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Defensin and application thereof in preparation of medicines for resisting aspergillus

An anti-Aspergillus and drug technology, applied in the direction of antifungal agents, pharmaceutical formulations, genetic material components, etc., can solve the problems of unsatisfactory treatment effect and low sensitivity

Inactive Publication Date: 2015-09-30
保罗生物园科技股份有限公司
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Type 2 herpes simplex virus (herpes simplex virus type2, HSV-2), vesicular stomatitis virus (vesicular stomatitis virus), influenza virus A / WSN (influenza virus A / WSN) are also easily infected by MCP-1 and MCP-2. Neutralizes, but MCP-1 and MCP-2 are ineffective against cytomegalovirus, echovirus type 11, and reovirus type 3
Aspergillus pyogenes infection may be of particular concern because A. pyogenes has poor susceptibility and poor response to many therapeutic fungal agents

Method used

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  • Defensin and application thereof in preparation of medicines for resisting aspergillus
  • Defensin and application thereof in preparation of medicines for resisting aspergillus
  • Defensin and application thereof in preparation of medicines for resisting aspergillus

Examples

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Embodiment 1

[0100] Embodiment 1. Expression vector construction method of Chlorella ellipsoides nitrate reductase mutant

[0101] Primers were designed according to the Ubiquitin promoter sequence (SEQ ID NO: 1), upstream primer: 5' CCGGAAGCTT GTGCAGCGTGACCCG3' (SEQ ID NO: 2); downstream primer: 5' GCCCGGATCC CTGCAGAAGT3' (SEQ ID NO: 3), wherein a Hind III restriction site (underlined part) is added to the upstream primer, and a BamH I restriction site (underlined part) is added to the downstream primer, and PCR method is used to obtain The Ubiquitin promoter was obtained in the maize genome, and the sequencing results showed that it was a Ubiquitin promoter sequence (SEQ ID NO: 4, which added Hind III restriction sites and BamH I respectively at the 5' end and 3' end of SEQ ID NO: 1 Restriction sites). The PCR reaction conditions were: pre-denaturation at 94°C for 3 min, denaturation at 94°C for 30 s, annealing at 55°C for 30 s, extension at 72°C for 2 min, and extension at 72°C for ...

Embodiment 2

[0102] Example 2. Using the pGreen0029 framework to construct an expression vector.

[0103] Design primers according to Nos terminator sequence (SEQ ID NO: 6), upstream primer: 5' ATAAGAATGCGGCCGC TCGAATTTCCCCGATCGTTCAAAC3' (SEQ ID NO: 7) downstream primer: 5' CGAGCTCGCCCGATCTAGTAACATAGATGA3' (SEQ ID NO: 8) wherein a Not I restriction site (underlined part) is added to the upstream primer, a Sac I restriction site (underlined part) is added to the downstream primer, and the PCR method is used The Nos terminator was obtained from pBI221 (Clontech). The PCR reaction conditions were: pre-denaturation at 94°C for 3 min, denaturation at 94°C for 30 s, annealing at 56°C for 30 s, extension at 72°C for 30 s, and extension at 72°C for 10 min after 30 cycles. The 268bp fragment of the PCR product was double-digested with Not I and Sac I endonucleases, and the plasmid pGreen0029( image 3 , from BBSRC) were also double-digested with Not I and Sac I endonucleases, and then the two d...

Embodiment 3

[0104] Example 3. Construction of the expression vector pGreen-NR-U-mNP1 of Chlorella ellipsoides nitrate reductase mutant.

[0105] According to conventional techniques, the Ubiquitin promoter (SEQ ID NO: 1) was extracted from the vector pbinUGUS ( figure 2 ) after being recovered by HindIII and BamHI double enzyme digestion, connected to the pGreen0029nos vector that was also subjected to HindIII and BamHI double enzyme digestion ( Figure 4 ) to obtain pGreen0029-U-nos primary intermediate vector ( Figure 5 ). The sequence with the target gene mNP-1 (its sequence is as SEQ ID NO: 13) was synthesized by chemical synthesis method. In order to improve the antiviral activity of NP-1, in the process of synthesis, the N-terminal of NP-1 added A methionine transforms NP-1 into mNP-1. Because the mNP-1 gene is too small, in order to facilitate the construction of the vector, a 75bp auxiliary sequence was added to the C-terminus of the gene. Two restriction sites BamH I and Not...

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Abstract

The invention relates to expression of improved rabbit defensin NP-1 (mNP-1) employing chlorella. The defensin mNP-1 expressed in the chlorella has a high inhibiting or killing effect. The result of the defensin can be applied to preparation of medicines for resisting aspergillus.

Description

technical field [0001] The invention relates to a defensin and its application in the preparation of anti-Aspergillus drugs. Specifically, it relates to the defensin mNP-1 produced by Chlorella, and its application in the preparation of anti-Aspergillus drugs. Background technique [0002] Structural Features and Classification of Defensins [0003] Defensins are a class of cationic small peptides widely present in animals, plants and humans with microbial resistance. Defensins generally consist of 29-54 amino acids with a molecular weight of 3-6KD. It has the following common characteristics in structure: (1) positively charged, (2) rich in arginine, (3) has a certain number of conserved cysteine, (4) forms intramolecular molecules through cysteine ​​molecules Disulfide bonds, cyclization of peptides to form antiparallel β-sheet structures. Since it was named by Professor Lehrer of the University of California in 1985 (Selsted et al., 1985), it has been widely concerned...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): A61K38/17A61K48/00A61P31/10
Inventor 武庆胡赞民陈宇红白丽莉王龙徐玲尹维波范成明崔晓磊揣文华辛秀明张圩玲张伟王谝
Owner 保罗生物园科技股份有限公司
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