类胡萝卜素
双加氧酶
劈理(地质)
底物特异性
基质(水族馆)
化学
生物化学
生物
酶
生态学
断裂(地质)
古生物学
作者
Zhipeng Qi,Xinyi Tong,Yangyang Zhang,Shutong Jia,Xianying Fang,Linguo Zhao
标识
DOI:10.1021/acs.jafc.3c06459
摘要
C13-apocarotenoids are naturally derived from the C9–C10 (C9′–C10′) double-bond cleavage of carotenoids by carotenoid cleavage dioxygenases (CCDs). As high-value flavors and fragrances in the food and cosmetic industries, the sustainable production of C13-apocarotenoids is emerging in microbial cell factories by the carotenoid cleavage dioxygenase 1 (CCD1) subfamily. However, the commercialization of microbial-based C13-apocarotenoids is still limited by the poor performance of CCD1, which severely constrains its conversion efficiency from precursor carotenoids. This review focuses on the classification of CCDs and their cleavage modes for carotenoids to generate corresponding apocarotenoids. We then emphatically discuss the advances for C13-apocarotenoid biosynthesis in microbial cell factories with various strategies, including optimization of CCD1 expression, improvement of CCD1's catalytic activity and substrate specificity, strengthening of substrate channeling, and development of oleaginous microbial hosts, which have been verified to increase the conversion rate from carotenoids. Lastly, the current challenges and future directions will be discussed to enhance CCDs' application for C13-apocarotenoids biomanufacturing.
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