Peony geranyl geranyl pyrophosphate synthase (plggps) gene and its encoded products and applications

A technology of geranyl pyrophosphate and enzyme gene, applied in application, genetic engineering, plant genetic improvement, etc., to achieve the effect of increasing the content of terpenoids

Inactive Publication Date: 2015-11-25
INST OF CHINESE MATERIA MEDICA CHINA ACAD OF CHINESE MEDICAL SCI
View PDF0 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Before the publication of the present invention, there was no disclosure or report of the geranylgeranyl pyrophosphate synthase gene and its amino acid sequence in Paeoniae alba mentioned in this patent application

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Peony geranyl geranyl pyrophosphate synthase (plggps) gene and its encoded products and applications
  • Peony geranyl geranyl pyrophosphate synthase (plggps) gene and its encoded products and applications
  • Peony geranyl geranyl pyrophosphate synthase (plggps) gene and its encoded products and applications

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0018] Embodiment 1, the construction of peony cDNA library

[0019] 1. Isolation and detection of peony total RNA

[0020] Take 2 g of the root of Paeonia lactiflora, quickly grind it into powder with liquid nitrogen in a mortar, and quickly transfer it to 10 mL of extraction buffer (CTAB (W / V) 2%, Tris-HCl (pH 8. 0) 100mmol·L -1 , EDTA25mmol·L -1 , NaCl2.0mol L -1 , PVP402%, spermidine 0.5g / L, mercaptoethanol 2%), fully shake and mix; extract twice with equal volume of chloroform, and centrifuge at 7500g for 15 minutes. Add 1 / 4 volume of 10MLiCl to the supernatant, mix well, and place it at 4°C to precipitate overnight; centrifuge at 7500g for 20 minutes, and use 500 μL SSTE (SDS0.5%, NaCl1mol L -1 , Tris-HCl (pH8.0) 10mmol L -1 , EDTA1mmol·L -1 , dissolved at 65°C for 5 minutes. Extract with an equal volume of chloroform, centrifuge at 13,000g for 5 minutes; add 2 times the volume of absolute ethanol to the supernatant, and store at -70°C for 2 hours; centrifuge at 1...

Embodiment 2

[0023] Example 2: Cloning of Paeoniae officinalis-related genes

[0024] Randomly pick 5000 single clones for colony PCR identification. Take an appropriate amount of PCR thin-walled tubes, place them on ice, and add 17.3ul of sterilized water to each tube. Use a sterilized 10ul small tip to pick up the monoclonal white spot into sterilized water, shake and mix. Add in sequence: Taqbuffer 2.5μL, MgCl 2 (25mM) 1.8μL, dNTP (2.5mM) 1μL, M13+ primer (10pmol) 1μL, M13-primer (10pmol) 1μL, Taq enzyme 0.4μL. The PCR reaction conditions were 5 minutes of pre-denaturation at 94°C, 40 seconds at 94°C, 40 seconds at 54°C, 4 minutes at 72°C, 35 cycles of extension at 72°C for 10 minutes, and storage at 4°C. After the PCR reaction enters 4°C, remove the PCR thin-walled tube, take 7ul of PCR product and add 3ul of bromofinland for agarose gel electrophoresis, take a picture half an hour later, observe the gel map, and roughly identify the size of the insert fragment and small fragments a...

Embodiment 3

[0025] Embodiment 3, the bioinformatics analysis of PLGGPS gene

[0026] The full-length cDNA of the peony geranylgeranyl pyrophosphate synthase gene involved in the present invention is 1110 bp in length, and the detailed sequence is shown in sequence 1 in the sequence list, wherein the open reading frame is located at 1-1110 bp. The full-length cDNA sequence of Peony was searched for nucleotide homology in Non-redundantGenBank+EMBL+DDBJ+PDB and Non-redundantGenBankCDStranslation+PDB+Swissprot+Superdate+PIR databases using BLAST program. The gene has high homology with GGPS in other species at the amino acid level, and has a typical Geranylgeranylpyrophosphatesynthase domain. Such as figure 1 .

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

PUM

No PUM Login to view more

Abstract

The invention discloses a PLGGPS gene and a coded protein and application thereof. The gene is cloned from Paeonia lactiflora by constructing a cDNA library for the first time, so a gap in separation and cloning of a geranylgeranyl diphosphate synthase gene from the traditional Chinese medicine--Paeonia lactiflora is filled in. The PLGGPS gene provided by the invention has a nucleotide sequence shown in SEQ ID NO. 1, or a homologous sequence obtained through addition, substitution, insertion or deletion of one or a plurality of nucleotides of the nucleotide sequence shown in SEQ ID NO. 1, or an allele of the gene or a nucleotide sequence derived from the allele. The protein coded by the gene has an amino acid sequence shown in SEQ ID NO. 2 or a homologous sequence obtained through addition, substitution, insertion or deletion of one or a plurality of amino acids of the amino acid sequence shown in SEQ ID NO. 2. The PLGGPS gene can increase the content of diterpene metabolites in Paeonia lactiflora through biotechnology and has good application prospects in aspects like quality improvement of the medicinal material Paeonia lactiflora and synthetic biology of active components of Paeonia lactiflora.

Description

technical field [0001] The invention belongs to the field of biotechnology, and mainly relates to cloning of geranylgeranyl pyrophosphate synthase gene and its coded product and application by using peony cDNA library, especially relates to the biosynthesis of organic acids and terpenoid enzyme genes with pharmacologically active ingredients. The coded product and application thereof belong to the field of genetic engineering of medicinal plants. Background technique [0002] The formation of medicinal plant active ingredients is the product of a unique group of genes in plant secondary metabolic pathways. With the extensive and in-depth study of plant functional genomes, the study of functional genes related to secondary metabolism synthesis of medicinal plants with unique characteristics and broad application prospects has gradually become a research hotspot. It provides a theoretical basis for the biosynthetic pathway and its regulation mechanism and explains the formati...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

Application Information

Patent Timeline
no application Login to view more
Patent Type & Authority Patents(China)
IPC IPC(8): C12N15/54C12N9/10C12N15/63A01H5/00
Inventor 黄璐琦袁媛汪周勇
Owner INST OF CHINESE MATERIA MEDICA CHINA ACAD OF CHINESE MEDICAL SCI
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap