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In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Results
  • Discussion
  • Disclosures
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

This protocol is designed to provide instructional information for the clonal propagation of Cannabis sativa L. by implementing aeroponic systems. The method described here includes all necessary supplies and protocols to successfully reproduce desirable morphological and chemical properties in the genus Cannabis.

Abstract

This protocol describes the standardization of an efficient clonal propagation technique of hemp by utilizing aeroponic systems. Primary shoot cuttings were excised from two hemp varieties, named "Cherry Wine" and "Red Robin" (17-20% w/w CBD), that served as 'mother plant'. An auxin precursor (indole-3-butyric acid) was applied to stimulate root development in the basal portion of the excised cuttings prior to placement in the system. Cuttings were lightly misted with the nutrient mist solution every three days to provide nutritional support as the solution contains the essential macronutrients, including nitrogen, phosphorus, and potassium. The aeroponic system water reservoir maintained a pH range between 5.0-6.0 and a water temperature between 20-22 °C. A submersible water pump was used to deliver water to the cuttings. The shoot tip cuttings were provided with 24 h of light per day for 10 days until root development occurred, upon which the rooted cuttings were transplanted for research purposes. These aeroponic systems have proven to generate desirable results for Cannabis propagation. The method described here alleviates potential time constraints that arise from traditional methods to allow for a more efficient means for the asexual propagation of Cannabis.

Introduction

Cannabis sativa L. is an annual, dioecious, flowering plant classified in the family Cannabaceae. Cannabinoids, produced predominantly within glandular trichomes located on the outer epidermal layer of bract tissues on female inflorescences1, are becoming an increasingly popular research topic, primarily due to their progressively recognized medicinal properties. Cannabidiol (CBD) is the second most prominent cannabinoid found in Cannabis after Δ9-tetrahydrocannabinol (THC) and is attributed to a host of medicinal benefits, including analgesic properties2, anti-seizure properties3, antidepressant properties4, reducing the risk of diabetes5, and treating various sleep disorders6. Due to the multitude of health benefits associated with the metabolites of the Cannabis plant, there is a growing demand for its commercial-scale production7. To meet this demand, cultivation methods are constantly being improved and reinvented to continuously supply consistent, high-quality plant material to the emerging Cannabis industry.

The propagation of Cannabis can be facilitated in two ways: sexual or asexual reproduction. An example of sexual reproduction is pollinating a female ovule with pollen from a male's stamen resulting in a seed that can be germinated. Seed germination is a reliable cultivation method that has been used for breeding and cultivation purposes where desirable phenotypical traits are selected in parental lines to improve the quality of the offspring Cannabis plants, including traits such as drought tolerance, insect resistance, increased yield, and increased potency8. However, unintended cross-pollination is an inherent risk when performing sexual reproduction, causing undesirable offspring, which leads to the potential loss of desirable traits or an introduction of unwanted traits. An example of this unintended pollination is highlighted by hemp growers receiving hemp seed pollinated with THC- producing pollen resulting in significant economic loss due to the non-compliant plants (>0.3% total THC w/w)9. Additionally, to generate a crop that consists of only females, a feminized seed must be sown instead of a non-feminized seed, which can lead to hermaphroditism and other undesirable traits leading to economic loss. To overcome the limitation of sexual reproduction of Cannabis, asexual reproduction has been widely practiced in commercial production models of the Cannabis industry10.

Asexual reproduction of Cannabis requires only a single plant, which allows for the multiplication of a single genotype that allows for commercial production of plants carrying desirable agronomic and pharmaceutical traits. A common form of asexual Cannabis reproduction is to cut and insert small portions of a female plant into a soilless substrate11 which is covered by a humidity dome to induce root formation. Although this method has proven successful, a common drawback is the accumulation of a high level of humidity (usually 80% or higher) inside the dome, providing an ideal growth environment for fungal pathogens, which can be detrimental to new, sensitive cuttings. Another form of asexual propagation is micropropagation using tissue culture, where sterile techniques allow for the propagation of insect, microbe, and virus-free Cannabis plant material in limited space12. This process, however, is expensive, time-consuming and requires trained laboratory technicians which are generally inaccessible for large-scale Cannabis facilities.

Very few published research reports exist on the clonal propagation of Cannabis. In order to provide a basis for the understanding of asexual reproduction of Cannabis for research purposes and industrial production, this study aimed to demonstrate the ease and accessibility of employing aeroponic systems for the clonal propagation of Cannabis. Aeroponic systems are ideal for the asexual propagation of Cannabis, consistently supplying nutrient-rich water to the cuttings, inducing early root formation in a timely manner, and allowing for a plant to be maintained indefinitely if needed.

Protocol

1. Generation of a mother plant for clonal propagation

  1. Select a healthy, female mother plant that exhibits desirable morphological and chemical characteristics specific to its intended use.
  2. Allow the mother plant to reach the appropriate size (roughly 25 mature shoots) for clonal propagation (i.e., cuttings).
  3. Allow the mother plants to remain in the vegetative growth stage (light: dark = 18 h:6 h) to promote shoot growth for future propagation.

2. Construction and preparation of aeroponic system

  1. Begin by positioning the lid on top of the container (38.1 cm x 25.4 cm x 30.48 cm). Drill the desired number of holes into the lid while providing adequate space (preferably 3 cm) between each.
  2. Position the water pump (Table of Materials) in the center of the container.
  3. Pour 7-8 L of distilled water into the container so that the pump nozzle remains roughly 2.5 cm above the waterline.
    NOTE: This ensures the submersible water pump (Table of Materials) is able to push water with enough force to spread across the container lid. Distilled water is recommended; however, regular tap water may also be used.
  4. Situate the appropriate amount of Rockwool cubes (3.81 cm) (Table of Materials) or media cubes of choice into each slot. Turn on the pump and allow it to run for 24 h.
    ​NOTE: Rockwool cubes are preferred due to their "anchoring" ability on the newly rooted cuttings that help keep plants upright following transplant.

3. Selecting and excising appropriate shoots

  1. Collect shoots near the apical meristem using a sterilized scalpel or scissor. Cuttings are ~10 cm in length, ideally with several nodes.
    NOTE: Cut the stem at a 45° angle. Cutting at a 45° angle increases the surface area of the basal portion of the cutting, allowing more space for root development. It's optional to make a small slit (1-2 cm) in the middle of the 45° cut to further increase surface area.
  2. Remove all foliage except foliage present on the top three nodes.
  3. Dip the newly excised cutting into the rooting solution containing indole-3-butyric acid (IBA) (Table of Materials) ~2-5 cm up from the base of the stem for ~5 s.
  4. Insert the cutting into the center of a Rockwool cube positioned in the aeroponic system.
    NOTE: The cutting insertion depth is to remain ~1-2 cm from the bottom of the Rockwool cube.
  5. Spray the unrooted cuttings with the nutrient mist solution (Table of Materials) every 3 days.
  6. Grow the cuttings with 18-24 h of light per day with a photosynthetic photon flux density (PPFD) of 100 µmol/m2/s at 24-29 °C and 40-60% relative humidity.

4. Aeroponic system maintenance and propagule health

  1. Replenish the system with water at a pH between 5.0- 6.0 every 2-5 days.
  2. Lightly mist the cuttings (one mist per cutting) with the nutrient mist solution (Table of Materials) every 3 days.
  3. Add 5 mL of each nutrient solution (Table of Materials) to the reservoir every 3-5 days.
    NOTE: The nutrient addition causes water to be brown and murky.
  4. Add 15 mL of the algae and bacteria cleaning solution containing hypochlorous acid (0.028%) per 10 L of water every 5 days (Table of Materials).

5. Transplanting propagules

  1. Select the cuttings with long, white, fibrous roots.
    NOTE: Avoid cuttings with brown, slimy, and short root systems as this is an indicator for the presence of root rot and will usually take longer to acclimate to the new growing medium and can bring unwanted diseases.
  2. Carefully dislodge the Rockwool cube from the system and untangle the roots.
  3. Transplant the Cannabis propagules to 4 L nursery pot filled with a nutritious soil mix (Table of Materials).
    ​NOTE: Watering immediately is recommended to prevent the roots from drying out.

6. Cleaning and storage of aeroponic system

  1. When the system is no longer in use, wash with water and clean with 70% ethanol or another disinfectant.
  2. Remove the filter from the water pump and rinse with water to remove debris.
  3. Dry the system by wiping it down with paper towels or a washcloth.
  4. Place the pump inside the tub with the lid on and store it until it is needed.

Results

To validate the efficiency of the described aeroponic system, a total of 10 and 12 healthy 14 cm long shoots were excised from the mother plants, 'Cherry Wine' and 'Red Robin', respectively (Figure 1A,B). After dipping into rooting induction media, the clones were placed into the system (Figure 2A). The construction and operation of an aeroponic system is shown as a schematic diagram in Figure 2A.

Discussion

With the increasing demand for Cannabis plants with consistent cannabinoid content, various clonal propagation methods have been exploited in Cannabis industry. The asexual propagation shows several advantages over sexual methods for large-scale, consistent production. An aeroponic propagation system is a modified version of a hydroponic system that utilizes an aerated nutrient-rich water mist to provide rapid root development. The described aeroponic system is composed of three critical steps, 1) gener...

Disclosures

The authors have no conflicts of interest.

Acknowledgements

This research was supported by the Institute of Cannabis Research at Colorado State University-Pueblo and the Ministry of Science and ICT (2021-DD-UP-0379), and Chuncheon city (Hemp R&D and industrialization, 2020-2021), The authors also wish to thank Justin Henderson at Summit CBD for the generous donation for "Cherry Wine" seeds.

Materials

NameCompanyCatalog NumberComments
1-part Fox FarmFox FarmSoil Mix
1-part PromixPromixSoil Mix
1-part Roots Organic OriginalAuora InnovationsSoil Mix
1-part Wiggle Worm Earth Worm CastingsUNCO IndustriesSoil Mix
Algae and Bacterial Cleaning Solution (Clear Rez)EZ CloneSKU#: 2258 fl. Oz.
Artificial LightingAgroBriteSKU#: 1399T5 324W 4' 6-Tube Fixture with Lamps
Cannabis Mother plant 1 (Cherry Wine)Summit CBDN/ADonated material
Cannabis Mother Plant 2 (Red Wine)TrilogeneSKU: 0101RR
Corresponding Plastic LidOffice DepotN/A38.1 cm x 25.4 cm
Drill Bit 1DewaltDW158638.1 mm spade drill bit
Drill Bit 2DewaltDW13083.175 mm drill bit
Flora/Bloom (Nutrient Solution)-5 mLGeneral HydroponicsSKU#: 726946 mL (1 Quart) 2.43 lbs. (1.1 kg) (Available Phosphate 5.0%, Soluble Potash 4.0%, Magnesium 1.5%, Sulfur 1.0%)
FloraGrow (Nutrient Solution)- 5 mLGeneral HydroponicsSKU#: 724946 mL (1 Quart) 2.43 lbs. (1.1 kg) ((Total Nitrogen 2.0% (0.25% Ammoniacal Nitrogen, 1.75% Nitrate Nitrogen), Available Phosphate 1.0%, Soluble Potash 6.0%, Magnesium 0.5%))
FloraMicro (Nutrient Solution)- 5 mLGeneral HydroponicsSKU#: 759946 mL (1 Quart) 2.43 lbs. (1.1 kg) ((Total Nitrogen 5.0% (0.3% Ammoniacal Nitrogen, 4.7% Nitrate Nitrogen), Soluble Potash 1.0%, Calcium 5.0%, Boron 0.01%, Cobalt 0.0005%, Copper 0.01%, Iron 0.1%, Manganese 0.05%, Molybdenum 0.0008%, Zinc 0.015%))
Horticultural ScissorsShear PerfectionSKU#: 12620Platinum Stainless Steel Bonsai Scissors (2.4")
Isopropyl AlcoholEquateWalmart # 57413356270% concentration
Nutrient Mist Solution (Clonex Mist)Growth TechnologySKU#: 488910.14 fl. Oz (300 ml) (Total Nitrogen: 5.9 × 10-4 %, Available Phosphate: 4.0 × 10-4 %, Soluble Potash: 5.0 × 10-4 %)
pH DownGeneral HydroponicsSKU#: 733946 ml (1 Quart) 2.43 lbs. (1.1 kg)
pH UpGeneral HydroponicsSKU#: 730946 ml (1 Quart) 2.43 lbs. (1.1 kg)
Plastic ContainerOffice DepotN/A38.1 cm x 25.4 cm x 30.48 cm
Power DrillDewaltDCD709B20-Volt Max ½” Drill
Rockwool CubesGrodanSKU#: 83038.1 mm
Rooting Solution (Clonex Rooting Gel)Growth TechnologySKU#: 9393.4 fl. Oz. (100 ml) (Indolebutyric Acid - 0.31%)
Statistic Software (Prism)GraphPad Inc.
Submersible Water PumpActiveAQUASKU: AAPW250Model: AAPW250, Voltage 120V, Power 16W

References

  1. ElSohly, M. A., Radwan, M. M., Gul, W., Chandra, S., Galal, A. Phytochemistry of Cannabis sativa L. Progress in the Chemistry of Organic Natural Products. 103, 1-36 (2017).
  2. Cunetti, L., et al. Chronic pain treatment with cannabidiol in kidney transplant patients in Uruguay. Transplantation Proceedings. 50 (2), 461-464 (2018).
  3. Hausman-Kedem, M., Menascu, S., Kramer, U. Efficacy of CBD-enriched medical cannabis for treatment of refractory epilepsy in children and adolescents - An observational, longitudinal study. Brain & Development. 40 (7), 544-551 (2018).
  4. Linge, R., et al. Cannabidiol induces rapid-acting antidepressant-like effects and enhances cortical 5-HT/glutamate neurotransmission: role of 5-HT1A receptors. Neuropharmacology. 103, 16-26 (2016).
  5. Lehmann, C., et al. Experimental cannabidiol treatment reduces early pancreatic inflammation in type 1 diabetes. Clinical Hemorheology and Microcirculation. 64 (4), 655-662 (2016).
  6. Shannon, S., Lewis, N., Lee, H., Hughes, S. Cannabidiol in anxiety and sleep: A large case series. The Permanente Journal. 23, 18-41 (2019).
  7. Russo, E. B. History of cannabis and its preparations in saga, science, and sobriquet. Chemistry & Biodiversity. 4 (8), 1614-1648 (2007).
  8. Vera, C. L., Hanks, A. Hemp production in Western Canada. Journal of Industrial Hemp. 9 (2), 79-86 (2004).
  9. . Hot hemp: How high THC levels can ruin a legal hemp harvest Available from: https://www.westword.com/marijuana/hot-hemp-how-high-thc-levels-can-ruin-a-legal-hemp-harvest-9963683 (2018)
  10. Lata, H., Chandra, S., Techen, N., Khan, I. A., ElSohly, M. A. Assessment of the genetic stability of micropropagated plants of Cannabis sativa by ISSR markers. Planta Medica. 76 (1), 97-100 (2010).
  11. Caplan, D., Dixon, M., Zheng, Y. Optimal rate of organic fertilizer during the flowering stage for Cannabis grown in two coir-based substrates. HortScience. 52 (12), 1796 (2017).
  12. Monthony, A. S., Page, S. R., Hesami, M., Jones, A. M. P. The past, present and future of Cannabis sativa tissue culture. Plants (Basel). 10 (1), 185 (2021).
  13. Clarke, R. C., Merlin, M. D. Cannabis domestication, breeding history, present-day genetic diversity, and future prospects. Critical Reviews in Plant Sciences. 35 (5-6), 293-327 (2016).

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