The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Jul. 31, 2007

Filed:

Sep. 03, 2002
Applicants:

Mohamad I. Farbood, State College, PA (US);

Robert W. Blocker, Brick, NJ (US);

Lynda B. Mclean, Matawan, NJ (US);

Mark A. Sprecker, Sea Bright, NJ (US);

Michael P. Mclean, Matawan, NJ (US);

Nicolas Kossiakoff, Les Arcs sur Argens, FR;

Augustine Yonghwi Kim, Morganville, NJ (US);

Myrna Hagedorn, Woodland Park, CO (US);

Inventors:

Mohamad I. Farbood, State College, PA (US);

Robert W. Blocker, Brick, NJ (US);

Lynda B. McLean, Matawan, NJ (US);

Mark A. Sprecker, Sea Bright, NJ (US);

Michael P. McLean, Matawan, NJ (US);

Nicolas Kossiakoff, Les Arcs sur Argens, FR;

Augustine Yonghwi Kim, Morganville, NJ (US);

Myrna Hagedorn, Woodland Park, CO (US);

Assignee:
Attorneys:
Primary Examiner:
Int. Cl.
CPC ...
A61K 8/00 (2006.01); A01N 37/00 (2006.01); A23L 1/226 (2006.01);
U.S. Cl.
CPC ...
Abstract

Described is a bioprocess for the high-yield production of food flavor-acceptable jasmonic acid and methyl jasmonate, as well as a novel jasmonic acid isomer produced thereby and organoleptic uses thereof. The process yields at least 5% of the 'cis' isomer defined according the structure: (wherein R is hydrogen or methyl) or at least 5% of the 'cis' isomer defined according to the structure: (wherein R is hydrogen or methyl). Compositions containing at least 98% of the isomer having the structure: with an optical rotation (α) of +58° are novel. Compositions containing at least 98% of the isomer having the structure: with an optical rotation (α) of +58° are also novel. The process of our invention comprises the cultivation under aerobic condition of one or more specific strain ofin a nutrient medium followed either by (1) isolation of the jasmonic acid product or (2) esterification of the jasmonic acid to form methyl jasmonate followed by the isolation of the methyl jasmonate and novel products produced by such process.


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