Nootkatone—a biotechnological challenge
Due to its pleasant grapefruit-like aroma and various further interesting molecular characteristics, (+)-nootkatone represents a highly sought-after specialty chemical. (+)-Nootkatone is accumulated in its producer plants in trace amounts only, and the demand of the food, cosmetics and pharmaceutica...
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description | Due to its pleasant grapefruit-like aroma and various further interesting molecular characteristics, (+)-nootkatone represents a highly sought-after specialty chemical. (+)-Nootkatone is accumulated in its producer plants in trace amounts only, and the demand of the food, cosmetics and pharmaceutical industry is currently predominantly met by chemical syntheses. These typically require environmentally critical reagents, catalysts and solvents, and the final product must not be marketed as a “natural flavour” compound. Both the market pull and the technological push have thus inspired biotechnologists to open up more attractive routes towards natural (+)-nootkatone. The multifaceted approaches for the de novo biosynthesis or the biotransformation of the precursor (+)-valencene to (+)-nootkatone are reviewed. Whole-cell systems of bacteria, filamentous fungi and plants, cell extracts or purified enzymes have been employed. A prominent biocatalytic route is the allylic oxidation of (+)-valencene. It allows the production of natural (+)-nootkatone in high yields under mild reaction conditions. The first sequence data of (+)-valencene-converting activities have just become known. |
doi_str_mv | 10.1007/s00253-009-1968-x |
format | Article |
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(+)-Nootkatone is accumulated in its producer plants in trace amounts only, and the demand of the food, cosmetics and pharmaceutical industry is currently predominantly met by chemical syntheses. These typically require environmentally critical reagents, catalysts and solvents, and the final product must not be marketed as a “natural flavour” compound. Both the market pull and the technological push have thus inspired biotechnologists to open up more attractive routes towards natural (+)-nootkatone. The multifaceted approaches for the de novo biosynthesis or the biotransformation of the precursor (+)-valencene to (+)-nootkatone are reviewed. Whole-cell systems of bacteria, filamentous fungi and plants, cell extracts or purified enzymes have been employed. A prominent biocatalytic route is the allylic oxidation of (+)-valencene. It allows the production of natural (+)-nootkatone in high yields under mild reaction conditions. The first sequence data of (+)-valencene-converting activities have just become known.</description><identifier>ISSN: 0175-7598</identifier><identifier>EISSN: 1432-0614</identifier><identifier>DOI: 10.1007/s00253-009-1968-x</identifier><identifier>PMID: 19333595</identifier><identifier>CODEN: AMBIDG</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Bacteria - enzymology ; Bacteria - metabolism ; Bioconversions. Hemisynthesis ; Biological and medical sciences ; Biosynthesis ; Biotechnology ; Biotechnology - methods ; Biotransformation ; Carcinogens ; Cell Extracts ; Chemical synthesis ; Citrus fruits ; Cosmetics ; Enzymes ; Flavoring Agents - metabolism ; Flavoring Agents - pharmacology ; Food ; Fundamental and applied biological sciences. Psychology ; Fungi - metabolism ; Kinases ; Life Sciences ; Methods. Procedures. 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Academic</collection><jtitle>Applied microbiology and biotechnology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fraatz, Marco A.</au><au>Berger, Ralf G.</au><au>Zorn, Holger</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Nootkatone—a biotechnological challenge</atitle><jtitle>Applied microbiology and biotechnology</jtitle><stitle>Appl Microbiol Biotechnol</stitle><addtitle>Appl Microbiol Biotechnol</addtitle><date>2009-05-01</date><risdate>2009</risdate><volume>83</volume><issue>1</issue><spage>35</spage><epage>41</epage><pages>35-41</pages><issn>0175-7598</issn><eissn>1432-0614</eissn><coden>AMBIDG</coden><abstract>Due to its pleasant grapefruit-like aroma and various further interesting molecular characteristics, (+)-nootkatone represents a highly sought-after specialty chemical. (+)-Nootkatone is accumulated in its producer plants in trace amounts only, and the demand of the food, cosmetics and pharmaceutical industry is currently predominantly met by chemical syntheses. These typically require environmentally critical reagents, catalysts and solvents, and the final product must not be marketed as a “natural flavour” compound. Both the market pull and the technological push have thus inspired biotechnologists to open up more attractive routes towards natural (+)-nootkatone. The multifaceted approaches for the de novo biosynthesis or the biotransformation of the precursor (+)-valencene to (+)-nootkatone are reviewed. Whole-cell systems of bacteria, filamentous fungi and plants, cell extracts or purified enzymes have been employed. A prominent biocatalytic route is the allylic oxidation of (+)-valencene. It allows the production of natural (+)-nootkatone in high yields under mild reaction conditions. 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subjects | Bacteria - enzymology Bacteria - metabolism Bioconversions. Hemisynthesis Biological and medical sciences Biosynthesis Biotechnology Biotechnology - methods Biotransformation Carcinogens Cell Extracts Chemical synthesis Citrus fruits Cosmetics Enzymes Flavoring Agents - metabolism Flavoring Agents - pharmacology Food Fundamental and applied biological sciences. Psychology Fungi - metabolism Kinases Life Sciences Methods. Procedures. Technologies Microbial Genetics and Genomics Microbiology Mini-Review Oxidation Pharmaceutical industry Plant extracts Plants - metabolism Reagents Sesquiterpenes - metabolism Sesquiterpenes - pharmacology Studies Termites |
title | Nootkatone—a biotechnological challenge |
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