Preservation method for mushroom strain
A technology for the preservation of strains and mushrooms, which is applied in the directions of microorganism-based methods, preservation of microorganisms, biochemical equipment and methods, etc., can solve the problems of operating contaminated strains, short storage time, inconvenient carrying, etc., and achieves improved low-temperature freezing resistance. properties, slowing down the loss of water, and wide application
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0020] (1) First prepare the culture medium, its composition formula includes: 20% wheat extract, 31% wood flour, 2% yeast extract, 0.8% sucrose, 2% lactose, buffer (calcium sulfate is used in this example) 0.5%, calcium chloride 0.7%, magnesium sulfate 1.2%, agar 1.2%, feed water 41%. The pH of the prepared solution is 6.8. Make a sterile plate, and when the medium is solidified, lay a layer of porous paper on the surface of the medium;
[0021] (2) Then increase the amount of filler to reduce the contact surface with the air; when the culture medium is cooled to 24°C, inoculate the mushroom strains on the carrier, cultivate in a sterile incubator at 22°C for 100 hours, and then put the carrier together with the strains Take it off together, and cut it according to the size of the bottom of the test tube to the corresponding size, place it in the test tube, compact it slightly, add a cotton plug, sterilize by high-pressure steam at 128°C for 45 minutes, and move the containe...
Embodiment 2
[0027] The preparation medium of this embodiment has a composition formula: 25% of wheat extract, 30% of wood flour, 1.6% of yeast extract, 1% of sucrose, 1.5% of lactose, buffer (calcium carbonate used in this embodiment) 0.8 %, calcium chloride 0.7%, magnesium sulfate 1.3%, agar 1.9%, feed water 44%, pH 6.5. , Calcium chloride 0.7%, magnesium sulfate 1.2%, agar 1.2%, feed water 41%.
[0028] The rest of the operation steps in this embodiment are the same as those in Embodiment 1, and will not be repeated here.
Embodiment 3
[0030] Preservation method of the present embodiment, its steps are:
[0031] (1) Medium preparation, its composition formula includes 30% of wheat extract, 15% of wood flour, 2.8% of yeast extract, 1.2% of sucrose, 2.5% of lactose, 0.6% of buffer (calcium carbonate or calcium sulfate), chloride Calcium 0.9%, magnesium sulfate 1%, agar 1.2%, feed water 37%, pH 6.7. Among them, the ratio of material to water is 1:1. Then make a sterile plate, and when the culture medium is solidified, lay a layer of porous paper on the surface of the culture medium.
[0032] (2) Increase the amount of filler to reduce the contact surface with the air; when the culture medium is cooled to 22°C, inoculate the mushroom strains on the carrier, cultivate in a sterile incubator at 22°C for 100 hours, and then put the carrier together with the strains And take it off, and cut it according to the size of the bottom of the test tube to the corresponding size, place it in the test tube, compact it slig...
PUM
Login to View More Abstract
Description
Claims
Application Information
Login to View More - R&D
- Intellectual Property
- Life Sciences
- Materials
- Tech Scout
- Unparalleled Data Quality
- Higher Quality Content
- 60% Fewer Hallucinations
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2025 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com