Thuringiensis bacillus strain for killing noctuidae pests and its preparing process
A technology for killing Bacillus chrysogenum and noctuids, applied in botany equipment and methods, bacteria, biocides, etc., can solve problems such as intractable pests of Noctuidae and affect the effective use of BT insecticides, and achieve great theoretical significance and practical value, the effect of strong insecticidal effect
Patent Information
- Authority / Receiving Office
- CN · China
- Patent Type
- Patents(China)
- Current Assignee / Owner
- Publication Date
- 2005-03-02
- Estimated Expiration
- Not applicable · inactive patent
Abstract
Description
technical field
[0001] The invention relates to a Bacillus thuringiensis strain with double toxicity (parasporal crystal and exotoxin protein) to efficiently kill Noctuidae pests. Bacillus thuringiensis (Bacillus thuringiensis) DL-5789 strain has a strong poisonous effect on noctuidae pests such as cotton bollworm, Spodoptera litura and Beet Spodoptera due to the composite effect of parasporal crystals and exotoxin protein. It also relates to the preparation method of the bacterial strain. Background technique
[0002] Bacillus thuringiensis (abbreviated as BT) has been used in large-scale production worldwide, and is widely used in the control of agricultural pests, forestry pests, storage pests and sanitation pests. It is an effective microbial insecticide in the world and plays an extremely important role in the practice of microbial control of pests. However, the currently commercialized BT insecticides are mainly used to control sensitive pest...
Examples
Embodiment Construction
[0021] 1. Strain isolation and cultivation
[0022] Put a little soil sample into a test tube containing 4.5ml of nutrient solution, and culture it with shaking for 48 hours at 78°C in a water bath for 15 minutes. Dilute the culture medium to 10 -7 -10 -8 times, spread it on the separation medium, culture it upside down in a 30°C incubator for 3 days, and select a single colony producing paraspora crystals by microscopic examination.
[0023] Nutrient medium: peptone 1% beef extract 0.3% NaCl 0.5% pH7.5.
[0024] Separation medium: peptone 1% beef extract 0.3% NaCl 0.5% agar 2% PH7.5.
[0025] 2. Strain shake flask fermentation