Engineering cellular dephosphorylation boosts (+)-borneol production in yeast

脱磷 冰片 酵母 生产(经济) 化学 计算机科学 细胞生物学 计算生物学 生物 生物化学 磷酸化 医学 宏观经济学 病理 经济 磷酸酶 中医药 替代医学
作者
Haiyan Zhang,Peng Cai,Juan Guo,Jiaoqi Gao,Linfeng Xie,Ping Su,Xiaoxin Zhai,Baolong Jin,Guanghong Cui,Yongjin J. Zhou,Luqi Huang
出处
期刊:Acta Pharmaceutica Sinica B [Elsevier BV]
卷期号:15 (2): 1171-1182 被引量:9
标识
DOI:10.1016/j.apsb.2024.12.039
摘要

(+)-Borneol, the main component of "Natural Borneol" in the Chinese Pharmacopoeia, is a high-end spice and precious medicine. Plant extraction cannot meet the increasing demand for (+)-borneol, while microbial biosynthesis offers a sustainable supply route. However, its production was extremely low compared with other monoterpenes, even with extensively optimizing the mevalonate pathway. We found that the key challenge is the complex and unusual dephosphorylation reaction of bornyl diphosphate (BPP), which suffers the side-reaction and the competition from the cellular dephosphorylation process, especially lipid metabolism, thus limiting (+)-borneol synthesis. Here, we systematically optimized the dephosphorylation process by identifying, characterizing phosphatases, and balancing cellular dephosphorylation metabolism. For the first time, we identified two endogenous phosphatases and seven heterologous phosphatases, which significantly increased (+)-borneol production by up to 152%. By engineering BPP dephosphorylation and optimizing the MVA pathway, the production of (+)-borneol was increased by 33.8-fold, which enabled the production of 753 mg/L under fed-batch fermentation in shake flasks, so far the highest reported in the literature. This study showed that rewiring dephosphorylation metabolism was essential for high-level production of (+)-borneol in S. cerevisiae , and balancing cellular dephosphorylation is also helpful for efficient biosynthesis of other terpenoids since all whose biosynthesis involves the dephosphorylation procedure. Boosting (+)-borneol production and proportion by identifying, characterizing phosphatases, and balancing cellular dephosphorylation metabolism. This strategy minimizes the impact of the side-reaction and the competition from cellular dephosphorylation process.
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