Method for improving Streptococcus thermophilus strains for dairy production
- Identification
- How does it work?
- What can it be used for?
- What can it not be used for?
- Implementation
- Related Facilities
- Further Information
Identification
Key words | Streptococcus thermophilus, natural transformation, competence state, DNA, peptide, dairy |
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Latest version | 2013/05/30 |
Completed by | INRA - IATE |
How does it work?
Primary objective | To improve the properties of Streptococcus thermophilus strains used as culture starter in dairy production | |||
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Working principle | Dairy manufacturers are always looking for Streptococcus thermophilus strains with new properties for improving the yoghurt and cheese production. The worldwide dairy market makes these S. thermophilus starter strains of a major economic importance.
Bacteria such as S. thermophilus are normally under a basic physiological state. Sometimes, they are under a specific physiological state, under which bacteria can transfer DNA with other bacteria. This state, which is called “competence state”, only occurs after a specific biological signal; this phenomenon is the induction.
Natural transformation is the transfer of DNA from a donor bacterium to a receptor bacterium, which is under a “competence state”. This transfer, which is partial and can only occur between a few bacterial species, makes the donor bacteria gain stable and transmissible new genetic characteristics.
The present method favours the natural transformation of S. thermophilus strains by inducing the required competence state. In a chemically defined, peptide-free culture medium, and at a particular moment of the cellular cycle, a specific peptide is used as a signal that makes the bacteria switch from basic state to competence state. The DNA transfer can then occur, giving modified properties (e.g. improved acidification rate, texture production, phage resistance, etc.) to the S. thermophilus strain.
(1)(2)
The method can work on strains that are naturally poorly or non competent (2) | |||
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Additional effects | ||||
Important process parameters | Chemical composition of the culture medium
Phase of the cellular cycle (short moment during the exponential growth phase) Properties of the DNA donor (1)(2) | |||
Important product parameters |
What can it be used for?
Products | Dairy products |
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Operations | Dairy production |
Solutions for short comings | Dairy strains with improved properties |
What can it NOT be used for?
Products | Any other than dairy products
Any other than Streptococcus thermophilus strains |
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Operations | Any other than dairy production |
Other limitations | To be transferred from one strain to another, the properties must be encoded by a limited number of loci on the chromosome of S. thermophilus (not any property can be obtained using this method) |
Risks or hazards | This technology is DNA transfer, but this transfer phenomenon occurs naturally. Moreover, the DNA that is transferred must be chromosomal DNA or plasmid DNA from S. thermophilus or a PCR product amplified from chromosomal DNA or plasmid DNA from S. thermophiles. |
Implementation
Maturity | The technology has been patented with a worldwide application, but still at lab-scale (2) |
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Modularity /Implementation | Once upscaled for industrial application, the transformation batch could be set up in addition to the existing dairy production line. |
Consumer aspects | Potential reluctance to consume products that could be interpreted as coming from GMO use. |
Legal aspects | Please check local legislation |
Environmental aspects | No problem is to be expected if DNA is transferred from one S. thermophilus strain to another S. thermophilus strain. |
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Further Information
Institutes | INRA - MICALIS |
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Companies | INRA Transfert |
References |
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