Method for quickly and efficiently extracting deoxyribonucleic acid (DNA) of wheat stripe rust directly from infected wheat leaf blades

Abstract

The invention discloses a method for quickly and efficiently extracting deoxyribonucleic acid (DNA) of wheat stripe rust directly from infected wheat leaf blades. The method is characterized in that 20mu l of prepared 20% chelex-100 suspension is drawn and injected into a 100mu l polymerase chain reaction (PCR) tube; 5mu l of chelex-100 supernate is drawn and dripped on the wheat leaf blades with wheat stripe rust uredispore and the spots of the leaf blades on which the chelex-100 supernate is dripped are smeared repeatedly to wash off the aecidiospore; the chelex-100 supernate containing the aecidiospore on the leaf blades is drawn back and added into the PCR tube containing 20mu l of 20% chelex-100 suspension; the mixture is drawn repeatedly and mixed evenly by a liquid-moving device; the mixture is put in boiling water bath for water bath for 2 minutes and then put in a vortex mixer to be oscillated and mixed evenly for 10 seconds; the mixture is subjected to water bath for 5 minutes and preserved at the temperature of minus 20 DEG C for later use; and the supernate can be used as templates of PCR. The invention provides an efficient and rapid method for extracting DNA of wheat stripe rust which is used as PCR amplification templates directly from infected wheat leaf blades.

Description

technical field [0001] The invention relates to a method for efficiently and rapidly extracting wheat stripe rust DNA directly from susceptible wheat leaves, belonging to the field of plant protection. Background technique [0002] Wheat stripe rust caused by Puccinia striiformis f.sp.tritici is one of the major diseases in wheat producing areas in the world. With the development of molecular biology, more and more researchers have rapidly increased their explorations at the level of proteins and DNA molecules related to wheat stripe rust, and the content of PCR-based research has gradually been enriched. The premise of PCR amplification is to extract relatively complete genomic DNA. The methods for extracting fungal DNA at home and abroad mainly include: CTAB method, SDS extraction method, urea extraction method, benzyl chloride extraction method and other chemical methods to break the cell wall, and then use organic solvents to extract DNA. These methods all have cumbers...

AI Technical Summary

Problems solved by technology

These methods all have cumbersome operation steps, time-consuming and labor-intensive, a large amount of bacterial cells, and low DNA acquisition rate.

For the obligate parasitic fungus that cannot be artificially cultivated——Wheat stripe rust, when extracting the single-spore pile DNA, it is necessary to obtain enough wheat stripe rust through the isolation and inoculation of the single-spore pi

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