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

Method for producing L-ornithine hydrochloride by genetic engineering bacteria

A technology of ornithine hydrochloride and genetically engineered bacteria, which is applied in the biological field and can solve problems such as filtration difficulties

Active Publication Date: 2011-09-21
WUHAN GRAND HOYO
View PDF6 Cites 13 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Because the method of chemically hydrolyzing L-arginine to generate L-ornithine often causes L-ornithine racemization, the method for preparing L-ornithine by weak base hydrolysis of L-arginine can reduce the degree of racemization, However, it is necessary to use sulfuric acid to precipitate weak alkali metal ions, which will encounter the problem of difficulty in filtration, and will produce certain solid waste

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 producing L-ornithine hydrochloride by genetic engineering bacteria
  • Method for producing L-ornithine hydrochloride by genetic engineering bacteria
  • Method for producing L-ornithine hydrochloride by genetic engineering bacteria

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0180] Design and synthesize a pair of TA cloning primers

[0181] Log in to GenBanK, obtain the complete coding sequence of the arginase gene (argBsub) of Bacillus subtilis (Bacillus Subtilis) 168 strain through Gene ID: 937760, and use Primerer 5.0 software to design a pair of PCR primers, p1 and p2, for amplifying subtilis The DNA sequence of the Bacillus arginase gene is TA-ligated with the pBAD / Thio-TOPO vector. Primers were synthesized by Yingwei Jieji (Shanghai) Trading Co., Ltd.

[0182] P1: 5'-GAAATGGATAAAACGATTTCGGTTAT-3', 26 bp in total.

[0183] P2: 5'-GGTCAGCAGCTTCTTCCCTAACA-3', 23 bp in total.

Embodiment 2

[0185] Extraction and determination of Bacillus subtilis genomic DNA

[0186] Genomic DNA of Bacillus subtilis was extracted by the improved method of Palva I et al.

[0187] (1). Pick a single bacterium colony cultured on the plate of Bacillus subtilis (preservation number CCTCC NO.AB93009), inoculate it into a test tube containing 10 ml of beef extract and peptone liquid medium, and culture it with shaking at 32° C. for 14 hours.

[0188] (2). Centrifuge at 5000rpm for 10min to obtain bacterial pellet, wash once with STE, centrifuge again, and resuspend the bacterial cell in 4ml TE solution.

[0189] (3). Add 8 μl of 50 mg / ml lysozyme solution (final concentration is 100 μg / ml), and keep warm at 37° C. for 20 minutes. Add 10 μl of RNase (10 mg / ml) to a final concentration of 25 μg / ml, then add 10% SDS to dissolve 0.5 ml, and incubate at 37° C. for 30 minutes. Add 10 μl of proteinase K (20 mg / ml) to a final concentration of 50 μg / ml, and keep at 37° C. for 60 minutes.

[0...

Embodiment 3

[0199] PCR Amplification of Arginase Gene of Bacillus subtilis

[0200] 1). Prepare 50 μl reaction system.

[0201] Template DNA, 2μl (50ng); 10X PCR Buf, 5μl; 50mMdNTPs, 0.5μl;

[0202] Primers p1 and p2, 1 μl each (100 ng); Taq DNA polymerase (1 unit / μl), 1 μl; add sterile pure water to a volume of 50 μl.

[0203] The program of the PCR reaction was as follows: pre-denaturation at 94°C for 4 min, denaturation at 94°C for 1 min, annealing at 56°C for 30 sec, extension at 72°C for 1.5 min; a total of 30 cycles, and a final extension at 72°C for 10 min. After the reaction was completed, temporarily store in ice until use.

[0204] 2). Take 2 μl of the amplification product and load it on 1.2% agarose gel electrophoresis to detect a DNA fragment with a size of 0.9 KB. The DNA band has a clear outline, which is suitable for direct TOPO-TA cloning reaction.

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 method for producing L-ornithine hydrochloride by TOP10 / PBAD / Thio-TOPO-Arg-Bsub colibacillus genetic engineering bacteria. The strain can express and generate excess bacillus subtilis arginase, and efficiently converts L-arginine into L-ornithine.

Description

technical field [0001] The invention belongs to the field of biotechnology and relates to the application of genetically engineered bacteria, in particular to a method for producing L-ornithine hydrochloride by using E. coli TOP10 / PBAD / Thio-TOPO-Arg-Bsub genetically engineered bacteria. Background technique [0002] 1. Physiological functions and health care value of L-ornithine: [0003] L-Ornithine is a non-protein amino acid, and it is a precursor for organisms to synthesize protein amino acids such as arginine and proline. L-Ornithine can be converted into polyamines such as putrescine, cadaverine, spermidine, and spermine in vivo, and polyamines can promote the growth of biological tissues. Positively charged polyamines can combine with negatively charged DNA and RNA to promote the transcription of DNA and translation of RNA in organisms; polyamines can combine with proteins or phospholipids on the cell membrane to maintain the stability of the membrane. [0004] L-or...

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): C12P13/10C12N1/21C12N15/60C12N15/70C12R1/19
Inventor 王炯王君英刘爱福易清明
Owner WUHAN GRAND HOYO
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