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

High yield L-leucine engineering bacterium and application thereof

A technology of Leucine and Corynebacterium glutamicum, applied in application, genetic engineering, bacteria, etc., can solve the problems of increased miscellaneous acids, long cycle, heavy workload, etc.

Active Publication Date: 2015-04-01
FUJIAN NORMAL UNIV +1
View PDF2 Cites 17 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

So far, industrialized L-leucine producing bacteria are mainly obtained through traditional mutagenesis screening. Although this classic breeding method can obtain excellent strains with relatively high L-leucine production, this method will also introduce harmful mutations, making the target The strain grows slowly and the heteroacids increase
In addition, this method has a large workload and a long cycle, and it is difficult to further increase the output of the target product in a short period of time.

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
  • High yield L-leucine engineering bacterium and application thereof
  • High yield L-leucine engineering bacterium and application thereof
  • High yield L-leucine engineering bacterium and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0031] Embodiment 1, the construction of engineering bacteria

[0032] 1. Exogenous high-level expression of leuA * Construction of recombinant vector

[0033] 1. Cloning and site-directed mutation of leuA gene

[0034] 1), using the genomic DNA of Corynebacterium glutamicum 13032 as a template, carrying out PCR amplification with primers composed of F1 and R1, to obtain a PCR amplification product (leuA gene fragment).

[0035] F1: 5'- GAATTC ATGCCAGTTAACCGCTACATGCCT-3';

[0036] R1: 5'- GTC GAC TTAAACGCCGCCAGCCAGGAC-3'.

[0037] Among them, F1 has an EcoR I restriction site, and R1 has a Sal I restriction site (the underlined partial sequence of the above primer).

[0038] PCR amplification conditions: pre-denaturation at 95°C for 5 minutes; denaturation at 94°C for 40 seconds, annealing at 59°C for 1 minute, extension at 72°C for 2 minutes, 30 cycles; reaction at 72°C for 10 minutes, and incubation at 4°C.

[0039] 2) Recovering the PCR amplified product of step 1)...

Embodiment 2

[0119] Embodiment 2, Corynebacterium glutamicum MD0032 produces L-leucine

[0120] 1. Preparation of culture medium

[0121] Seed medium (pH=6.5-7.0): Take 100g glucose, 5g corn steep liquor, 10g brown sugar, 50g molasses, 100ml soybean meal hydrolyzate (purchased from Shandong Yangcheng Biotechnology Co., Ltd., catalog number DP001), 3g yeast extract , 25g (NH 4 ) 2 SO 4 , 0.2g MgSO 4 ·7H 2 O, 0.05g FeSO 4 ·7H 2 O, 0.3g KH 2 PO 4 ·3H 2 O. Dissolve 0.025g of kanamycin monosulfate and 10g of calcium carbonate in deionized water and adjust the volume to 1L; sterilize at 125°C for 25min.

[0122] Fermentation medium (pH=6.5-7.5): take 120g glucose, 150ml soybean meal hydrolyzate, 27g (NH 4 ) 2 SO 4 , 5.5g KH 2 PO 4 ·3H 2 O, 2.5g K 2 HPO 4 ·3H 2 O, 0.2g MgSO 4 ·7H 2 O, 0.05g FeSO 4 ·7H 2 O, 0.02gMnSO 4 ·H 2 O, 200 μg vitamin H, 200 μg vitamin B1, 100 μg vitamin B2, 100 μg vitamin B6, 0.025 g kanamycin monosulfate, 30 g CaCO 3 Dissolve in deionized water a...

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 high yield L-leucine engineering bacterium and an application of the bacterium.The invention provides a method for preparing a recombinant bacterium. The method comprises the following step of importing an alpha-isopropylmolic acid synthetase mutant encoding gene into a target bacterium to form the recombinant bacterium, wherein an alpha-isopropylmolic acid synthetase mutant is enzyme obtained by mutating 494th arginine of alpha-isopropylmolic acid synthetase into histidine, 497th glycine into aspartic acid and 499th leucine into valine.The high yield L- leucine engineering bacterium, particularly corynebacterium glutamicum MD0032, has higher L-leucine yield than bacterial strains produced at home at present, has a unique identification label and is a L-leucine production strain with a high production and application value.

Description

technical field [0001] The invention relates to the field of biotechnology, in particular to a high-yielding L-leucine engineering bacterium and its application. Background technique [0002] The molecular structure of L-leucine, L-isoleucine (L-isoleucine) and L-valine (L-valine) contains a methyl side chain, so it is called branched chain amino acid (branched chain amino acid). acids, BCAA). As one of the eight essential amino acids for the human body, L-leucine is a raw material for the synthesis of human hormones and enzymes. It has the effect of promoting protein synthesis and inhibiting decomposition, but it cannot be synthesized in the body. Therefore, L-leucine has a wide range of applications and commercial value in the fields of food, medicine, feed and sports health care, and with the continuous development of the function of L-leucine, its application fields are gradually expanding, and the market is also continuing rising. [0003] At present, the production ...

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): C12N1/21C12N15/54C12P13/06C12R1/15
CPCC07K14/34C12N9/0006C12N9/1025C12N9/1096C12N9/88C12N9/93C12P13/06C12Y203/03013C12Y206/01002C12Y403/01019
Inventor 黄钦耿黄建忠梁玲翁雪清吴伟斌黄祥峰施巧琴吴松刚
Owner FUJIAN NORMAL 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