DOCSLIB.ORG

A Terpene for Everyone Maximizing Your Cannabis Experience Author: Caitlin Nelson | Editors: Erica Freeman & Amanda Woods

Total Page：16

File Type：pdf, Size：1020Kb

Download full-text PDF Read full-text
A Terpene for Everyone Maximizing Your Cannabis Experience Author: Caitlin Nelson | Editors: Erica Freeman & Amanda Woods A Terpene for Everyone Maximizing your Cannabis Experience Author: Caitlin Nelson | Editors: Erica Freeman & Amanda Woods Let’s take a moment to re-hash our topic—terpenes! The essential oils that create the familiar scent that fills your nose when you open your jar of Sour Diesel, and maybe even makes your mouth water. (Just a little, not drooling status or anything) The compounds are inhaled through the nose, and transported to the hypothalamus in the limbic brain, which controls heart rate, blood pressure, hunger, and thirst. Terpene test results are broken down by each terpene as a percentage of the total terpene profile (i.e., some percentage out of 100%). There are hundreds of terpenes and countless combinations; each combination carrying a unique set of characteristics working to unlock your bodies cannabinoid receptors like a key. An “herban” legend rumors that eating a Mango before smoking cannabis would get you “more high”. This sounds like a delicious myth and current research suggest there is some truth to this after all. It turns out that Mangos contain a high percentage of the compound β-Myrcene, which “…has been shown to allow more absorption of cannabinoids by the brain, by changing the permeability of cell membranes. Eating a fresh mango 45 minutes before smoking could increase the effects”, Steep Hill Lab states. (buys stock in Mangos) β–Myrcene gets its name from a medicinal shrub from Brazil, the Myrcia sphaerocarpa, which contains very high amounts of β–Myrcene. According to many sources, extracts of the roots have been used there to treat hypertension, diabetes, diarrhea and dysentery. β-Myrcene plays an important role forming other terpenes, and is found in small amounts of nearly every essential oil and plant. About half of Choice Organics strains tested at 50% β–Myrcene or higher. Afgooey made the loudest statement at 85%. β–Myrcene’s smell can be hypnotic, and it can relax your muscles, and act as a sedative with anti-inflammatory properties. It is naturally found in high concentrations in lemongrass, hops, thyme, citrus, and of course, mango. As you can see with Myrcene, each terpene plays a unique and harmonious role in the effect you feel. Pinene makes up 10% of Afgooey’s terpene profile, and provides the crucial biosynthetic base of our endocannabinoid system—CB2 receptors. Terpenes help amplify the effects of cannabinoids. Pinene helps to build the biosynthetic base and β-Myrcene permeates the cell membranes, both helping with the uptake of potent cannabinoids. All of Choice Organics’ strains tested at 6% to 35% Pinene. This makes sense because α-Pinene and β-Pinene are the most common terpenes in plants. It is a bronchodilator, which helps open respiratory pathways in the lungs and is great for those with asthma or chronic lung problems. Like many terpenes, Pinene is an anti-inflammatory so it may help with most aches and pains as well. It also promotes awareness and memory retention, which is surprising because some cannabis properties will make you forget you just ate a whole bag of Cheetos and two slices of cake. Another terpenoid that is growing a reputation quickly is β-Caryophyllene, and it’s not because of the length of its name. It is very effective for pain relief, and it has an affinity for the CB2 receptor, similarly to CBD. Since β-Caryophyllene is absorbed by the endocannabinoid system it is known as a “phytocannabinoid”, meaning it acts like a cannabinoid but it is not. Black pepper has high concentrations of β-Caryophyllene, and is a strong anti-inflammatory and has pain relieving effects. Green, leafy vegetables also have great amounts of β-Caryophyllene. While Pinene builds our endocannabinoid receptors, Myrcene is permeating the cell walls to increase absorption, and β-Caryophyllene activates the CB2 receptors, all increasing efficacy of your cannabinoids. So in theory, these terpenes don’t make you feel high, but they do help to increase the absorption of your cannabinoids, and in turn you will feel a better effect from your cannabis. Toking Tips: Terpenes act on our limbic system through inhalation. According to our on-site Aromatherapist, Lori Reeves, research in essential oils shows that the boiling point changes the effects of terpenes. Lighters burn around 2,000F. At that temperature you may not get some of the described therapeutic benefits described with traditional smoking or dabbing. β–Myrcene boils at 330F, β-Caryophyllene at 266F, and Pinene at 311F. It’s believed that smelling, eating, and vaping lower than those temperatures will be most efficient way to receive those benefits. References: Ethan Russo, MD., “Taming THC: potential cannabis synergy and phytocannabinoid- terpenoid entourage effects.” CMT Laboratories Cannabis and Cannabis Extracts: Greater Than the Sum of Their Parts? John M. McPartland And Ethan B. Russo. .
Load more

Recommended publications
  • Biosynthesis of Natural Products
    63 2. Biosynthesis of Natural Products - Terpene Biosynthesis 2.1 Introduction Terpenes are a large and varied class of natural products, produced primarily by a wide variety of plants, insects, microoroganisms and animals. They are the major components of resin, and of turpentine produced from resin. The name "terpene" is derived from the word "turpentine". Terpenes are major biosynthetic building blocks within nearly every living creature. Steroids, for example, are derivatives of the triterpene squalene. When terpenes are modified, such as by oxidation or rearrangement of the carbon skeleton, the resulting compounds are generally referred to as terpenoids. Some authors will use the term terpene to include all terpenoids. Terpenoids are also known as Isoprenoids. Terpenes and terpenoids are the primary constituents of the essential oils of many types of plants and flowers. Essential oils are used widely as natural flavor additives for food, as fragrances in perfumery, and in traditional and alternative medicines such as aromatherapy. Synthetic variations and derivatives of natural terpenes and terpenoids also greatly expand the variety of aromas used in perfumery and flavors used in food additives. Recent estimates suggest that over 30'000 different terpenes have been characterized from natural sources. Early on it was recognized that the majority of terpenoid natural products contain a multiple of 5C-atoms. Hemiterpenes consist of a single isoprene unit, whereas the monoterpenes include e.g.: Monoterpenes CH2OH CHO CH2OH OH Myrcens
    [Show full text]
  • Use the Right Citrus-Based Cleaning Products to Avoid Corrosion Or Rust Bob Beckley, Project Leader
    United States Department of Agriculture Facilities Forest Service Technology & Development Program March 2006 0673–2319–MTDC 7300/7100/5100/2400/2300 Use the Right Citrus-Based Cleaning Products to Avoid Corrosion or Rust Bob Beckley, Project Leader itrus-based cleaning products are commonly found in metal on their chain saws. The crew stopped using citrus-based residential and commercial settings. The ingredients in products because they believed citric acid was causing the these products vary widely (figure 1). While some of damage. However, the damage probably was caused by a C water-based citrus cleaning product. What To Look for in a Citrus-Based Cleaning Product The Material Safety Data Sheets (MSDSs) for chemical products list their ingredients. The MSDS for a citrus-based cleaner should list D-Limonene among the ingredients. D- Limonene is in the terpene family, which includes citrus and pine oils. Terpenes are generally not corrosive or harmful to metals or most plastics and polymers. Terpenes won’t cause rusting, pitting, etching, or staining. Citrus-based terpenes can dissolve heavy petroleum greases and residues in about 30 Figure 1—Citrus-based cleaners are commonly used in residential and minutes when they are used at ambient temperatures. commercial settings, but users often are unaware of the difference between citrus oil-based cleaning products and water-based products. A citrus oil-based cleaning product will not cause corrosion these products can cause corrosion or rust, others do not. The or rust. Such products are made from the oil found in the difference is based on the ingredients. Hundreds of cleaning orange peel, rather than the pulp and juice of the orange.
    [Show full text]
  • (C5–C20) Emissions of Downy Birches
    Atmos. Chem. Phys., 21, 8045–8066, 2021 https://doi.org/10.5194/acp-21-8045-2021 © Author(s) 2021. This work is distributed under the Creative Commons Attribution 4.0 License. Sesquiterpenes and oxygenated sesquiterpenes dominate the VOC (C5–C20) emissions of downy birches Heidi Hellén1, Arnaud P. Praplan1, Toni Tykkä1, Aku Helin1, Simon Schallhart1, Piia P. Schiestl-Aalto2,3,4, Jaana Bäck2,3, and Hannele Hakola1 1Atmospheric Composition Research Unit, Finnish Meteorological Institute, P.O. Box 503, 00101 Helsinki, Finland 2Institute for Atmospheric and Earth System Research/Forest Sciences, Helsinki, Finland 3Faculty of Agriculture and Forestry, University of Helsinki, Helsinki, Finland 4Department of Forest Ecology and Management, SLU, 901 83 Umeå, Sweden Correspondence: Heidi Hellén (heidi.hellen@fmi.fi) Received: 2 December 2020 – Discussion started: 16 December 2020 Revised: 23 March 2021 – Accepted: 28 April 2021 – Published: 26 May 2021 Abstract. Biogenic volatile organic compounds (BVOCs) 24 % and 17 % of the total SQT and OSQT emissions, re- emitted by the forests are known to have strong impacts in spectively. A stressed tree growing in a pot was also stud- the atmosphere. However, lots of missing reactivity is found, ied, and high emissions of α-farnesene and an unidentified especially in the forest air. Therefore better characterization SQT were detected together with high emissions of GLVs. of sources and identification/quantification of unknown re- Due to the relatively low volatility and the high reactivity of active compounds is needed. While isoprene and monoter- SQTs and OSQTs, downy birch emissions are expected to pene (MT) emissions of boreal needle trees have been studied have strong impacts on atmospheric chemistry, especially on quite intensively, there is much less knowledge on the emis- secondary organic aerosol (SOA) production.
    [Show full text]
  • Medically Useful Plant Terpenoids: Biosynthesis, Occurrence, and Mechanism of Action
    molecules Review Medically Useful Plant Terpenoids: Biosynthesis, Occurrence, and Mechanism of Action Matthew E. Bergman 1 , Benjamin Davis 1 and Michael A. Phillips 1,2,* 1 Department of Cellular and Systems Biology, University of Toronto, Toronto, ON M5S 3G5, Canada; [email protected] (M.E.B.); [email protected] (B.D.) 2 Department of Biology, University of Toronto–Mississauga, Mississauga, ON L5L 1C6, Canada * Correspondence: [email protected]; Tel.: +1-905-569-4848 Academic Editors: Ewa Swiezewska, Liliana Surmacz and Bernhard Loll Received: 3 October 2019; Accepted: 30 October 2019; Published: 1 November 2019 Abstract: Specialized plant terpenoids have found fortuitous uses in medicine due to their evolutionary and biochemical selection for biological activity in animals. However, these highly functionalized natural products are produced through complex biosynthetic pathways for which we have a complete understanding in only a few cases. Here we review some of the most effective and promising plant terpenoids that are currently used in medicine and medical research and provide updates on their biosynthesis, natural occurrence, and mechanism of action in the body. This includes pharmacologically useful plastidic terpenoids such as p-menthane monoterpenoids, cannabinoids, paclitaxel (taxol®), and ingenol mebutate which are derived from the 2-C-methyl-d-erythritol-4-phosphate (MEP) pathway, as well as cytosolic terpenoids such as thapsigargin and artemisinin produced through the mevalonate (MVA) pathway. We further provide a review of the MEP and MVA precursor pathways which supply the carbon skeletons for the downstream transformations yielding these medically significant natural products. Keywords: isoprenoids; plant natural products; terpenoid biosynthesis; medicinal plants; terpene synthases; cytochrome P450s 1.
    [Show full text]
  • Isoprene Rule Revisited 242:2 R9–R22 Endocrinology REVIEW Terpenes, Hormones and Life: Isoprene Rule Revisited
    242 2 Journal of S G Hillier and R Lathe Isoprene rule revisited 242:2 R9–R22 Endocrinology REVIEW Terpenes, hormones and life: isoprene rule revisited Stephen G Hillier1 and Richard Lathe2 1Medical Research Council Centre for Reproductive Health, University of Edinburgh, The Queen’s Medical Research Institute, Edinburgh, UK 2Division of Infection and Pathway Medicine, University of Edinburgh Medical School, Edinburgh, UK Correspondence should be addressed to S G Hillier or R Lathe: [email protected] or [email protected] Abstract The year 2019 marks the 80th anniversary of the 1939 Nobel Prize in Chemistry awarded Key Words to Leopold Ruzicka (1887–1976) for work on higher terpene molecular structures, including f isoprene the first chemical synthesis of male sex hormones. Arguably his crowning achievement f terpene was the ‘biogenetic isoprene rule’, which helped to unravel the complexities of terpenoid f steroid biosynthesis. The rule declares terpenoids to be enzymatically cyclized products of f evolution substrate alkene chains containing a characteristic number of linear, head-to-tail f great oxidation event condensed, C5 isoprene units. The number of repeat isoprene units dictates the type of f Ruzicka terpene produced (i.e., 2, monoterpene; 3, sesquiterpene; 4, diterpene, etc.). In the case of triterpenes, six C5 isoprene units combine into C30 squalene, which is cyclized into one of the signature carbon skeletons from which myriad downstream triterpenoid structures are derived, including sterols and steroids. Ruzicka also had a keen interest in the origin of life, but the pivotal role of terpenoids has generally been overshadowed by nucleobases, amino acids, and sugars.
    [Show full text]
  • Terpene Esters from Natural Products: Synthesis and Evaluation of Cytotoxic Activity
    Anais da Academia Brasileira de Ciências (2017) 89(3): 1369-1379 (Annals of the Brazilian Academy of Sciences) Printed version ISSN 0001-3765 / Online version ISSN 1678-2690 http://dx.doi.org/10.1590/0001-3765201720160780 www.scielo.br/aabc | www.fb.com/aabcjournal Terpene Esters from Natural Products: Synthesis and Evaluation of Cytotoxic Activity MAURICIO M. VICTOR1,2, JORGE M. DAVID1,2, MARIA C.K. SAKUKUMA1,2, LETÍCIA V. COSTA-LOTUFO3,4, ANDREA F. MOURA3 and ANA J. ARAÚJO3,5 1Instituto de Química, Universidade Federal da Bahia, Depto de Química Orgânica, Rua Barão do Jeremoabo, s/n, Campus de Ondina, Ondina, 40170-115 Salvador, BA, Brazil 2Instituto Nacional de Ciência e Tecnologia/INCT de Energia e Ambiente,Universidade Federal da Bahia/UFBA, Rua Barão de Geremoabo, 147, Campus de Ondina, 40170-290 Salvador, BA, Brazil 3Departamento de Fisiologia e Farmacologia, Universidade Federal do Ceará, Centro de Ciências da Saúde, Av. Coronel Nunes de Melo, 1127, Rodolfo Teófilo, 60430-270 Fortaleza, CE, Brazil 4Departamento de Farmacologia, Universidade de São Paulo, Av. Professor Lineu Prestes, 1524, Cidade Universitária, Butantã, 05508-900 São Paulo, SP, Brazil 5Universidade Federal do Piauí, Av. São Sebastião, 2819, São Benedito, Campus Ministro Reis Velloso, 64202-020 Parnaíba, PB, Brazil Manuscript received on November 16, 2016; accepted for publication on February 22, 2017 ABSTRACT Natural steroids and triterpenes such as β-sitosterol, stigmasterol, lupeol, ursolic and betulinic acids were transformed into its hexanoic and oleic esters, to evaluate the influence of chemical modification towards the cytotoxic activities against tumor cells. The derivatives were evaluated against five tumor cell lines [OVCAR-8 (ovarian carcinoma); SF-295 (glioblastoma); HCT-116 (colon adenocarcinoma); HL-60 (leukemia); and PC-3 (prostate carcinoma)] and the results showed only betulinic acid hexyl ester exhibits cytotoxic potential activity.
    [Show full text]
  • Limonene and (+)-Α-Pinene on Bacterial Cells
    biomolecules Article The Mode of Action of Cyclic Monoterpenes (−)-Limonene and (+)-α-Pinene on Bacterial Cells Olga E. Melkina 1, Vladimir A. Plyuta 2 , Inessa A. Khmel 2 and Gennadii B. Zavilgelsky 1,* 1 State Research Institute of Genetics and Selection of Industrial Microorganisms of the National Research Centre “Kurchatov Institute”, Kurchatov Genomic Center, 117545 Moscow, Russia; [email protected] 2 Institute of Molecular Genetics of the National Research Center “Kurchatov Institute”, 123182 Moscow, Russia; [email protected] (V.A.P.); [email protected] (I.A.K.) * Correspondence: [email protected] Abstract: A broad spectrum of volatile organic compounds’ (VOCs’) biological activities has attracted significant scientific interest, but their mechanisms of action remain little understood. The mechanism of action of two VOCs—the cyclic monoterpenes (−)-limonene and (+)-α-pinene—on bacteria was studied in this work. We used genetically engineered Escherichia coli bioluminescent strains harboring stress-responsive promoters (responsive to oxidative stress, DNA damage, SOS response, protein damage, heatshock, membrane damage) fused to the luxCDABE genes of Photorhabdus luminescens. We showed that (−)-limonene induces the PkatG and PsoxS promoters due to the formation of reactive oxygen species and, as a result, causes damage to DNA (SOSresponse), proteins (heat shock), and membrane (increases its permeability). The experimental data indicate that the action of (−)- limonene at high concentrations and prolonged incubation time makes degrading processes in cells irreversible. The effect of (+)-α-pinene is much weaker: it induces only heat shock in the bacteria. Moreover, we showed for the first time that (−)-limonene completely inhibits the DnaKJE–ClpB bichaperone-dependent refolding of heat-inactivated bacterial luciferase in both E.
    [Show full text]
  • Plant Terpenoids: Applications and Future Potentials Sam Zwenger
    University of Northern Colorado Scholarship & Creative Works @ Digital UNC School of Biological Sciences Faculty Publications School of Biological Sciences 2008 Plant Terpenoids: Applications and Future Potentials Sam Zwenger Chhandak Basu University of Northern Colorado Follow this and additional works at: http://digscholarship.unco.edu/biofacpub Part of the Plant Sciences Commons Recommended Citation Zwenger, Sam and Basu, Chhandak, "Plant Terpenoids: Applications and Future Potentials" (2008). School of Biological Sciences Faculty Publications. 4. http://digscholarship.unco.edu/biofacpub/4 This Article is brought to you for free and open access by the School of Biological Sciences at Scholarship & Creative Works @ Digital UNC. It has been accepted for inclusion in School of Biological Sciences Faculty Publications by an authorized administrator of Scholarship & Creative Works @ Digital UNC. For more information, please contact [email protected]. Biotechnology and Molecular Biology Reviews Vol. 3 (1), pp. 001-007, February 2008 Available online at http://www.academicjournals.org/BMBR ISSN 1538-2273 © 2008 Academic Journals Standard Review Plant terpenoids: applications and future potentials Sam Zwenger and Chhandak Basu* University of Northern Colorado, School of Biological Sciences, Greeley, Colorado, 80639, USA. Accepted 7 February, 2008 The importance of terpenes in both nature and human application is difficult to overstate. Basic knowledge of terpene and isoprene biosynthesis and chemistry has accelerated the pace at which scientists have come to understand many plant biochemical and metabolic processes. The abundance and diversity of terpene compounds in nature can have ecosystem-wide influences. Although terpenes have permeated human civilization since the Egyptians, terpene synthesis pathways are only now being understood in great detail.
    [Show full text]
  • Monoterpenes in the Glandular Trichomes of Tomato Are Synthesized
    Monoterpenes in the glandular trichomes of tomato SEE COMMENTARY are synthesized from a neryl diphosphate precursor rather than geranyl diphosphate Anthony L. Schilmillera,1, Ines Schauvinholdb,1, Matthew Larsonc, Richard Xub, Amanda L. Charbonneaua, Adam Schmidtb, Curtis Wilkersona,d, Robert L. Lasta,d, and Eran Picherskyb,2 aDepartments of Biochemistry and Molecular Biology and dPlant Biology, and cBioinformatics Core, Research Technology Support Facility, Michigan State University, East Lansing, MI 48824-1319; and bDepartment of Molecular, Cellular, and Developmental Biology, University of Michigan, Ann Arbor, MI 48109-1048 Communicated by Anthony R. Cashmore, University of Pennsylvania, Philadelphia, PA, April 20, 2009 (received for review December 19, 2008) We identified a cis-prenyltransferase gene, neryl diphosphate (FPP), and diterpene synthases use the C20-diphosphate inter- synthase 1 (NDPS1), that is expressed in cultivated tomato (Sola- mediate E,E,E-geranylgeranyl diphosphate (GGPP) (7). The num lycopersicum) cultivar M82 type VI glandular trichomes and enzymes that synthesize these intermediates are designated as encodes an enzyme that catalyzes the formation of neryl diphos- trans-prenyltransferases, and they consist of a family of struc- phate from isopentenyl diphosphate and dimethylallyl diphos- turally related proteins with representatives found in all branches phate. mRNA for a terpene synthase gene, phellandrene synthase of life (8). 1 (PHS1), was also identified in these glands. It encodes an enzyme In contrast, the isoprene units of some long-chain plant that uses neryl diphosphate to produce ␤-phellandrene as the terpenoids such as rubber and dolichols (the latter group of major product as well as a variety of other monoterpenes. The compounds is present in bacteria, fungi, and animals as well) are profile of monoterpenes produced by PHS1 is identical with linked to each other in the cis (Z) conformation (9, 10).
    [Show full text]
  • Biochemistry of Terpenes and Recent Advances in Plant Protection
    International Journal of Molecular Sciences Review Biochemistry of Terpenes and Recent Advances in Plant Protection Vincent Ninkuu , Lin Zhang, Jianpei Yan, Zhenchao Fu, Tengfeng Yang and Hongmei Zeng * State Key Laboratory for Biology of Plant Diseases and Insect Pests, Institute of Plant Protection, Chinese Academy of Agricultural Sciences (IPP_CAAS), Beijing 100193, China; [email protected] (V.N.); [email protected] (L.Z.); [email protected] (J.Y.); [email protected] (Z.F.); [email protected] (T.Y.) * Correspondence: [email protected]; Tel.: +86-10-82109562 Abstract: Biodiversity is adversely affected by the growing levels of synthetic chemicals released into the environment due to agricultural activities. This has been the driving force for embracing sustainable agriculture. Plant secondary metabolites offer promising alternatives for protecting plants against microbes, feeding herbivores, and weeds. Terpenes are the largest among PSMs and have been extensively studied for their potential as antimicrobial, insecticidal, and weed control agents. They also attract natural enemies of pests and beneficial insects, such as pollinators and dispersers. However, most of these research findings are shelved and fail to pass beyond the laboratory and greenhouse stages. This review provides an overview of terpenes, types, biosynthesis, and their roles in protecting plants against microbial pathogens, insect pests, and weeds to rekindle the debate on using terpenes for the development of environmentally friendly biopesticides and herbicides. Keywords: terpenes; biosynthesis; phytoalexin; insecticidal; allelopathy Citation: Ninkuu, V.; Zhang, L.; Yan, J.; Fu, Z.; Yang, T.; Zeng, H. Biochemistry of Terpenes and Recent 1. Introduction Advances in Plant Protection. Int. J. Plants and a multitude of pathogenic microbes are in a constant battle for supremacy.
    [Show full text]
  • Investigation of the Role of Gene Clusters in Terpene Biosynthesis in Sorghum Bicolor Rebecca Hay [email protected]
    University of Missouri, St. Louis IRL @ UMSL Theses UMSL Graduate Works 5-8-2018 Investigation of the role of gene clusters in terpene biosynthesis in Sorghum bicolor Rebecca Hay [email protected] Follow this and additional works at: https://irl.umsl.edu/thesis Part of the Plant Biology Commons Recommended Citation Hay, Rebecca, "Investigation of the role of gene clusters in terpene biosynthesis in Sorghum bicolor" (2018). Theses. 320. https://irl.umsl.edu/thesis/320 This Thesis is brought to you for free and open access by the UMSL Graduate Works at IRL @ UMSL. It has been accepted for inclusion in Theses by an authorized administrator of IRL @ UMSL. For more information, please contact [email protected]. Investigation of the role of gene clusters in terpene biosynthesis in Sorghum bicolor by Rebecca F. K. Hay B. S. Biology, University of Guelph 2012 A Thesis/Dissertation Submitted to The Graduate School of the University of Missouri-St. Louis in partial fulfillment of the requirements for the degree Master of Science in Biology May 2018 Advisory Committee Bethany Zolman, Ph.D. Chairperson Toni M. Kutchan, Ph.D. Elizabeth Kellogg, Ph.D. Wendy Olivas, Ph.D. Abstract The staple crop Sorghum bicolor shows potential as a source of secondary metabolite- based biofuels due to its diverse phenotype and chemical profile. S. bicolor produces a variety of high-energy metabolites, including terpenes which are a potential renewable source of fuel additives. Information on the biosynthetic and genetic pathways by which S. bicolor terpenes are produced is limited and these pathways must be better understood before they can be engineered for human applications.
    [Show full text]
  • Terpene and Isoprenoid Biosynthesis in Cannabis Sativa
    TERPENE AND ISOPRENOID BIOSYNTHESIS IN CANNABIS SATIVA by Judith Booth B.Sc., The University of King’s College, 2012 A THESIS SUBMITTED IN PARTIAL FULFILLMENT OF THE REQUIREMENTS FOR THE DEGREE OF DOCTOR OF PHILOSOPHY in The Faculty of Graduate and Postdoctoral Studies (Genome Science and Technology) THE UNIVERSITY OF BRITISH COLUMBIA (Vancouver) September 2020 © Judith Booth, 2020 The following individuals certify that they have read, and recommend to the Faculty of Graduate and Postdoctoral Studies for acceptance, the dissertation entitled: Terpene and Isoprenoid Biosynthesis in Cannabis sativa submitted by Judith Booth in partial fulfillment of the requirements for the degree of Doctor of Philosophy in Genome Science and Technology Examining Committee: Dr. Joerg Bohlmann, Professor, Michael Smith Laboratories, UBC Supervisor Dr. Anne Lacey Samuels, Professor, Botany, UBC Supervisory Committee Member Dr. Murray Isman, Professor Emeritus, Land and Food Systems, UBC University Examiner Dr. Corey Nislow, Professor, Biochemistry and Molecular Biology, UBC University Examiner Additional Supervisory Committee Members: Dr. Jonathan Page, Adjunct Professor, Botany, UBC Supervisory Committee Member Dr. Reinhard Jetter, Professor, Professor, Botany, UBC Supervisory Committee Member ii Abstract Cannabis sativa (cannabis, marijuana, hemp) is a plant species grown widely for its psychoactive and medicinal properties. Cannabis products were made illegal in most of the world in the early 1900s, but regulations have recently been relaxed or lifted in some jurisdictions, notably Canada and parts of the United States. Cannabis is usually grown for the resin produced in trichomes on the flowers of female plants. The major components of that resin are isoprenoids: cannabinoids, monoterpenes, and sesquiterpenes. Terpene profiles in cannabis flowers can vary widely between cultivars.
    [Show full text]