SmFPS (Salviamiltiorrhizabge Farnesyl Pyrophosphate Synthase) gene as well as coded protein and application thereof

A technology based on pyrophosphate synthase and salvia miltiorrhiza, applied in the fields of application, genetic engineering, plant genetic improvement, etc.

Inactive Publication Date: 2010-12-29
INST OF CHINESE MATERIA MEDICA CHINA ACAD OF CHINESE MEDICAL SCI
View PDF0 Cites 15 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Before the present invention was published, there was no disclosure or report of the Danshen terpenoid enzyme gene and its amino acid sequence 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
  • SmFPS (Salviamiltiorrhizabge Farnesyl Pyrophosphate Synthase) gene as well as coded protein and application thereof
  • SmFPS (Salviamiltiorrhizabge Farnesyl Pyrophosphate Synthase) gene as well as coded protein and application thereof
  • SmFPS (Salviamiltiorrhizabge Farnesyl Pyrophosphate Synthase) gene as well as coded protein and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0042] Embodiment 1, the making of Danshen cDNA chip

[0043] 1. Isolation and detection of total RNA from Salvia miltiorrhiza

[0044] Take 2 g of Shaanxi Shangluo Salvia (Salvia Miltiorrhiza Bge) roots, quickly grind them into powder with liquid nitrogen in a mortar, and quickly transfer them to 10 mL of extraction buffer (CTAB (W / V) 2%, Tris-HCl (pH8.0)100mmol·L -1 , EDTA 25mmol·L -1 , NaCl 2.0mol·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 10M LiCl 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 (SDS 0.5%, NaCl 1mol L -1 , Tris-HCl (pH8.0) 10mmol L -1 , EDTA 1mmol·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 ...

Embodiment 2

[0054] Example 2: Cloning of Salvia miltiorrhiza-related genes

[0055] 1. Chip hybridization analysis

[0056] The hairy roots of Salvia miltiorrhiza were induced by Ri-plasmid transformation by direct infection with Agrobacterium rhizogenes 15834. Well-grown hairy roots of Salvia miltiorrhiza (0.1 g each) were subcultured on 6, 7V solid medium, placed in an incubator at 25°C for dark culture, and harvested at 30 days, 45 days, and 60 days, respectively. The 30-day-old material was used as a reference, and hybridization was carried out with the 45-day-old and 60-day-old material respectively, and was repeated twice. Each group was labeled positively and negatively to eliminate the error of the dye.

[0057] The indirect labeling method is used for probe labeling, including double-stranded cDNA synthesis, T7-mediated RNA in vitro transcription to synthesize cRNA, random primer reverse transcription, and cDNA labeling with KLENOW enzyme.

[0058] (1) Synthesis of double-stran...

Embodiment 3

[0070] Embodiment 3, the bioinformatics analysis of SmFPS gene

[0071] The full-length cDNA of the salvia miltiorrhiza diterpene synthase gene involved in the present invention has a length of 1494bp, and the detailed sequence is shown in sequence 1 in the sequence list, wherein the open reading frame is located at 58-1107bp. The full-length cDNA sequence of Salvia miltiorrhiza was searched for nucleotide homology in Non-redundant GenBank+EMBL+DDBJ+PDB and Non-redundant GenBank CDS translation+PDB+Swissprot+Superdate+PIR databases with BLAST program. The gene has high homology with FPS in other species at the amino acid level, and has a typical DXXDD domain of terpenoid enzymes. like figure 1 and 2 .

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 farnesyl pyrophosphate synthase gene as well as a coded protease and application thereof. The gene is obtained by clone from salviamiltiorrhizabge by utilizing a cDNA chip technology, which fills the blank of separating and cloning the farnesyl pyrophosphate synthase gene from a rare traditional Chinese medicine of salviamiltiorrhizabge. The farnesyl pyrophosphate synthase gene has a nucleotide sequence shown as SEQ ID NO.1, or a homological sequence adding, substituting, inserting or lacking one or more nucleotides or allelic genes and derived nucleotide sequence thereof. The protein coded by the gene has an amino acid sequence shown as SEQ ID NO.2 or a homological sequence adding, substituting, inserting or lacking one or more amino acids. The farnesyl pyrophosphate synthase gene can improve the content of tanshinone which is diterpene active element in the salviamiltiorrhizabge by the biotechnology, is beneficial to the quality improvement of the salviamiltiorrhizabge medicine, can be used for the breeding selection and has good application prospect.

Description

technical field [0001] The invention belongs to the field of biotechnology, mainly relates to the use of cDNA chip technology to clone the Danshen terpenoid enzyme gene and its coded product and its application, especially relates to the biosynthesis of the terpenoid enzyme gene with pharmacologically active ingredients and its coded product and its application, belonging to medicinal plants field of genetic engineering. Background technique [0002] The formation of active ingredients (secondary metabolites) of medicinal plants 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 forma...

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 Applications(China)
IPC IPC(8): C12N15/54C12N9/10C12N15/63C12N5/10C12N15/82
Inventor 黄璐琦戴住波崔光红袁媛王学勇张夏楠
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