Oxidoreductase reaction control and use thereof

Patent metadata

Field	Value
Publication number	US-9777299-B2
Application number	US-201314408127-A
Country	US
Kind code	B2
Filing date	Jun 13, 2013
Priority date	Jun 16, 2012
Publication date	Oct 3, 2017
Grant date	Oct 3, 2017

Abstract

The present invention is intended to prove a technique useful for controlling the reaction of oxidoreductase, and to provide a reaction system allowing efficient conversion from carbon dioxide to formic acid, and an efficient methanol production system including the reaction system. The reverse redox reaction is selectively promoted by carrying out the reaction catalyzed by an oxidoreductase using an artificial electron carrier. The reaction system is used for the production of methanol.

First claim

The invention claimed is:

1. A method for selectively promoting a reverse redox reaction, comprising:
contacting an artificial electron carrier with an electron donor and photosensitizer and applying light to form a reduced artificial electron carrier, or contacting an artificial electron carrier with a reducing agent to form a reduced artificial electron carrier, wherein the artificial electron carrier is the compound of any one of the formulae (1) to (5):

wherein R1 is a alkyl group substituted by a substituted or unsubstituted amino group, a aryl group substituted by a substituted or unsubstituted amino group, or a arylalkyl group substituted by a substituted or unsubstituted amino group, and the alkyl group has 1 to 12 carbon atoms, the aryl group has 6 to 20 carbon atoms, and the arylalkyl group has 7 to 20 carbon atoms,
wherein R2 is a substituted or unsubstituted alkyl group, a substituted or unsubstituted aryl group, or a substituted or unsubstituted arylalkyl group, and the alkyl group has 1 to 12 carbon atoms, the aryl group has 6 to 20 carbon atoms, and the arylalkyl group has 7 to 20 carbon atoms,

wherein n is an integer of 1 to 10, wherein R3 is a alkyl group substituted by a substituted or unsubstituted amino group, a aryl group substituted by a substituted or unsubstituted amino group, or a arylalkyl group substituted by a substituted or unsubstituted amino group, and the alkyl group has 1 to 12 carbon atoms, the aryl group has 6 to 20 carbon atoms, and the arylalkyl group has 7 to 20 carbon atoms,
wherein R4, R5, and R6 are each independently a substituted or unsubstituted alkyl group, a substituted or unsubstituted aryl group, or a substituted or unsubstituted arylalkyl group, the alkyl group has 1 to 12 carbon atoms, the aryl group has 6 to 20 carbon atoms, and the arylalkyl group has 7 to 20 carbon atoms;

wherein n is an integer of 1 to 10, wherein R4 is a alkyl group substituted by a substituted or unsubstituted amino group, a aryl group substituted by a substituted or unsubstituted amino group, or a arylalkyl group substituted by a substituted or unsubstituted amino group, and the alkyl group has 1 to 12 carbon atoms, the aryl group has 6 to 20 carbon atoms, and the arylalkyl group has 7 to 20 carbon atoms,
wherein R3, R5, and R6 are each independently a substituted or unsubstituted alkyl group, a substituted or unsubstituted aryl group, or a substituted or unsubstituted arylalkyl group, the alkyl group has 1 to 12 carbon atoms, the aryl group has 6 to 20 carbon atoms, and the arylalkyl group has 7 to 20 carbon atoms;

wherein n is an integer of 0 to 10, R7 is a substituted or unsubstituted amino group;

wherein n is an integer of 1 to 10, R8 is a substituted or unsubstituted amino group;
contacting a substrate, the reduced artificial electron carrier, and NAD-dependent dehydrogenase to produce a reduced substrate.

2. The method of claim 1 , wherein the NAD-dependent dehydrogenase is selected from the group consisting of formate dehydrogenase, aldehyde dehydrogenase, alcohol dehydrogenase, lactate dehydrogenase, and glutamate dehydrogenase.

3. The method of claim 1 , wherein the artificial electron carrier is the compound of the formula (8) or (9):

4. The method of claim 1 , wherein the reducing agent is selected from the group consisting of sodium dithionate, sodium dithionite, ascorbic acid, and hydrazine.

5. A method of converting carbon dioxide into formic acid, comprising:
contacting an artificial electron carrier with an electron donor and photosensitizer and applying light to form a reduced artificial electron carrier, or contacting an artificial electron carrier with a reducing agent to form a reduced artificial electron carrier, wherein the artificial electron carrier is the compound of any one of the formulae (1) to (5):

wherein R1 is a alkyl group substituted by a substituted or unsubstituted amino group, a aryl group substituted by a substituted or unsubstituted amino group, or a arylalkyl group substituted by a substituted or unsubstituted amino group, and the alkyl group has 1 to 12 carbon atoms, the aryl group has 6 to 20 carbon atoms, and the arylalkyl group has 7 to 20 carbon atoms,
wherein R2 is a substituted or unsubstituted alkyl group, a substituted or unsubstituted aryl group, or a substituted or unsubstituted arylalkyl group, and the alkyl group has 1 to 12 carbon atoms, the aryl group has 6 to 20 carbon atoms, and the arylalkyl group has 7 to 20 carbon atoms,

wherein n is an integer of 1 to 10, wherein R3 is a alkyl group substituted by a substituted or unsubstituted amino group, a aryl group substituted by a substituted or unsubstituted amino group, or a arylalkyl group substituted by a substituted or unsubstituted amino group, and the alkyl group has 1 to 12 carbon atoms, the aryl group has 6 to 20 carbon atoms, and the arylalkyl group has 7 to 20 carbon atoms,
wherein R4, R5, and R6 are each independently a substituted or unsubstituted alkyl group, a substituted or unsubstituted aryl group, or a substituted or unsubstituted arylalkyl group, the alkyl group has 1 to 12 carbon atoms, the aryl group has 6 to 20 carbon atoms, and the arylalkyl group has 7 to 20 carbon atoms;

wherein n is an integer of 1 to 10, wherein R4 is a alkyl group substituted by a substituted or unsubstituted amino group, a aryl group substituted by a substituted or unsubstituted amino group, or a arylalkyl group substituted by a substituted or unsubstituted amino group, and the alkyl group has 1 to 12 carbon atoms, the aryl group has 6 to 20 carbon atoms, and the arylalkyl group has 7 to 20 carbon atoms,
wherein R3, R5, and R6 are each independently a substituted or unsubstituted alkyl group, a substituted or unsubstituted aryl group, or a substituted or unsubstituted arylalkyl group, the alkyl group has 1 to 12 carbon atoms, the aryl group has 6 to 20 carbon atoms, and the arylalkyl group has 7 to 20 carbon atoms;

wherein n is an integer of 0 to 10, R7 is a substituted or unsubstituted amino group;

wherein n is an integer of 1 to 10, R8 is a substituted or unsubstituted amino group;
contacting carbon dioxide, the reduced artificial electron carrier, and formate dehydrogenase to produce formic acid.

6. The method of claim 5 , wherein the artificial electron carrier is the compound of the formula (8) or (9):

7. The method of claim 5 , wherein the reducing agent is selected from the group consisting

Assignees

• Amano Enzyme Inc

Inventors

• Amao Yutaka
• IKEYAMA Shusaku
• Nakanishi Yuji
• Takahashi Tetsuya
• Koikeda Satoshi

Classifications

• C12P7/24

  containing a carbonyl group · CPC title

• C12P7/40 Primary

  containing a carboxyl group {including Peroxycarboxylic acids} · CPC title

• C12M21/18

  Apparatus specially designed for the use of free, immobilized or carrier-bound enzymes · CPC title

• C12P7/04

  acyclic · CPC title

• C12N11/14

  Enzymes or microbial cells immobilised on or in an inorganic carrier · CPC title