Improvement and breeding
Najmeh Hadi; Razieh Azimi; Mahdi Yahyazadeh; Maryam Mackizadeh; S. Fekri Qomi; Simin Mohit
Abstract
Background and objectives: Chamomile (Matricaria chamomilla L.) is a valuable medicinal plant with many applications in the food, pharmaceutical, and cosmetic health industries. Chamomile's biological properties are attributed to its essential oil (EO) compounds, especially chamazulene and a-bisabolol ...
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Background and objectives: Chamomile (Matricaria chamomilla L.) is a valuable medicinal plant with many applications in the food, pharmaceutical, and cosmetic health industries. Chamomile's biological properties are attributed to its essential oil (EO) compounds, especially chamazulene and a-bisabolol oxide A, and flavonoids, esp. apigenin and luteolin. Evaluation of wild plant populations belonging to different geographical regions in situ (study on wild samples) and ex-situ (study on wild samples under agricultural conditions) is a crucial step in plant breeding and selection of promising genotypes. On the other hand, cultivation and domestication of wild plants under agricultural conditions improve plant yield and prevent unnecessary harvesting and extinction of the plant. In the present study, the quantitative and qualitative EO diversity of some wild chamomile was investigated.Methodology: Flowers and seeds of 15 wild chamomile populations were collected from Iran's natural habitats, including 12 populations from Khuzistan province (Kh1-12), 2 populations from Fars province (F1-2), and 1 population from Bushehr province (F3) in 2021 (February-May). Flowers were used for essential oil extraction, and seeds were planted in a randomized complete block design (treatment = genotype) with three replications. The research farm located at Alborz Research Station, affiliated with the Research Institute of Forests and Rangelands, Alborz province, was considered a cultivation site without adding fertilizer to the soil. The seeds were sown directly in the field with a 15 cm distance between the planting lines and 15 cm between the plants on the lines (April 2021). Drip irrigation was used, and weeding was done mechanically. Flowers with less than 5 cm of peduncles were harvested manually at the 70% full bloom stage. The shade-dried flower EOs were extracted by water distillation (Clevenger) for 3 hours, and their quantitative and qualitative analysis was done using GC and GC/MS.Results: The results showed that sesquiterpene hydrocarbons, oxygenated sesquiterpenes, and diacetylenes made the highest EO compounds percentage in both wild and cultivated samples. Chamazulene (from sesquiterpene hydrocarbons) and a-bisabolol oxide A (from oxygenated sesquiterpenes), as two important chamomile EO compounds, showed an increase from wild to cultivated samples. Among the wild samples, the highest chamazulene (5.3%) and a-bisabolol oxide A (21.5%) contents were assigned to the populations Kh8 and Kh4, respectively. In the cultivated samples, the highest amount of these compounds (11.1 and 32.3%, respectively) was obtained in the populations Kh7 and F2, respectively. In general, the main EO compounds (%) in the wild and cultivated populations included α-bisabolone oxide A (wild: 31.3 (F1) to 64.5 (Kh3) and cultivated: 29.8 (F2) to 56 (Kh3)), α-bisabolol oxide A (wild: 5.8 (Kh5) to 21.5 (Kh4) and cultivated: 10.3 (Kh3) to 32.3 (F2)), E-β-farnesene (wild: 6.1 (Kh3) to 23.3 (Kh8) and cultivated: 6.9 (Kh1) to 15.6 (F3)), Z-spiroether (wild: 0 (F1) to 16.1 (Kh1) and cultivated: 9.1 (Kh7) to 15.1 (Kh13)), and chamazulene (wild: 1.6 (F1) to 5.3 (Kh8) and cultivated: 4.7 (Kh6) to 11.1 (Kh7)). Also, the EO% was obtained more in the cultivated samples (0.9 (Kh5) to 1.4% (Kh13)) than in the wild ones (0.1 (Kh6) to 0.5% (Kh10).Conclusion: The results of this research showed that by cultivating wild populations under agricultural conditions and water and crop management, it is possible to have essential oil in the desired quantity and quality compared to wild ones. It should be noted that the results of repeating population cultivation under the same conditions in the following years will be reported in proportion to the data output.
N. Hadi; F. Sefidkon; A. Shojaeiyan; A.A. Jafari
Abstract
The genus Nepeta is one of the largest genera of the Lamiaceae family, and Iran, particularly, is one of the main centers of origin of this genus. Nepetalactones and flavonoids were reported as major constituents of Nepeta species, and the main cause of their medicinal value and biological properties. ...
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The genus Nepeta is one of the largest genera of the Lamiaceae family, and Iran, particularly, is one of the main centers of origin of this genus. Nepetalactones and flavonoids were reported as major constituents of Nepeta species, and the main cause of their medicinal value and biological properties. There are lots of reports related to biological activities of secondary metabolites of genus Nepeta showing the importance of this genus. In this work, the essential oil (EO) diversity of 21 wild populations from Nepeta kotschyi Boiss., Iranian endemic species, was investigated. For removing the environmental effect, the seeds of populations were planted in one place. Plant aerial parts were harvested at full flowering stage, and after shade-drying, their EO was extracted by hydrodistillation method. EO was quantitatively and qualitatively analyzed by GC and GC/MS. After botanical study and EO analysis, it was revealed that the populations were from two different varieties. Two populations including buyer-ahmad1 and Buyer-Ahmad2, were from N. kotschyi var. kotschyi, and others were stood in N. kotschyi var. persica. Twenty-four components were characterized in the EO of N. kotschyi. The highest amount of EO yield (w/w) was obtained in populations of var. kotschyi (0.5-0.7%). Three main chemotypes were identified among populations of var. persica based on the main component(s) of EO, including a containing NepI (4aα,7α,7aα-nepetalactone), b containing NepII (4aα,7α,7aβ-nepetalactone) and cubenol, and c containing geranyl acetate and cubenol. Except of semirom and Taft5 which were stood in b-chemotype, and Taft4 which was placed in c-chemotype, other populations of var. persica, also populations of var. kotschyi, were stood in a-chemotype. In addition, based on the main component of EO, the populations of var. kotschyi were put in a-chemotype. In a-chemotype, the amount of NepI was obtained between %53.9 (Chelgard) and %84.8 (Buyer-Ahmad2), and NepII was measured between %1 (Taft1) and %13.7 (Chelgard). In b-chemotype, the amount of NepI was measured between %0.3 (Taft5) and %4.9 (Semirom), and NepII was obtained between %13.4 (Taft5) and 44.7% (Semirom). NepIII (4aα,7β,7aα-nepetalactone) (1.3-3.3%) was characterized only in the EO of var. Kotschyi populations.
