Termitomyces albuminosus strain with high yield of cerebroside compounds and mycelium cultivation method for termitomyces albuminosus strain
A technology of cerebrosides and gallinaceous fungi, applied in the field of microorganisms, can solve the problems of low content of cerebrosides A and B and the like
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0058] This example illustrates mycelium induction and strain purification.
[0059] 1. Collection of fruiting bodies of wild Gallus teratum
[0060] The fruiting bodies of Gallinarum albumen were collected from the mountainous area of Jianshui County, Honghe Prefecture, Yunnan Province in August 2013, numbered, and stored in a refrigerator at 4-10°C.
[0061] 2. Hyphae induction
[0062] Clean and sterilize the collected fruiting body of the wild Gallus luteum, take the tissue of the fruiting body with a scalpel, and cut into about 0.1cm 3 of small pieces. The tissue pieces (86 pieces in total) were respectively connected to test tubes equipped with slant medium, placed in a constant temperature incubator at 25° C. for 5-16 days, and hyphae of each tissue were induced. The slant medium was prepared as follows. Recipe (g / L): Potato extract powder 15, glucose 20, agar 20, yeast extract powder 2, pH 5; sterilize at 121°C for 20 minutes; cool to about 60°C at room temperatu...
Embodiment 2
[0066] This example illustrates the screening of strains.
[0067] 1. Cell culture.
[0068] strain 51-S M -2 / P2, 51-S T -1 / P1 and 51-P-3 / P1 were used as objects for strain screening.
[0069] Try to select colonies with the same growth potential, punch holes at the edge of the plate colony with a sterile puncher with a pore diameter of 5 mm, take out circular colony slices with a diameter of 5 mm, and inoculate to a new plate medium (formula (g / L): potato Extract powder 15, glucose 20, agar 20, yeast extract powder 2, pH5). Each bacterial strain was connected with 6 plate mediums, and each plate medium was connected with 3 bacterial blocks. Cultivate at a constant temperature of 28°C, measure the diameter of the colony regularly, and observe the color, shape and growth of the colony.
[0070] figure 1 Indicates the change of colony diameter of each strain during plate culture. 27 days before plate culture, strain 51-S M -2 / P2, 51-S TThere was no significant differenc...
Embodiment 3
[0095] This example illustrates the identification of bacterial species.
[0096] 1. Morphological identification.
[0097] The conidia of the strain CTM-1 were oval, with a size of 5-10 μm×10-15 μm. The mycelium is less branched, with a diaphragm, no lock joints, and the diameter of mycelium is about 5-7μm; The characteristics of mycelium and conidia of this strain are consistent with those of Termitomyces albuminosus (Nie Xiaodong, optimization of submerged fermentation conditions for mycelia and saponins [D]. Jiangnan University, 2009). like Figure 5 shown.
[0098] 2. Molecular biological identification.
[0099] The 18SrRNA sequence of the fruiting body raw material (Fruiting body-5) used for mycelia induction is as follows:
[0100]
[0101] The 18S rRNA sequence of strain CTM-1 is as follows:
[0102]
[0103] Using the sequence local similarity query system BLAST (National Center for Biotechnology Information, USA), the 18S rRNA sequences of fruiting body ...
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com