Sutellaria viscidula phenyl alanine ammonialyase protein coded sequence

A technology of phenylalanine ammonia-lyase protein and coding sequence, which is applied in the field of genetic engineering, and can solve problems such as the cloning of the flavonoid pal gene of Scutellaria baicalensis, which has not been seen and has not yet been discovered.

Inactive Publication Date: 2009-09-16
SOUTHWEST UNIVERSITY
View PDF0 Cites 3 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0004] In the analysis of existing documents, there is no cloning of the pal gene on the biosynthetic pathway of Scutellaria ba

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
  • Sutellaria viscidula phenyl alanine ammonialyase protein coded sequence
  • Sutellaria viscidula phenyl alanine ammonialyase protein coded sequence
  • Sutellaria viscidula phenyl alanine ammonialyase protein coded sequence

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0076] Cloning of phenylalanine ammonia-lyase from Scutellaria baicalensis

[0077] 1. Tissue separation (isolation)

[0078] Scutellaria baicalensis was purchased from Shanxi University, and the seeds were sown in the greenhouse. When the Scutellaria baicalensis seedlings grew to a height of 10 cm, DNA or RNA was prepared to be extracted.

[0079] 2. RNA isolation (RNA isolation)

[0080] Take part of the tissue, grind it with a mortar, add it to a 1.5mL EP tube filled with lysate, shake it fully, and then transfer it into a glass homogenizer. After homogenization, transfer to 1.5mL EP tube, and extract total RNA (TRIzol Reagents, GIBCO BRL, USA). The quality of total RNA was identified by formaldehyde denaturing gel electrophoresis, and then the RNA content was determined on a spectrophotometer.

[0081] 3. Cloning of Full-length cDNA

[0082] According to the nucleotide conservative sequence of the phenylalanine ammonia-lyase gene of various plants, using the principle ...

Embodiment 2

[0093] Sequence information and homology analysis of phenylalanine ammonia lyase gene from Scutellaria baicalensis

[0094] The full-length cDNA of the new phenylalanine ammonia-lyase gene sequence of the present invention is 2406bp in length, and the detailed sequence is shown in SEQID NO.3, wherein the open reading frame is located at 129-2261 nucleotides (2133 nucleotides). According to the full-length cDNA, the amino acid sequence of phenylalanine ammonia-lyase from Scutellaria baicalensis was deduced, with a total of 711 amino acid residues, a molecular weight of 77.18kDa, and an isoelectric point (PI) of 5.97. See SEQ ID NO.4 for the detailed sequence.

[0095] The full-length cDNA sequence related to the phenylalanine ammonia-lyase gene gene of Scutellaria baicalensis and its encoded protein were published in Non-redundant GenBank+EMBL+DDBJ+PDB and Non-redundant GenBankCDS translations+PDB+SwissProt+Superdate+ Nucleotide and protein homology search was carried out in t...

Embodiment 3

[0097] The protein or polypeptide of Scutellaria baicalensis phenylalanine ammonia-lyase was expressed in eukaryotic cells in Scutellaria baicalensis and the content of baicalin in transgenic plants was detected.

[0098] The construction of the expression vector containing the target gene, according to the Scutellaria baicalensis phenylalanine ammonia-lyase gene coding sequence (SEQID NO.3), design and amplify the primers for the complete coding reading frame, and introduce them on the upstream and downstream primers respectively Restriction endonuclease sites (this can be selected depending on the carrier), in order to construct expression vectors. Using the amplified product obtained in Example 1 as a template, after PCR amplification, the Scutellaria baicalensis phenylalanine ammonia-lyase gene cDNA was cloned into an intermediate vector (such as pBluescript), and further cloned into a binary expression vector (such as pBI121 and improved pCAMBIA1304), the expression vecto...

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 provides a sutellaria viscidula phenyl alanine ammonialyase protein coded sequence belonging to the genetic engineering field. Polypeptide nucleotide sequences having phenyl alanine ammonialyase activity are coded. The nucleotide sequences are composed of nucleotide sequences from positions 129 to 2261 in the SEQ ID NO.3 or simplified sequences. The sequences code polypeptide having amino acid sequences showed by SEQ ID NO.3. The invention obviously improves content of flavonoid compounds for instance scutelloside in sutellaria viscidula plants and has great application value.

Description

technical field [0001] The invention relates to a protein coding sequence, in particular to a protein coding sequence of Scutellaria baicalensis phenylalanine ammonia-lyase, which belongs to the field of genetic engineering. Background technique [0002] Scutellaria baicalensis is a perennial medicinal herb belonging to the genus Scutellariae of the Lamiaceae. There are more than 300 species of plants in this genus, which are widely distributed in the world. There are more than 100 species in my country. There are about 7 species that can be used as Scutellaria baicalensis, and Scutellaria baicalensis is one of them. The main medicinal component of this plant is baicalin, which has been proved by modern pharmacology to have the functions of clearing heat and detoxifying, stopping bleeding and preventing miscarriage, antibacterial and anti-inflammatory, protecting liver and gallbladder, reducing blood pressure and desensitization, sun protection and whitening. With the conti...

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
IPC IPC(8): C12N15/55C12N9/78C12N1/19C12N5/10
Inventor 孙敏雷桅
Owner SOUTHWEST UNIVERSITY
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