Relevant enzymes for preparing mannitol by performing anabolism on Chinese caterpillar fungus and hirsutella sinensis, gene and application thereof
A Chinese technology of Trichosporum and Cordyceps sinensis, applied in the fields of application, genetic engineering, plant genetic improvement, etc., can solve the problem of rare research on the biosynthesis and metabolism of mannitol, and achieve the effect of high expression
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Embodiment 1
[0033] Example 1: Cultivation of "Bailing" production fungus Cordyceps sinensis
[0034] Source of the strain: firstly collect the natural Cordyceps sinensis from Qinghai, and bring it back to Hangzhou for isolation and screening, and obtain the L0106 strain, which is identified as Hirsrtella Sinensis by strain identification. This strain is preserved in a typical culture in China Collection Center, address: China, Wuhan, Wuhan University, 430072, deposit number is CCTCCNo: M 2011278, deposit date: August 5, 2011.
[0035] The bacterial classification is inoculated on the slant, and the culture medium formula (this is the liquid formula before solidification, and the slant is made after being prepared according to the following ratio) is glucose 2.0% (w / v, 1% means that 100mL medium contains 1g , the same below), corn flour 1.0%, potato juice 0.5%, dextrin 0.5%, yeast powder 0.5%, bran 1.0%, silkworm chrysalis powder 2.0%, peptone 1.0%, magnesium sulfate 0.05%, potassium dihyd...
Embodiment 2
[0036] Example 2: Extraction of total RNA of "Bailing" production fungus Cordyceps sinensis
[0037] The total RNA was extracted with TRIzol reagent, and the steps were as follows: 1) Grinding with liquid nitrogen: Take 1 g of wet bacteria and put it into a mortar, add liquid nitrogen repeatedly and grind until powdery, then pack it into a pre-cooled 1.5mL centrifuge tube, Add 1mL TRIzol reagent, mix well, and let stand on ice for 5min to completely separate the nucleic acid-protein complex. 2) RNA isolation: Add 0.2 mL of chloroform, shake vigorously for 15 s, let stand on ice for 2-3 min, centrifuge at 4°C, 12000 rpm for 15 min, separate the layers, and take the upper aqueous phase, about 600 μL. 3) RNA precipitation: add 500 μL of isopropanol, let stand on ice for 10 minutes, centrifuge at 12000 rpm at 4°C for 10 minutes, and discard the supernatant. 4) RNA washing: add 1 mL of 75% ethanol, suspend the precipitate, let stand on ice for 10 min, centrifuge at 4°C, 7500 rpm for...
Embodiment 3
[0038] After extracting the total RNA from the sample, the mRNA was enriched with Oligo(dT) magnetic beads. Add fragmentation buffer to break mRNA into short fragments (200-700bp), use mRNA as a template, use six-base random primers (random hexamers) to synthesize the first cDNA strand, then synthesize the second cDNA strand, and then pass through QiaQuick PCR After the kit is purified and eluted with EB buffer, end repair is performed, polyA is added and sequencing adapters are connected, and then agarose gel electrophoresis is used for fragment size selection, and finally PCR amplification is performed, and the built sequencing library is sequenced with Illumina GAIIx . The original image data obtained by sequencing is converted into sequence data through base calling, that is, raw data or raw reads. The reads containing only the adapter sequence in the original sequencing reads were removed for subsequent analysis.
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