is demonstrated through operating a HACCP-based food safety system, complying with labelling rules and not exceeding contaminant, residue and microbiological limits. A test result produces evidence not for a certificate but for a functioning system.

Allergen management carries particular weight. The presence of an undeclared allergen in a product is one of the most frequent causes of food recalls. Analysis here runs together with cleaning validation: it is shown that the line has been cleaned adequately after a production run containing an allergen and that the risk of cross-contamination is under control.

Voluntary schemes have become effectively mandatory in this field. Retail chains require their suppliers to hold a certificate under a GFSI-recognised scheme (BRCGS, IFS, FSSC 22000); without it, getting onto the shelf is practically impossible.

Method groups in this field

  • Pathogen detection

    Detection of Salmonella, Listeria monocytogenes, Campylobacter, Cronobacter and Shiga toxin-producing E. coli; culture-based and molecular methods.

  • Indicator counts

    Total mesophilic aerobic count, Enterobacteriaceae, coliforms and E. coli, coagulase-positive staphylococci, yeasts and moulds, lactic acid bacteria, sulphite-reducing Clostridia.

  • Pesticide and veterinary residues

    Multi-residue screening by LC-MS/MS and GC-MS/MS with QuEChERS extraction.

  • Mycotoxins and contaminants

    Aflatoxins, ochratoxin A, deoxynivalenol, patulin; heavy metals (ICP-MS), acrylamide and PAH compounds.

  • Nutritional composition

    Kjeldahl protein, fat and fatty acid profile, moisture, ash, dietary fibre, sugar profile, vitamin and mineral analyses.

  • Allergens and authenticity

    Gluten, milk, egg, nut and soy allergen analyses; molecular methods for species identification and adulteration detection.

Commonly confused in this field

  • Sampling is half the result. A sample transported at the wrong temperature or delayed gives an invalid result even if it is analysed correctly in the laboratory.
  • The absence of a pathogen does not show that hygiene is good; indicator counts give separate information and the two are read together.
  • A result from a sample taken from a lot can be generalised to the whole lot only if the sampling plan was set up statistically.
  • Limits are defined in separate regulations by product group and are updated regularly; a conformity decision based on an outdated limit table may be wrong.
  • For exports, the limits of the destination country may differ from EU limits; the same product may be compliant in one market and non-compliant in another.

Which decisions these results support

  • Verification of the HACCP plan and process monitoring
  • The basis for the nutrition declaration and allergen information on the label
  • Health certificates before export and compliance with destination market limits
  • Supplier and lot-based acceptance control
  • Shelf-life studies and determining storage conditions
  • Producing evidence for audits under GFSI-recognised schemes

Related Tests

Frequently Asked Questions About Bacillus

Why does it come off even though we cook it?

Bacillus cereus forms spores, and the spores survive normal cooking temperatures. If the product is cooled slowly or kept at room temperature after cooking, the spores will germinate and reproduce rapidly. The critical point is not the cooking speed but the cooling speed.

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