Bacillus thuringiensis and application thereof
A technology of Bacillus aureus and strains, applied in the field of biological control, can solve the problems of difficult practical application and poor control effect in the field, and achieve the effects of good drug effect persistence, strong specialization and high control effect
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Embodiment 1
[0039] Embodiment 1 The process of collection and screening of bacterial strain DK49 of the present invention
[0040]In August 2015, the Institute of Plant Protection, Hebei Academy of Agriculture and Forestry Sciences collected more than 2,000 soil samples in Hebei Province, and isolated more than 100 Bt strains from them. More than 100 isolated Bt strains were mixed in 30mL LB liquid medium (composed of: tryptone 10g, yeast extract 5g, sodium chloride 10g, add water to 1L), at 30°C, 220rpm Cultivate under conditions until the cell crystals are separated, and after counting, transfer the bacterial suspension to a 50mL centrifuge tube, centrifuge at 4°C and 8000rpm for 5min, and collect the bacterial cells; resuspend the bacterial cells with sterile water to reach a final concentration of 1×10 7 spores / mL. The indoor biological activity of Flea beetle adults was measured by dip feeding method, and finally a Bt strain with high insecticidal activity against Flea beetle was ob...
Embodiment 2
[0041] Example 2 According to the morphological characteristics, the bacterial strain DK49 of the present invention is initially classified and identified
[0042] Inoculate the DK49 strain on LB solid medium (its composition and ratio are: tryptone 10g, yeast extract 5g, sodium chloride 10g, agar powder 15g, add water to 1L), and culture at 30°C , Sampling at different times for microscopic examination to observe the morphological characteristics and crystal characteristics of the colonies. Observation results at different culture stages on LB medium are as follows: vegetative bodies: rod-shaped, blunt at both ends, about 1.1-1.5×0.5 μm in size; single or more than two exist in chains. Spores: oval, about 1.0-1.2×0.5μm in size, dormant; have strong resistance to adverse environments such as high temperature or dryness. Paraspora crystals: spherical, about 0.4 μm in diameter, with insecticidal activity. These morphological characteristics are basically consistent with the mo...
Embodiment 3
[0043] Example 3 Classification and Identification of DK49 at the Molecular Level
[0044] (1) Identification and classification of DK49 strains using gyrB gene sequence:
[0045] Inoculate the DK49 strain in LB culture medium, shake overnight at 30°C, take 1mL of the bacterial liquid into an Eppenddorf tube, centrifuge, discard the supernatant, suspend with 200μL ultrapure water, treat at 100°C for 10min, centrifuge at 12000rpm for 5min, and take Qing is the DNA template of the DK49 strain. The general primers gyrB-F and gyrB-R were used as primers for PCR amplification to obtain PCR amplification products; wherein the primers were: gyrB-F: 5'-TTGRCGGHRGYGGHTATAAAGT-3', gyrB-R: 5'-TCCDCCSTCAGARTCWCCCTC -3'. Wherein the PCR reaction system (50μL) is: 10×PCR Buffer (Mg 2+ ) 5 μL; dNTPMixture (2.5mM) 5 μL, primers (10 μmol / L) 1 μL each, template 1 μL, Taq polymerase (5U / μL) 1 μL, and ultrapure water to 50 μL. The PCR reaction program was: 95°C for 5min; 30 cycles of 95°C for...
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