Bibenzyl synthesis in Cannabis sativa L. (6th December 2021)

• Record Type: Journal Article
• Authors: Boddington, Kelly F.; Soubeyrand, Eric; Van Gelder, Kristen; Casaretto, José A.; Perrin, Colby; Forrester, Taylor J.B.; Parry, Cameron; Al‐Abdul‐Wahid, M. Sameer; Jentsch, Nicholas G.; Magolan, Jakob; Bozzo, Gale G.; Kimber, Matthew S.; Rothstein, Steven J.; Akhtar, Tariq A.
• Is Part Of: Plant journal. Volume 109:Number 3(2022)
• Page Start: 693
• Page End: 707
• Publication Date: 2021-12-06
• Subjects: Cannabis sativa L. -- bibenzyl synthase -- 4‐coumarate‐CoA ligase -- inflammation -- dihydroresveratrol -- canniprene; Plant molecular biology -- Periodicals; Plant cells and tissues -- Periodicals; Botany -- Periodicals; 580
• DOI: 10.1111/tpj.15588
• Languages: English
• ISSNs: 0960-7412

Abstract

SUMMARY: This study focuses on the biosynthesis of a suite of specialized metabolites from Cannabis that are known as the 'bibenzyls'. In planta, bibenzyls accumulate in response to fungal infection and various other biotic stressors; however, it is their widely recognized anti‐inflammatory properties in various animal cell models that have garnered recent therapeutic interest. We propose that these compounds are synthesized via a branch point from the core phenylpropanoid pathway in Cannabis, in a three‐step sequence. First, various hydroxycinnamic acids are esterified to acyl‐coenzyme A (CoA) by a member of the 4‐coumarate‐CoA ligase family (Cs4CL4). Next, these CoA esters are reduced by two double‐bond reductases (CsDBR2 and CsDBR3) that form their corresponding dihydro‐CoA derivatives from preferred substrates. Finally, the bibenzyl backbone is completed by a polyketide synthase that specifically condenses malonyl‐CoA with these dihydro‐hydroxycinnamoyl‐CoA derivatives to form two bibenzyl scaffolds: dihydropiceatannol and dihydroresveratrol. Structural determination of this 'bibenzyl synthase' enzyme (CsBBS2) indicates that a narrowing of the hydrophobic pocket surrounding the active site evolved to sterically favor the non‐canonical and more flexible dihydro‐hydroxycinnamoyl‐CoA substrates in comparison with their oxidized relatives. Accordingly, three point mutations that were introduced into CsBBS2 proved sufficient to restore some enzymatic activity with an oxidized substrate, in vitro . Together, the identification of this set of Cannabis enzymes provides a valuable contribution to the growing 'parts prospecting' inventory that supports the rational metabolic engineering of natural product therapeutics. Significance Statement: The medicinal properties of Cannabis sativa have long been attributed to Δ 9 ‐tetrahydrocannabinol and the pharmacologically related cannabinoids, but a growing body of evidence points to another class of specialized metabolites, known as the bibenzyls, which contribute to the therapeutic potential of Cannabis . Here, we characterize the biosynthetic pathway towards a core group of Cannabis bibenzyls, thereby opening the door to the production of these Cannabis compounds that are not easily accessible from nature.