Acid xylanase XYNB, genes and application thereof
A technology of acid xylanase and xylanase, applied in the field of genetic engineering
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0117] Example 1 Isolation of acidophilic fungus Bispora sp.X-1
[0118] After the uranium mine wastewater sample from a mine in Jiangxi was enriched and cultured (enrichment medium: (NH 4 ) 2 SO 4 5g / L, KH 2 PO 4 1g / L, MgSO 4 ·7H 2 O 0.5g / L, FeSO 4 ·7H 2 O 0.01g / L, CaCl 2 0.2g / L, 0.5% corncob powder, 0.5% bran, pH2.5), and spread it on the enzyme-producing medium ((NH 4 ) 2 SO 4 5g / L, KH 2 PO 4 1g / L, MgSO 4 ·7H 2 O 0.5g / L, FeSO 4 ·7H 2 O 0.01g / L, CaCl 2 0.2g / L, 1% xylan, 1.5% agarose, pH 2.5) on a plate, culture at 30°C for 5-6 days, pick colonies that produce transparent circles and streak them on the enzyme-producing medium plate, and repeat the streaking and separation process 3 rounds to purify the strain. The strain that secretes xylanase is screened by this method.
[0119] This strain was cultured on PDA at 30°C for 7 days, and the colony diameter was 2-3cm, gray-black or gray-brown, circular and radial, with velvet-like wrinkles on the surface ...
Embodiment 2
[0120] Example 2 Cloning of the gene xynB encoding the acidophilic fungus Bispora sp.X-1 xylanase
[0121] Extraction of acidophilic fungus Bispora sp.X-1 genomic DNA:
[0122] Filter the mycelium cultured in liquid for 3 days with sterile filter paper, put it into a mortar, add 2mL of extract, grind for 5min, then put the grinding solution in a 50mL centrifuge tube, lyse in a water bath at 65°C for 20min, and mix every 10min. Homogenize once and centrifuge at 10,000 rpm for 5 min at 4°C. The supernatant was extracted in phenol / chloroform to remove impurity proteins, and then an equal volume of isopropanol was added to the supernatant. After standing at room temperature for 5 minutes, centrifuge at 10,000 rpm for 10 minutes at 4°C. The supernatant was discarded, the precipitate was washed twice with 70% ethanol, dried in vacuum, dissolved by adding an appropriate amount of TE, and stored at -20°C for later use.
[0123] Degenerate primers P1, P2 were designed and synthesized...
Embodiment 3
[0132] The RT-PCR analysis of embodiment 3 xylanase gene
[0133] Extract the total RNA of Bispora sp.X-1, use reverse transcriptase to obtain a strand of cDNA, and then design appropriate primers (XynB F: 5′-ATGCATGCATTCTCATACTTGGCTGTGGCG-3′, XynB R: 5′-CTAATTCGACACAGTCTGATACGCATTTCCACTCC-3′) The single-stranded cDNA was amplified to obtain the cDNA sequence of xylanase, and the amplified product was recovered and sent to Sanbo Biotechnology Co., Ltd. for sequencing.
[0134] By comparing the genome sequence and cDNA sequence of xylanase, it was found that the gene has an intron, the cDNA is 693bp long, encoding 231 amino acids, and the N-terminal 19 amino acids are its signal peptide sequence. The deduced amino acid sequence has high sequence similarities with xylanases from Hypocrea jecorina, Penicillium funiculosum and Phanerochaetechrysosporium, which are 57.1, 49.8 and 44.4%, respectively. It was proved that the gene encoding xylanase isolated and cloned from Bispora sp...
PUM
Property | Measurement | Unit |
---|---|---|
molecular weight | aaaaa | aaaaa |
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