Method for preparing young pine infected by armillaria matsutake
一种松树、蘑菌的技术,应用在植物学设备和方法、园艺方法、真菌类等方向,能够解决复杂实验技术、没有高产量等问题
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Embodiment 1
[0044] Example 1 Preparation of young pine trees infected with matsutake mushrooms using a culture vessel for Flammulina velutipes
[0045] In order to obtain such Figure 4 Young pine trees infected with Matsutake mushroom shown, sterilized K-solid medium, which is usually used for cultivating Flammulina velutipes mushrooms, was poured into a sterilized culture vessel and allowed to harden . After covering the K-solid medium with filter paper, the mycelium and 5ml sterile water were inoculated on the filter paper with a dry weight of 0.075mg. A mixture of perlite and sphagnum peat moss was added to the inoculated fungal mycelia and K-broth pH 5.6 was added to the soil to form an infection medium. Then, the sprouts obtained from germinating pine sub-germinations under aseptic conditions were planted on the infection medium containing mixed soil and K-liquid medium, and the culture container was covered with a cover, and then the pine trees were grown at 20° C. under the ligh...
preparation example 1
[0049] Preparation Example 1: Preparation of Tricholoma matsutake inoculum from liquid culture
[0050] The matsutake fungus used as an inoculum in the present invention was isolated from a naturally occurring matsutake mushroom just before its cap opened from Gyeongju, Gyeongsangbuk-do, Korea. -si) Collected from 10 hectares (ha) of Doyoo Forest in Namsan-dong. Within 8 hours after collection, the part between the cap and the gills in the collected mushrooms was cut into 0.5 mm sized pieces, and planted on the MMN medium of pH 5.5 according to the composition shown in Table 2 below. Then, the isolated mycelia were further cultured on PDA medium for 60 days at the optimum growth temperature for matsutake mushroom growth, 23±0.5°C. The matsutake fungus was successfully isolated from about 98% of the cultured mycelia. It was found that the isolated mycelia had more than 99% homology with the known ITS sequence, the entire 5.8S rRNA and part of the 18S DNA sequence. The identi...
preparation example 2
[0053] Preparation Example 2: Preparation of Infection Medium Using Mixed Soil and K-Liquid Medium
[0054] Perlite and peat moss peat bog were used as bed soil for cultivating pine sprouts. After mixing in a ratio of 80:1.5, they were sterilized in containers. On the ultra-clean bench, pour the sterilized mixed soil into the culture container inoculated with the matsutake mycelium to a suitable height.
[0055] K-liquid medium was prepared according to the composition shown in Table 1 above. After autoclaving at high temperature, pour 100 ml of K-liquid medium onto the mixed soil on a clean bench.
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