Nootkatone-a biotechnological challenge

被引:113
作者
Fraatz, Marco A. [1 ]
Berger, Ralf G. [2 ]
Zorn, Holger [1 ]
机构
[1] Univ Giessen, Inst Food Chem & Food Biotechnol, D-35392 Giessen, Germany
[2] Leibniz Univ Hannover, Inst Food Chem, D-30167 Hannover, Germany
关键词
Valencene; Flavour; Biosynthesis; Bioconversion; PHOTOMIXOTROPHIC CELL-CULTURES; ACETYLCHOLINESTERASE ACTIVITY; FUNCTIONAL-CHARACTERIZATION; VOLATILE CONSTITUENTS; EFFICIENT PRODUCTION; RACEMIC NOOTKATONE; ALPINIA-OXYPHYLLA; CITRUS-PARADISI; ESSENTIAL OILS; YELLOW-CEDAR;
D O I
10.1007/s00253-009-1968-x
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 [微生物学]; 090105 [作物生产系统与生态工程];
摘要
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.
引用
收藏
页码:35 / 41
页数:7
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