IP Library Granted Patent US 8,945,890
Granted Patent B2
US 8,945,890 · App. 13/775,860 · Granted Feb 3, 2015

Method for producing monoterpene and monoterpinoid compounds and use thereof

Inventors: Claus Tittiger (Reno, NV); Rubi Figueroa-Teran (Reno, NV); Gary J. Blomquist (Sparks, NV)
Assignee: Board of Regents of the Nevada System of Higher Education, on behalf of the University of Nevada, Reno
C12P7/04C12N9/0004C12P41/002C12P7/26A01N49/00
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Quick Facts
Patent No.
US 8,945,890
App. No.
13/775,860
Granted
Feb 3, 2015
Kind
B2
Abstract

In various embodiments, the present disclosure provides a method and enzyme for forming various compounds, such as monoterpenes and monoterpenoid compounds. In a specific example, the present disclosure provides a method for producing one or more of (−)-ipsdienol, (−)-ipsenol, ipsenone, and ipsdienone. The present disclosure also provides methods of using compounds formed from the disclosed method and enzyme.

Claims (17)

1. A method of catalyzing the oxidation of ipsenol or ipsdienol comprising contacting a sample comprising ipsenol or ipsdienol with an isolated, synthetic or transgenically expressed polypeptide having oxidation activity encoded by a polynucleotide sequence at least 95% homologous to the sequence of SEQ ID NO:1.

2. A method of catalyzing the reduction of ipsenone or ipsdienone comprising contacting a sample comprising ipsenone or ipsdienone with an isolated synthetic or transgenically expressed polypeptide having reduction activity encoded by a polynucleotide sequence at least 95% homologous to the sequence of SEQ ID NO:1.

3. A process for resolving an enantiomeric mixture of ipsenol or ipsdienone comprising:

providing an enzymatically active isolated, synthetic or transgenically expressed polypeptide having oxidation reduction or oxidoreductase activity encoded by a polynucleotide sequence at least 95% homologous to the sequence of SEQ ID NO:1;

providing a mixture comprising at least one of ipsenol or ipsdienol;

contacting the mixture with the polypeptide under conditions wherein the polypeptide can oxidize the alcohol;

contacting the mixture with the polypeptide under conditions wherein the polypeptide can reduce the previously oxidized alcohol; and

recovering a mixture of alcohols enriched in one enantiomer or a mixture of alcohols enriched in the opposite enantiomer.

4. The method of claim 1 , wherein the polynucleotide sequence is at least about 99% homologous to the sequence of SEQ ID NO:1.

5. The method of claim 1 , wherein the polynucleotide sequence is the sequence of SEQ ID NO:1.

6. The method of claim 1 , wherein the polypeptide is encoded by a fragment of a polynucleotide sequence at least 95% homologous to the sequence of SEQ ID NO:1.

7. The method of claim 2 , wherein the polynucleotide sequence is at least about 99% homologous to the sequence of SEQ ID NO:1.

8. The method of claim 2 , wherein the polynucleotide sequence is the sequence of SEQ ID NO:1.

9. The method of claim 2 , wherein the polypeptide is encoded by a fragment of a polynucleotide sequence at least 95% homologous to the sequence of SEQ ID NO:1.

10. The method of claim 3 , wherein the polynucleotide sequence is at least about 99% homologous to the sequence of SEQ ID NO:1.

11. The method of claim 3 , wherein the polynucleotide sequence is the sequence of SEQ ID NO:1.

12. The method of claim 3 , wherein the polypeptide is encoded by a fragment of a polynucleotide sequence at least 95% homologous to the sequence of SEQ ID NO:1.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 27, 2013
From: TITTIGER, CLAUS; BLOMQUIST, GARY; FIGUEROA-TERAN, RUBI
To: BOARD OF REGENTS OF THE NEVADA SYSTEM OF HIGHER EDUCATION, ON BEHALF OF THE UNIVERSITY OF NEVADA, RENO
Reel/Frame 030099/0313 →
Continuity (3)
Division 12947708 · Nov 17, 2009
Provisional Application 61115623 · Nov 18, 2008
Related Publication 20130230878A1 · Sep 5, 2013