SimplePath: A Cell-free Enzymatic Platform for Cannabinoid Boisynthesis - Project Summary
Cannabinoids are bioactive natural products with many current and potential theoretical therapeutic uses that
are generally extracted from natural plant sources. While the cannabinoids tetrahydrocannabinolic acid (THCA),
and cannabidiolic acid (CBDA) are the highest abundance and therefore the most well studied, there are many
other low abundant (rare) cannabinoids that are also made in plants (e.g. the “varins” cannabidivarinic acid,
CBDVA, and tetrahydrocannabivarinic acid, THCVA). Plant production of cannabinoids, particularly rare
cannabinoids, is problematic because of crop variability, purification challenges and environmental concerns.
Consequently, there is considerable interest in producing both common and rare cannabinoids by metabolic
engineering of microbes. Microbial production of cannabinoids also faces daunting challenges, however, and
published titers so far are several orders of magnitude below cost competitive levels (8 mg/L).
Invizyne Technologies is developing an alternative, cell-free method to produce common and rare cannabinoids
(and other natural products) using enzymatic transformations. Our primary focus is production of the central
cannabinoid precursors cannabigerolic acid (CBGA) and cannabigerovarinic acid (CBGVA), because a variety
of important cannabinoids can be produced from CBGA/CBGVA in single enzymatic steps. Moreover, CBGA
itself is bioactive and shows promise for treatment of glaucoma, inflammatory bowel disease, and Huntington’s
disease.
A key barrier to cell-based and cell-free production of cannabinoids has been reliance on the native enzyme that
makes CBGA/CBGVA, Geranyl:Olivetolate Transferase (GOT), which is a membrane protein. In a major
development, we were able to design a highly active, specific and water soluble GOT enzyme. With this GOT
enzyme in hand, we have designed a 7 enzyme system for the production of CBGA/CBGVA, that we call
SimplePath. Not only is a 7 enzyme system tractable for commercial development, but initial tests provide CBGA
titers well over 1 g/L, already far exceeding cell-based methods by several orders of magnitude.
Our goal in this Phase I application is to expand our SimplePath approach and make necessary improvements
to lower costs and improve titers even further. At the end of Phase I we will perform techno-economic analysis
on the optimized SimplePath system to guide commercialization efforts (and identify weak points) that will be
addressed in a Phase II project. Phase I work is necessary for establishing a consistent, highly pure supply of
cannabinoids to be used as therapeutics.