Bacteria genome DNA extraction liquid, preparation and application thereof

An extract and genome technology, applied in the field of bacterial genome DNA extract and its preparation and application, can solve the problem of complex operation of bacterial genome extraction kits, ineffective release of genomic DNA, contamination of bacteria or their genomic DNA, etc. problems, to achieve the effects of reducing physical health damage, high extraction efficiency, and sufficient cracking

Active Publication Date: 2008-12-10
SHANGHAI BLOOD CENT
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

However, for some bacteria with special cell wall structure, such as Staphylococcus aureus, the genomic DNA cannot be released effectively, so lysozyme cannot be used for lysis
[0004] In addition, the routinely used bacter

Method used

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  • Bacteria genome DNA extraction liquid, preparation and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0028] Make bacterial genomic DNA extract according to the following formula:

[0029] ①Add an appropriate amount of SDS, NP-40 and Tween into water and mix, then filter and sterilize with a 0.22 μm filter, and finally add an appropriate amount of chelex-100 to make the final concentration 5% (g / m1), adjust SDS, NP-40 and The concentration of Tween is 0.03% (g / ml), 1% (ml / ml) and 1% (ml / ml) respectively, and the mixture A solution is obtained;

[0030] ②Mix the stock solutions of lysostaphin, wall-breaking enzyme and proteinase K at a volume ratio of 1:5:1.25, filter through a YM-100 protein filter column at 14,000 g / min, and centrifuge at 4°C for 24 minutes to obtain liquid B;

[0031] ③ Add 230ul of the liquid obtained in step ① to 100ul of the liquid obtained in step ② to obtain the product bacterial genome DNA extract.

[0032] Follow the procedure below to extract bacterial genomic DNA:

[0033] ①Take 200ul of platelet products, centrifuge at 13000g / min for 10 minutes, ...

Embodiment 2

[0039] Make bacterial genomic DNA extract according to the following formula:

[0040] ① Add appropriate amount of SDS, NP-40 and Tween to water and mix, then filter and sterilize with a 0.22 μm filter, and finally add appropriate amount of chelex-100 to make the concentration 10% (g / ml), SDS, NP-40 and Tween Make up concentration to be 0.05% (g / ml), 1.5% (ml / ml) and 1.5% (ml / ml) respectively, make A solution;

[0041] ②Mix the stock solutions of lysostaphin, wall-breaking enzyme and proteinase K at a ratio of 1.5:4.5:1.75, filter through a YM-100 protein filter column at 14,000 g / min, and centrifuge at 4°C for 24 minutes to obtain liquid B;

[0042] ③ Add 400ul of the liquid obtained in step ① to 200ul of the liquid obtained in step ② to obtain the product bacterial genome DNA extract.

[0043] Follow the procedure below to extract bacterial genomic DNA:

[0044] ① Take 800ul of plasma, centrifuge at 13000g / min for 10 minutes, and collect bacteria;

[0045] 2. Abandon the ...

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Abstract

The invention discloses a bacteria genome DNA extracting solution in a blood and platelet product and a preparation method and an application method thereof. The bacteria genome DNA extracting solution consists of chelex-100, tween, NP-40, SDS, lysostaphin, a wall-breaking enzyme, a protease K and water. The extracting solution can be effectively used for extracting a bacteria genome DNA with high extraction efficiency. The preparation method and the application method are simple and convenient for operation.

Description

technical field [0001] The invention relates to an extraction solution and a preparation method for extracting bacterial genome DNA from blood and platelet products and a method for using the extract solution to extract bacterial genome DNA. Background technique [0002] Bacterial contamination in blood and platelet products has become a major hidden danger threatening the safety of blood products. In recent years, it has received much attention. In the past, the detection of bacterial contamination was based on the traditional culture method. This method generally takes 24 hours to obtain the preliminary report and seven days to obtain the final report. For some bacteria with small amount of bacteria or difficult to culture, false negative results are easy to be produced, which endangers the safety of blood transfusion. With the development of molecular biology techniques, PCR and fluorescent quantitative PCR techniques are widely used in the diagnosis of bacteria. This ...

Claims

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Application Information

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IPC IPC(8): C12N15/10C12N15/31
Inventor 刘晓颖马敏王迅郑岚钱开诚
Owner SHANGHAI BLOOD CENT
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