Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Terpene fragrance gene Hctps1 from hedychium coronarium and use thereof

A technology of terpenoids and genes, which is applied to the ginger flower terpenoid floral fragrance gene Hctps1 and its application field, can solve the problem of not finding common structural elements, etc., and achieve the effect of shortening the breeding time

Inactive Publication Date: 2013-01-09
SOUTH CHINA AGRI UNIV
View PDF1 Cites 4 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

This signal peptide contains a large number of serine and threonine residues and less acidic amino acid residues, but no common structural elements were found

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
  • Terpene fragrance gene Hctps1 from hedychium coronarium and use thereof
  • Terpene fragrance gene Hctps1 from hedychium coronarium and use thereof
  • Terpene fragrance gene Hctps1 from hedychium coronarium and use thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0029] Example 1 Hctps1 Acquisition of gene cNDA and full-length DNA:

[0030] Ginger flower material: The ginger flower uses the petals of white ginger flower in full bloom. Weigh about 10g of the sample in a mortar, grind it into a powder with liquid nitrogen quick-freezing, and then transfer it to a sterile 50 mL centrifuge tube; immediately add 20 mL of boric acid buffer solution preheated at 80°C, incubate at 42°C and extract with slight shaking for 2 hours ; add 1 / 3 volume of 2.4 mol / L KCl solution and place in ice bath at 4°C for more than 1 h; centrifuge at 20,000 rpm and 4°C for 30 min; take the supernatant and add 8 mol / L LiCl solution to make the final concentration of LiCl become 2 mol / L, precipitate RNA overnight in ice bath at 4°C; centrifuge at 10,000 rpm for 30 min and remove the supernatant; wash the precipitate with 2 mol / L LiCl solution 1-3 times; add 10 mmol / L Tris-HCl (pH7.5) Buffer solution to dissolve the precipitate; add 2mol / L KOAc solution and mix o...

Embodiment 2

[0041] Example 2 Hctps1 Gene expression analysis:

[0042] Take 1 μL of the total RNA solution and dilute it 100 times, measure its concentration on the Eppendorf Biophotometer Nucleic Acid Protein Analyzer, calculate the volume of RNA solution used to take 10 μg RNA, make up to 10 μL with sterilized ultrapure water, add 10 μL EB-containing RNA electrophoresis and load the sample The buffer was denatured at 70°C for 10 minutes, cooled rapidly in ice, and subjected to denaturing gel electrophoresis (50V, 60min) with 1.2% agarose gel containing formaldehyde. After electrophoresis, observe whether the bands are consistent in depth under the gel imaging system. If they are inconsistent, adjust the amount of total RNA loaded. After adjusting the total RNA bands to be basically consistent, put the gel pieces in a 2×SSC solution, shake and wash twice on a decolorizing shaker at room temperature, about 20 minutes each time. The denatured RNA was transferred from the gel to a nylon m...

Embodiment 3

[0048] Example 3 Hctps1 Gene prokaryotic expression:

[0049] According to the obtained full-length cDNA, the signal peptide fragment was removed, and the S alI and N otI restriction site-specific primers for PCR amplification. The PCR product was recovered with the Takara recovery kit, and the recovered product was directly used S alI and N otI restriction endonuclease was used for double digestion, and 1% agarose gel was used to recover the target fragment. For pET-28a prokaryotic expression vector S alI and N otI restriction enzyme was used for double digestion and 1% agarose gel was used to recover large fragments. After ligation overnight at 16°C, the ligation product was transformed into Escherichia coli ( E. coli ) DH5α competent cells; the recombinant prokaryotic expression vector was obtained after the extracted plasmid was identified by enzyme digestion and sequencing.

[0050] Transform Escherichia coli (BL21) competent cells with the identified recombinan...

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

PropertyMeasurementUnit
molecular weightaaaaaaaaaa
Login to View More

Abstract

The invention discloses a terpene fragrance gene Hctps1 from hedychium coronarium and use thereof. The nucleotide sequence of the terpene fragrance gene from hedychium coronarium is shown by SEQ ID No.1; and the amino acid sequence of the protein coded by the gene is shown by SEQ ID No.2. The terpene fragrance gene Hctps1 from hedychium coronarium can be expressed in flower tissues of fragrant hedychium coronarium and expressed under induction by damage in laminae of hedychium coronarium, but cannot be expressed in non-fragrant hedychium coronarium varieties; and the expression of the gene isassociated with the growth process of flowers. The terpene fragrance gene Hctps1 from hedychium coronarium disclosed by the invention can be connected to any plant conversion vector and then transferred into cells of hedychium coronarium and other plants to produce transgenic fragrant or resistance varieties in which the gene is expressed, and thus, the gene can be used in production. In addition, specific molecular markers can be produced according to the sequence information of the gene and used to identify the fragrance gene types of hedychium coronarium and other plants or used in molecular marker-assisted selective breeding for improving selection rate in breeding.

Description

technical field [0001] The invention relates to the technical field of genetic engineering, in particular to a ginger flower terpene floral aroma gene Hctps1 and its application. Background technique [0002] Floral fragrance plays an important role in the process of plant reproduction, which can not only improve the yield and quality of crops, but also increase the aesthetic characteristics of ornamental plants and cut flowers, and terpenoids are one of the main components of floral fragrance. Terpenoids are a general term for a class of compounds composed of several isoprene (C5) structural units, which can be divided into monoterpene (monoterpene, C10), sesquiterpene (C15) and Diterpene (diterpene, C20), etc. There are many kinds of terpenoids with various structures, and more than 25,000 kinds have been found in plants so far, which is the most diverse category of plant secondary metabolites. Terpenes are not only the main components of floral fragrance, but also have...

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): C12N15/52C12N9/00C12N15/63A01H5/00C12N15/82C12Q1/68
Inventor 范燕萍徐婧兰建彬卢保兰余让才
Owner SOUTH CHINA AGRI UNIV
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products

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