Cherry gummosis bacteria inhibitor and preparation method thereof
The technology of a bacteriostatic agent and a preparation method is applied in the field of a bacteriostatic agent for cherry gum flow bacteria and its preparation, and achieves the effects of non-toxicity in prevention and control costs and reduction in prevention and control costs.
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0013] Pour the slightly cooled PDA medium after sterilization into a petri dish (diameter 9cm) to make a plate, use a puncher (diameter 6mm) to punch a hole in the center of the plate, and the inhibitor (proportioning: fresh garlic 10g, fresh Onion 10g, cinnamon 10g, fennel 10g, crushed and distilled to 2000ml with distilled water, let stand for leaching for 12 hours, and the filtrate is used for later use) Add to the hole, inoculate the bacteria plate of cherry tree gummosis bacteria around the hole, put it in 28℃ for constant temperature cultivation Box culture, with the treatment of adding sterilized water as the control, each treatment was repeated 5 times. When the control plate was full, the size of the inhibition zone of each treatment was measured and statistically analyzed.
Embodiment 2
[0015] Pour the slightly cooled PDA medium after sterilization into a petri dish (diameter 9cm) to make a plate, punch a hole in the center of the plate with a puncher (diameter 6mm), and mix the inhibitor (proportioning: fresh garlic 15g, fresh Onion 15g, cinnamon 15g, fennel 15g, crushed and distilled to 1500ml with distilled water, let stand for leaching for 48 hours, and the filtrate is used for later use) into the hole, inoculate cherry tree gelatinous bacteria plate around the hole, and put it into 28 ℃ constant temperature culture Box culture, with the treatment of adding sterilized water as the control, each treatment was repeated 5 times. When the control plate was full, the size of the inhibition zone of each treatment was measured and statistically analyzed.
Embodiment 3
[0017] Pour the slightly cooled PDA medium after sterilization into a petri dish (diameter 9cm) to make a plate, punch a hole in the center of the plate with a puncher (diameter 6mm), and mix the inhibitor (proportioning: fresh garlic 30g, fresh 30g of onion, 30g of cinnamon, 30g of fennel, crushed and distilled to 1000ml with distilled water, let stand for leaching for 36 hours, and the filtrate will be used for later use) into the hole, inoculate the bacteria tray of cherry tree gummosis bacteria around the hole, and put it in a constant temperature culture at 28°C Box culture, with the treatment of adding sterilized water as the control, each treatment was repeated 5 times. When the control plate was full, the size of the inhibition zone of each treatment was measured and statistically analyzed.
PUM
Login to View More Abstract
Description
Claims
Application Information
Login to View More 


