Trichomes are kind of a big deal. Why? Because they deliver the goods
Though you may not know exactly what they are, you’ve probably noticed the tiny hairs that cover the cannabis plant, giving it a crystal-like sheen and sticky feel. These glandular hairs are called trichomes, and they’re responsible for practically everything you love about cannabis.
Trichomes are glandular hairs found on the surface of plants and are responsible for producing the cannabis plant’s cannabinoids and terpenes. Trichomes contain resin glands that make the terpenes, flavonoids, THCA, CBDA, and other phytocannabinoids for which cannabis is known.
The crystal-like sheen and sticky feeling of cannabis buds are caused by high accumulations of trichomes. While they’re most visible to the naked eye on cannabis flower, trichomes can also be found on the leaves and stems of the plant.
There are two primary categories for trichomes: glandular and nonglandular. The glandular type produces cannabinoids while the nonglandular type does not. Within the glandular trichomes, there are three main types: bulbous, capitate sessile and capitate-stalked. Nonglandular trichomes are called cystoliths.
Bulbous trichomes are tiny bulbs that dot the surface of the plant. They cannot be seen without a microscope. While their production of cannabinoids is still in question, they add a crystal-like sheen to the cannabis plant and add to the stickiness of the flower. Bulbous trichomes aren’t restricted to particular areas of cannabis; they are evenly distributed throughout the surface of the plant.
Capitate Sessile trichomes are more abundant than bulbous trichomes, but still typically only visible with the aid of a microscope. Like bulbous trichomes, capitate sessile trichomes have large bulbs, but with more of the classic “mushroom” structure. This type of trichome is primarily found on the underside of the sugar and fan leaves.
Capitate-Stalked trichomes are shaped like mushrooms and contain a large bulb at the head of the stalk. These are the largest and most abundant trichomes in cannabis and the shape with which consumers are most familiar because they can be easily seen with the naked eye. The stalked trichome is primarily found of the surface of cannabis flowers and rarely seen on sugar or fan leaves.
How Cannabinoids Are Created in the Trichome
Cannabinoids, terpenes, and flavonoids are produced within the trichome cells through biosynthesis, in which enzymes catalyze a series of chemical reactions to produce complex molecules from simple (smaller) molecules. A quick review: Cannabinoids produced by the cannabis plant, or phytocannabinoids, interact with our body’s receptors to produce numerous psychotropic and therapeutic effects. Terpenes are compounds responsible for the aroma and flavors of cannabis, and support cannabinoids in producing desired effects. Flavonoids are similar to terpenes in that they contribute to a plant’s aroma and flavor profile, but may offer their own therapeutic effects.
The three basic steps for cannabinoid biosynthesis are binding, prenylation, and cyclization. On a molecular level, the activity is as follows: Nanoscale macromolecules called enzymes bind to one or two small molecules (substrates), attach the substrates to each other (prenylation, catalytic chemical conversion of the substrates), then pass the small molecule (transformed substrate) down an assembly line to another enzyme that processes it, making sequential changes to the small molecule (cyclization). Think of enzymes as biological nanomachines that use chemical energy rather than mechanical energy to build structures. Enzymes have inspired numerous studies in nanotechnology, biology, and other fields.
The following figures depict some of the molecular structures involved in cannabinoid biosynthesis. In these figures, each line is a bond between atoms. When two lines meet at a point and no letter is written, the atom is, by default, carbon. Oxygen and phosphorus atoms are explicitly indicated. Hydrogen atoms are only drawn in when bonded to oxygen or on the aromatic ring, they are not drawn on the alkyl chains. The curved arrows that point from one atom to another indicate that a new bond is formed between those atoms during the reaction, they also indicate the motion or exchange of electrons which make up a bond. Not all steps are shown, so there are some bonds that break and by-products formed which are not displayed.
The precursors to all natural cannabinoids, geranyl pyrophosphate, and olivetolic acid, are produced themselves by a complex series of biosynthetic reactions. Geranyl pyrophosphate and olivetolic acid bond to one another with the assistance of an enzyme in the prenyltransferase category known as GOT, thus creating the first cannabinoid, CBGA (see Figure 1). The CBGA contains a carboxylic acid group with the molecular formula COOH, and due to the presence of that acidic group, an “A” is placed at the end of CBGA. This is true for the rest of the cannabinoids whose acronym ends with the letter A (THCA, CBDA, etc.). The carboxylic acid groups spontaneously break off the cannabinoid structures as carbon dioxide (CO2) gas when heated. This process is called decarboxylation, after which the “A” designation is lost. For example, decarboxylated CBGA becomes CBG. This is considered a degradation process because it does not require enzymes and occurs after the plant is harvested. The CBG type of cannabinoids have one ring in the molecular structure, it’s the aromatic ring that came from the olivetolic acid (see Figure 1).
So, CBGA is the first cannabinoid formed from a biosynthetic reaction that joined two smaller pieces together — it is also the precursor to all other natural cannabinoids. Next, CBGA is cyclized into THCA, CBDA, or CBCA via the enzymes known as THCA synthase, CBDA synthase, and CBCA synthase. The presence and relative quantities of the specific enzymes are what controls which cannabinoid is the major product from each particular strain, and each particular cell. Remember, the CBG type cannabinoids have only one ring in their structure. After the cyclization reactions, the THCA, CBDA, and CBCA cannabinoids have more rings in their structures (see Figure 2).
For THCA, two new rings are formed by creation of two new covalent bonds, a carbon-oxygen bond and a carbon-carbon bond. The CBDA synthase enzyme catalyzes a reaction that creates one new carbon-carbon (C-C) bond at the same position that the C-C bond formed in THCA, but without the new C-O bond, thus forming CBDA. The formation of CBCA occurs by the formation of one carbon-oxygen bond at a different position of the molecule than the carbon-oxygen bond formed in THCA. Compounds with two rings fused to one another, such as in CBCA and CBC, are said to be bicyclic. That’s how THCA, CBDA, and CBCA are made through biosynthesis.
When cannabis flower is dried and cured properly, the most prominent cannabinoid will be the acidic form of the cannabinoid (THCA, CBDA, CBCA or CBGA). When smoked, or baked into edibles, these molecules decarboxylate (decarboxylated forms might be produced to a small extent biosynthetically and while drying, but acidic forms are the major product). The decarboxylation products are Δ9-THC, CBD, and CBC (see Figure 2).
As you can see, cannabis’ effects are the result of complex developments of cannabinoids, flavonoids, and terpenes that take place in the plant’s trichomes.
Burke, Anthony. “Cannabinoid Biosynthesis Part 1 – CBG, THC, CBD and CBC.” www.marijuana.com, 23 June 2014.
Fellermeier, Monica, et al. “Biosynthesis of cannabinoids: Incorporation experiments with 13C-Labeled glucoses.” European Journal of Biochemistry, no. 268, 2001, pp. 1596–1604.
ElSohly, Mahmoud A., editor. Marijuana and the Cannabinoids. Humana Press, 2007.