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Screening microbially produced Δ9-tetrahydrocannabinol using a yeast biosensor workflow.


ABSTRACT: 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 Δ9-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 Δ9-tetrahydrocannabinol acid synthase (THCAS) mutants.

SUBMITTER: Shaw WM 

PROVIDER: S-EPMC9489785 | biostudies-literature | 2022 Sep

REPOSITORIES: biostudies-literature

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Screening microbially produced Δ<sup>9</sup>-tetrahydrocannabinol using a yeast biosensor workflow.

Shaw William M WM   Zhang Yunfeng Y   Lu Xinyu X   Khalil Ahmad S AS   Ladds Graham G   Luo Xiaozhou X   Ellis Tom T  

Nature communications 20220920 1


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 Δ<sup>9</sup>-tetrahyd  ...[more]

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