Paecilomyces lilacinus PlTS01 strain and application thereof in bemisia tabaci control
A technology for Paecilomyces lilacinus and Bemisia tabaci, applied to Paecilomyces lilacinus PlTS01 and its application field in the control of Bemisia tabaci, can solve the problems of no reports on the prevention and control of Bemisia tabaci, and achieve good promotion and application Value, the effect of sustainable development promotion
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Embodiment 1
[0030] Example 1 Isolation and screening of Paecilomyces lilacinus strain PlTS01
[0031] The soil was collected from Zhongchuan Town, Yongdeng County, Gansu Province. The soil samples were sieved to remove stones and sundries. Take 10g of pure soil and suspend in 90mL of 0.05% Tween 80 solution. Shake well, let stand for 15min, and take the supernatant 2mL was diluted in 8mL0.05% Tween 80.
[0032] Selective culture: Inoculate 0.1mL of the above suspension on the surface of the selective medium plate and spread evenly with a triangular glass rod. At 25°C, culture at constant temperature for 3-6 days, then use an inoculation loop to pick mycelium from a single colony, inoculate it on a PDA plate to continue culturing, and store it in a refrigerator at 4°C after purification.
[0033] After the above operations, a fungus with pathogenic effect on Bemisia tabaci was screened out from the soil, numbered PlTS01.
Embodiment 2
[0034] Example 2 Identification of strain PlTS01
[0035] The bacterial strain PlTS01 screened in Example 1 was on the Chapei medium, initially the colony was regular and round, raised, with white hyphae, and the back was light yellow or nearly beige; after prolonged cultivation, the colony was still round and formed a pale pink spore layer; After 14 days of culture, the colony diameter was 44~46mm.
[0036] Microstructure: mycelium is long and thin, colorless and transparent, with septa, width 1.58~3.61μm; 2~5 phialides grow on the conidiophores, phialides are oval or fusiform inflated, gradually thin tube upward, 6.07~7.44μm long, 2.77~3.66μm wide; a large number of conidia are produced on it, the conidia are strung together, colorless and transparent, and the single cells are oval to oval, 2.51~3.66μm long, 1.77~2.66μm wide μm.
[0037] Molecular phylogeny: The rDNA-ITS gene sequence of the PlTS01 strain (as shown in SEQ ID NO: 1) was amplified with universal primers IT...
Embodiment 3
[0041] Preparation of conidia suspension: pick conidia from the slant strains, insert them into 0.05% Tween-80 solution that has been sterilized, measure the concentration of spores with a hemocytometer, and adjust to 10 7 conidia / mL. spare.
[0042] Seed culture: inoculate 2mL spore suspension in 98mL seed medium, at 180r / m and 26 0 Shake flask culture under C condition for 2-3 days and serve as seed solution. Seed medium is the Czapek-Dox medium of 0.5% peptone, and its composition is: albumen 5g, NaN0 3 3g, K 2 HP0 4 1g, MgS0 4 7H 2 00.5g, KCl0.5g, FeS0 4 7H 2 00.01g, molasses 30g, agar 15-20g, water 1000mL.
[0043] Solid fermentation: steam the rice first, put it into a fresh-keeping bag, and inoculate the above seed liquid after it is cooled to normal temperature, the inoculation ratio is 5-15% (V / W), and the inoculation ratio is 5-15% (V / W), at 25-28 0 C culture for about 2 weeks, until the surface of the rice grains is covered with conidia, the conidia are sepa...
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