Microbial production of cannabinoids promises to provide a consistent, cheaper, and more sustainable supply of these important therapeutic molecules. However, scaling production to compete with traditional plant-based sources is challenging. Our ability to make strain variants greatly exceeds our capacity to screen and identify high producers, creating a bottleneck in metabolic engineering efforts. Here, we present a yeast-based biosensor for detecting microbially produced Î(9)-tetrahydrocannabinol (THC) to increase throughput and lower the cost of screening. We port five human cannabinoid G protein-coupled receptors (GPCRs) into yeast, showing the cannabinoid type 2 receptor, CB2R, can couple to the yeast pheromone response pathway and report on the concentration of a variety of cannabinoids over a wide dynamic and operational range. We demonstrate that our cannabinoid biosensor can detect THC from microbial cell culture and use this as a tool for measuring relative production yields from a library of Î(9)-tetrahydrocannabinol acid synthase (THCAS) mutants.
Screening microbially produced Î(9)-tetrahydrocannabinol using a yeast biosensor workflow.
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作者:Shaw William M, Zhang Yunfeng, Lu Xinyu, Khalil Ahmad S, Ladds Graham, Luo Xiaozhou, Ellis Tom
| 期刊: | Nature Communications | 影响因子: | 15.700 |
| 时间: | 2022 | 起止号: | 2022 Sep 20; 13(1):5509 |
| doi: | 10.1038/s41467-022-33207-x | ||
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