ORIGINAL RESEARCH article
Sec. Plant Metabolism and Chemodiversity
Volume 10 - 2019 | https://doi.org/10.3389/fpls.2019.01265
Phytochemical and Ecological Analysis of Two Varieties of Hemp (Cannabis sativa L.) Grown in a Mountain Environment of Italian Alps
- 1Centre of Applied Studies for the Sustainable Management and Protection of Mountain Areas–CRC Ge.S.Di.Mont., University of Milan, Edolo, Italy
- 2Department of Agricultural and Environmental Sciences–Production, Landscape and Agroenergy–DISAA, University of Milan, Milan, Italy
- 3Department of Veterinary Science and Public Health–VESPA, Università degli Studi di Milano, Milan, Italy
- 4Department of Life Sciences, University of Modena and Reggio Emilia, Modena, Italy
- 5Department of Sciences and Technological Innovation–DiSIT, Università del Piemonte Orientale, Vercelli, Italy
Hemp (Cannabis sativa L.) is a multifunctional crop that is capable of prompt environmental adaptation. In this study, a monoecious cultivar (Futura 75) and a dioecious one (Finola) were tested in a mountain area in Valsaviore (Rhaetian Alps, Italy; elevation: 1,100 m a.s.l.) during the growing season 2018. Phytochemical behavior was evaluated by different analytical approaches: HPLC-high-resolution mass spectrometry, SDS-PAGE LC-MS/MS, HS-SPME GC-MS, and GC-FID in order to obtain complete profile of two varieties cultivated in altitude. CSR functional strategy used for ecological evaluation revealed that both genotypes are mainly competitors, although Finola is more stress tolerator (C:S:R = 57:26:17%) than Futura (C:S:R = 69:15:16%). The Finola inflorescences were characterized by higher quantities of β-ocimene and α-terpinolene, while α- and ß-pinene accompanied by extremely high ß-myrcene were found as predominant in Futura. Both varieties were rich in sesquiterpenes (45 recognized) among which trans-caryophyllene and α-humulene were the most abundant. Total tetrahydrocannabinol level was lower than 0.1%, while the most abundant cannabinoid was cannabidiolic acid (CBDA): 2.3% found in Finola vs. 2.7% revealed for Futura. The level of corresponding neutral form, cannabidiol, varied drastically: 0.27% (Finola) vs. 0.056% (Futura). Finola showed the unique cannabinoid profile with unexpectedly high cannabidivarin, 2-fold higher that corresponding acidic analogue, whereas the particularity of Futura 75 was the occurrence of cannabigerolic acid (CBGA) in the quantities that was double than those exposed for Finola. The seeds from both chemovars proved to be rich in polyunsaturated fatty acids, and Finola showed a higher ratio ω6/ω3. No difference was found in the protein content, and the SDS-PAGE profile was similar. The most abundant protein was edestin, followed by heat shock protein 70, ß-conglycinin, and vicilin. In conclusion, comprehensive phytochemical and ecological study of two fiber-type varieties cultivated in Italian Alps displayed specific, legal, and safe cannabinoids profile, followed by particular terpene composition, polyunsaturated fatty acids content, and favorable protein profile. This postulates that geographical provenience of hemp should be considered in selecting a variety that would be suitable for a specific end-use nutraceutical application.
Hemp (cannabis, Cannabis sativa L.) has been emerging as a resourceful plant that is highly adaptable to the most of European climate and geographical conditions (Salentijn et al., 2015). Plenty of advantageous ecological, agronomical, and pharmaceutical properties that this multifunctional crop possesses qualifies it as a convenient raw material for various traditional (fiber, food, oil, medicine) or innovative industrial application (new biomaterials and biofuels) (Amaducci et al., 2015, Bonini et al., 2018). A modest, non-demanding cultivation accompanied by a sustainability of cannabis-derived products are the main reasons of its evident agronomic expansion. Historically, hemp was frequently grown in 1930s/40s mainly for the production of technical textiles, but despite its versatility, the cultivation of hemp was prohibited in the beginning of the 1950s by reason of problematic presence of psychoactive substance Δ-9-tetrahydrocannabinol (THC) that is produced by some hemp varieties. Nowadays, this has been partly abolished and the European Union permits the cultivation of hemp with THC content being less than 0.20% (EU Regulation, 2013) In Italy, regulation published on 14th of January 2017 delineates the conditions for hemp production, its commercialization and utilization in for specific industrial purposes (Legge 242/2016). Different genotypes have been selected and registered along with standardized cultivation methods.
The uniform taxonomy of the Cannabis sativa L. has been proven rather challenging and often confusing, due to the huge variability within the same genus (McPartland, 2018). Recently, a simple and practical classification into few different chemotypes on the base of the cannabinoids profile has been proposed (Aizpurua-Olaizola et al., 2016). However, two main phenotypes according to THC content are most frequently taken into consideration: the first one is drug-type cannabis with high THC amount issued for medical and recreational purposes and the second one is fiber-type (industrial) hemp with THC less than 0.2%.
Cannabis sativa L. is naturally dioecious, with the staminate plants that are usually slender, taller, and that come to flower earlier that the pistillate ones. Hemp is wind pollinated, and the male plants die after producing millions of pollen grains. A small percentage of monoecious plant can naturally occur, particularly in short-day conditions. Monoecious varieties have been selected in modern times to reduce the agronomic problems related to the sexual vegetative dimorphism present in dioecious varieties, in particular the lack of an efficient mechanization for harvesting the seeds, and the lower fiber quality and yield losses encountered when harvesting dioecious varieties at seed maturity (Faux et al., 2013). Usually seeds in monoecious varieties are smaller than in dioecious ones.
Currently, the European Union has regulated commercial production and distribution of about 70 hemp varieties (Plant Variety Catalogues, Databases & Information Systems, 1995). Among all those varieties, two are particularly spread in Italy: Finola and Futura 75. Finola is dioecious, an auto-flowering hemp variety with a short stature, adaptation to high latitudes, high yield, and it is presently one of the most popular seed cultivar (Schluttenhofer and Yuan, 2017). Futura 75 (French monoecious) has been the most cultivated hemp variety in Italy in the last 5 years (Frassinetti et al., 2018). Generally, monoecious variates are a result of long breading efforts and are driven by the search of tall stalks that would give a high fiber output.
As mentioned previously, industrial hemp has been traditionally cultivated as a source of fibers but increasing concern in the nutritional properties of the seeds has promoted its further development, especially for the fatty acid (Callaway, 2004) and protein portions (Tang et al., 2006). Furthermore, there is a growing interest about the valorization of a hemp inflorescence that could display potential pharmacological effects (Amaducci et al., 2015). To this regard, hemp essential oil is reported to have an intriguing antimicrobial activity, whereas the whole decocted plant is used against migraine, or as pain-relieving substance (Zengin et al., 2018, Bonini et al., 2018).
Hemp is also a prolific producer of bioactive secondary metabolites, and their recovery from inflorescences contributes to identification of this plant as a multipurpose crop. The most important secondary metabolites are phytocannabinoids that have received attention owing to their biomedical relevance. Acidic forms of cannabinoids are exclusively biosynthesized in the trichromes: inflorescences of industrial hemp varieties are particularly rich in cannabidiolic acid (CBDA) that is susceptible to the spontaneous decarboxylation to cannabidiol (CBD) under favorable environmental/conservational conditions, such as heat and light. CBD is responsible for a variety of pharmacological actions that could have some remarkable applications, but unlike THC, CBD does not possess any psychoactive effects (Russo, 2011). That is the reason why the CBD dietary supplements obtained from different industrial cannabis chemotypes have become particularly widespread (Pavlovic et al., 2018).
Although CBD and THC are the key molecules, the plant itself is capable of generating a whole series of phytocannabinoids: about 120 have been isolated to date (ElSohly et al., 2017). Based on the diversity of their structure, phytocannabinoids are classified into 11 general types (Hanuš et al., 2016). The biosynthetic pathway of the most abundant members of the phytocannabinoid class (with appurtenant enzymes involved) is presented in the Figure 1. This metabolic sequence includes the production of central precursor cannabigerolic acid (CBGA) that is synthesized from geranyl diphosphate and olivetolic acid. The activities of specific synthases lead to the production of tetrahydrocannabiolic acid (THCA), CBDA, and cannabichromenic acid (CBCA). Corresponding chemically neutral, but physiologically active counterparts are produced following decarboxylation in order to generate cannabigerol (CBG), THC, CBD, or cannabichromene (CBC). Other phytocannabinoids detected in plant samples include principal oxidation products of THC(A) and CBD(A): cannabinol (CBN) and cannabinolic acid (CBNA) obtained from THC(A) and cannabielsoin (CBE) and cannabielsoinic acid that derive from CBD(A) (Figure 1). Furthermore, the important phytocannabinoids family, so-called “cannabivarin” class, that regularly accompanies the main ones, is produced from condensation of geranyl diphosphate with divarinic acid, which results in a propyl instead of the pentyl side chain.
Figure 1 Biosynthesis of main phytocannabinoids. Cannabigerolic acid (CBGA), synthetized from geranyl diphosphate and olivetolic acid, is the central precursor of tetrahydrocannabinolic acid (Δ9-THCA), cannabidiolilc acid (CBDA), and cannabichromenic acid (CBCA), which contain an n-pentyl side chain. Decarboxylation of acidic precursors gives respectively Δ9-tetrahydrocannabinol (Δ9-THC), cannabidiol (CBD), and cannabichromene (CBC). Cannabinol (CBN) and cannabinolic acid (CBNA) are formed by non-enzymatic oxidation of THC(A), while cannabielsoin (CBE) and cannabielsoinic acid (CBEA) are produced by intramolecular CBD(A) modifications.
Although the attention of scientific community has been focused on major phytocannabinoids, the phytochemical characterization of cannabis highlights the presence of various non-cannabinoids constituents including flavonoids, spiroindans, dihyrostilbenes, dihydrophenanthrenes, lignanamides, steroids, and alkaloids (Pollastro et al., 2018). Their characterization is scarce and random, especially when the inflorescences of industrial hemp is concerned.
On the other hand, one non-phytocannabinoid class that is studied in much more details is terpene category. They represent the volatile component that has been claimed to have a synergic action with cannabinoids (Russo, 2019). Hemp plants produce and accumulate a terpene-rich resin in glandular trichomes, which are abundant on the surface of the female inflorescence. Bouquets of different monoterpenes and sesquiterpenes are important components of cannabis resin as they define some of the unique organoleptic properties and may also influence medicinal qualities of different cannabis strains and varieties (Lewis et al., 2018).
Choosing a genotype suitable for a specific end-use application and adapted to an environment is of paramount importance to the success of hemp cultivation. Hemp is a plant adaptable to various growing and ecological conditions, but there is no data available in literature that concern the mountain environment. A higher altitude could affect the secondary metabolites profile of flowers (cannabinoids and terpenes) and main nutritional components of seeds (fatty acids and proteins). In this research, a monoecious cultivar, Futura 75, and a dioecious one, Finola, were studied in a mountain environment of Italian Alps (Valsaviore, 1100 m a.s.l.) during the growing season 2018 for their potential to provide nutraceutical substances and to study their behavior from an ecological and phytochemical point of view to assess their usefulness as mountain crop. The special attention was given to the inflorescences that were studied by new metabolomic, untargeted analytical approach by means of high-resolution mass spectrometry (HRMS), which enabled the detection of a whole series of secondary metabolites.
Materials and Methods
Experimental Fields and Sample Collection
Valsaviore is an alpine valley on the orographic left of the upper-middle Valle Camonica; experiments were carried out on two terraced fields of two local farms (Dimensione Natura and Shanty Maè) in the municipality of Saviore dell’Adamello (latitude 46°4’53”04 N, Longitude 10°24’2”52 E, elevation 1,100 m a.s.l.) during the season 2018. This area belongs to the Temperate Oceanic bioclimate (Rivas-Martinez and Rivas-Saenz, 2009). It has a rainfall of 1.100 mm per year, concentrated mainly in the spring and the autumn; the annual average temperature is about 8,9°C; minimum temperatures and precipitation are during the winter months (data source: Centro Meteo Lombardo). According to Blasi et al. (2014), the area is within the Northeastern Alps Ecoregional Subsection (Central and Eastern Alps Section, Alpine Province, Temperate Division).
The experimental fields were obtained from terraced mountainside, from abandoned fields that had not been cultivated for more than 60 years. Thus, fertilization was not done, and soil was prepared ploughing with an excavator at depth 70–80 cm without soil tipping, manual removal of weed roots, and successive mechanical milling. No irrigation supplies were needed after sowing either in summer period thanks to the natural soil water availability. Plants were maintained under identical fertilization conditions throughout the field experiments. Finola (FINOLA DE 166 -2700754 11-2016) and Futura 75 (FUTURA 75 FR 484520 AA COD. B 174613 02/2018) seeds were donated by Hemp Farm Italia in February 2018.
The two varieties were planted in six randomized blocks: 3 blocks of Finola variety plus 3 blocks of Futura 75 (for final surface of about 130 m2 for each variety) in the two terraced fields; in both cases, Finola had a planting pattern of 10 cm between rows and at intervals of 10 cm within the row, while Futura 75, a higher and larger variety, requested a more spacious planting pattern of 20 cm between rows and at intervals of 20 cm within the row. Crop was protected against weeds by frequent hand weeding, but no pesticides were supplied.
Finola seeds were sown the 23rd of May 2018, while Futura 75 seeds were sown the 30th of May 2018 in both farms. The seeds were sown with manually 3–4 inches deep. It was decided to use experimental fields from Dimensione Natura farm to concentrate data analysis about inflorescences, while experimental fields from Shanty Maè farm were designated to obtain seeds.
For both cultivars, it took about 5 days to obtain over the 50% germination of seeds. In the Dimensione Natura farm, male plants of dioecious cultivar Finola were eliminated (to obtain the maximum concentration of secondary metabolites in the inflorescences trichomes) starting from the third week from sowing (15th of June 2018) and removing them every 3 days. Male plants were estimated being about 50% of total plants and reached a final height from 15 to 70 cm (measured on 30 plants randomized) before being removed. The final crop density, considering removing males and other factors as snails and mice, was about 10 plants per m2. The height of Finola female plants was calculated on a randomized sample of 30 plants (Table 1).
Table 1 Height of Finola and Futura 75 plants for inflorescence harvesting (average of 30 plants randomly selected).
Futura 75, as monoecious plant, started producing male flowers the second week of August, after the complete flowering of Finola. No plants were removed, and the final crop density was about 20 plants per m2 in both experimental fields. Futura 75 male and female flowers appeared from the second week of August until the second week of September. The male flowers of Futura were also removed in Dimensione Natura farm, but it was not possible to completely avoid some pollination. Visual estimation of flowering calendar for both chemotypes is presented in Table 2.
Harvest of inflorescences was carried out at flowering, corresponding to the phenological codes 2202 and 2302 (Mediavilla et al., 1998) for dioecious and monoecius varieties, respectively. The fresh inflorescences were manually sampled from the same plants, cutting the 30 cm upper part of the stem, from 10 to 20 plants per plot randomly chosen. Then they were left to air-dry, protected from light in open containers on room temperature (25°C) for 2 weeks (Hillig, 2004). Afterwards, dried inflorescences were collected, placed in the plastic bags, put under the vacuum, and stored in cool room until analysis. Low temperature was kept, avoiding as much as possible changes in metabolites, as cannabinoids and terpenes.
Harvest of seeds was performed at the start of September for Finola and start of October for Futura 75 in Shanty Maè farm. The seeds were manually sampled cutting the 30 cm upper part of the stem of every plant (phenological codes: 2204 and 2306, Mediavilla et al., 1998), then left to dry in a cool and dry room for 2 weeks. Seeds were then sieved, and a random sample of about 30 grams of each variety was chosen for laboratory tests.
The analysis of the CSR (C—competitors, S—stress-tolerators, R—ruderals) functional strategy of Grime, 1974, Grime, 1977, Grime, 2001 of the two varieties of Cannabis sativa L. was performed according to the method proposed by Pierce et al. (2017). In detail, 10 fully expanded leaves for each variety were collected in July 2018. The leaf samples were wrapped in moist tissue paper and stored in the dark overnight at 4°C. Leaf fresh weight (LFW) was determined from these saturated organs using analytical balance Precisa XB 220A and the leaf area (LA) was measured using ImageJ software (Schneider et al., 2012) after scanning the leaves with high resolution digital scanner (hp Scanjet 3670). Leaf dry weight (LDW) was measured after oven drying at 105°C for 24 h. CSR values and functional strategy were determined using “StrateFy” tool (Pierce et al., 2017). Finally, CSR coordinates were projected in the CSR ternary graph using the “ggplot2” package of R (R Development Core Team, 2018) and one-way ANOVA was performed considering C, S, and R values as dependent variables and varieties as independent variables.
Seed Weight and Proteins Analysis
The seed weight was assessed by weighing (using analytical balance Precisa XB 220A) a sample of 50 seeds per genotype. The test was performed for the commercial seeds and for the seeds obtained from the experimental fields of both varieties and was done in triplicate.
Hempseed (1 g) were ground in a mortar at 4°C, added with 20 ml of a solution of 10% trichloroacetic acid (TCA) in cold acetone (−20°C), containing 20 mM dithiothreitol and 1% protease inhibitors cocktail (Sigma), filtered, and incubated overnight at −20°C. Seed protein precipitate was obtained by centrifugation (18,000g, 1 h, 4°C), and the pellet was washed (three times) with acetone and dried. The protein precipitate was extracted with a solution of 7 M urea, 2 M thiourea, 4% w/v CHAPS, 100 mM DTT, IPG-buffer (pH 3–10). Protein content was estimated by Bradford (1976).
Protein characterization was realized performing sodium dodecyl sulphate–polyacrylamide gel electrophoresis (SDS-PAGE) and direct protein identification by LC-MS/MS analysis. For SDS-PAGE, 10 µg of hempseed proteins were mixed with Laemmli buffer (2% w/v SDS, 10% glycerol, 5% b-mercaptoethanol,62 mM Tris-HCl pH 6.8), boiled for 5 min, and loaded on 10 × 8 cm vertical 12% polyacrylamide gels. SDS-PAGE was performed at 15 mA for 30 min and 30 mA for 3 h at 10°C with a Mini Protean II Xi System (Bio-Rad). The running buffer was 25 mM Tris-HCl, 200 mM glycine, 0.1% w/v SDS. Gels were stained with Colloidal Coomassie brilliant blue G250 (Bio-Rad Laboratories).
Protein bands of interest were manually excised and in-gel trypsin digested as described in Spertino et al. (2012). Proteins were identified by liquid chromatography tandem mass spectrometry (LC-MS/MS) analysis by a micro-LC Eksigent Technologies (Dublin, USA) system (Spertino et al., 2018). Briefly, the mass spectrometer worked in information dependent acquisition (IDA) mode. MS data were acquired with Analyst TF 1.7 (ABSCIEX, Concord, Canada). The mass spectrometry files were searched using Mascot v. 2.4 (Matrix Science Inc., Boston, MA, USA). A search tolerance of 0.6 Da was specified for the peptide mass tolerance, and 100 ppm for the MS/MS tolerance.
Seeds Fatty Acid Composition
Seed samples of the investigated varieties were grinded using superfine grinding extractor—intensive vibrational mill (Model MM400, Retsch GmbH, Haan, Germany). To obtain a representative seed powder, a 50 ml jar with 20 mm stainless steel balls at a frequency of 25 Hz for 1 min was used.
Lipid extraction (Bligh and Dyer, 1959) was performed using 7.0 g of powdered seeds. The seed oil was extracted by a Soxhlet extractor and petroleum ether for 6 h at 60°C. n-Hexane was used as the solvent, and following the extraction method oil was separated from n-hexane using a rotator apparatus. The fatty acid composition of hemp seeds was determined using GC. In this method, the fatty acids were turned volatile using the method of methyl esterification (Metcalf et al., 1996). The prepared solution was injected into a GC Trace Ultra (ThermoFisher Scientific) equipped with a flame ionization detector (FID) detector, with the following specifications. Capillary column RTX-2560 (100 m × 0.25 mm id, 0.20 μm); the carrier gas was nitrogen, with the purity of 99.9%. The injector and the detector temperature were equal to 260 and 280°C, respectively. The oven temperature was kept at 100°C for 5 min and increased to 240°C at the rate of 4°C per minute and maintained at 240°C for 30 min (Tang et al., 2015; Zhang et al., 2015). The chromatographic profiles of analyte were elaborated with an Azur Software (Analytical Technology, Brugherio, Italia). Identification and quantitative evaluation of fatty acids was realized confronting retention times and areas with the ones of standard mixes FAMEs (fatty acid methyl esters). All analyses were done in three biological replicates.
Chemical and Reagents
All HPLC or analytical grade chemicals were from Sigma (Sigma–Aldrich, St. Louis, MO, USA). Formic acid 98–100% was from Fluka (Sigma–Aldrich, St. Louis, MO, USA). Ultrapure water was obtained through a Milli-Q system (Millipore, Merck KGaA, Darmstadt, Germany). For head-space (HS) analysis, the SPME coating fiber (DVB/CAR/PDMS, 50/30 µm) was from Supelco (Bellefonte, PA, USA). Acetonitrile, 2-propanol, and formic acid LC-MS grade were purchased from Carlo Erba (Milan, Italy). CBD, THC, CBN, CBG, CBC, cannabidivarin (CBDV), tetrahydrocannabivarin (THCV), CBDA, THCA, CBNA, CBGA, CBCA, cannabidivarinic acid (CBDVA), and tetrahydrocannabivarinic acid (THCVA) were purchased from Sigma Aldrich (Round Rock, Texas). All cannabinoids were analytical standards at concentration 1 mg ml−1 delivered as solutions in methanol.
Superfine Grinding (SFG) Sample Preparation
Superfine Finola and Futura 75 inflorescence powder was prepared using mechanical grinding-activation in an energy intensive vibrational mill. Five biological replicates (1.0 g each) were ground in a high intensity planetary mill. The mill was vibrating at a frequency of 25 Hz for 1 min, using two 50 ml jars with 20 mm stainless steel balls. Prior to use, jars were precooled with liquid nitrogen. The speed differences between balls and jar result in the interaction of frictional and impact forces, releasing high dynamic energies. The interplay of all these forces results in the very effective energy input of planetary ball mills. Mechano-chemical technology has been developed and successfully adopted in different fields (synthesis of superfine powder, surface modification, drug and pharmaceutical applications) and could represent a novel research tool.
Accelerated Solvent Extraction (ASE) for Cannabinoid Profiling
The extraction procedure was done according to the already published procedure (Calvi et al., 2018a, Calvi et al., 2018b). Briefly, all extractions to delineate the cannabinoid profile were performed by accelerated solvent extraction apparatus using an ASE 350 (Thermo-Fisher Scientific, Waltham, MA, USA) with 34-ml stain steel cells. Inflorescence powder (100 mg) obtained by using SFG was weighed and then homogenized with an equal weight of diatomaceous earth and transferred into the cell. Then, 100 μl of extraction solution containing the IS (diazepam 1 mg ml−1) was added. Afterwards, the remaining empty part of the cell was filled-up with diatomaceous earth. Room temperature of 25°C, pressure (1500 psi), number of static cycles (2 cycles, 5 min each), purging time (60 s with nitrogen), and rinse volume (90%) were used for the study. Organic extracts (25 ml) were obtained using pure methanol and were dried under vacuum in a centrifugal evaporator. The residue was dissolved in 1 ml of acetonitrile, and after proper dilution (1:10) in starting mobile phase, 2 μl were submitted to analysis by HPLC-Q-Exactive-Orbitrap-MS. To obtain the matrix-matched calibration curves, blank samples (100 mg of commercially available officinal plants mixture previously analyzed for the absences of cannabinoids) were used and spiked with appropriate standard solution of 14 commercially available cannabinoids listed above covering the two concentration range from 0.1 to 10 μg g−1 and from 10 to 1000 μg g−1.
Cannabinoids LC-Q-Exactive-Orbitrap-MS Analysis
The cannabinoid profile in both cultivars was evaluated applying the method recently published by us (Pavlovic et al., 2018) with modification that was essential for the untargeted analysis. In order to perform HPLC-Q-Exactive-Orbitrap®-MS analysis, samples extracted with ASE were prepared as specified in paragraph 2.5.3. Chromatography was accomplished on an HPLC Surveyor MS quaternary pump, a Surveyor AS autosampler with a column oven, and a Rheodyne valve with a 20 μl loop system (Thermo Fisher Scientific, San Jose, CA, USA). Analytical separation was carried out using a reverse-phase HPLC column 150 × 2 mm i.d., 4 μm, Synergi Hydro RP, with a 4 × 3 mm i.d. C18 guard column (Phenomenex, Torrance, CA, USA). The mobile phase was run as a gradient that consisted of water and acetonitrile both acidified with 0.1% formic acid. The gradient was initiated with 95% eluent 0.1% aqueous formic acid with a linear decrease up to 95% in 30 min. The mobile phase was returned to initial conditions at 35 min, followed by a 5-min re-equilibration period. This condition was maintained for 5 min. The flow rate was 0.3 ml/min. The column and sample temperatures were 30°C and 5°C, respectively. The mass spectrometer Thermo Q-Exactive Plus (Thermo Scientific, San Jose, CA, USA) was equipped with a heated electrospray ionization (HESI) source. Capillary temperature and vaporizer temperature were set at 330 and 380°C, respectively, while the electrospray voltage operating in positive was adjusted at 3.30 kV. Sheath and auxiliary gas were 35 and 15 arbitrary units, with S lens RF level of 60. The mass spectrometer was controlled by Xcalibur 3.0 software (Thermo Fisher Scientific, San Jose, CA, USA). The exact mass of the compounds was calculated using Qualbrowser in Xcalibur 3.0 software. The FS-dd-MS2 (full scan data-dependent acquisition) in positive mode was used for both screening and quantification purposes. Resolving power of FS adjusted on 70,000 FWHM at m/z 200, with scan range of m/z 100–900. Automatic gain control (AGC) was set at 3e6, with an injection time of 200 ms. A targeted MS/MS (dd-MS2) analysis operated in both positive and negative mode at 35,000 FWHM (m/z 200). The AGC target was set to 2e5, with the maximum injection time of 100 ms. Fragmentation of precursors was optimized as three-stepped normalized collision energy (NCE) (20, 40, and 40 eV). Detection was based on retention time and on calculated exact mass of the protonated molecular ions, with at least one corresponding fragment of target compounds (Pavlovic et al., 2018). Good peak shape of extracted ion chromatograms (EICs) for targeted compounds was ensured by manual inspection, as well.
Untargeted Metabolomics Approach
Raw data from Xcalibur 3.0 software were processed with Compound Discoverer™ (Thermo Scientific). In particular, this platform applies peak detection, retention time, profile assignment, and isotope annotation. A list of potential compounds was suggested for each chromatographic peak depending on the mass fragmentation of the parent pseudomolecular ion. Accurate mass determination generating elemental composition within a narrow mass tolerance window for identification based on accurate precursor mass. For some signals, the putative identification was confirmed by analysis performed on authentic standard. Metabolite identification was based on accurate mass and mass fragmentation pattern spectra against MS-MS spectra of compounds available on mzCloud database (HighChem LLC, Slovakia). The ChemSpider Web services platform was used as additional confirmation tool. If mass fragmentation pattern did not correspond to any of databases annotated by Compound Discoverer™ software, manual confirmation of their fragments was performed.
HS-SPME and GC-MS Analysis for Terpenes Examination
Exhaustive analytical procedures were described in detail in our recently published article (Calvi et al., 2018b). In brief, inflorescence powder (100 mg) previously grinded was weighed and put into 20 ml glass vials along with 100 μl of the IS (4-metil-2-pentanone, 20 mg/ml in 2-propanol). Each vial was fitted with a cap equipped with a silicon/PTFE septum (Supelco, Bellefonte, PA, USA). To keep the temperature constant during analysis (37°C), the vials were maintained in a cooling block (CTC Analytics, Zwingen, Switzerland). At the end of the sample equilibration time (30 min), a conditioned (60 min at 280°C) SPME fiber was exposed to the headspace of the sample for 120 min using a CombiPAL system injector autosampler (CTC Analytics, Zwingen, Switzerland).
Analyses were performed with a Trace GC Ultra coupled to a Trace DSQII quadrupole mass spectrometer (MS) (Thermo-Fisher Scientific, Waltham, MA, USA) equipped with an Rtx-Wax column (30 m × 0.25 mm i.d. × 0.25 µm film thickness) (Restek, Bellefonte, PA, USA). The oven temperature program was: from 35°C, held for 8 min, to 60°C at 4°C/min, then from 60 to 160°C at 6°C/min and finally from 160 to 200 at 20°C/min. Helium was the carrier gas, at a ﬂow rate of 1 ml/min. Carry over and peaks originating from the fibers were regularly assessed by running blank samples. After each analysis, fibers were immediately thermally desorbed in the GC injector for 5 min at 250°C to prevent contamination. The MS was operated in electron impact (EI) ionization mode at 70 eV. An alkanes mixture (C8-C22, Sigma R 8769, Saint Louis, MO, USA) was run under the same chromatographic conditions as the samples to calculate the Kovats Retention Indices (RI) of the detected compounds (Giorgi et al., 2012, Giorgi et al., 2013a; Giorgi et al., 2015). The mass spectra were obtained by using a mass selective detector, a multiplier voltage of 1456 V, and by collecting the data at a rate of 1 scan/s over the m/z range of 35–350. Compounds were identified by comparing the retention times of the chromatographic peaks with those of authentic compounds analyzed under the same conditions when available, by comparing the Kovats retention indices with the literature data and through the National Institute of Standards and Technology (NIST) MS spectral database. The quantitative evaluation was achieved using the internal standard procedure, and the results were finally expressed as µg/g. For both chemotype, all analyses were done in five biological replicates.
Differences between two varieties for the quantitative analysis were determined using a two-tailed Student’s t-test from the BioVinci statistical program (Version 1.1.4., BioTurning Inc 2018). A p-value of less than 0.05 was considered statistically significant.
Figure 2 reports the triangular diagram obtained by CSR analysis. Both the varieties are competitors, although Finola is more stress tolerator (C:S:R = 57:26:17%) than Futura (C:S:R = 69:15:16%), meaning for stress all those conditions able to reduce the photosynthetic activity in plants (Grime, 2001). This difference was confirmed from the results of the ANOVA test (Table 3) showing how the two varieties are significantly different (p < 0.01) for what concerns C (competitiveness) and S (stress tolerance.
Figure 2 CSR classification of the two variety of Cannabis sativa. Mean CSR strategy of Futura 75 = C/CR (C:S:R: = 69:15:16%); mean CSR strategy of Finola = C/CSR (C:S:R: = 57:26:17%). ANOVA test revealed significant differences (p < 0.01) for what concerns C (competitiveness) and S (stress tolerance).
Protein Yield and Characterization
As shown in Table 4, the seeds of Finola and Futura 75 are consistently smaller than the commercial seeds used to set up experimental fields. The protein yield resulted of 19.96 ± 2.20 mg/ml for Futura 75, for a total content of 39.9 mg of protein starting from 1 g of seeds. For Finola, the protein yield was of 19.69 ± 3.02 mg/ml for a total content of 39.4 mg of protein starting from 1 g of seeds. No difference was found in the protein content, and the SDS-PAGE profile was similar. The most abundant protein was the storage protein edestin, directly identified by mass spectrometry; some other proteins such as heat shock protein 70, beta conglycinin, and vicilin were also found. As shown in Figure 3, in fact, MS/MS analysis of the principal bands revealed the two subunits (35 and 18 kDa) of the reserved protein edestin as recently reported (Mamone et al., 2019); moreover, we can detect edestin at higher molecular weight, together with the heat shock protein (70 kDa) and conglycinin (around 50 kDa).
Figure 3 SDS-PAGE profile of hemp seed proteins. Resolved proteins were detected by Colloidal Coomassie staining and identified by MS/MS analysis.
Seeds Fatty Acid Profile
In Table 5, the results of fatty acid profiling of Finola and Futura 75 seeds and the total of saturated fatty acids (SFA), monounsaturated (MUFA), polyunsaturated (PUFA), and omega-3 (ω3) and omega-6 (ω6) fatty acids are shown.
The principal SFA was palmitic acid (PA; 16:0) for Futura 75 (6.4%) and pentadecanoic acid (C15:0) for Finola (6.08%), then followed by stearic acid (SA; 18:0) that was in similar percentage in both varieties (the 2.18% in Finola and 2.91% in Futura 75). Also, if with a different composition, the total SFA content showed to be in analogous quantity in the two varieties (9.33% in Finola and 10.27% in Futura 75). The most abundant unsaturated fatty acids in the seeds of the two varieties proved to be linoleic acid (LA; C18:2 ω6c), in average percentage of 57.69% for Finola and 57.22% for Futura 75 and oleic acid (OA; C18:1 ω9c), and 9.41% and 11.50% for Finola and Futura 75, respectively. Another fatty acid contained in high quantity was the ω3 linolenic acid (C18:3ω3) that was found in higher quantity in Futura 75 (18.42%) compared to Finola (9.96%). Cis-11-eicosenoic acid (C20:1) was found in a significative percentage only in Finola, while only 0.37% in Futura 75. This affected the total MUFA percentage, which resulted higher in Finola (18.7%), while in Futura 75 it was 12.13%.
It is clearly shown how the seeds of both varieties are rich in PUFA, which are 71.98% for Finola and 77.61% for Futura 75. Both the genotypes are exceptionally rich source of the two essential fatty acids (EFAs) LA (18:2 ω6) and α-linolenic acid (18:3 ω3). However, as expected, the Finola showed the highest content of γ-linolenic (GLA, 4.22%), accompanied with higher average values of ω6/ω3 ratio (6.22 Finola vs. 3.21 for Futura).
Quantification of Cannabinoids: Targeted Metabolomics With Commercially Available Phytocannabionids
In the presented work, the absolute quantification of 14 cannabinoids (7 acids with appurtenant neutral counterpart) in Finola and Futura 75 inflorescences was performed. Extracted ion chromatograms (EICs) were obtained with an accuracy of 2 ppm m/z from total ion chromatogram engaging the m/z corresponding to the molecular ions. EICs of the acidic forms found in Finola chemovar are shown in Figure 4. According to this chromatogram, the observed relative order of elution of the detected acidic forms of pentyl phytocannabinoids is as follows: CBDA > CBGA > CBNA > Δ9-THCA > CBCA. This order of elution is due to increased polarity according to the increased number of polar phenolic groups (CBGA vs. Δ9-THCA, for example) as well as due to and formation of chromene moiety, which increased the lipophilcity of CBCA. CBDVA and Δ9-THCVA, the propyl homologues of CBDA and Δ9-THCA, respectively, have faster retention times compared to their respective pentyl analogues because of shorter (C-3) aliphatic chain. CBCA and Δ9-THCA, the acid precursors of CBC (RT-29.82min) and Δ9-THC (RT-29.43min), respectively, have longer retention times. On the contrary, CBDA and CBDVA elute before the corresponding neutral forms (CBD and CBDV), which appeared at RT-27.38min and 25.29min, respectively. This chromatographic behavior of the available standards, accompanied with characteristic mass fragmentation, enabled putative identification of additional 43 cannabinoids that express the analogous chromatographical elution behavior and analogous mass fragmentation pattern. For example, the peak that appeared at RT 29.63 was identified as CBCVA (Figure 4).
Figure 4 Extracted ion chromatogram for the acidic forms of phytocannabionids (CBGA, CBDA, THCA, CBDVA, and THCVA) identified according to analytical standards. The retrospective data analysis reveals the presence of CBCVA.
Based on the disposability of commercially available standards, the absolute quantification of phytocannabinoids in inflorescence extracts was performed by applying our validated method with external calibrations as it was explained in detail in experimental section (Calvi et al., 2018a; Calvi et al., 2018b). Quantitative data related to the content of phytocannabinoids in two hemp inflorescences determined by means of the HPLC-HRMS method are shown in Table 6. Since both varieties analyzed belong to the fiber-type hemp, it is not surprising that the most abundant phytocannabinoids were CBDA and CBD. The CBDA content did not vary drastically, although Futura inflorescence contained slightly higher concentration. On the contrary, the level of CBD was 5-times higher in Finola samples. Besides, the Finola showed the unique phytocannabinoid profile with unexpectedly high CBDV, twice higher than the corresponding acidic form (CBDVA). Futura exhibited the same trend regarding the “varin” phytocannabinoids, although not as accentuated as for Finola. Both varieties contained the neglected levels of THCA and THC, with corresponding C3 analogues detected under the limit of quantification (LOQ). The content of CBNA especially in Futura should not be underestimated, as CBNA is formed from THCA by non-enzymatic oxidation. Characteristically, Finola presented the small amount of CBCA, whereas the particularity of Futura was the occurrence of CBGA in the quantities that was double that those exposed for Finola.
Table 6 Phytocannabinoids content (µg/g) in investigated hemp inflorescences (average ± SD, n = 5 independent biological replicates).
Un-Targeted Metabolomics: Phytocannabinoid Profiling and Putative Identification of Non-Phytocannabinoic Compounds by Means of HPLC-HRMS
Two chemovars (each in five biological replicates) after being analyzed by LC-HRMS in FS-dd-MS2 acquisition mode were further processed by Compound Discoverer platform that enabled differential analysis applying Volcano plot model (Figure 5).
Figure 5 Differential analysis for the comparison between the relative intensity of chromatographic peak from Finola and Futura 75 samples. P-value (PV) was set on 0.05. Red region contains up-regulated signal, where the quantities from Futura were significantly higher than those found in Finola and were greater than the upper fold-change (FC) threshold. The green region comprises down-regulated peaks, where the quantity from Futura was significantly lower than that from Finola and was less than the lower FC threshold.
After performing differential analysis, the chromatographical signals were then subjected to the putative identification according to exact mass of the pseudomolecular ion (M+1)+ with appropriate mass fragmentation pattern found in the available databases (mzCloud, ChemSpider, FooDB) metabolomics platforms (MyCompoundID, Li et al., 2013) and/or reported in the literature (Brighenti et al., 2018; Calvi et al., 2018a; Berman et al., 2018; Citti et al., 2019). Our initial experiment data analysis involved about 100 known phytocannabionids that are listed in the recently published inventories (Hanus at al., 2016; Berman et al., 2018; ElSohly et al., 2017). The overall 43 additional phytocannabinoids from the seven phytocannabinoid subclasses were recognized in this study. In Table 7, the compounds that characterize the Cannabis sativa L. inflorescences have been by listed/identified by applying the CompoundDiscover platform. Both chemovars displayed a similar phytocannabinoids profile with some exceptions that are evident for the quantitative analysis presented above. The most abundant class was CBC-type with the C-1 and C-3 side chain length that was up-regulated in Finola, while the both neutral and acidic forms of C4 (Nor) and C-5 were found to be higher in Futura 75. The ample class of CBL-type (that derives from the CBC-counterparts) was also worth of noting, as the signals attributed to this class did not differ significantly between two varieties. The solid signals with the particular fragmentation of the cannabicitrans (CBCT-type) were observed in the both varieties without statistical significance. CBCT itself was identified according to the m/z cloud database spectrum, while other members of this group showed the analogous fragmentation, taking into account the structural differences concerning the side chain length and the carboxylic function for the acidic forms. A substantial, power signal designated the presence of cannabielsoinic acid, both C3 and C5 analogues, that are considered as main oxidation products of CBDVA and CBDA, respectively. Also, it is important to note the occurrence of the compounds that are produced by non-enzymatic, post-biosynthetical oxidative modifications of main phytocannabinoids: cannabifouranic acid, cannabicoumaronone, cannabichromanone, cannabiripsol, as well as acidic and neutral forms of 6,7-epoxycanabigerol.
Table 7 Putative identification of phytocannabinoids, flavonoids, lignans, stilbenoids, and alkaloids based on (full scan data dependent) FS-dda-MS2 characterization and chromatographical behavior.
As far as non-phytocannabinoid secondary metabolites are concerned, untargeted metabolomic approach enabled the identification of the cannaflavines A, B, and C (Table 7). As it was not possible to find (neither in the literature nor in the available databases) their high resolution MS/MS spectrum done in positive mode, we have proposed the fragmentation outline as it was shown in the Figure 6 for the cannaflavin A and C found in Futura 75. Those two isoprenic flavones are the isomeric compounds, displayed almost identical fragmentation pattern (with differences in relative abundance of pseudomolecular ion), but they can be distinguished very well by the chromatography. Position of isprenyl chain in the molecule cannaflavin A contributes to its higher lipophilicity compared to the cannaflavin C, which is more polar due to its compact structural aspect. Therefore, cannaflavin A had been eluted almost 2 min after the cannaflavin C. Futura 75 had been shown as much more affluent regarding all three cannaflavines (Table 7). The important issue is that cannaflavin C content was extremely high in Futura 75 than in Finola inflorescences where practically was present in traces.
Figure 6 Extracted ion LC-HRMS chromatogram of Futura 75 inflorescence with the respective ful-MS2 spectra illustrating the presence of two isomeric compounds: Cannaflavin A and Cannaflavin C in Futura 75 inflorescence.
Regarding the data obtained in positive ionization, it was possible to detect other secondary metabolites, already identified in some cannabis species (Pollastro et al., 2018). Between non-phytocannabinoid phenols, structurally unique compounds exist as lignans, spiroindan type, dihydrostilbene-type, dihydrophenantrene derivatives, stilbenoids, and cannabispirans. Lignans belong to two main groups: phenolic amides and lignanamides (Yan et al., 2015). Both varieties included in this study exhibited the analogous phenolic amides profile: the substantial amount of N-trans-coumaroyltyramine and N-trans-feruloyltyramine accompanied with approximately 10 times lower signal for the N-trans-caffeoyltyramine. N-trans-coumaroyltyramine and N-trans-feruloyltyramine found in Cannabis sativa L. are recognized as precursor of unique arylnapthalene bis-amides, cannabisins. The inflorescences of both genotypes contained substantial amount of cannabisin D and grossamide, while the presence of another 12 compounds of this class that was previously reported for the hemp seeds/fruits was not detected in our Futura 75 and Finola samples.
Stilbenoids identified in Cannabis sativa L. could be divided into three main structural types: phenanthrenes, dihydrostilbenes, and spiroindans. A rare quinoid stilbenoid denbinobin was well-defined in both chemovars, and intensity of its signals reveals that it is one of the major constituents of phenanthrene-type with Futura 75 as preponderate chemovar. This was accompanied with significant decline of 4,5-dihydroxy-2,3,6-trimethoxy-9,10-dihydrophenanthrene in Futura 75 compared to Finola, which implies toward divergent metabolic routes reserved for phenanthrenes. Furthermore, the differential analysis revealed that the content of dihydroresveratrol, which is considered as dyhydrostylbenes precursor, was unaffected, while the level of its derivates, cannithrenes, was significantly higher in Futura 75. The sub-class of cannbisilbenes was not significantly represented, apart cannabistilbene I that was featured for Finola. Noteworthy results emerged for the spiroindans: Futura 75 inflorescences were particularly reached in cannabispiran and its oxidation analouges, while their concentration in Futura turns out to be neglected. Alkaloids were not detected, with the exception of hordenine, predominately observed in Futura 75 samples. Anyway, here we have to underline that, bearing in mind alkaloids prominent polarity, the absence of this previously well-defined compounds belonging to this group may be attributed to the limitation of our chromatographic conditions to retain and reveal the polar nitrogen species.
Terpenoids Profile Evaluated by HS-SPME- GC-MS Methodology
The untargeted HPLC-HRMS approach has revealed also the presence of some terpenoids in the inflorescence exanimated herein, but due to its non-polar and high-volatile characteristics the HS-SPME-GC-MS analytical strategy remains the best methodology for comprehensive profiling of terpenoid fraction. Complete data concerning the terpenes profile are summarized and reported in Table 8. Overall, up to 83 volatile compounds composed the terpene fingerprint and are further divided in the classes. The sum of mono/di/tri terpenes did not vary significantly, but the two genotypes expressed qualitatively different profile: Finola inflorescences were characterized by higher quantities of β-ocimene and α-terpiolene, while in Futura 75 α- and β-pinene accompanied by extremely high β-myrcene were found as predominated. Both chemovars were partiality rich in sesquiterpenes: 45 different compounds from this subclass were identified, among which trans-caryophyllene and α-humulene were most abundant. The importance of ample sesquiterpene subclass is also reflected in the occurrence of sesqui-CBG that was documented during the HPLC-HRMS data elaboration (Table 7). The total content of sesquiterpenes was more than double in Finola than those discovered for Futura, while oxygenated products were more pronounced in Futura 75. Concretely, it should be noticed that fenchone and α-fenchyl alcohol were, from quantitative point of view, the most important oxygenated terpenes found. Although rather speculative, we have to indicate the possibility that α-fenchyl alcohol also exists in ester form coupled with CBD as we have recorded a strong signal that with the pseudomolecular ions (C32H47O4, 495.34689) and fragmentation pattern (CBDA structure) corresponds to the fenchyl-cannabidiolate.
To support a sustainable development of industrial hemp in mountain areas, proper agronomic techniques should be optimized to preserve inflorescence and/or seed quality during the plant seasoning. This would enable suitable industrial processing and would improve high-added value applications, especially for the nutraceutical and homoeopathic purposes (Calzolari et al., 2017). Hemp has a wide range of environmental adaptation, but varieties tend to perform better in their instinctive areas of growth (Dempsey, 1975) what was confirmed by our results regarding the functional strategy. Particularly, Finola has been proven as more stress-tolerant variety in comparison with Futura 75. These data contribute to fill the lack of studies of intraspecific variation of CSR strategy; in fact, until now, only May et al. (2017), Giupponi and Giorgi 2019a; Giupponi and Giorgi et al., 2019b, and Giupponi et al., 2017; Giupponi et al., 2019 have studied this intraspecific variation in Arabidopsis thaliana, Linaria tonzigii, and Fagopyrum tataricum, respectively. Finola is a Finnish short-cycle variety, considered as a self-flourishing for its ability to bloom in about 3 months and with a high germinability (Baldini et al., 2018). Having been conceived for northern Europe, it remains short and therefore more manageable, more “compact,” and more stress tolerant. Futura as monoic French variety of medium height (2–3 mt) with intermediate flowering is suitable for fabric transformation and with discrete levels of seed production as a main product.
Nowadays, environmental concerns and multi-purpose production have brought renewed interest in industrial hemp; however, there is little information that concerns phytochemical composition to support hemp cultivation in mountain areas. Besides hemp fiber production, there is growing interest in cultivating industrial hemp for other purposes such as using its inﬂorescence for extracting essential oils and its seeds for alimentary oil and ﬂour production (Campiglia et al., 2017). However, few studies have compared the performance of the current commercial chemovar of industrial hemp (Tang et al., 2016) and there is little available information regarding agronomical practices. Therefore, considering the lack of information on hemp genotypes, it is difficult for mountain farmers to select the most suitable genotype for different kinds of utilization.
The result that regards qualitative analysis of inflorescence phytocannabinoids profile in the inflorescences points out that, under same environmental conditions that yield the major cannabinoid, CBDA is similar in both varieties. The difference that is significant regarding the neutral derivate CBD indicated the higher amount revealed in Finola could be indirectly caused by genetic predisposition of Finola to flower in the full summer season when the average daily temperatures are higher than those that are present when Futura 75 develops its inflorescences (late summer/early autumn). Therefore, flowering season, itself, may have led to a partial conversion of the parent CBDA into its neutral counterpart, via a decarboxylation process, which naturally occurs under the action of heat and light. The sum of problematic, potentially toxic THC and THCA was found to be low (under 0.1%), which confirms the possibility to use inflorescences in nutraceuticals purposes. Notable amount of neutral CBDV for Finola opens possibility to exploit this variety for the medicinal (galenic) preparation as CBDV is considered to express a beneficial effect on human health (Iannotti et al., 2014).
Apart from the 14 phytocannabinoids that were quantified, untargeted metabolomics approached offered in-depth recognitions of the possible dissimilarities in the chemical profile between two chemovars. For the cannabinoids fraction, apart for the evident alterations that are produced by genetic differences (alterations found for CBC class, for example), it is important to consider also the phytocannabionoids that are produced due to non-enzymatic modifications of main phytocannabionids. In the first place, there is a substantial power signal that designates the presence of cannabielsoinic acid, both C3 and C5 analogues, that are considered as main oxidation products of CBDVA and CBDA, respectively. Also, the presence of four compounds from the miscellaneous type indicates that cultivation under uniform, mountain growing environment has led to the biotransformation of main phytocannabionids to the particular oxidation forms that were revealed as cannabifouranic acid (CBDFA) that derives from the CBDA, and the cannabicoumaronone and cannabichromanone originating from THC. Also, the appearance of cannabiripsol that is specific glycolic forms of THC indicates toward prompt hydroxylation of mayor phytocannabinoids. The presence of the 6,7-epoxycanabigerol acidic and neutral form with significantly higher amount in the Finola inflorescence should not be undervalued as it is not still clear weather the epoxidation had occurred as the part of the early phytocannabinoids metabolic pathway during the flowering, or it had aroused as result of the post-harvest CBG oxidative modifications.
Cannflavins, which belong to the class of prenylflavonoids, are secondary metabolite exclusive for the Cannabis genus and were detected in both varieties. Their notable presence points towards metabolic pathway at the outgoings of the polyketide cannabinoid machinery (Calzolari et al., 2017). The notably higher level of cannaflavin C detected in Futura 75 could be a consequence of the lower average temperature combined with high solar radiation experienced at the beginning of plant flowering. In fact, it was reported that different classes of flavonoids are involved in plant protection mechanisms, specifically for their radical scavenger activity and screening ability against short wavelength UV-B light (Agati and Tattini, 2010). Furthermore, Futura 75 inflorescences was characteristically rich in cannabispiran and its oxidation analogues, which can be in relation with the fact that Futura 75 is more susceptible to oxidative stress.
Considering the terpenoids fraction, our results are qualitatively comparable with those reported by others (Bertoli et al., 2010; Elzinga et al., 2015; Aizpurua-Olaizola et al., 2016; Benelli et al., 2018, Namdar et al., 2018). The particularity of both chemovars presented in this study is the presence of the strong signal of sesqui-CBG accompanied with very reach sesquiterpenes fraction, indicating that geographic origin accompanied with environmental conditions is one of the important variables that determine the terpene fingerprint (Giorgi et al., 2013b; Marchini et al., 2014; Giupponi et al., 2017). The presumed appearance of fenchyl-cannabidiolate might also be defined as possible discrimination factor that concerns cultivation/ecological conditions. Apart from environmental impact, a genetic predisposition of variety could thoughtfully affect the terpene family: the qualitative profile of our Futura inflorescence is similar to this recently reported by Benelli et al. (2018). The significant differences found in the quali-quantitative terpenes profile (such as α- and β-pinene, myrcene, terpinolene, β-ocimene, trans-caryophyllene, and α-humulene) between Futura and Finola inflorescences reported herein permit to distinguish monoecious from dioecious hemp cultivars (Bertoli et al., 2010).
The fatty acid composition is a primary value of hemp seed. The composition of the fatty acid profile has been demonstrated to vary according to the plant cultivars. Both varieties grown in mountain have been shown as a good resource of PUFA (71.98% for Finola and 77.61% for Futura 75). Fundamentally, ω6/ω3 is found to be in range 2.5–3:1 (Simopoulos, 2008), which has been claimed as ideal for human nutrition. In fact, the value of 3.21 calculated for Futura 75 qualifies this genotype as favorable for human diet (Callaway, 2004, Galasso et al., 2016), Particularly, the level of ω6 is thus an interesting resource for manufacturing dietary supplement (Mölleken and Theimer, 1997). Finola contained much lower amount of ω3, which influenced final ω6/ω3 (6.25), which is higher than values reported recently (Galasso et al., 2016) for Finola and for the other varieties of industrial hemp (Petrović et al., 2015). The principal difference in ω3 PUFA profile involves the linolenic acid, which was surprisingly two times lower in Finola than in Futura 75. On the other hand, our findings have demonstrated that Finola has an important content of GLA if grown in an mountain area of the Alps, which is in accordance with results published by Mölleken and Theimer (1997) that the cultivars from the cooler regions displaying a higher concentration of GLA (Callaway, 2004; Vonapartis et al., 2015).
Our results confirmed that about 65% of the total hemp protein consists of a single storage protein, edestin, a hexamer composed of acidic and basic subunits linked by disulfide bonds. It has been stated that, differently from soybean seeds that are abundant in trypsin inhibitors that require thermal treatment for inactivation, hemp seeds present very low amounts of these anti-nutritional factors and are therefore more digestible (Malomo et al., 2015). Due to the high content in essential amino acids of edestin, hemp seed proteins could be considered as a superfood, possessing a health-promoting property that might reduce a risk of disease or improving some aspect of well-being.
Hemp is recognized as a crop that could be cultivated in different surroundings, exploiting marginal land. Generally, it can be grown without pesticides (Desanlis et al., 2013) and with a low input technique (Struik et al., 2000), so it becomes a very interesting option for farm working in organic regime in very delicate environments as mountain areas. That is reason why it is considered as alternative viable crop for sustainable agriculture (Amaducci et al., 2015). As a multifunctional crop, it can have different end use: traditional ones as fiber but also innovative ones as the use of seeds and inflorescences as sources of interesting bioactive secondary metabolites for nutraceutical (Frassinetti et al., 2018), medicinal (Calvi et al., 2018b), and cosmetic (Sapino et al., 2005) purposes or for producing essential oils as natural flavor and fragrance additives (Bertoli et al., 2010). Comprehensive quality study of two fiber-type hemp varieties cultivated in Italian Alps points out a specific, legal, and safe cannabinoids profile and particular terpene composition in the inflorescences that is followed by a favorable polyunsaturated fatty acids and protein content in the seeds.
Due to its different application and since this crop was abandoned for long time in mountain environment, geographical provenience of hemp should be considered in selecting a variety that would be suitable for a specific nutraceutical destination. Further and targeted studies should be addressed to the ecological and phytochemical behavio of most popular varieties in diverse edaphic and environmental conditions. This would be important for the possible end-use of the hemp and to support mountain farmers to select the correct variety for their purposes and agronomic environment. Additionally, due to its ecological and phytochemical complexity, the comprehensive chemical profiling of this plant could be an interesting case study for investigations on plant physiology and plant behavior in response to different biotic and abiotic environmental factors.
Data Availability Statement
The raw data supporting the conclusions of this manuscript will be made available by the authors, without undue reservation, to any qualified researcher.
AG, RP, VL, SP, LG, and MC conceived and designed the study and interpreted the results. RP, VL, MC, CCi, and CCa performed phytochemical analyses and statistical analyses. VL and LG followed the experimental fields and performed ecological and statistical analyses. RP and CCi completed metabolomic examination. All the authors contributed to writing, with AG as the leading author.
This research was supported by the “FISR-MIUR Italian Mountain Lab” project.
Conflict of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
We want to thank Paolo Messali of Shanty Maè Farm, and Fabrizio Bresciani of Dimensione Natura Farm.
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Keywords: Futura 75, Finola, plant metabolomics, Terpenes, functional strategy
Citation: Pavlovic R, Panseri S, Giupponi L, Leoni V, Citti C, Cattaneo C, Cavaletto M and Giorgi A (2019) Phytochemical and Ecological Analysis of Two Varieties of Hemp (Cannabis sativa L.) Grown in a Mountain Environment of Italian Alps . Front. Plant Sci. 10:1265. doi: 10.3389/fpls.2019.01265
Received: 07 May 2019; Accepted: 11 September 2019;
Published: 15 October 2019.
Edited by:Flavia Guzzo, University of Verona, Italy
Reviewed by:Mohamed M. Radwan, University of Mississippi, United States
Andrea Anesi, Centro Ricerca e Innovazione, Fondazione Edmund Mach, Italy
Copyright © 2019 Pavlovic, Panseri, Giupponi, Leoni, Citti, Cattaneo, Cavaletto and Giorgi. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Luca Giupponi, email@example.com