Fraatz Marco A, Berger Ralf G, Zorn Holger
Institute of Food Chemistry and Food Biotechnology, Justus Liebig University Giessen, Heinrich-Buff-Ring 58, 35392 Giessen, Germany.
Appl Microbiol Biotechnol. 2009 May;83(1):35-41. doi: 10.1007/s00253-009-1968-x. Epub 2009 Mar 31.
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.
由于其具有类似葡萄柚的宜人香气以及其他各种有趣的分子特性,(+)-诺卡酮是一种备受追捧的特殊化学品。(+)-诺卡酮在其生产植物中仅以微量积累,目前食品、化妆品和制药行业的需求主要通过化学合成来满足。这些合成通常需要对环境有危害的试剂、催化剂和溶剂,并且最终产品不能作为“天然香料”化合物进行销售。因此,市场需求和技术推动都促使生物技术专家开辟更具吸引力的途径来生产天然(+)-诺卡酮。本文综述了从头生物合成或前体(+)-瓦伦烯生物转化为(+)-诺卡酮的多方面方法。已采用细菌、丝状真菌和植物的全细胞系统、细胞提取物或纯化酶。一条重要的生物催化途径是(+)-瓦伦烯的烯丙基氧化。它能够在温和的反应条件下高产率地生产天然(+)-诺卡酮。关于(+)-瓦伦烯转化活性的首批序列数据刚刚公布。