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

Method for enzymatically synthesizing nicotinamide uracil dinucleotide

A technology for uracil dinucleotide and uridine triphosphate, which is applied in the field of enzymatic synthesis of nicotinamide uracil dinucleotide, can solve the problems of difficulty in NUD entering cells, difficulty in separation and purification, and complicated steps.

Active Publication Date: 2020-10-16
DALIAN INST OF CHEM PHYSICS CHINESE ACAD OF SCI
View PDF2 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0009] Aiming at the disadvantages of cumbersome chemical synthesis of NUD, difficult separation and purification, NUD is difficult to enter cells, etc., and no enzyme that can efficiently catalyze the synthesis of NUD has been found so far. The purpose of the present invention is to provide a method for enzymatic synthesis of NUD. The mutant of nucleotide adenosyltransferase is used as a catalyst to catalyze the synthesis of NUD with nicotinamide mononucleotide and uridine triphosphate as substrates, and transfer NUD by expressing nicotinamide mononucleotide adenosine in the cell Enzyme mutants can directly synthesize NUD in cells, which can be used to selectively regulate metabolic processes and increase the yield of target metabolites

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 enzymatically synthesizing nicotinamide uracil dinucleotide
  • Method for enzymatically synthesizing nicotinamide uracil dinucleotide
  • Method for enzymatically synthesizing nicotinamide uracil dinucleotide

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0071] Example 1 NadD 3G10 Catalytic synthesis of NUD

[0072] 1. Construction of mutant library

[0073] The mutation library was constructed by RF cloning (F. van den Ent, et al. Journal of Biochemical and Biophysical Methods. 2006, 67, 67). In the first step, the template is a wild-type NadD expression vector (see Comparative Example 1), and the primers replace the base of the amino acid site to be mutated with a degenerate base NNK, and the PCR product is recovered; in the second step, the template is the same as the first step, The primers were the PCR products recovered in the first step, and the obtained products were digested with DpnI restriction enzyme, and transferred into BL21(DE3) competent cells, and the obtained transformants were the mutant library expressing NadD mutants, each mutant The expression bacteria were named BL21(DE3)(pET-NadD-xxx), and the expressed protein product was named NadD xxx . Among them, xxx is a combination of numbers and letters, and...

Embodiment 2

[0080] Example 2 NadD 3G10 Pure Enzyme Preparation of NUD

[0081] 10mL pure enzyme NadD 3G10 The reaction system for synthesizing NUD contains Tris 50mM, UTP 2mM, NMN 4mM, MgCl 2 10mM, MnCl 2 5mM, pure enzyme NadD3G10 10mg, pH 8.0, reacted at 37°C, 200rpm for 1h, then centrifuged at 5000g, 4°C for 15min with an ultrafiltration centrifuge tube to remove protein, reference method (D.Ji, et al.Journal of the American Chemical Society.2011, 133, 20857), isolated and purified to obtain 5.8 mg of NUD with a yield of 45%.

[0082] Product NMR data: 1 H NMR (D20, 400MHz): δ9.36(s, 1H), 9.20(d, J=6.2Hz, 1H), 8.88(d, J=8.1Hz, 1H), 8.22(pseudo t, J=6.6Hz , 1H), 7.79(d, J=8.2Hz, 1H), 6.10(d, J=5.4Hz, 1H), 5.82-5.80(m, 2H), 4.52(brs, 1H), 4.48-4.46(m, 1H), 4.39-4.37(m, 1H), 4.34-4.32(m, 1H), 4.25-4.21(m, 2H), 4.18-4.15(m, 3H), 4.07-4.04(m, 1H).13C NMR (D20, 100MHz): δ166.1, 165.6, 151.7, 146.1, 142.6, 141.7, 139.9, 133.9, 128.7, 102.5, 99.9, 88.5, 87.0, 82.9, 77.6, 73.7, 70.7, 69....

Embodiment 3

[0083] Example 3 NadD 3G10 Preparation of NUD from crude enzyme solution

[0084] NadD 3G10 The expression engineered bacteria BL21(DE3)(pET-NadD-3G10) was streak cultured, and a single colony was picked and inoculated in 5mL LB (containing kanamycin 50ng / μL) liquid medium, activated overnight at 37°C and 200rpm, All of them were inoculated in 50 mL of fresh LB (containing 50 ng / μL of kanamycin and 1 mM of IPTG), and cultured at 30° C. and 200 rpm for 24 h. The cells were collected by centrifugation, added with 5 mL of cell lysate (50 mM HPEPS pH 7.5, 1% Triton X-100, 1 mg / mL lysozyme), and lysed at 37° C. for 1 h at 200 rpm. Centrifuge (12000g) for 10min, collect the supernatant to get NadD 3G10 crude enzyme solution.

[0085] 300μL crude enzyme solution reaction system contains: Tris 50mM, UTP 100μM, NMN 4mM, MgCl 2 10mM, MnCl 2 5mM, NadD 3G10 50 μL of crude enzyme solution, pH 8.0, reacted at 37°C, 200 rpm for 2 hours. Add 150 μL of ice-cold 1.2M HClO 4 After mixin...

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 relates to a method for enzymatically synthesizing nicotinamide uracil dinucleotide and its application. The nicotinamide mononucleotide adenosyltransferase mutant is used as a catalyst to catalyze the coupling reaction of nicotinamide mononucleotide and uridine nucleoside triphosphate to prepare nicotinamide uracil dinucleotide. Express the coding gene of nicotinamide mononucleotide adenylyltransferase mutant in microbial cells, engineered bacteria use endogenous metabolites to synthesize nicotinamide uracil dinucleotide, and intracellular nicotinamide uracil dinucleotide can be As a coenzyme, it selectively mediates redox reactions and increases the yield of target metabolites. In a typical example, succinic acid production was increased by 35%.

Description

technical field [0001] The invention belongs to the technical field of bioengineering, and relates to a method for enzymatically synthesizing nicotinamide uracil dinucleotide (NUD) and its application, and expressing a mutant of nicotinamide mononucleotide adenylyltransferase in microbial cells The coding gene of the engineered bacteria uses endogenous metabolites to synthesize NUD, and intracellular NUD can act as a coenzyme to selectively mediate redox reactions and increase the yield of target metabolites. Background technique [0002] Nicotinamide adenine dinucleotide (NAD) and its reduced state (NADH) all play a very important role in cell reproduction, growth, differentiation, apoptosis and other life activities (W.Ying, et al.Antioxidants RedoxSignaling .2008, 10, 179). In addition, NAD is also the coenzyme of many important redox enzymes, which plays the role of transferring hydrogen and electrons. Its structural formula is as follows: [0003] [0004] Since N...

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 Patents(China)
IPC IPC(8): C12P19/36
CPCC12P19/36
Inventor 赵宗保王雪颖刘玉雪
Owner DALIAN INST OF CHEM PHYSICS CHINESE ACAD OF SCI
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