Method for obtaining ophiocordyceps sinensis by infecting hirsutella sinensis with host insects of hepialus armoricanus oberthiir larvae
A technology of bat moth larvae and Trichosporum sinensis, applied in botany equipment and methods, horticulture, plant cultivation, etc., can solve the problems of low mortality, shorten infection ossified time, and high larval mortality, and achieve low mortality, The effect of shortening the zombification time of infection
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Embodiment 1
[0026] The bat moth used in this example is Thitarodes gonggaensis collected from Sichuan.
[0027] 1. Preparation of Chinese hairy sporozoites
[0028] The medium for cultivating blastospores is PDA medium: each liter contains 20g of glucose, 200g of potato, 5g of peptone, KH 2 PO 4 3g, MgSO 4 ·7H 2 O 1.5g and VB 1 0.02g, the rest is H 2 O (natural pH). After accurate molecular identification, the conidia of Trichosporum sinensis were inserted into the above-mentioned PDA medium, cultured in a shaker (120rpm, 9°C) for 60 days, and the blastospores of Trichosphaera sinensis were collected by centrifugation for injection to infect bat moths larva.
[0029] 2. Breeding of bat moth larvae
[0030] The larvae of the bat moth were mixed and fed with carrots, Polygonum villosa and Potentilla velvet in a mass ratio of 1:1:1 to obtain healthy 5th instar bat moth larvae for infection.
[0031] 3. Injection infection and post-injection care
[0032] Inject the 5th instar bat...
Embodiment 2
[0039] The bat moth used in this example is Thitarodes gonggaensis collected from Sichuan.
[0040] 1. Preparation of Chinese hairy sporozoites
[0041] The medium for cultivating blastospores is PDA medium: each liter contains 20g of glucose, 200g of potato, 5g of peptone, KH 2 PO 4 3g, MgSO 4 ·7H 2 O 1.5g and VB 1 0.02g, the rest is H 2 O (natural pH). After accurate molecular identification, the conidia of Trichosporum sinensis were inserted into the above-mentioned PDA medium, cultured in a shaker (120rpm, 9°C) for 60 days, and the blastospores of Trichosphaera sinensis were collected by centrifugation for injection to infect bat moths larva.
[0042] 2. Breeding of bat moth larvae
[0043] The larvae of the bat moth were mixed and fed with carrots, Polygonum villosa and Potentilla velvet in a mass ratio of 1:1:1 to obtain healthy 5th instar bat moth larvae for infection.
[0044] 3. Injection infection and post-injection care
[0045] Inject the 5th instar bat m...
Embodiment 3
[0052] The bat moth used in this example is Thitarodes gonggaensis collected from Sichuan.
[0053] 1. Preparation of Chinese hairy sporozoites
[0054] The medium for cultivating blastospores is PDA medium: each liter contains 20g of glucose, 200g of potato, 5g of peptone, KH 2 PO 4 3g, MgSO 4 ·7H 2 O 1.5g and VB 1 0.02g, the rest is H 2 O (natural pH). After accurate molecular identification, the conidia of Trichosporum sinensis were inserted into the above-mentioned PDA medium, cultured in a shaker (120rpm, 9°C) for 60 days, and the blastospores of Trichosphaera sinensis were collected by centrifugation for injection to infect bat moths larva.
[0055] 2. Breeding of bat moth larvae
[0056] The larvae of the bat moth were fed with carrots, Polygonum villosa and Potentilla velvet in a mass ratio of 1:1:1 to obtain healthy, infected 2nd instar larvae of the bat moth.
[0057] 3. Injection infection and post-injection care
[0058] The 2nd instar bat moth larvae i...
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