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A kind of alginate lyase sha-2 gene and its expression vector

A technology of alginate lyase and gene, which is applied in the direction of genetic engineering, plant gene improvement, and the introduction of foreign genetic material using vectors, etc. It can solve the problems of low enzyme production, difficulty in meeting application requirements, and high cost of wild-type alginate-decomposing bacteria. problems, achieve broad substrate specificity, facilitate industrial production, and be easy to operate

Active Publication Date: 2018-07-24
KUNMING UNIV OF SCI & TECH
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the wild-type alginate-decomposing bacteria have low enzyme production and high cost, and it is difficult to meet the actual application requirements.

Method used

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  • A kind of alginate lyase sha-2 gene and its expression vector
  • A kind of alginate lyase sha-2 gene and its expression vector
  • A kind of alginate lyase sha-2 gene and its expression vector

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0039] Example 1: Marinicatena alginatilytica Preparation and Detection of SH-52 Genomic DNA

[0040] used in the present invention Marinicatena alginatilytica SH-52 is a strain screened by our laboratory. The preparation of SH-52 genomic DNA adopts the extraction method of common bacterial genome. The specific content is as follows: Take 2 mL of overnight culture liquid and centrifuge at 4000 rpm for 2 min at 4 ° C. Discard the supernatant and collect the bacteria. Add 100μl Solution I suspension bacteria, 30ul 10% SDS and 1μl 20mg / ml proteinase K, mix well, and incubate at 37°C for 1 hour; add 100μl 15mol / L NaCl, mix well; add 20μl CTAB / NaCl solution (CTAB 10%, NaCl 0.7mol / L), mix well, 65℃, 10 minutes; add an equal volume of phenol / chloroform / isoamyl alcohol (25:24:1) to mix, centrifuge at 12000rpm for 5 minutes; take the supernatant, add 2 times the volume of Water ethanol, 0.1 times the volume of 3mol / L NaOAC, placed at -20°C for 30 minutes; centrifuged at 12000rpm fo...

Embodiment 2

[0041] Example 2: Alginate Lyase SHA-2 Gene amplification and TA cloning

[0042] alginate lyase SHA-2 gene amplification and cloning figure 2 As shown, first find out from the whole genome sequencing results SHA-2 The full-length gene sequence, and design a pair of specific primers, the sequence is as follows:

[0043] SHA-2-F: GGATCC ATGAAAAAATCAAGCTTTTTAC

[0044] SHA-2-R: GCGGCCGC TCAATCCTGACCAGGCG

[0045] The 5' end primer has the GGATCC characteristic sequence, and thus forms the BamH I restriction site; the 3' end adds the GCGGCC characteristic sequence, forming the Not I restriction site.

[0046] Add 5-10ng of Marinicatena alginatilytica SH-52 genomic DNA is used as a template, and 30-50ng of specific primers SHA-2-F and SHA-2-R, 2.5μl dNTP (10mM), 0.5-3.0μl of Pfu reaction buffer and 0.5-1.0μl of pfu (5U / μl) polymerase (Beijing Quanshijin Biotechnology Co., Ltd.), add double distilled water to make the final volume 25μl. Heated at 94°C for 3 minutes on...

Embodiment 3

[0047] Example 3: Prokaryotic expression vector pGEX-4T-1- SHA-2 build

[0048] pGEX-4T-1- SHA-2 A build strategy such as Figure 6 As shown, the purified prokaryotic expression vectors pGEX-4T-1 (purchased from GE Healthcare) and pMD19T- SHA-2 , separated the cleaved vector and insert fragments by agarose gel electrophoresis, and recovered the vector fragments pGEX-4T-1 (4.9kb) and pMD19- SHA-2 produced by cutting SHA-2 The DNA fragment of the gene (about 1.0kb), and then use the ligase kit of TaKaRa to connect the pGEX-4T-1 vector fragment and SHA-2 The DNA fragment of the gene produces the prokaryotic expression vector pGEX-4T-1- SHA-2 . Use the ligation reaction mixture to transform high-efficiency E. coli competent cells Trans1-T1 (Beijing Quanshijin Biotechnology Co., Ltd.), and spread the transformed E. coli on a plate added with ampicillin (Amp, 100mg / L). Cultivate overnight at 37°C, screen Amp-resistant recombinant colonies, and extract plasmids from Amp-resist...

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Abstract

The invention discloses an alginate lyase SHA‑2 gene, the nucleotide sequence of which is shown in SEQ ID NO: 1; the invention constructs a prokaryotic expression vector of the alginate lyase gene SHA‑2, the prokaryotic expression vector The expression product alginate lyase SHA‑2 can be obtained in a short period of time, and it has a wide range of substrate specificity, and can utilize both polymannuronate (Poly‑mannuronate, PolyM) and polyguluronic acid (Poly-guluronate, PolyG) is the substrate, and the enzyme activity reaches 5.2U / mg. It is a bifunctional enzyme with wide application prospects. The prokaryotic expression vector and the overall expression system of the present invention are easy to operate and convenient for industrial production.

Description

technical field [0001] The invention belongs to the field of microbial genetic engineering, in particular to an alginate lyase SHA-2 gene and its prokaryotic expression vector pGEX-4T-1- SHA-2 , the vector highly expresses the alginate lyase protein SHA-2. Background technique [0002] In recent years, the development and utilization of marine resources has gradually become a research hotspot. Because of its unique physical and chemical properties, alginic acid has broad application prospects in the fields of food, medicine and chemical industry. Alginate oligosaccharides have become the focus of new drug development because of their various physiological activities. At the same time, as one of the most abundant marine biomass, alginic acid has the following advantages: (1) high photosynthetic efficiency, fast growth, high yield, and abundant resources; (2) growth does not occupy arable land; (3) hardly contains wood The content of cellulose is low, the pretreatment is sim...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C12N15/60C12N15/70
Inventor 伊日布斯何漫漫李勤超吴铭杰严金平
Owner KUNMING UNIV OF SCI & TECH
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