Engineering strain capable of producing high-content zeaxanthine or astaxanthin and application thereof

A technology of zeaxanthin and engineering bacteria, which is applied in the field of genetic engineering, can solve the problems of non-specific substrates, difficulty in separation and purification, and limit the preparation of a single type of zeaxanthin or astaxanthin, and achieve the effect of increasing input costs

Active Publication Date: 2017-06-06
SUN YAT SEN UNIV
View PDF4 Cites 7 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, due to the nonspecificity and substrate nonspecificity of these two enzymes, crtZ and crtW, a series of intermediate metabolites are often generated during the reaction, such as lycopene, β-carotene, canthaxanthin, marigold Anthocyanin, cryptoxanthin and echinenone, etc., lead to the content of the target products zeaxanthin and astaxanthin in the total carotenoids below 80%. These intermediate products belong to the same carotenoids as the target products, and their molecular structures Very similar, it is difficult to separate and purify by ordinary chemical methods, even if high-yielding zeaxanthin and astaxanthin strains are obtained, the low content of the target product limits the preparation of high-purity single zeaxanthin or astaxanthin

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
  • Engineering strain capable of producing high-content zeaxanthine or astaxanthin and application thereof
  • Engineering strain capable of producing high-content zeaxanthine or astaxanthin and application thereof
  • Engineering strain capable of producing high-content zeaxanthine or astaxanthin and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0022] Example 1 Using lycopene-producing Escherichia coli as the starting bacterium to construct a plasmid-free engineering bacterium producing high-content zeaxanthin

[0023] Lycopene-producing Escherichia coli itself carries the crtE gene, crtB gene, and crtI gene, and introduces the crtY gene and crtZ gene (genbankD90087) of a specific source and copy number. The steps are as follows:

[0024] (1) Using the Pantoea ananatis genome or the expression plasmid pQE-crtYZ containing the crtY and crtZ genes of Pantoea ananatis as a template, use the primers in Table 1 below to amplify the crtY fragment gene and the crtZ gene fragment respectively.

[0025] Table 1 Amplification primers of crtY gene and crtZ gene

[0026]

[0027] (2) connecting the above-mentioned crtY fragment gene and crtZ gene fragment to the assembly plasmid pZSABP to obtain pZSABP-crtY recombinant plasmid and pZSABP-crtZ recombinant plasmid respectively;

[0028] (3) Digest pZSABP-crtZ with AvrII / SalI, ...

Embodiment 2

[0030] Example 2 Using Escherichia coli producing β-carotene as the starting bacterium to construct a plasmid-free engineering bacterium producing high-content zeaxanthin

[0031] Escherichia coli producing β-carotene itself carries crtE gene, crtB gene, crtI gene, crtY gene, and introduces crtY gene and crtZ gene of specific source and copy number, the steps are as follows:

[0032] (1) The amplification of crtY and crtZ gene fragments, the preparation of pZSABP-crtY recombinant plasmid and pZSABP-crtZ recombinant plasmid are the same as in Example 1;

[0033] (2) digest pZSABP-crtZ with AvrII / SalI, and recover the crtZ fragment; connect it to the XbaI / SalI of pZSABP-crtZ to obtain pZSABP-2*crtZ; use the same method to combine 2*crtZ and the crtY- 2*crtZ were assembled together to obtain pZSABP-crtY-4*crtZ;

[0034] (3) Digest pZSABP-2*crtZ and pZSABP-crtY-4*crtZ with MluI / SalI, recover the gene fragments, connect them to the integration vector pHKKP37b, and obtain the integ...

Embodiment 3

[0035] Example 3 produces high-content astaxanthin-free engineering bacteria

[0036] On the basis of the Escherichia coli ZEAX-4 with high yield of zeaxanthin constructed in Example 1, the crtW gene was introduced, and the steps were as follows:

[0037] (1) In order to improve the expression level of the gene in Escherichia coli, the codons of the gene were optimized according to the codon preference of Escherichia coli. The codon-optimized Brevundimonas crtW gene (see SEQ ID NO: 5 for the nucleotide sequence) was entrusted to Suzhou Jinweizhi Biotechnology Co., Ltd. to synthesize the whole gene, and connected to the pUC57 vector to obtain pUC57-crtW BSP ;

[0038] (2) Digest pUC57-crtW with NheI / PstI BSP, recycle crtW BSP fragment, ligated into the assembly vector pZS5P37 to obtain pZS-5P37-crtW BSP ; Digest pZS-5P37-crtW with BglII / SalI BSP , recycle crtW BSP fragment, ligated into pZS-5P37-crtW BSP Between BamHI / SalI, pZS-2*(5P37-crtW BSP );

[0039] (3) Digest p...

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 an engineering strain capable of producing high-content zeaxanthine or astaxanthin and application thereof. The engineering strain capable of producing the high-content zeaxanthine or astaxanthin carries a crtE gene, a crtB gene, a crtI gene, a crtY gene and a crtZ gene, wherein the copy number ratio of the crtY gene to the crtZ gene is preferably 1 to 2; the engineering strain capable of producing the high-content zeaxanthine or astaxanthin also carries at least one crtW gene, the copy number ratio of the crtW gene, the crtZ gene and the crtY gene is preferably 1 to 2 to 1; the used crtY gene and crtZ gene are preferably selected from pantoea ananatis, the crtW gene is preferably selected from brevundimonas, and plasmid-free engineering escherichia coli is preferably selected as the engineering strain. The content of the zeaxanthine or astaxanthin produced by the built engineering strain accounts for more than 90 percent of total carotenoids, the problems that the content of target products is low, the purification is difficult are solved, and the engineering strain can be applied to preparation of high-purity zeaxanthine or astaxanthin.

Description

technical field [0001] The invention relates to the field of genetic engineering, in particular to engineering bacteria producing high-content zeaxanthin or astaxanthin and applications thereof. Background technique [0002] Zeaxanthin and astaxanthin are important carotenoids. Among them, zeaxanthin is clinically used to treat age-related macular degeneration. Astaxanthin, as the antioxidant with the strongest antioxidant capacity found, has anti-oxidation, skin and eye protection, radiation resistance, cardiovascular aging, senile dementia and cancer effects in clinical practice. [0003] The heterologous synthesis of zeaxanthin and astaxanthin by microorganisms has become a research hotspot, generally by introducing exogenous carotenoid synthesis pathway genes into the chassis bacteria. The synthesis of zeaxanthin and astaxanthin starts from FPP and passes through crtE, crtB, crtI , crtY continuous catalysis to generate β-carotene, β-carotene is catalyzed by crtZ to pro...

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): C12N1/21C12P23/00C12R1/19
CPCC12N9/001C12N9/0069C12N9/0073C12N9/0083C12N9/1085C12P23/00C12Y103/05005C12Y205/01029C12Y205/01032
Inventor 刘建忠鲁骞步依繁申洪杰
Owner SUN YAT SEN UNIV
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