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将毕赤酵母开发为高效从头生产β-石竹烯的细胞工厂。

Development of Komagataella phaffii as a cell factory for efficient de novo production of β-caryophyllene.

作者信息

Cheng Jintao, Chen Jiali, Chen Dingfeng, Li Baoxian, Wen Zhengshun, Jin Yuanxiang, Sun Chenfan, Yang Guiling

机构信息

Xianghu Laboratory, Hangzhou 310027, China.

Xianghu Laboratory, Hangzhou 310027, China.

出版信息

N Biotechnol. 2025 Mar 25;85:52-58. doi: 10.1016/j.nbt.2024.12.002. Epub 2024 Dec 7.

DOI:10.1016/j.nbt.2024.12.002
PMID:39653076
Abstract

β-Caryophyllene is a natural bicyclic sesquiterpene found in a large number of plants around the world. It has anti-inflammatory, anticancer and analgesic biological activities associated with its important medicinal value, and has also attracted attention in the field of bioenergy with high energy density. Due to the low amount of β-caryophyllene in plants and complex purification process, microbial biosynthesis is considered as a promising alternative for the industrial development of β-caryophyllene. Komagataella phaffii has a robust transcriptional regulatory system and has many advantages in protein expression, high-density culture, making it suitable for large-scale industrial production. However, there are no systematic studies on the efficient biosynthesis of β-caryophyllene in K. phaffii. In this study, firstly, farnesyl diphosphate synthase ERG20 and β-caryophyllene synthase AaCPS were fused and expressed with different linkers. Secondly, we enhanced the mevalonate pathway and inhibited the branch pathway. At last, the copy number of ERG20-(PA)5-AaCPS were adjusted for the biosynthesis of β-caryophyllene, a highly efficient β-caryophyllene production strain AaCPS16 was constructed. AaCPS16 could produce 136.4 mg/L β-caryophyllene in shake flask level, which was 37 times higher than the initial strain AaCPS1. To the best of our knowledge, this is the first report of caryophyllene biosynthesis in Komagataella phaffii. This established a good foundation for the synthesis of sesquiterpenes in K. phaffii.

摘要

β-石竹烯是一种天然的双环倍半萜,存在于世界上大量的植物中。它具有抗炎、抗癌和镇痛等生物活性,具有重要的药用价值,同时因其高能量密度在生物能源领域也受到关注。由于植物中β-石竹烯含量低且纯化过程复杂,微生物生物合成被认为是β-石竹烯工业开发的一种有前景的替代方法。毕赤酵母具有强大的转录调控系统,在蛋白质表达、高密度培养方面有诸多优势,适合大规模工业生产。然而,关于毕赤酵母中β-石竹烯的高效生物合成尚无系统研究。在本研究中,首先,将法尼基二磷酸合酶ERG20和β-石竹烯合酶AaCPS与不同接头融合表达。其次,增强甲羟戊酸途径并抑制分支途径。最后,调整ERG20-(PA)5-AaCPS的拷贝数用于β-石竹烯的生物合成,构建了高效β-石竹烯生产菌株AaCPS16。AaCPS16在摇瓶水平可产生136.4 mg/L的β-石竹烯,比初始菌株AaCPS1高37倍。据我们所知,这是毕赤酵母中石竹烯生物合成的首次报道。这为毕赤酵母中倍半萜的合成奠定了良好基础。

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