Selenium-enriched pleurotus eryngii cultivation and ingredient detecting methods
A technology for detecting king oyster mushrooms and components, which is applied in the fields of botanical equipment and methods, measuring devices, color/spectral characteristic measurement, etc. Benefit, increase yield, increase the effect of selenium enrichment capacity
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0048] Embodiment 1: the cutting and cultivating method of selenium-enriched Pleurotus eryngii
[0049] (1) Preparation medium: a, take the following raw materials by weight: 50 corncobs, 30 miscellaneous sawdust, 17 bran, 8 nutrient granules, 1 lime, 1 white sugar, 1 gypsum powder, 0.0001 sodium selenite; b 1. Crush the non-mildewed corncobs into the size of soybean grains and set aside; c. Mix sodium selenite and white sugar evenly, then add an appropriate amount of water and stir in a mixer for 1 minute to fully dissolve it, then add corncobs, Mix sawdust, bran, nutrient granules, lime, and gypsum powder for 5 minutes to make the compost fully absorb water; d. Spread the well-mixed medium on the cement floor for 24 hours, and turn it twice in the middle;
[0050] (2) Bagging: put the culture medium into a 17×33 cm polypropylene bag, each bag contains 1.5 kg of culture medium, compact it when filling the bag, put a collar on it, plug it with a silicone plug, and use a punche...
Embodiment 2
[0059] Embodiment 2: the selenium composition determination method of Pleurotus eryngii
[0060] (1) Determination of Selenium Content in Fruiting Body of Pleurotus eryngii
[0061] Mark the fully grown fruiting body and put it away as a sample. Wash the sample with distilled water for three times, dry it at 50°C, cool, pulverize, grind and weigh it. Because in this test, the quality of the obtained sample is less after drying, it is called The amount to be taken is also reduced as appropriate, accurately weigh 0.25 sample fine powder, add the volume ratio of HNO 3 : HClO 3 = 5ml of mixed acid solution composed of 2:1, soak and dissolve, bathe in a water bath at 100°C until the powder is completely dissolved, the mixed acid solution is clear, dilute the acid solution to 50ml, take 10ml of the diluted solution, put it into a conical flask, add 5 Mix %EDTA-2Na5ml, then adjust the pH to 2 with dilute nitric acid, add 3ml of 1% o-phenylenediamine solution, shake and shake for on...
Embodiment 3
[0066] Embodiment 3: the amino acid composition determination method of Pleurotus eryngii
[0067] (1) Pleurotus eryngii sample pretreatment
[0068] Clean the Pleurotus eryngii sample, dry it, separate the stipe and the cap, put the stipe and the cap respectively in a DHG-9240A electric heating constant temperature blast drying oven to dry to constant weight at 110°C, cool, and place in the laboratory Grind into fine powder in a bowl, pass through a 60-mesh sieve, and store in a desiccator for later use;
[0069] (2) Determination of amino acid content
[0070]Grind the above-mentioned different experimental materials, pass through 80 mesh sieve, accurately weigh 100mg of the analysis sample, put it into the hydrolysis tube, add 15-20ml of 6mol / L hydrochloric acid into the tube, vacuumize, and fill with 2000g / m 2 High-purity nitrogen, repeat this 3 times, seal the nozzle under nitrogen and place it at 110°C for 22 hours, take it out and cool it, filter the hydrolyzate, rins...
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