Multiple PCR detection kit for main pathogenic bacteria of cucurbit and detection method thereof
A detection kit and technology for pathogenic bacteria, which are applied in the directions of microorganism-based methods, microbial determination/inspection, biochemical equipment and methods, etc., can solve the problem of heavy workload, single identification of melon anthracnose, and increase the difficulty of disease detection and identification. and other problems, to achieve the effect of economical simplicity and saving testing costs
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment
[0053] 1 Materials and methods:
[0054] 1.1 Bacteria and disease samples:
[0055] Table 1 below lists the tested fungal strains and amplification results used for specific primer screening.
[0056] Table 1
[0057]
[0058]
[0059] Note: + means amplified product; - means no amplified product.
[0060] 1.2 Mycelium culture and collection
[0061] Put the tested watermelon wilt bacteria, watermelon wilt bacteria, watermelon sclerotinia and watermelon anthracnose bacteria on PDA (potato dextrose agar medium) plate, after 7 days of culture at 26 ° C, cut mycelium pieces from the edge of the colony and transfer them to potato dextrose In liquid culture medium (100ml of culture medium per 250ml Erlenmeyer flask), 28°C, 100rpm shaking culture for 7 days, filter to collect mycelia, freeze-dry and grind into mycelium powder, store at -20°C for future use.
[0062] 1.3 Genomic DNA extraction
[0063] 1.3.1 Extraction of mycelia genomic DNA, according to Sun et al. [5] M...
PUM
Login to View More Abstract
Description
Claims
Application Information
Login to View More 