Next Article in Journal
Studies of Dopamine Oxidation Process by Atmospheric Pressure Glow Discharge Mass Spectrometry
Previous Article in Journal
Synthesis and Photocatalytic Properties of Four Coordination Compounds Constructed from Two Benzimidazole-Based Asymmetric Polyazocyclic Ligands
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

The Potential Use of Plant Growth Regulators for Modification of the Industrially Valuable Volatile Compounds Synthesis in Hylocreus undatus Stems

1
Department of Plant Breeding and Seed Production, University of Environmental and Life Sciences, Grunwaldzki Square 24a, 50-363 Wrocław, Poland
2
Department of Food Chemistry and Biocatalysis, Wrocław University of Environmental and Life Sciences, Norwida 25, 53-375 Wrocław, Poland
*
Author to whom correspondence should be addressed.
Molecules 2023, 28(9), 3843; https://doi.org/10.3390/molecules28093843
Submission received: 30 March 2023 / Revised: 21 April 2023 / Accepted: 27 April 2023 / Published: 1 May 2023
(This article belongs to the Section Analytical Chemistry)

Abstract

:
The pitaya (dragon fruit) Hylocereus is a genus which belongs to the Cactaceae family. It is native to Mexico, occurring also in other regions of Central and South America. Pitaya fruit is mainly intended for consumption and for this reason the species is grown commercially. The fruit is a rich source of vitamins, biologically active compounds, and dietary fibre. Using in vitro culture can accelerate the process of reproduction and growth of pitaya plants. Profiling of volatile compounds contained in the stem of Hylocereus undatus was carried out using the SPME-GC-MS technique. The main compounds present were hexanal, 2-hexenal and 1-hexanol. The results showed differences in the occurrence of volatile compounds between plants grown in media with an addition of BA (6-benzylaminopurine) and IAA (indole-3-acetic acid), which have been used as plant growth regulators. Statistically significant differences between the contents of volatile compounds were observed in the case of 2-hexenal and 1-hexanol. The effect of BA on reducing the amount of volatile compounds was observed. However, introduction of IAA to the in vitro medium resulted in more compounds being synthesized. This study is the first to describe the volatile compounds in the pitaya stem. The results indicate that plant hormones are able to modify the profile of volatile compounds.

1. Introduction

Hylocereus ssp. are perennial succulents, growing as epiphytes. The genus originates from tropical and subtropical forests of Mexico and other areas within Central and South America (e.g., Guatemala, Salvador, Panama, Costarica, Colombia or Brazil). From its native localities the plant has been spread to Near East and Australia. Nowadays, the industrial plantations of pitaya are mostly located in Asian countries, namely, Thailand, Malesia and Taiwan. The pitaya is a cactus genus characterized by long triangular green stems, equipped with thorns on the edges. The fruit is an elongated berry. The peel’s characteristic feature is intense dark pink or reddish purple coloration with green scales resembling leaves. Pitaya fruit is mostly used for consumption and therefore the plant is cultivated for commercial purposes. It is a rich source both of vitamins (C—20.5–33 mg/100 g pulp, B3—0.2–2.8 mg/100 g pulp) and dietary fibre (69 g/100 g of dried pulp). Its pH value reaches 4.4–5.1. The predominating acid is malic acid [1,2].
Full production of raw material falls on the fifth year of land use. It is possible to incessantly obtain fruit for 10–15 years. Depending on the region of cultivation, the yield from 1 ha plantation can reach as much as 16–80 tons of fruit annually [2,3,4,5,6,7,8,9]. Plantlets for establishing a plantation can be acquired on generative way from seeds and vegetatively from in vivo or in vitro cultures. The seedlings raised from seeds grow slower and need a longer time to reach the reproductive phase, while the individual specimens obtained are diverse. The second method, which is easier and cheaper, is vegetative propagation by cuttings. It consists in in vivo cutting of plants to acquire 15–60 cm-long segments (the longer the fragment the faster the regeneration time). Whereas using in vitro culture, one can accelerate the process of vegetative propagation and growth of the dragon fruit plants. Thanks to this method it is possible to acquire healthy pathogen-free plant material in a very short time [3,5,7]. So far research with the use of plant in vitro cultures in this species concentrated on acquisition of effective micropropagation and acclimatization [9].
From the perspective of different branches of bio-economy, modification of metabolic paths in plants finds a wide array of applications. Alterations to the chemical composition can be induced under in vivo and in vitro conditions. Increased production by plants of biologically active compounds can be applicable in industry. In the tissues of many Hylocereus species it was possible to enhance the production of betacyans through triggering auto-polyploidization and also by using tyrosine or methyl jasmonate, whereas the synthesis of betalins was intensified with the use of elicitors, tyrosine or leucine as well as when raising the plants in red light conditions Table S1 [10,11,12,13,14,15,16,17,18,19,20,21,22].
It was not only in species falling within the genus Hylocereus that synthesis of valuable chemical compounds was effectively enhanced. Table S1 provides examples of species representing different plant genera and families for which such modifications have been reported [23,24,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44]. Besides, in species belonging to the genus pitaya, namely H. monacanthus, H. undatus and Hylocereus polyrhizus, as well as in represenatives of other plant genera, such as Andrographis paniculata, Phoenix dactylifera L. or Artemisia argyi, intensified production of flavonoids was successfully initiated Table S1. Consequences of the presence of plant growth regulators (PGR) and their possible impact on changes in the synthesis of volatile compounds in pitaya stems have not been analyzed as yet. So far modification to the profile of volatile compounds with the use of plant hormones was successfully performed in a few plant species representing other genera. Application of jasmonic acid in the narrow-leaved lavender (L. angustifolia ‘Luoshen’) under in vitro conditions caused an increase in the content of volatile substances—monoterpenoids and sesquiterpenoids Table S1. A similar effect was obtained in the Pyrenees oak, in which application of the above mentioned compound resulted in enhanced emission of volatile compounds, although the overall chemical composition did not change. In the case of the orange Citrus sinensis L. ‘Osbeck’ alterations in the contents of volatile compounds were recorded, but also emission of E-β-ocimen and indole was found intensified. Taking into consideration the present state of knowledge, the herein discussed research was an attempt at defining the impact of two chosen plant growth regulators representing different groups—BA (cytokinin) and IAA (auxin)—on the profile and percentage of particular volatile compounds in pitaya stems coming from in vitro culture. These plant hormones allowed pitayas to be maintained in in vitro cultures. In addition, there are reports on these regulators that may have consequences of secondary metabolites in plants [45]. The hitherto reported data on volatile compounds in the pitaya are very scarce in the literature.

2. Results

The main compounds occurring in Hylocereus undatus tissues coming from both types of culture were: hexanal (6.87–4.53%), 2-hexenal (22.53–25.48%) and 1-hexanol (40.89–36.44%). The profile of volatile compounds in plants bred on media with an addition of plant hormones differed. The plants which were cultivated on a medium supplemented with IAA were characterized by occurrence of the following compounds: 1-heptanol, 1-octen-3-ol, octanal, o-cymene, ethanol, 2-(2-butoxyethoxy), 2-decenal, tetradecane and geranyl acetone, which were not detected in plants bred on media enriched with BA. Whereas in the tissues of pitaya cultured in vitro on a medium containing BA heptanoic acid, octanoic acid and hexyl ester were detected, which were not found in plant tissues grown on a medium with IAA added. A clearly negative impact of BA on the synthesis of volatile compounds was observed. Unlike, addition of IAA to the cultivation medium induced synthesis of a larger number of compounds. Statistically significant differences in the shares of volatile compounds were revealed Table 1. Mean values have been qualified into seven homogeneous groups based on Tukey’s test. The mean values of the following compounds: 1-hexanol coming from plants cultivated on a medium with an addition of BA, 1-hexanol from plants bred on a medium enriched with IAA, 2-hexenal coming from plants growing on a medium with IAA and 2-hexenal from plants grown on a medium containing BA have been qualified with distinct homogeneous groups (a–d). Most compounds identified—taking into consideration plant growth regulators added—did not exceed a mean share of over 5%.

3. Discussion

In their research based on in vivo material of Hylocereus megalanthus fruit, the team of Quijano-Célis et al., (2012) [46] identified the same compounds as those found in the present study, namely hexanal, 2-hexenal, 1-hexanol, 1-octen-3-ol, octanal, hexanoic acid, limonene, 1-octanol, nonanal, octanoic acid, decanal, 2-decenal, nonanoic acid, tetradecane, geranyl acetone, 1-dodecanol. However, our research revealed occurrence of 2-decenal, tetradecane and geranyl acetone only in plant tissues cultivated on a medium enriched with IAA and not that containing BA. Compounds such as linear alcohols and aldehydes (LAs, e.g., 1-hexanol, 2-hexanal) that occurs in plant are synthesized mainly from ω-3 and ω-6 carboxilic acids via hyper-peroxidation reaction (LOX). It was found, that they could play an important role in plant defense against herbivores and pathogens. Although the biosynthetic pathway of Las is not directly triggered with auxins or BA mode of action Escobar-Bravo found the relation between emission of 3-hexenyl acetate with changes in auxin concentration in maize. Also [47] (2013) proven that BA and IAA could directly effect on LOX activity, and in LAs emission as a response to stress. In grapes [48]. proven that cytokins effect on hexenals and hexenols biosynthesis, although it’s pathway is unclear. Due to their activity, the most interesting volatile compounds, applicable in industry, including pharmaceuticals production or plant protection, which were detected in the tissues of Hylocereus undatus were hexanal, 2-hexenal, 1-hexenol, o-cymene, limonene, eucalyptol, β-linalool and thymol.
Recent years, more and more volatile compounds from plants have been identified as protective compounds against pests [49,50,51]. Hexanal induces early apoptosis of saprophytic fungus (Aspergillus flavus) conidia and have actively inhibits the growth of Aspergillus and Penicillium species. In addition, it is one of the attracting compounds for Holotrichia parallela [52,53,54,55]. Another component of the fresh green fragrance is 2-hexenal found in green plants. It is a typical defense compound of many insects, but it is also a component of the pheromone in several insects of the genus Podisus and in the species C. lectularius [56,57,58]. 1-hexanol was identified during the analysis of volatile compounds of fruits, among others, of species from the genus Pyrus spp. And Prunus spp. Moreover, this compound has an antagonistic effect on the sex pheromones of Adelphocoris lineolatus, while it attracts the insect Lobesia botrana [59,60,61,62]. Regarding the activities of hexanal and 2-hexenal, the abundance of those compounds in in vitro cultivations of pitaya supported with growth regulators may be a valuable feature for biotechnological production of agents dedicated for pest and fungi management.
Moreover, the interesting result was the observation that samples cultivated on the medium with IAA were able to synthesis other compounds, like o-cymene than cultures with BA. o-Cymene is one of the major the main components (65.2%) of the essential oils from Bursera simaruba (L.) Sarg., Thymus vulgaris ((56.2%) and Nigella sativa L. seeds (37.82%). The latter essential oil exhibits anti-oxidative properties, anti-microbial effect against clinically significant strains of bacteria and fungi whereas the thyme oil possesses potential activity against fungi causing the brown rot disease, what again brings the perspective of use of in vitro pitaya cultures industrial importance, however it has to be highlighted that for this purpose further optimalization of the process would be required due to low share of this compound in the present study Besides, o-cymene shows anti-viral effect against the virus of human influenza H1N1 [63,64,65,66,67].
In the case of limonene, eucalyptol, β-linalool and thymol the difference was observed between BA and IAA cultures, in favor for BA ones—the share of listed volatiles were higher. First of them -limonene is the most important volatile obtained from citrus peels essential oils, in which the content of limonene can reach as much as 97–98%. Limonene has been reported to control the development of S. aureus. What is more, in pre-clinical investigations this compound was revealed to have an inhibitory effect on the development of cancers, including the melanoma. Studies in vitro yield similar results. Limonene is characterized by anti-viral activity against the bird flu virus H5N1 type A and against COVID-19. At present it is possible to acquire limonene from citrus wastes [68,69,70,71,72,73]. Moreover, C. reticulata leaf essential oil from cultivars Cara mandarin, Kishu mandarin and Willow leaf mandarin—whose one of the main components is d-limonene—was reported to have a promising inhibitory impact on the tested aging enzymes [74]. Furthermore, eucalyptol is a component of the essential oil of a few eucalyptus species, i.e., E. longicornis (84.2%), E. wandoo (73.6%), E. Lesouefii (40.8%). The essential oils from eucalyptuses are reported as highly effective in controlling the adhesion by gram-negative (Pseudomonas aeruginosa, Escherichia coli and Acinetobacter baumannii) and gram-positive (Staphylococcus aureus and Listeria monocytogenes) bacteria. Eucalyptus oil displays also anti-inflammatory quality and anti-viral activity, e.g., against influenza A (H1N1) virus. Besides, this oil can potentially act as an Mpro inhibitor of COVID-19. What is more, it has been found to show phytotoxicity to Sinapis arvensis and Raphanus sativus [75,76,77,78,79,80,81]. Eucalyptol alone belongs to compounds having a potential for treatment of influenza [82]. Another compound, which is present plentifully in the aroma profile of two night-blooming species representing the genus Silene (Caryophyllaceae), namely S. chlorantha (40.5%) and S. italica (14.5%), is β-linalool. It is also present in Osmanthus fragrans var. thunbergi (27.71%) [83,84] and cardamom (0.44–11.0%) [85]. And this is mainly linalool that is responsible for the fragrance of the lychee fruit [86]. This compound, also one of the basic components of Citrus reticulata leaves essential oil, possesses promising attributes as an additive to anti-aging cosmetics for skin care [74]. Fumigation with linalool hinders significantly the growth of Botrytis cinerea mycelium and expansion of this pathogen on tomato fruit [87]. Thymol is the main component of essential oils emitted by plants falling within the family Lamiaceae. In Thymus vulgaris L. essential oil the percentage of this compound ranges from 10 to 64%. Numerous varied types of activity of thymol have been revealed, including anti-oxidant, anti-inflammatory, molocally anaesthetic, anti-nociceptive, scarring, anti-septic, anti-bacterial, anti-fungal, anti-cancerogenic, antispasmodic, anti-Leishmanial, anti-biofilm, anti-viral properties, and also its effect as a growth stimulator and immunomodulator. It also shows therapeutic attributes against different cardio-vascular, neurological, rheumatic and gastro-intestinal diseases [88,89,90,91]. What is more, thymol was found causing the weakening of Nosema ceranae individuals, infesting the honey bee Apis mellifera, and a decline in the productive and reproductive capabilities of their microsporidians [92]. As shown in our investigations and also other authors’ research Table S1 [22,28,29,30,31,32,33,34,35,36,37] addition of plant hormones to the breeding medium in plant in vitro cultures affects the composition and share of particular compounds in the case of various species of plants, Hylocereus undatus for example. Our results may be a starting point for further investigations and optimization to improve the potential of in vitro pitaya cultures for biotechnological production of valuable for numerous industries, such as pharmaceutical or plant protection ones, volatile compounds.

4. Materials and Methods

4.1. Biological Material

Initial material for chemical analysis were stems of Hylocereus undatus comprized within the plant collection run under in vitro conditions at the Faculty of Genetics, Plant Breeding and Seed Production (Figure 1). Two pools of explants bred on the MS (Murashige and Skoog) medium with an addition of different PGRs (BA—for multiplication and IAA—for elongation) with concentration 0.5 mg·L−1, which is the standard concentration used for preliminary in vitro studies. The multiplication of the material without a control (MS basic medium without hormones) was performed due to poor plant growth and vitality on it [7,93,94]. Then plants were selected for the analyses of volatile compounds.

4.2. Aroma Profiling

The analysis of the stem chemical composition was performed with the use of a gas chromatograph coupled with a mass spectrometer (single quadrupole mass spectrometer; gas chromatograph Shimadzu GC-MS QP 2020, Shimadzu, Kyoto, Japan) with using solid-phase micro extraction (SPME) technique. Each sample (~500 mg of fresh plant material respectively) was placed in a vial of the head-space type, volume of 20 mL. The polymer coating of the fibre was a mixture of divinylbenzene, WR carboxene and polydimethylsiloxane (DVB/C-WR/PDMS). The volatile extraction was performed at 80 °C for 10 min; before the extraction sample was preincubated for 10 min at extraction temperature. The desorption of extracted volatile was carried out in the apparathus injector for 3 min. The injector temperature was 250 °C. As the carrier gas, helium at flow 1.0 mL/min, with split 5, was applied. Separation was reached using a capillary column Zebron ZB-5 (30 m, 0.25 mm, 0.25 µm of stationary phase; Phenomenex, Torrance, CA, USA). The temperature program of the column was as follows: 50 °C, an increase by 4.0 °C min−1 to 130 °C, then 10 °C min−1 to 180 °C then 20 °C min−1 to 280 °C. The MS analysis was performed using scans from 40 to 300 m/z with the application of electron ionization (EI) at 70 eV. The analysis was carried out in four replications.
The compounds were identified with the help of two different analytic methods in order to compare the retention times of authentic chemical compounds (standard of saturated alkanes Supelco C6–C30) with the mass spectra acquired from the available library (Willey NIST 17, match indicator; 90%). The identification of compounds was performed through a comparison of the experimentally obtained linear retention indices calculated relative to the mixture of n-alkanes C6–C30 (SigmaAldrich, Saint Louis, MO, USA) and mass spectra with the ones available at libraries (NIST 17 Mass Spectral and Retention Index Library (NIST17) and NIST WebBook) or in literature [95].

4.3. Statistical Analysis

The results were expressed as the mean of the measurements and reported as mean ± SD (standard deviation). The data reported in the present study are the mean values of at least four replicates. A one-way analysis of variance (ANOVA) was conducted to verify the lack of significance of PGRs (plant growth regulators). The hypothesis assumed no impact of medium (supplemented with various PGRs) on the chemical content of pitaya. The significant differences were assessed at levels of 0.05 and 0.01. When an analysis of variance gave a significant result, Tukey’s honestly significant difference (HSD) test was performed to compare mean values [96]. Data obtained during aroma profiling were subjected to a one-way analysis of variance using Tukey’s test (p < 0.05). The obtained results were statistically analyzed with the use of the Statistica programme, version 13.3. Tukey’s HSD test was performed in those cases where the hypothesis was rejected.

5. Conclusions

The present study revealed effect of cytokinin BA (6-6-benzylaminopurine) and auxin IAA (indolyl-3-acetic acid) on modification of the volatile compounds profile in the overground part of the white pitaya plants coming from in vitro cultures. And thus, plant hormones display properties leading to alterations in the profile of volatile compounds. Furthermore, they possess a potential for increasing the percentage of particular valuable compounds in plants.
The hitherto conducted investigations were focused on analysis of compounds in particular parts of fruit of different species representing the genus Hylocereus, while only the present research pertains to volatile compounds contained in stems of the white pitaya. Our research, based on in vitro cultures, was performed in the context of future application of the technique itself to purposeful and directed modification of the chemical composition in plants.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/1420-3049/28/9/3843/s1, Table S1: Modification the chemical composition using chemical and physical factor in plants under the conditions.

Author Contributions

Conceptualization, M.J. and R.G.; methodology, J.Ł., R.G. and A.S.; software, M.J., K.Z. and R.G.; validation, J.Ł., R.G. and A.S.; formal analysis M.J. and K.Z.; investigation, M.J., J.Ł. and K.Z.; resources, J.Ł., R.G. and A.S.; data curation, M.J. and J.Ł.; writing—original draft preparation, M.J., J.Ł. and R.G.; writing—review and editing, M.J., J.Ł. and R.G; supervision, R.G. and A.S.; project administration, R.G. All authors have read and agreed to the published version of the manuscript.

Funding

The APC is financed by Wrocław University of Environmental and Life Sciences.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Data is contained within the article or supplementary material or data is available on request.

Conflicts of Interest

The authors declare no conflict of interest.

Sample Availability

Samples of the compounds are not available from the authors.

References

  1. Cheah, L.K.; Eid, A.M.; Aziz, A.; Ariffin, F.D.; Elmahjoubi, A.; Elmarzugi, N.A. Phytochemical Properties and Health Benefits of Hylocereusundatus. Nanomed. Nanotechnol. Open Access 2016, 1, 1–10. [Google Scholar] [CrossRef]
  2. Liaotrakoon, W. Characterization of Dragon Fruit (Hylocereus spp.) Components with Valorization Potential. Ph.D. Thesis, Ghent University, Ghent, Belgium, 2013; p. 217. [Google Scholar]
  3. Drew, R.A.; Azimi, M. Micropropagation of Red Pitaya (Hylocereous undatus). Acta Hortic. 2002, 575, 93–98. [Google Scholar] [CrossRef]
  4. ElObeidy, A.A. Mass Propagation of Pitaya (Dragon Fruit). Fruits 2006, 61, 313–319. [Google Scholar] [CrossRef] [Green Version]
  5. Gunasena, H.P.M.; Pushpakumara, D.K.N.G.; Kariyawasam, M. Dragon Fruit Hylocereus undatus (Haw.) Britton and Rose. In Underutilized Fruit Trees in Sri Lanka; World Agroforestry Centre: New Delhi, India, 2007; pp. 110–141. [Google Scholar]
  6. Hoa, T.T.; Clark, C.J.; Waddell, B.C.; Woolf, A.B. Postharvest Quality of Dragon Fruit (Hylocereus undatus) Following Disinfesting Hot Air Treatments. Postharvest Biol. Technol. 2006, 41, 62–69. [Google Scholar] [CrossRef]
  7. Hua, Q.; Chen, P.; Liu, W.; Ma, Y.; Liang, R.; Wang, L.; Wang, Z.; Hu, G.; Qin, Y. A Protocol for Rapid in Vitro Propagation of Genetically Diverse Pitaya. Plant Cell Tissue Organ Cult. 2015, 120, 741–745. [Google Scholar] [CrossRef]
  8. Zee, F.; Yen, C.-R.; Nishina, M. Pitaya (Dragon Fruit, Strawberry Pear). In Fruits and Nuts; University of Hawaii: Honolulu, HI, USA, 2004; pp. 1–3. [Google Scholar]
  9. Mohamed-Yasseen, Y. Micropropagation of Pitaya (Hylocereus undatus Britton et Rose). Vitr. Cell. Dev. Biol. Plant 2002, 38, 427–429. [Google Scholar] [CrossRef]
  10. Hua, Q.; Zhou, Q.; Gan, S.; Wu, J.; Chen, C.; Li, J.; Ye, Y.; Zhao, J.; Hu, G.; Qin, Y. Proteomic Analysis of Hylocereus polyrhizus Reveals Metabolic Pathway Changes. Int. J. Mol. Sci. 2016, 17, 1606. [Google Scholar] [CrossRef]
  11. Cohen, H.; Fait, A.; Tel-Zur, N. Morphological, Cytological and Metabolic Consequences of Autopolyploidization in Hylocereus (Cactaceae) Species. BMC Plant Biol. 2013, 13, 173. [Google Scholar] [CrossRef] [Green Version]
  12. Li, X.; Zhang, Y.; Wu, Y.; Li, B.; Sun, J.; Gu, S.; Pang, X. Lipid Metabolism Regulated by Superoxide Scavenger Trypsin in Hylocereus undatus through Multi-omics Analyses. J. Food Biochem. 2022, 46, e14144. [Google Scholar] [CrossRef]
  13. Jiao, Z.; Xu, W.; Nong, Q.; Zhang, M.; Jian, S.; Lu, H.; Chen, J.; Zhang, M.; Xia, K. An Integrative Transcriptomic and Metabolomic Analysis of Red Pitaya (Hylocereus polyrhizus) Seedlings in Response to Heat Stress. Genes 2021, 12, 1714. [Google Scholar] [CrossRef]
  14. Li, X.; Li, B.; Min, D.; Ji, N.; Zhang, X.; Li, F.; Zheng, Y. Transcriptomic Analysis Reveals Key Genes Associated with the Biosynthesis Regulation of Phenolics in Fresh-Cut Pitaya Fruit (Hylocereus undatus). Postharvest Biol. Technol. 2021, 181, 111684. [Google Scholar] [CrossRef]
  15. Wu, Q.; Gao, H.; Zhang, Z.; Li, T.; Qu, H.; Jiang, Y.; Yun, Z. Deciphering the Metabolic Pathways of Pitaya Peel after Postharvest Red Light Irradiation. Metabolites 2020, 10, 108. [Google Scholar] [CrossRef] [Green Version]
  16. Huang, W.; Yang, G.; Liu, D.; Li, Q.; Zheng, L.; Ma, J. Metabolomics and Transcriptomics Analysis of Vitro Growth in Pitaya Plantlets with Different LED Light Spectra Treatment. Ind. Crops Prod. 2022, 186, 115237. [Google Scholar] [CrossRef]
  17. Wang, A.; Ma, C.; Ma, H.; Qiu, Z.; Wen, X. Physiological and Proteomic Responses of Pitaya to PEG-Induced Drought Stress. Agriculture 2021, 11, 632. [Google Scholar] [CrossRef]
  18. Winson, K.W.S.; Chew, B.L.; Sathasivam, K.; Subramaniam, S. Effect of Amino Acid Supplementation, Elicitation and LEDs on Hylocereus Costaricensis Callus Culture for the Enhancement of Betalain Pigments. Sci. Hortic. 2021, 289, 110459. [Google Scholar] [CrossRef]
  19. Fadzliana, N.A.F.; Rogayah, S.; Shaharuddin, N.A.; Janna, O.A. Addition of L-Tyrosine to Improve Betalain Production in Red Pitaya Callus. Pertanika J. Trop. Agric. Sci. 2017, 40, 521–532. [Google Scholar]
  20. Mustafa, M.A.; Ali, A.; Seymour, G.; Tucker, G. Treatment of Dragonfruit (Hylocereus polyrhizus) with Salicylic Acid and Methyl Jasmonate Improves Postharvest Physico-Chemical Properties and Antioxidant Activity during Cold Storage. Sci. Hortic. 2018, 231, 89–96. [Google Scholar] [CrossRef]
  21. Winson, K.W.S.; Chew, B.L.; Sathasivam, K.; Subramaniam, S. The Establishment of Callus and Cell Suspension Cultures of Hylocereus costaricensis for the Production of Betalain Pigments with Antioxidant Potential. Ind. Crops Prod. 2020, 155, 112750. [Google Scholar] [CrossRef]
  22. Wee, C.; Sekeli, R.; Asari, N.H.C.; Yahya, S.F.; Machap, C. Select Record Enhancement of Bioactive Compounds in Hylocereus polyrhzus Callus Mediated by Plant Growth Regulators and Elicitors. Malays. Soc. Plant Physiol. 2018, 10, 1–10. [Google Scholar]
  23. Biddington, N.L.; Thomas, T.H. Interactions of Abscisic Acid, Cytokinin and Gibberellin in the Control of Betacyanin Synthesis in Seedlings of Amaranthus Caudatus. Physiol. Plant 1977, 40, 312–314. [Google Scholar] [CrossRef]
  24. Biddington, N.L.; Thomas, T.H. A Modified Amaranthus Betacyanin Bioassay for the Rapid Determination of Cytokinins in Plant Extracts. Planta 1973, 111, 183–186. [Google Scholar] [CrossRef] [PubMed]
  25. Ray, S.D.; Guruprasad, K.N.; Laloraya, M.M. Reversal of Abscisic Acid-Inhibited Betacyanin Synthesis by Phenolic Compounds in Amaranthus Caudatus Seedlings. Physiol. Plant 1983, 58, 175–178. [Google Scholar] [CrossRef]
  26. Ewas, M.; Gao, Y.; Ali, F.; Nishawy, E.M.; Shahzad, R.; Subthain, H.; Amar, M.; Martin, C.; Luo, J. RNA-Seq Reveals Mechanisms of SlMX1 for Enhanced Carotenoids and Terpenoids Accumulation along with Stress Resistance in Tomato. Sci. Bull. 2017, 62, 476–485. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  27. Steiner, U.; Schliemann, W.; Böhm, H.; Strack, D. Tyrosinase Involved in Betalain Biosynthesis of Higher Plants. Planta 1999, 208, 114–124. [Google Scholar] [CrossRef]
  28. Rodrigues-Brandão, I.; Kleinowski, A.M.; Einhardt, A.M.; Lima, M.C.; do Amarante, L.; Peters, J.A.; Braga, E.J.B. Salicylic Acid on Antioxidant Activity and Betacyan in Production from Leaves of Alternanthera tenella. Ciência Rural 2014, 44, 1893–1898. [Google Scholar] [CrossRef] [Green Version]
  29. Badrhadad, A.; Piri, K.; Ghiasvand, T. Increase Alpha-Tocopherol in Cell Suspension Cultures Elaeagnus angustifolia L. Int. J. Agric. Crop Sci. 2013, 5, 1–4. [Google Scholar]
  30. Saw, N.M.M.T.; Riedel, H.; Kütük, O.; Ravichandran, K.; Smetanska, I. Effect of Elicitors and Precursors on the Synthesis of Anthocyanin in Grape Vitis Vinifera Cell Cultures. Energy Res. J. 2010, 1, 189–192. [Google Scholar] [CrossRef] [Green Version]
  31. Mendhulkar, V.D.; Moinuddin, M. Ali Vakil Elicitation of Flavonoids by Salicylic Acid and Penicillium expansum in Andrographis paniculata (Burm. f.) Nees. Cell Culture. Res. Biotechnol. 2013, 4, 1–9. [Google Scholar]
  32. Łyczko, J.; Piotrowski, K.; Kolasa, K.; Galek, R.; Szumny, A. Mentha piperita L. Micropropagation and the Potential Influence of Plant Growth Regulators on Volatile Organic Compound Composition. Molecules 2020, 25, 2652. [Google Scholar] [CrossRef]
  33. Al-Khayri, J.M.; Naik, P.M. Influence of 2iP and 2,4-D Concentrations on Accumulation of Biomass, Phenolics, Flavonoids and Radical Scavenging Activity in Date Palm (Phoenix dactylifera L.) Cell Suspension Culture. Horticulturae 2022, 8, 683. [Google Scholar] [CrossRef]
  34. Clapa, D.; Nemeș, S.-A.; Ranga, F.; Hârța, M.; Vodnar, D.-C.; Călinoiu, L.-F. Micropropagation of Vaccinium Corymbosum L.: An Alternative Procedure for the Production of Secondary Metabolites. Horticulturae 2022, 8, 480. [Google Scholar] [CrossRef]
  35. Koprna, R.; Humplík, J.F.; Špíšek, Z.; Bryksová, M.; Zatloukal, M.; Mik, V.; Novák, O.; Nisler, J.; Doležal, K. Improvement of Tillering and Grain Yield by Application of Cytokinin Derivatives in Wheat and Barley. Agronomy 2020, 11, 67. [Google Scholar] [CrossRef]
  36. Yang, L.; Yan, Y.; Zhao, B.; Xu, H.; Su, X.; Dong, C. Study on the Regulation of Exogenous Hormones on the Absorption of Elements and the Accumulation of Secondary Metabolites in the Medicinal Plant Artemisia argyi Leaves. Metabolites 2022, 12, 984. [Google Scholar] [CrossRef] [PubMed]
  37. Rogowska, A.; Stpiczyńska, M.; Pączkowski, C.; Szakiel, A. The Influence of Exogenous Jasmonic Acid on the Biosynthesis of Steroids and Triterpenoids in Calendula officinalis Plants and Hairy Root Culture. Int. J. Mol. Sci. 2022, 23, 12173. [Google Scholar] [CrossRef] [PubMed]
  38. Meza, S.L.R.; de Castro Tobaruela, E.; Pascoal, G.B.; Magalhães, H.C.R.; Massaretto, I.L.; Purgatto, E. Induction of Metabolic Changes in Amino Acid, Fatty Acid, Tocopherol, and Phytosterol Profiles by Exogenous Methyl Jasmonate Application in Tomato Fruits. Plants 2022, 11, 366. [Google Scholar] [CrossRef] [PubMed]
  39. Elahi, N.N.; Raza, S.; Rizwan, M.S.; Albalawi, B.F.A.; Ishaq, M.Z.; Ahmed, H.M.; Mehmood, S.; Imtiaz, M.; Farooq, U.; Rashid, M.; et al. Foliar Application of Gibberellin Alleviates Adverse Impacts of Drought Stress and Improves Growth, Physiological and Biochemical Attributes of Canola (Brassica napus L.). Sustainability 2022, 15, 78. [Google Scholar] [CrossRef]
  40. Didi, D.A.; Su, S.; Sam, F.E.; Tiika, R.J.; Zhang, X. Effect of Plant Growth Regulators on Osmotic Regulatory Substances and Antioxidant Enzyme Activity of Nitraria tangutorum. Plants 2022, 11, 2559. [Google Scholar] [CrossRef]
  41. Wu, P.; Liu, A.; Zhang, Y.; Feng, K.; Zhao, S.; Li, L. NnABI4-Mediated ABA Regulation of Starch Biosynthesis in Lotus (Nelumbo nucifera Gaertn). Int. J. Mol. Sci. 2021, 22, 13506. [Google Scholar] [CrossRef]
  42. Dong, Y.; Li, J.; Zhang, W.; Bai, H.; Li, H.; Shi, L. Exogenous Application of Methyl Jasmonate Affects the Emissions of Volatile Compounds in Lavender (Lavandula angustifolia). Plant Physiol. Biochem. 2022, 185, 25–34. [Google Scholar] [CrossRef] [PubMed]
  43. Patt, J.M.; Robbins, P.S.; Niedz, R.; McCollum, G.; Alessandro, R. Exogenous Application of the Plant Signalers Methyl Jasmonate and Salicylic Acid Induces Changes in Volatile Emissions from Citrus Foliage and Influences the Aggregation Behavior of Asian Citrus Psyllid (Diaphorina citri), Vector of Huanglongbing. PLoS ONE 2018, 13, e0193724. [Google Scholar] [CrossRef] [Green Version]
  44. Amo, L.; Mrazova, A.; Saavedra, I.; Sam, K. Exogenous Application of Methyl Jasmonate Increases Emissions of Volatile Organic Compounds in Pyrenean Oak Trees, Quercus pyrenaica. Biology 2022, 11, 84. [Google Scholar] [CrossRef]
  45. Jamwal, K.; Bhattacharya, S.; Puri, S. Plant Growth Regulator Mediated Consequences of Secondary Metabolites in Medicinal Plants. J. Appl. Res. Med. Aromat. Plants 2018, 9, 26–38. [Google Scholar] [CrossRef]
  46. Quijano-Célis, C.; Echeverri-Gil, D.; Pino, J.A. Characterization of Odor-Active Compounds in Yellow Pitaya (Hylocereus megalanthus (Haw.) Britton et Rose). Rev. CENIC Cienc. Químicas 2012, 43, 1–7. [Google Scholar]
  47. Scala, A.; Allmann, S.; Mirabella, R.; Haring, M.; Schuurink, R. Green Leaf Volatiles: A Plant’s Multifunctional Weapon against Herbivores and Pathogens. Int. J. Mol. Sci. 2013, 14, 17781–17811. [Google Scholar] [CrossRef] [Green Version]
  48. Tyagi, K.; Maoz, I.; Kochanek, B.; Sela, N.; Lerno, L.; Ebeler, S.E.; Lichter, A. Cytokinin but Not Gibberellin Application Had Major Impact on the Phenylpropanoid Pathway in Grape. Hortic. Res. 2021, 8, 51. [Google Scholar] [CrossRef] [PubMed]
  49. Dudareva, N.; Negre, F.; Nagegowda, D.A.; Orlova, I. Plant Volatiles: Recent Advances and Future Perspectives. CRC Crit. Rev. Plant Sci. 2006, 25, 417–440. [Google Scholar] [CrossRef]
  50. Brilli, F.; Loreto, F.; Baccelli, I. Exploiting Plant Volatile Organic Compounds (VOCs) in Agriculture to Improve Sustainable Defense Strategies and Productivity of Crops. Front. Plant Sci. 2019, 10, 264. [Google Scholar] [CrossRef] [PubMed]
  51. Hammerbacher, A.; Coutinho, T.A.; Gershenzon, J. Roles of Plant Volatiles in Defence against Microbial Pathogens and Microbial Exploitation of Volatiles. Plant Cell Env. 2019, 42, 2827–2843. [Google Scholar] [CrossRef] [Green Version]
  52. Wang, X.; Wang, S.; Yi, J.; Li, Y.; Liu, J.; Wang, J.; Xi, J. Three Host Plant Volatiles, Hexanal, Lauric Acid, and Tetradecane, Are Detected by an Antenna-Biased Expressed Odorant Receptor 27 in the Dark Black Chafer Holotrichia Parallela. J. Agric. Food Chem. 2020, 68, 7316–7323. [Google Scholar] [CrossRef] [PubMed]
  53. Schade, F.; Thompson, J.E.; Legge, R.L. Use of a Plant-Derived Enzyme Template for the Production of the Green-Note Volatile Hexanal. Biotechnol. Bioeng. 2003, 84, 265–273. [Google Scholar] [CrossRef]
  54. Li, S.-F.; Zhang, S.-B.; Zhai, H.-C.; Lv, Y.-Y.; Hu, Y.-S.; Cai, J.-P. Hexanal Induces Early Apoptosis of Aspergillus flavus Conidia by Disrupting Mitochondrial Function and Expression of Key Genes. Appl. Microbiol. Biotechnol. 2021, 105, 6871–6886. [Google Scholar] [CrossRef] [PubMed]
  55. Zhang, S.; Zheng, M.; Zhai, H.; Ma, P.; Lyu, Y.; Hu, Y.; Cai, J. Effects of Hexanal Fumigation on Fungal Spoilage and Grain Quality of Stored Wheat. Grain Oil Sci. Technol. 2021, 4, 10–17. [Google Scholar] [CrossRef]
  56. Francke, W.; Schulz, S. Pheromones. In Comprehensive Natural Products Chemistry; Elsevier: Amsterdam, The Netherlands, 1999; pp. 197–261. [Google Scholar]
  57. Francke, W.; Schulz, S. Pheromones of Terrestrial Invertebrates. In Comprehensive Natural Products II; Elsevier: Amsterdam, The Netherlands, 2010; pp. 153–223. [Google Scholar]
  58. Hatanaka, A. Biosynthesis of So-Called “Green Odor” Emitted by Green Leaves. In Comprehensive Natural Products Chemistry; Elsevier: Amsterdam, The Netherlands, 1999; pp. 83–115. [Google Scholar]
  59. Koczor, S.; Vuts, J.; Caulfield, J.C.; Withall, D.M.; Sarria, A.; Pickett, J.A.; Birkett, M.A.; Csonka, É.B.; Tóth, M. Sex Pheromone of the Alfalfa Plant Bug, Adelphocoris lineolatus: Pheromone Composition and Antagonistic Effect of 1-Hexanol (Hemiptera: Miridae). J. Chem. Ecol. 2021, 47, 525–533. [Google Scholar] [CrossRef] [PubMed]
  60. Von Arx, M.; Schmidt-Büsser, D.; Guerin, P.M. Plant Volatiles Enhance Behavioral Responses of Grapevine Moth Males, Lobesia botrana to Sex Pheromone. J. Chem. Ecol. 2012, 38, 222–225. [Google Scholar] [CrossRef] [PubMed]
  61. Roussos, P.A.; Efstathios, N.; Intidhar, B.; Denaxa, N.-K.; Tsafouros, A. Plum (Prunus domestica L. and P. salicina Lindl.). In Nutritional Composition of Fruit Cultivars; Elsevier: Amsterdam, The Netherlands, 2016; pp. 639–666. [Google Scholar]
  62. Li, X.; Li, X.; Wang, T.; Gao, W. Nutritional Composition of Pear Cultivars (Pyrus spp.). In Nutritional Composition of Fruit Cultivars; Elsevier: Amsterdam, The Netherlands, 2016; pp. 573–608. [Google Scholar]
  63. Najar, B.; Nardi, V.; Stincarelli, M.A.; Patrissi, S.; Pistelli, L.; Giannecchini, S. Screening of the Essential Oil Effects on Human H1N1 Influenza Virus Infection: An in Vitro Study in MDCK Cells. Nat. Prod. Res. 2022, 36, 3149–3152. [Google Scholar] [CrossRef] [PubMed]
  64. Zouirech, O.; Alyousef, A.A.; El Barnossi, A.; El Moussaoui, A.; Bourhia, M.; Salamatullah, A.M.; Ouahmane, L.; Giesy, J.P.; Aboul-soud, M.A.M.; Lyoussi, B.; et al. Phytochemical Analysis and Antioxidant, Antibacterial, and Antifungal Effects of Essential Oil of Black Caraway (Nigella sativa L.) Seeds against Drug-Resistant Clinically Pathogenic Microorganisms. Biomed. Res. Int. 2022, 2022, 5218950. [Google Scholar] [CrossRef]
  65. Elshafie, H.S.; Mancini, E.; Camele, I.; De Martino, L.; De Feo, V. In Vivo Antifungal Activity of Two Essential Oils from Mediterranean Plants against Postharvest Brown Rot Disease of Peach Fruit. Ind. Crops Prod. 2015, 66, 11–15. [Google Scholar] [CrossRef]
  66. Setzer, W.N. Leaf and Bark Essential Oil Compositions of Bursera simaruba from Monteverde, Costa Rica. Am. J. Essent. Oils Nat. Prod. 2014, 1, 34–36. [Google Scholar]
  67. Pourbafrani, M.; Forgács, G.; Horváth, I.S.; Niklasson, C.; Taherzadeh, M.J. Production of Biofuels, Limonene and Pectin from Citrus Wastes. Bioresour. Technol. 2010, 101, 4246–4250. [Google Scholar] [CrossRef]
  68. Andrade, M.A.; Barbosa, C.H.; Shah, M.A.; Ahmad, N.; Vilarinho, F.; Khwaldia, K.; Silva, A.S.; Ramos, F. Citrus By-Products: Valuable Source of Bioactive Compounds for Food Applications. Antioxidants 2022, 12, 38. [Google Scholar] [CrossRef]
  69. Han, Y.; Sun, Z.; Chen, W. Antimicrobial Susceptibility and Antibacterial Mechanism of Limonene against Listeria monocytogenes. Molecules 2019, 25, 33. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  70. Suri, S.; Singh, A.; Nema, P.K. Current Applications of Citrus Fruit Processing Waste: A Scientific Outlook. Appl. Food Res. 2022, 2, 100050. [Google Scholar] [CrossRef]
  71. Nagoor Meeran, M.F.; Seenipandi, A.; Javed, H.; Sharma, C.; Hashiesh, H.M.; Goyal, S.N.; Jha, N.K.; Ojha, S. Can Limonene Be a Possible Candidate for Evaluation as an Agent or Adjuvant against Infection, Immunity, and Inflammation in COVID-19? Heliyon 2021, 7, e05703. [Google Scholar] [CrossRef]
  72. Nagy, M.M.; Al-Mahdy, D.A.; Abd El Aziz, O.M.; Kandil, A.M.; Tantawy, M.A.; El Alfy, T.S.M. Chemical Composition and Antiviral Activity of Essential Oils from Citrus reshni Hort. Ex Tanaka (Cleopatra mandarin) Cultivated in Egypt. J. Essent. Oil Bear. Plants 2018, 21, 264–272. [Google Scholar] [CrossRef]
  73. Shojaei, S.; Kiumarsi, A.; Moghadam, A.R.; Alizadeh, J.; Marzban, H.; Ghavami, S. Perillyl Alcohol (Monoterpene Alcohol), Limonene. In The Enzymes; Academic Press: Cambridge, MA, USA, 2014; pp. 7–32. [Google Scholar]
  74. Fahmy, N.M.; Elhady, S.S.; Bannan, D.F.; Malatani, R.T.; Gad, H.A. Citrus reticulata Leaves Essential Oil as an Antiaging Agent: A Comparative Study between Different Cultivars and Correlation with Their Chemical Compositions. Plants 2022, 11, 3335. [Google Scholar] [CrossRef]
  75. Polito, F.; Kouki, H.; Khedhri, S.; Hamrouni, L.; Mabrouk, Y.; Amri, I.; Nazzaro, F.; Fratianni, F.; De Feo, V. Chemical Composition and Phytotoxic and Antibiofilm Activity of the Essential Oils of Eucalyptus bicostata, E. Gigantea, E. Intertexta, E. Obliqua, E. Pauciflora and E. Tereticornis. Plants 2022, 11, 3017. [Google Scholar] [CrossRef]
  76. Khedhri, S.; Polito, F.; Caputo, L.; Manna, F.; Khammassi, M.; Hamrouni, L.; Amri, I.; Nazzaro, F.; De Feo, V.; Fratianni, F. Chemical Composition, Phytotoxic and Antibiofilm Activity of Seven Eucalyptus Species from Tunisia. Molecules 2022, 27, 8227. [Google Scholar] [CrossRef] [PubMed]
  77. Juergens, L.J.; Worth, H.; Juergens, U.R. New Perspectives for Mucolytic, Anti-Inflammatory and Adjunctive Therapy with 1,8-Cineole in COPD and Asthma: Review on the New Therapeutic Approach. Adv. Ther. 2020, 37, 1737–1753. [Google Scholar] [CrossRef] [Green Version]
  78. Sharma, A.D.; Kaur, I. Molecular Docking Studies on Jensenone from Eucalyptus Essential Oil as a Potential Inhibitor of COVID 19 Corona Virus Infection. arXiv 2020, arXiv:2004.00217. [Google Scholar]
  79. Seol, G.H.; Kim, K.Y. Eucalyptol and Its Role in Chronic Diseases. In Eucalyptol and Its Role in Chronic Diseases; Springer: Cham, Switzerland, 2016; pp. 389–398. [Google Scholar]
  80. Usachev, E.V.; Pyankov, O.V.; Usacheva, O.V.; Agranovski, I.E. Antiviral Activity of Tea Tree and Eucalyptus Oil Aerosol and Vapour. J. Aerosol. Sci. 2013, 59, 22–30. [Google Scholar] [CrossRef]
  81. Astani, A.; Reichling, J.; Schnitzler, P. Comparative Study on the Antiviral Activity of Selected Monoterpenes Derived from Essential Oils. Phytother. Res. 2010, 24, 673–679. [Google Scholar] [CrossRef] [PubMed]
  82. Oriola, A.O.; Oyedeji, A.O. Essential Oils and Their Compounds as Potential Anti-Influenza Agents. Molecules 2022, 27, 7797. [Google Scholar] [CrossRef] [PubMed]
  83. Deng, C.; Song, G.; Hu, Y. Application of HS-SPME and GC-MS to Characterization of Volatile Compounds Emitted from Osmanthus Flowers. Ann. Chim. 2004, 94, 921–927. [Google Scholar] [CrossRef]
  84. Jürgens, A.; Witt, T.; Gottsberger, G. Flower Scent Composition in Night-Flowering Silene Species (Caryophyllaceae). Biochem. Syst. Ecol. 2002, 30, 383–397. [Google Scholar] [CrossRef]
  85. Ashokkumar, K.; Vellaikumar, S.; Murugan, M.; Dhanya, M.K.; Ariharasutharsan, G.; Aiswarya, S.; Akilan, M.; Warkentin, T.D.; Karthikeyan, A. Essential Oil Profile Diversity in Cardamom Accessions from Southern India. Front. Sustain. Food Syst. 2021, 5, 639619. [Google Scholar] [CrossRef]
  86. Liu, Z.; Zhao, M.; Li, J. Aroma Volatiles in Litchi Fruit: A Mini-Review. Horticulturae 2022, 8, 1166. [Google Scholar] [CrossRef]
  87. Shen, Q.; Li, H.; Wang, Q.; Wang, J.; Ge, J.; Yang, X.; Wang, X.; Li, X.; Zhang, Y.; Zhang, R.; et al. Alleviating Effects of Linalool Fumigation on Botrytis Cinerea Infections in Postharvest Tomato Fruits. Horticulturae 2022, 8, 1074. [Google Scholar] [CrossRef]
  88. Marchese, A.; Orhan, I.E.; Daglia, M.; Barbieri, R.; Di Lorenzo, A.; Nabavi, S.F.; Gortzi, O.; Izadi, M.; Nabavi, S.M. Antibacterial and Antifungal Activities of Thymol: A Brief Review of the Literature. Food Chem. 2016, 210, 402–414. [Google Scholar] [CrossRef]
  89. Salehi, B.; Mishra, A.P.; Shukla, I.; Sharifi-Rad, M.; del Contreras, M.M.; Segura-Carretero, A.; Fathi, H.; Nasrabadi, N.N.; Kobarfard, F.; Sharifi-Rad, J. Thymol, Thyme, and Other Plant Sources: Health and Potential Uses. Phytother. Res. 2018, 32, 1688–1706. [Google Scholar] [CrossRef] [PubMed]
  90. Nagoor Meeran, M.F.; Javed, H.; Al Taee, H.; Azimullah, S.; Ojha, S.K. Pharmacological Properties and Molecular Mechanisms of Thymol: Prospects for Its Therapeutic Potential and Pharmaceutical Development. Front Pharm. 2017, 8, 380. [Google Scholar] [CrossRef] [Green Version]
  91. Kowalczyk, A.; Przychodna, M.; Sopata, S.; Bodalska, A.; Fecka, I. Thymol and Thyme Essential Oil—New Insights into Selected Therapeutic Applications. Molecules 2020, 25, 4125. [Google Scholar] [CrossRef]
  92. Glavinic, U.; Blagojevic, J.; Ristanic, M.; Stevanovic, J.; Lakic, N.; Mirilovic, M.; Stanimirovic, Z. Use of Thymol in Nosema ceranae Control and Health Improvement of Infected Honey Bees. Insects 2022, 13, 574. [Google Scholar] [CrossRef] [PubMed]
  93. Trivellini, A.; Lucchesini, M.; Ferrante, A.; Massa, D.; Orlando, M.; Incrocci, L.; Mensuali-Sodi, A. Pitaya, an Attractive Alternative Crop for Mediterranean Region. Agronomy 2020, 10, 1065. [Google Scholar] [CrossRef]
  94. Lee, Y.-C.; Chang, J.-C. Development of an Improved Micropropagation Protocol for Red-Fleshed Pitaya ‘Da Hong’ with and without Activated Charcoal and Plant Growth Regulator Combinations. Horticulturae 2022, 8, 104. [Google Scholar] [CrossRef]
  95. Adams, R.P. Identification of Essential Oils by Ion Trap Mass Spectroscopy; Academic Press: Cambridge, MA, USA, 2012. [Google Scholar]
  96. Abdi, H.; Lynne, J. Williams Tukey’s Honestly Significant Difference (HSD) Test. Encycl. Res. Des. 2010, 3, 1–5. [Google Scholar]
Figure 1. Hylocereus undatus motherplant in vitro cultures.
Figure 1. Hylocereus undatus motherplant in vitro cultures.
Molecules 28 03843 g001
Table 1. Comparison of percentage use for volatile pitaya plants grown in vitro on two variants of MS medium with the addition of BA or IAA.
Table 1. Comparison of percentage use for volatile pitaya plants grown in vitro on two variants of MS medium with the addition of BA or IAA.
No.CompoundExperimental Retention
Index
Litrature Retention IndexBA [%]SD IAA
[%]
SD
1Hexanal8078066.87 e*±1.134.53 ef±0.45
22-Hexenal85886022.53 d±3.7425.48 c±2.77
31-Hexanol86286840.89 a±3.5836.44 d±2.02
42-Heptenal, (Z)-9619641.12 g±0.180.79 g±0.09
52-Hexenoic acid, methyl ester, (E)-9709661.94 fg±0.840.99 g±0.49
61-Heptanol974970--0.24 g±0.25
71-Octen-3-ol983980--0.35 g±0.32
83-Octanone, 2-methyl-9879850.59 g±0.442.67 fg±1.72
9Hexanoic acid9899810.91 g±0.691.05 g±0.53
10Furan, 2-pentyl-9929930.67 g±0.270.39 g±0.08
11Octanal10041007--1.04 g±1.01
12o-Cymene10291022--0.82 g±0.64
13Limonene103410311.26 g±0.310.95 g±0.22
14Eucalyptol103610331.66 g±0.110.93 g±0.18
15Pyrazine, 3-methoxy-2.5-dimethyl-105710540.39 g±0.260.43 g±0.09
161-Octanol107410820.70 g±0.350.60 g±0.26
17Heptanoic acid108210780.45 g±0.30--
18Pyrazine, 2-methoxy-3-(1-methylethyl)-109610931.27 g±0.092.07 fg±0.36
19Linalool110011031.49 g±0.240.57 g±0.07
20Nonanal110511040.67 g±0.171.30 g±1.29
21Hexanoic acid, 2-ethyl-11261123--0.85 g±0.64
22Benzene, 1.2-dimethoxy-114911491.13 g±0.230.78 g±0.12
23Pyrazine, 2-methoxy-3-(1-methylpropyl)-117511752.55 fg±0.982.45 fg±0.71
24Octanoic Acid117911820.66 g±0.350.98 g±0.40
25Pyrazine, 2-methoxy-3-(2-methylpropyl)-118211921.03 g±0.221.31 g±0.07
26Ethanol, 2-(2-butoxyethoxy)-11901196--0.36 g±0.23
27Decanal120512060.89 g±0.230.51 g±0.08
282-Decenal12631270--0.60 g±0.76
29Nonanoic acid127712801.24 g±0.321.06 g±0.90
30Thymol129312910.67 g±0.111.60 g±1.18
31Unknow 11359-0.74 g±0.370.65 g±0.20
32Unknow 21375-0.55 g±0.221.49 g±0.69
33Unknow 31379-1.07 g±0.610.63 g±0.59
34Tetradecane13991400--0.59 g±0.51
35Geranyl acetone14571452--0.27 g±0.05
361-Dodecanol147814732.42 fg±1.121.33 g±0.26
37β-Ionone149014940.51 g±0.100.59 g±0.05
38Octanoic acid,
hexyl ester
158415800.53 g±0.28--
39Unknow 41638-0.43 g±0.440.78 g±0.09
40Octyl ether166716570.66 g±0.180.27 g±0.06
41Unknow 51680-0.60 g±0.250.54 g±0.15
42Norphytan170717030.10 g±0.030.30 g±0.08
43Phytan181118110.84 g±0.580.41 g±0.16
* Values followed by the different letter are significantly different (p > 0.05, Tukey’s test); SD standard deviation.
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Jakobina, M.; Łyczko, J.; Zydorowicz, K.; Galek, R.; Szumny, A. The Potential Use of Plant Growth Regulators for Modification of the Industrially Valuable Volatile Compounds Synthesis in Hylocreus undatus Stems. Molecules 2023, 28, 3843. https://doi.org/10.3390/molecules28093843

AMA Style

Jakobina M, Łyczko J, Zydorowicz K, Galek R, Szumny A. The Potential Use of Plant Growth Regulators for Modification of the Industrially Valuable Volatile Compounds Synthesis in Hylocreus undatus Stems. Molecules. 2023; 28(9):3843. https://doi.org/10.3390/molecules28093843

Chicago/Turabian Style

Jakobina, Maciej, Jacek Łyczko, Kinga Zydorowicz, Renata Galek, and Antoni Szumny. 2023. "The Potential Use of Plant Growth Regulators for Modification of the Industrially Valuable Volatile Compounds Synthesis in Hylocreus undatus Stems" Molecules 28, no. 9: 3843. https://doi.org/10.3390/molecules28093843

Article Metrics

Back to TopTop