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

Method for increasing fermentation yield of polyketone compounds

A technology for polyketide compounds and synthase, which is applied in the biological field, can solve the problems of difficulty in meeting practical application requirements and insufficient fermentation yield of polyketide compounds, and achieves the effects of simple and easy operation, low cost and good application prospect.

Active Publication Date: 2015-04-15
SHANGHAI INST OF PHARMA IND +1
View PDF5 Cites 3 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] The technical problem to be solved by the present invention is to provide a method for increasing the fermentation yield of polyketides in view of the fact that the fermentation yield of the existing polyketides is not high enough to meet the actual application requirements

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
  • Method for increasing fermentation yield of polyketone compounds
  • Method for increasing fermentation yield of polyketone compounds
  • Method for increasing fermentation yield of polyketone compounds

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0033] Example 1 Extraction of Streptomyces roseosporus Genome

[0034] Genome extraction includes the following steps:

[0035] (1) Cultivation of Streptomyces roseospora: inoculate Streptomyces roseospora into 50ml liquid YEME medium, said YEME medium includes: 0.3% yeast extract, 0.5% peptone, 0.3% maltose extract, 1% glucose , 10% sucrose and 5mM MgCl 2 , the stated percentages are mass volume percentages (W / V), cultivated at 28°C (300rpm), so that the bacteria grow to the middle and late logarithmic stages.

[0036] (2) Collection of Streptomyces roseospora: Take 1ml of the culture in a 1.5ml EP tube, centrifuge at room temperature and 8000rpm for 5min, discard the supernatant, and resuspend the pellet in 1ml TE (pH8.0) buffer.

[0037] (3) Phytolysis: add 6 μl of 50 mg / ml lysozyme and react at 37°C for 30 minutes. Add 50 μl of 2mol / L NaCl, 110 μl of 10% SDS, and 3 μl of proteinase K at 20 mg / ml, and act for 3 hours at 50°C or overnight at 37°C (the bacterial liquid sh...

Embodiment 2

[0042] Example 2 Construction of recombinant expression vector pSET152erm*E-DptEF:

[0043] 1. Cloning of DptEF gene:

[0044] Using the Streptomyces roseospore genome obtained in Example 1 as a template, primers p1 and p2 were used to carry out high-fidelity PCR amplification to obtain a fragment of about 2461bp, which contained complete DptE and DptF genes, and its complete sequence was as SEQ ID NO. 6. Wherein, the sequences of primers p1 and p2 are respectively shown in SEQ ID NO.7 and SEQ ID NO.8.

[0045] (1) The reaction system (50μl) includes: 5μl 10×KOD NEO plus buffer, 3μl 25mM MgCl2, 1.5μl 2.5mmol / L dNTP solution, 2.5μl DMSO, 30pmol P1, 30pmol P2, 1U KOD NEO plus DNA polymerase, 50ng genome , add double distilled water to 50 μl.

[0046] (2) The PCR reaction program is: 95°C for 5min, 30 cycles (94°C for 30s, 56°C for 30s, 72°C for 120s), 72°C for 10min.

[0047] PCR fragments were purified and recovered by agarose gel electrophoresis and gel recovery kit.

[0...

Embodiment 3

[0057] Example 3. Transformation of pSET152erm*E-DptEF into Actinomycetes mobilis:

[0058] Preparation of Actinomycetes spore suspension: About 5 days before the conjugation transfer, take 3 μl of the glycerin preservation solution of Actinomycetes and coat I-Isp2 solid medium, which includes 1% Maltose extract, 0.4% yeast extract yeast extract, 0.4% glucose, 2% agar powder, the stated percentages are mass volume percentages (W / V), and the pH is 7.0. Cultivate at 28°C for about 120 hours, use without Scrape the surface bacteria with a bacteria scraper, wash with 15-20ml of sterile water and shake 10 times on a vortex oscillator through glass beads. After 10 seconds each time, pass the suspension through a sterile syringe with a cotton plug, filter After the liquid is centrifuged at 7000 rpm, the supernatant is discarded, and the spore suspension is obtained by resuspending with an appropriate amount of 0.4-1.0ml sterile water.

[0059] The recombinant expression vector pSET1...

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
Wavelengthaaaaaaaaaa
Login to View More

Abstract

The invention discloses a method for increasing fermentation yield of polyketone compounds. The method includes steps of: (1) culturing genetically engineered bacteria of an overexpressed acyl-coenzyme A synthesizing enzyme and an acyl carrier protein in a culture medium added with natural grease; and (2) extracting the polyketone compounds from a fermented product. The genetically engineered bacteria are a recombination expression transformant of the overexpressed acyl-coenzyme A synthesizing enzyme and the acyl carrier protein, which is prepared through conjugational transfer by an actinomycete onto recombinant escherichia coli containing a recombinant expression vector expressing the overexpressed acyl-coenzyme A synthesizing enzyme and the acyl carrier protein. In the method, an exogenetic acyl-coenzyme A synthesizing enzyme and an exogenetic acyl carrier protein are overexpressed in the bacteria generating the polyketone compounds through gene engineering technologies, so that by means of cheap natural grease as a raw material, the fermentation yield of the polyketone compounds is increased, wherein the method is never reported in references. The method is simple in operations, can provide precursors for synthesizing the polyketone compounds through the cheap natural grease, is low in cost and is convenient to popularize.

Description

technical field [0001] The invention belongs to the field of biotechnology, and in particular relates to a method for increasing the fermentation yield of polyketide compounds. Background technique [0002] Polyketides are an important class of secondary metabolites, which are produced from simple fatty acids through a synthetic pathway similar to long-chain fatty acids. The resulting compounds have a series of complex structures, and the diversity of structures leads to the diversity of biological activities. sex. There are about 20,000 natural polyketide substances found in nature, and most antibiotics and some other important drugs such as anticancer drugs and immunosuppressants belong to this family. Such compounds used as therapeutic drugs include clinically used erythromycin, tetracycline, rifamycin, amphotericin, doxorubicin, lovastatin, rapamycin and other important antibiotics, as well as agricultural and animal husbandry Avermectin and monensin, tylosin and so on...

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): C12P17/18C12N1/20C12N15/03C12R1/045C12R1/55
Inventor 胡海峰黄鹤
Owner SHANGHAI INST OF PHARMA IND
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