Growth and volatiles in the micropropagation of Santa Maria herb¹

Crescimento e voláteis na micropropagação de Erva-de-Santa-Maria

ABSTRACT

The aims of this study were to establish micropropagation for Chenopodium ambrosioides L. and analysis of volatile constituents in vitro as a function of different salt concentrations of MS medium and sucrose. The apical buds were established on MS medium added with 3% sucrose. The vegetative growth of nodal segments was tested in different salt concentrations of MS basic medium (0.25, 0.50, 1.00, 1.50, and 2.00) and of sucrose (5, 10, 20, 30, and 40 g L^-1). Nodal and apical segments were tested in vertical and horizontal orientations. Different volumes of culture medium (20; 35, 50, 65, and 80 mL) were examined in the growth of nodal segments. Plants were acclimatized in three different substrates. The apical segments collected from matrices plants were successful when established in MS medium. A multiplication rate of 8.5 was obtained with nodal and apical segments without using growth regulator. MS medium with its salt concentration reduced by half (0.50 MS) and sucrose at the concentration of 30 g L^-1 provided better in vitro growth of nodal segments. Four major volatile compounds (α-terpinene, p-cymene, Z-ascaridole, and E-ascaridole) varied at different salt concentrations and only α-terpinene showed difference for sucrose concentrations. Apical segments in vertical orientation and nodal segments in horizontal with 50 mL of culture medium showed better responses for the in vitro cultivation of C. ambrosioides L.

Key words:
Chenopodium ambrosioides L.; Medicinal plant; Tissue culture

RESUMO

Objetivou-se com o presente trabalho estabelecer a micropropagação para Chenopodium ambrosioides L. e análise de constituintes voláteis in vitro em função de diferentes concentrações de sais do meio MS e de sacarose. As gemas apicais foram estabelecidas em meio MS acrescido de 3% de sacarose. O crescimento vegetativo dos segmentos nodais foi testado em diferentes concentrações de sais do meio básico MS (0,25; 0,50; 1,00; 1,50 e 2,00) e de sacarose (5; 10; 20; 30 e 40 g L^-1). Segmentos nodais e apicais foram testados nas orientações vertical e horizontal. Diferentes volumes de meio de cultura (20; 35; 50; 65 e 80 mL) foram examinados no crescimento de segmentos nodais. As plantas foram aclimatizadas em três diferentes substratos. Os segmentos apicais coletados de plantas matrizes obtiveram sucesso ao estabelecerem-se em meio MS. Uma taxa de multiplicação de 8,5 foi obtida com segmento nodal e apical sem a utilização de regulador de crescimento. O meio MS com sua concentração de sais reduzida pela metade (0,50 MS) e a sacarose na concentração de 30 g L^-1 proporcionaram melhor crescimento in vitro de segmentos nodais. Quatro principais compostos voláteis (α-terpineno, p-cimeno, Z-ascaridol e E-ascaridol) variaram nas diferentes concentrações de sais e para as concentrações de sacarose, apenas o α-terpineno apresentou diferença. Segmentos apicais na orientação vertical e segmentos nodais na horizontal, com 50 mL de meio de cultura, apresentaram melhores respostas para o cultivo in vitro de C. ambrosioides L.

Palavras-chave:
Chenopodium ambrosioides L.; Planta medicinal; Cultura de tecidos

INTRODUCTION

Chenopodium ambrosioides L. is a medicinal herb and spice popularly known worldwide, by names: Mexican tea, wormseed, "epazote", "mastruz" and "Erva-de-santa-Maria" (BLANCKAERT et al., 2012). It is used as anthelmintic, anti-inflammatory, anti-Leishmania, antidiarrheal, among other (CYSNE et al., 2016). The plant's anthelmintic property has been attributed to the presence of the monoterpene ascaridole, with few species showing capacity to produce it (SÁ; SOARES; RANDAU, 2015). Its therapeutic potential was recognized in such a way that the Brazilian Ministry of Health included it in the National List of Medicinal Plants of Interest to the SUS (Relação Nacional de Plantas Medicinais de Interesse ao SUS - RENISUS)(VERISSIMO et al., 2011).

C. ambrosioides L. seeds present a high dormancy degree revealed by low germinative power (MARTINS; SILVA; JUNIOR, 2010). Medicinal plants are usually collected in their natural habitats and this practice harms the environment and can cause the extinction of species (DEBNATH; MALIK; BISEN, 2006). Thus, micropropagation represents a viable alternative for the rapid propagation of large numbers of clones in a small space, besides preserving germplasm and producing compounds of secondary metabolism.

According to Morais et al. (2012), micropropagation allows studying the accumulation of secondary metabolites and choosing of new species sources of bioactive compounds, improving the phytopharmaceutical production. Still according to these authors, the agricultural production of medicinal plants in pharmaceutical standards can be compromised by the heterogeneity of individuals due to the genetic and biochemical variability and difficulty of multiplication.

In the in vitro cultivation, a large amount of plant biomass can be obtained by using bioreactors and thus increasing the content of secondary metabolites of interest. When comparing in vitro and in vivo essential oil composition, Manan et al. (2016) observed that the amount of methyl chavicol of Ocimum basilicum in vitro (93.71%) exceeded the amount found in plants in vivo (66.29%). According to Mendes et al. (2013), the amount of monoterpene sabinene was higher in shoots of Thymus caespititius cultivated in vitro (40-45%) than in plants grown in vivo (18%).

In order to conduct in vitro studies, factors as the type and concentration of the culture medium must be studied and adjusted for each species, making available mineral elements essential for plant metabolism and the sucrose concentration suitable for energy supply and precursor carbons for the biosynthesis of structural and functional components (JO et al., 2009; PIVETTA et al., 2010; REIS et al., 2009).

The aim of this study was to establish micropropagation for C. ambrosioides L. and to study the influence of different salt concentrations of MS medium and sucrose on the growth of species and their relationships with volatile constituents in vitro.

MATERIAL AND METHODS

General conditions of the experiments

In all experiments, autoclaving of the culture medium was performed at 120ºC and 1 atm for 20 min. The tubes or flasks were kept in a growth room with photoperiod of 16 h of light, temperature of 25 ± 2 ºC and photon flux density of 32 µmol m^-2 s^-1 (PAR Photon Flux Sensor, ProCheck -Decagon devices); the pH of the culture medium was adjusted to 5.7 ± 0.1 before autoclaving and the culture medium was supplemented with 0.6% agar.

The growth variables shoot length (SL), number of shoots (NS) and leaves (NL), leaf (LDW), shoot (SDW), root (RDW), and total dry weight (TDW) were evaluated after 40 days. SL variable expresses the size of the main shoot measured from its base to the apical bud. The evaluation was performed with the aid of a digital caliper. LDW, SDW and RDW were measured on a precision scale after drying in a convection oven at 35 ºC for three days. TDW was obtained by the sum of RDW, SDW and LDW.

Establishment of explant

Wild plants from C. ambrosioides L. species located in the medicinal herb garden of UFLA were used as seed source. The exsiccate was deposited in the herbarium of the Department of Biology of this Institution under record 10137. The seeds were collected and sowed in a polystyrene tray of 128 cells, containing commercial Plantmax^® substrate in order to obtain matrix plants. After 60 days, the germinated plants were transplanted into 3.6 L polyethylene pots, containing the same substrate and kept in a greenhouse with irrigation.

After 30 days, the apical segments were collected from these transplanted plants and washed in running water and neutral soap for 30 min. In a laminar flow cabinet, the explants were immersed in 70% ethyl alcohol for 30 s, followed by a 40% bleach solution for 10 min and finally washed five times in distilled and autoclaved water. At the end of the asepsis, the explants were inoculated into 120 test tubes containing 15 mL of MS culture medium (MURASHIGE; SKOOG, 1962) and 3% sucrose. The tubes were capped and sealed with paraffin film and kept in the growth room. At 40 days, the percentage of contamination and plants established in vitro was evaluated.

Concentrations of salts, sucrose, and volume of culture medium

Nodal segments of, approximately, 2 cm length obtained from plants established in vitro were used as explants for all the three experiments. For each experiment, a completely randomized design (CRD) with four replications was used. The experimental unit was represented by three flasks containing three segments per replicate.

For the study of salt and sucrose concentrations of the MS medium, nodal segments were inoculated vertically in, 250 mL, flasks containing 35 mL of the medium at five different MS concentrations (2.00, 1.50, 1.00, 0.50, and 0.25) and five sucrose concentrations (5, 10, 20, 30, and 40 g L^-1). Nodal segments were inoculated vertically in flasks containing different solution volumes (20; 35, 50, 65, and 80 mL) of the culture medium.

Orientations of apical and nodal segments

Nodal and apical segments were inoculated in the vertical and horizontal orientations in the half of the MS salt concentration and supplemented with 30 g L^-1 sucrose. The experimental design was completely randomized (CRD) in a 2x2 factorial design, being the explant type factor with two levels (apical and nodal) and the explant orientation factor (vertical and horizontal). Five replicates were used and the experimental unit consisted of three flasks, containing three segments per replicate.

Acclimatization of plants

After 40 days, the micropropagated plants were removed from the culture flasks, washed in running water, transferred to 53 cm³ plastic tubes containing three types of substrates (ProVaso^®, vermiculite, and sand) and kept in a greenhouse with irrigation. The used experimental design was the completely randomized (CRD) with seven replications. The experimental unit was represented by four tubes containing, one plant each. After 30 days, the percentage of surviving plants was evaluated.

Chemical analysis by headspace GC/MS

The leaves were collected from plants at 40 days of in vitro culture from experiments of different salt concentrations of MS and sucrose. Samples were dried in a convection oven at 35 ºC. For analysis of the volatile constituents, 60 mg of dry leaves were used in triplicate.

The chemical analyses were performed by headspace -CG/MS, using an Agilent^® 7890A gas chromatograph coupled to an Agilent^® MSD 5975C mass selective detector. The operating conditions were established with the following parameters: sample incubation temperature of 110 ºC for 30 min, syringe temperature at 120 ºC. A HP-5MS fused silica capillary column (30 m long x 0.25 mm internal diameter x 0.25 µm film thickness) was used.

Volatile fraction constituents were identified by comparing their retention indices relative to the co-injection of a standard solution of n-alkanes (C8-C20, Sigma-Aldrich®, St. Louis, USA) and by comparing mass spectra from the database of NIST/EPA/NHI (NATIONAL INSTITUTE OF STANDARDS TECHNOLOGY, 2008) and of the literature (ADAMS, 2007).

Statistical analysis

Statistical analyses were performed using R software and the statistical package ExpDes (FERREIRA; CAVALCATI; NOGUEIRA, 2011), according to R DEVELOPMENT CORE TEAM (2012). The regression analysis for quantitative factors and the Tukey test, for qualitative factors were used for treatments whose averages showed significant differences at a 5% probability level.

RESULTS AND DISCUSSION

The establishment and asepsis of apical segments inoculated in complete MS medium, supplemented with 30 g L^-1 sucrose were efficient with 98.3% survival. Apical segments inoculated in the MS medium had an approximate growth of 4 cm after 40 days, with a greenish staining.

The established plants were inoculated at different salt concentrations of MS medium and sucrose in order to study the influence of these factors on the growth of species and its relationships with the in vitro volatile constituents. Differences in herb growth were observed for the proposed treatments (Figure 1).

Figure 1
Micropropagated plants of C. ambrosioides L. cultivated in: A- different salt concentrations of the MS medium and Bdifferent concentrations of sucrose in the medium

The MS medium has a macronutrient and micronutrient composition of 4.41 g L^-1. It is considered as a culture medium with high salt concentrations (MONFORT et al., 2015). Thus, the MS medium in its original, lower and higher salt concentrations were tested. The analyzed explant growth variables showed significant differences in the salt concentrations of MS medium (Figure 2).

Figure 2
Effect of different salt concentrations of MS medium in: A- shoot length (SL), B- number of leaves (NL), C- number of shoots (NS), D- leaf dry weeight (LDW), E- shoot dry weight (SDW), F- root dry weight (RDW), and G- total dry weight (TDW) of C. ambrosioides L plants cultivated in vitro

RDW declined linearly in increasing salt concentrations. For the other analyzed variables, significance for quadratic regression was verified and the maximum points were calculated for each function. The estimated maximum shoot length was 61.84 mm at the concentration of 0.54 MS. The maximum number of leaves (24.27) and shoots (2.13) were obtained at concentrations of 0.90 and 0.88 MS, respectively. In relation to the dry weight, 22.13, 10.17, and 14.89 mg at the salt concentrations 1.05, 0.74, and 0.25 MS were verified for leaf, shoot, and root, respectively.

The lower salt concentration (0.25 MS) affected root growth. RDW decreased significantly from 0.25 MS to 2.00 MS. George, Hall and Klerk (2008) state that the addition of components to the culture medium, especially macronutrients and carbon sources, represents a considerable decrease in the osmotic potential of the medium. The effect of salt concentration of the medium can affect the availability of water to the roots (osmotic stress) and absorption of salts by the plant can reach a toxic level in the tissue (ionic stress). In general, the effect of salt stress on growth can reduce dry weight, leaf area, root length, shoot length, and senescence if the concentration is beyond the tolerated limit (TAIZ; ZEIGER, 2009).

Monfort et al. (2015) observed higher root length using low salt level (0.25 MS), which may be mainly due to the decrease in nitrogen level. The MS, 0.5 MS, and 0.25 MS media contain 60 mM, 30 mM, and 15 mM nitrogen, respectively. Also according to these authors, root growth is inhibited by NH4⁺ and promoted by NO₃^-. A higher nitrate/ammonium ratio in medium with lower nitrogen concentration may have occurred to aid in rooting.

TDW of the plant was between half and the original salt concentration of the MS medium, reaching a maximum of 0.89 of the MS concentration, with a weight gain of 45.82 mg.

The reduction or gain in growth of the explant grown under salt conditions is a consequence of several physiological responses, including changes in ionic balance, water availability, mineral nutrition, photosynthetic efficiency, and carbon allocation and utilization. Qiu, Lu and Lu (2003) report that the reduction in growth observed in several species subjected to salt concentration is often associated with a decrease in photosynthetic capacity.

In relation to nutrient absorption, lower concentrations (0.25 MS) may limit some nutrient essential for plant metabolism (EPSTEIN; BLOOM, 2005). On the other hand, the excess of one ion reduces the absorption of another. According to Paula et al. (2015), the K absorption is inhibited when the Mg concentration is high (competitive inhibition). Moreira et al. (2003) observed that in the presence of high concentrations of Mg²⁺, the absorption of Zn and Mn is impaired. According to these authors, the inhibition of Mg²⁺ on the absorption of Zn and Mn refers to the non-competitive type. Zinc is a very important element, since it is directly responsible for the synthesis of tryptophan, a precursor of auxin (indoleacetic acid), and indirectly for protein synthesis(VILLA et al., 2009).

Regarding the volatile chemical composition, four constituents represented 92.27% of the total relative area of chromatographic peaks in the plant samples grown at different salt concentrations of MS medium. The constituents were α-terpinene (20.06%), p-cymene (16.65%), Z-ascaridole (45.81%), and E-ascaridole (9.75%), being that the indicated contents indicate the average of treatments. Cavalli et al. (2004) identified five constituents in the essential oil of Chenopodium ambrosioides L., characterized by Z -ascaridole (58.38%), p-cymene (16.2%), α-terpinene (9.7%), E-ascaridole (4.3%) and limonene (3.8%).

Comparing the volatile chemical composition of the cultivated plant in the normal MS medium and the other concentrations, there were significant differences among the relative areas of the constituent peaks (Figure 3).

Figure 3
Relative area (%) of chromatographic peaks of the main constituents of the volatile fraction of C. ambrosioides L. grown in vitro in different salt concentrations of MS medium

The compounds were shown in greater relative area percentage for salt concentrations of MS medium in 1.79 MS (α-terpinene), 2.00 MS (p-cymene) 0.79 MS (Z-ascaridole), and 0.71 MS (E-ascaridole). It can also be observed that the decrease in α-terpinene content resulted in increases in ascaridole (Z) and its isomer (E), as well as the opposite. This relationship occurred because terpinene is a precursor of ascaridole biosynthesis (DEMBITSKYA; SHKROBB; HANUSA, 2008). For the monoterpenes Z and E -ascaridol, the maximum content was observed in the concentration of culture medium that provided the greatest growth of nodal segments (between 0.50 and 1.00 MS).

Studies on the factors that affect the volatile composition of C. ambrosioides L. are important to obtain plants with higher accumulation of the compounds of interest. The variability in the content of major and/or active constituents is one of the main difficulties of developing herbal medicines with action reproducibility (SÁ; SOARES; RANDAU, 2015).

The culture medium should be supplemented with carbohydrates due to the low photosynthetic activity and irradiation and to the limited gas exchange. It was observed that plants showed maximum growth up to a sucrose concentration limit, followed by a reduction in the evaluated parameters, except for SDW and NS, where they occurred linearly (Figure 4).

Figure 4
Effect of different sucrose concentrations on: A- shoot length (SL), B- number of leaves (NL), C- number of shoots (NS), D- leaf dry weight (LDW), E- shoot dry weight (SDW), F- root dry weight (RDW), and G- total dry weight (TDW) of C. ambrosioides L. plants cultivated in vitro. ^*ns Not significant by F test

Plants showed maximum growth (65.38 mm) at the concentration of 24.25 g L^-1 sucrose, followed by a reduction. The highest LDW estimated was 30.92 mg at the concentration of 33.75 g L^-1. The most efficient concentration of sucrose for RDW accumulation was 34 g L^-1 for a gain of 10.97 mg. The maximum sucrose concentration for TDW accumulation was 29.88 g L^-1 with, a gain of 47.72 mg by regression curve analysis (Figure 4).

Monfort et al. (2015) studied the effect of interactions between three MS variations (MS, 0.5 MS, and 0.25 MS) and three sucrose concentrations (0, 15, and 30 g L^-1) on the growth of in vitro nodal segments of Ocimum selloi. According to these researchers, there was no effect of the MS medium on the length and weight of shoots in the absence of sucrose. This result demonstrated the importance of sucrose in the basic medium in order to provide energy for shoot growth.

For the environmental conditions of the present study, it was observed that the low sucrose concentration (5 g L^-1) culminated in lower results for all variables with significant differences. In the in vitro culture, sucrose acts as a source of energy and provides carbons that will be used during respiration and are precursors for the biosynthesis of structural and functional components, such as oligosaccharides, amino acids and other molecules necessary for growth (TORRES; CALDAS; BUSO, 1998).

The highest concentration of this carbohydrate (40 g L^-1) did not interfere in SDW and NS. However, there was inhibition of explant growth in the other parameters.

It is observed a decrease in the weight gain by the behavior of the regression curve in concentrations above 30 g L^-1 of sucrose. According to Desjardins, Dubuc and Badr (2009) and Villa et al. (2006), excess sucrose may be harmful because the presence of carbohydrate in the culture medium inhibits the synthesis of chlorophyll and increases the osmotic potential of the medium. Therefore, it reduces the photosynthetic capacity of the crops, even being essential for growth.

Similarly to the experiment with the salt concentration of the MS medium, the presence of the same four volatile constituents (α-terpinene, p-cymene, Z-ascaridole, and E-ascaridole) were observed. However, different concentrations of sucrose did not significantly influence the content of p-cymene, Z-ascaridole, and E-ascaridole. In sucrose additions, only the α-terpinene content increased linearly (Figure 5).

Figure 5
Relative area (%) of chromatographic peaks of the main constituents of the volatile fraction of C. ambrosioides L. grown in vitro at different sucrose concentrations. ^*ns Not significant by F test

Figure 6A shows the growth of plants resulting from the inoculation of nodal and apical segments in the vertical and horizontal orientations. In Figure 6B, nodal segments were inoculated vertically in flasks containing different solution volumes of medium (20; 35, 50, 65, and 80 mL).

Figure 6
Micropropagated plants of C. ambrosioides L. after 40 days, cultivated in: A- different orientations of nodal and apical segments and B- different volumes of medium (mL)

For NS and NL, there was not significant interaction between orientation and explant type. In the vertical orientation, there was higher leaf production per plant and NS was not statistically influenced, as well as the explant type (apical and nodal) for these variables. However, the interaction was significant for SL, SDW, RDW, and LDW (Table 1).

Table 1
Shoot length, shoot, leaf and root dry weight of apical buds and nodal segments of C. ambrosioides L. grown in vitro in vertical and horizontal orientations

Variables	Types	Orientation
		Vertical	Horizontal
Shoot length (mm)	Apical	57.75 Aa	39.23 Bb
	Nodal	51.34 Aa	50.10 Aa
Shoot dry weight (mg)	Apical	10.74 Aa	7.80 Ab
	Nodal	8.50 Ba	16.04 Aa
Leaf dry weight (mg)	Apical	21.36 Aa	15.28 Ba
	Nodal	15.56 Ab	16.78 Aa
Root dry weight (mg)	Apical	12.42 Aa	7.84 Ba
	Nodal	8.54 Ab	9.96 Aa
Total dry weight (mg)	Apical	44.52 Aa	30.92 Bb
	Nodal	32.66 Bb	42.78 Aa

• Averages followed by the same capital letter on the line and lowercase on the column do not differ significantly among themselves by Tukey test at 5% significance

It is observed that, in absolute values, the apical segment inoculated in the culture medium in the vertical position obtained greater growth gain, which not occurred in the horizontal position (Table 1). In these segments, the highest growth may be due to apical dominance. It is known that auxin is synthesized at the shoot apical and transported towards the base, giving greater development. This transport is called polar auxin transport. Therefore, it does not occur when the apical segment is inoculated in the horizontal position.

In relation to nodal segments, the horizontal position favored the growth in relation to apical segments. According to Erig and Schuch (2002), obtaining a higher number of shoots with the nodal segment in the horizontal orientation is mainly due to the breakdown of apical dominance, which in this orientation may have inhibited the auxin polar translocation, with a higher sprouting in nodal segments.

The response to plant growth depends on the genotype. Papafotiou and Martini (2009), studied leaf explants of Zamioculcas zamiifolia and observed that the horizontal explant orientation provided less development compared to the vertical orientation. However, Botrel et al. (2015) observed in Hyptis marrubioides and Silva et al. (2017) in Aloysia triphylla, higher dry weight gain in the horizontal position.

Nodal segments were inoculated vertically in flasks containing different solution volumes (20; 35, 50, 65, and 80 mL) of the 0.5 MS culture medium, supplemented with 30 g L^-1 sucrose. The studied response variables showed significant differences. SL showed cubic behavior and the other quadratic behavior (Figure 7).

Figure 7
A- shoot length (SL), B-log of number of leaves (NL)*, C- number of shoots (NS), D- leaf dry weight (LDW), Eshoot dry weight (SDW), and F- root dry weight (RDW) of C. ambrosioides L. grown in vitro in different volumes of culture solution. *Variable transformed by log (Y)

The maximum values for SL (62.48 mm), NL (43.82), and NS (5.03), occurred in volumes 42.25, 64.31, and 60.34 mL, respectively. The most efficient volume for accumulation of LDW (28.86 mg), SDW (22.11 mg), and RDW (28.57 mg) was observed at 60.53, 60.06, and 63.02 mL, respectively.

The type of vial and the amount of used culture medium are variables that have received little attention, although they directly affect the surface area of the culture medium-atmosphere interface, the depth and the volume of air over the culture medium, being that the use of ideal container for each species can optimize its production speed (MORAES et al., 2010). Pereira et al. (2006) and Reis et al. (2007) studied the proliferation of 'curauá' in vitro (Ananas erectifolius) and the micropropagation of lemon balm (Melissa officinalis), respectively, using growing volumes of culture medium. These researchers observed that the increase in volume (30-40 mL) positively affected the growth of micropropagated plants.

The economic feasibility study was not performed. However, it can be observed generically that volumes of culture medium higher than 50 mL did not provide increasing increments in the explant growth. It is also worth noting that, when multiplying this species, either by apical or nodal segments, there will be no great differences in the number of plants that will be obtained between the volumes of 50 and 80 mL based on NS (apical buds) and NL (axillary buds) from both treatments. However, it will use 1.6 x more of culture medium, 80 mL when compared to 50 mL, in order to obtain the same multiplication rate.

The multiplication rate through the apical and nodal segments presented an average of 8.50, reflecting a satisfactory methodology of micropropagation. It is also emphasized the non-use of growth regulators. The most important is to obtain a satisfactory multiplication rate with the minimum variation among explants, the culture medium being one of the variables that can be used for this study (REIS et al., 2008).

Nodal and apical culture is considered as ideal to reduce the risks of genetic irregularity. Since cellular dedifferentiation is not necessary, there is a lower probability of regeneration of plants with somaclonal variation. The plants of the species were acclimatized in sand, vermiculite and ProVaso^® substrate with a survival percentage of 100%.

CONCLUSIONS

1. Apical segments of C. ambrosioides L. matrix plants can be established in vitro with MS medium and 3% sucrose;

2. For better growth and multiplication of nodal segments, the explants should be inoculated in the MS culture medium, with half the original salt concentration and 3% sucrose;

3. Nodal segments can be inoculated in vertical or horizontal orientations. However, the horizontal position allows greater TDW. The apical segments should be inoculated vertically. For greater multiplication efficiency, it is recommended to use 50 mL of culture medium;

4. The percentage of relative area of the major volatiles constituents (α-terpinene, p-cymene, Z-ascaridole, and E -ascaridole) is influenced by the different salt concentrations of the MS medium. The different concentrations of sucrose influence only the α-terpinene content.

• 1
  Pesquisa financiada pelas agências de fomento CAPES, CNPq e FAPEMIG

ACKNOWLEDGEMENTS

The authors would like to thank the National Council for Scientific and Technological Development (CNPq - Conselho Nacional de Desenvolvimento Científico e Tecnológico), the Coordination for the Improvement of Higher Education Personnel (CAPES - Coordenação de Aperfeiçoamento de Pessoal de Nível Superior) and the Minas Gerais State Research Foundation (FAPEMIG - Fundação de Pesquisa do Estado de Minas Gerais) for the financial support (scholarships and research grants).

REFERENCES

• ADAMS, R. P. Identification of essential oil components by gas chromatography/mass spectrometry Illinois: Allured Publishing Corporation, 2007. 804 p.
• BLANCKAERT, I. et al Ethnobotanical, morphological, phytochemical and molecular evidence for the incipient domestication of Epazote (Chenopodium ambrosioides L.: Chenopodiaceae) in a semi-arid region of Mexico. Genetic Resources and Crop Evolution, v. 59, n. 4, p. 557-573, 2012.
• BOTREL, P. P. et al Factors affecting in vitro propagation and chromatographic analysis of compounds in Hyptis marrubioides epl., a threatened medicinal plant. Acta Horticulturae, n. 1083, p. 319-325, 2015.
• CAVALLI, J. F. et al Combined analysis of the essential oil of Chenopodium ambrosioides by GC, GC-MS and 13C-NMR spectroscopy: quantitative determination of ascaridole, a heat-sensitive compound. Phytochemical Analysis, v. 15, n. 5, p. 275-279, 2004.
• CYSNE, D. N. et al Antimalarial potential of leaves of Chenopodium ambrosioides L. Parasitology Research, v. 115, n. 11, p. 4327-4334, 2016.
• DEBNATH, M.; MALIK, C. P.; BISEN, P. S. Micropropagation: a tool for the production of high quality plant-based medicines. Curr Pharm Biotechnol, v. 7, n. 1, p. 33-49, 2006.
• DEMBITSKYA, V.; SHKROBB, I.; HANUSA, L. O. Ascaridole and related peroxides from the genus Chenopodium Biomedical Papers of the Medical Faculty of the UniversityPalacky,Olomouc Czech Republic, v. 152, n. 2, p. 209-215, 2008.
• DESJARDINS, Y.; DUBUC, J. F.; BADR, A. In vitro culture of plants: a stressful activity. Acta Horticulturae, v. 812, p. 29-50, 2009.
• EPSTEIN, E.; BLOOM, A. J. Mineral nutrition of plants: principles and perspectives Davis: University of California, 2005. 380 p.
• ERIG, A. C.; SCHUCH, M. W. Multiplicação in vitro do porta-enxerto de macieira cv. Marubakaido: efeito da orientação do explante no meio de cultura. Revista Brasileira de Fruticultura, v. 24, p. 293-295, 2002.
• FERREIRA, E. B.; CAVALCANTI, P. P.; NOGUEIRA, A. Experimental designs: um pacote R para análise de experimentos. Revista da Estatística da UFOP, v. 1, n. 1, p. 1-9, 2011.
• GEORGE, E. F.; HALL, M. A.; KLERK, G. J. Plant propagation by tissue culture. Volume 1 The background Dordrecht: Springer Science & Business Media, 2008.
• JO, E. A. et al In vitro sucrose concentration affects growth and acclimatization of Alocasia amazonica plantlets. Plant Cell, Tissue and Organ Culture, v. 96, n. 3, p. 307-315, 2009.
• MANAN, A. A. et al In vitro flowering, glandular trichomes ultrastructure, and essential oil accumulation in micropropagated Ocimum basilicum L. In Vitro Cellular & Developmental Biology - Plant, v. 52, n. 3, p. 303-314, 2016.
• MARTINS, G. N.; SILVA, F. D.; ALMASSY JUNIOR, A. A. Superação de dormância em sementes de Chenopodium ambrosioides L. Magistra, v. 22, n. 3/4, p. 205-209, jul./dez., 2010.
• MENDES, M. D. et al Essential oil production in shoot cultures versus field-grown plants of Thymus caespititius Plant Cell, Tissue and Organ Culture, v. 113, n. 2, p. 341-351, 2013.
• MONFORT, L. E. F. et al Micropropagação e germinação de sementes in vitro de atroveran. Revista Ceres, v. 62, p. 215-223, 2015.
• MORAES, C. P. et al Desenvolvimento in vitro de Dendrobium nobile Lindl.(Orchidaceae) em recipientes de diferentes volumes. Revista Brasileira de Biociências, v. 8, n. 2, 2010.
• MORAIS, T. P. et al Aplicações da cultura de tecidos em plantas medicinais. Revista Brasileira de Plantas Medicinais, v. 14, p. 110-121, 2012.
• MOREIRA, A. et al Influência do magnésio na absorção de manganês e zinco por raízes destacadas de soja. Pesquisa Agropecuaria Brasileira, v. 38, p. 95-101, 2003.
• MURASHIGE, T.; SKOOG, F. A revised medium for rapid growth and bio assays with tobacco tissue cultures. Physiologia Plantarum, v. 15, p. 473-497, 1962.
• NATIONAL INSTITUTE OF STANDARDS TECHNOLOGY. PC version 2.0 of the NIST/EPA/NIH mass spectral library Gaithersburg, 2008.
• PAPAFOTIOU, M.; MARTINI, A. N. Effect of position and orientation of leaflet explants with respect to plant growth regulators on micropropagation of Zamioculcas zamiifolia Engl. (ZZ). Scientia Horticulturae, v. 120, n. 1, p. 115-120, 2009.
• PAULA, Y. C. M. et al Micropropagação de bananeira sob diferentes concentrações de potássio e magnésio. Tecnologia & Ciencia Agropecuária, v. 9, n. 3, p. 43-47, 2015.
• PEREIRA, F. D. et al Proliferação in vitro de brotos de curauá utilizando diferentes volumes de meio. Plant Cell Culture and Micropropagation, v. 2, n. 2, p. 53-106, 2006.
• PIVETTA, K. F. L. et al Crescimento in vitro de plântulas de Caularthron bicornutum em diferentes concentrações de sacarose. Ciencia Rural, v. 40, p. 1897-1902, 2010.
• QIU, N.; LU, Q.; LU, C. Photosynthesis, photosystem II efficiency and the xanthophyll cycle in the salt-adapted halophyte Atriplex centralasiatica New Phytologist, v. 159, n. 2, p. 479-486, 2003.
• R DEVELOPMENT CORE TEAM. R: a language and environment for statistical computing. Vienna: R Foundation for Statistical Computing, 2012.
• REIS, E. S. et al Tipos de explantes e volumes de meio de cultura no cultivo in vitro de Melissa officinalis L. Plant Cell Culture and Micropropagation, v. 3, n. 2, p. 83-88, 2007.
• REIS, É. S. et al Influência do meio de cultura na germinação de sementes in vitro e taxa de multiplicação de Melissa officinalis L. Revista Ceres, v. 55, n. 3, 2008.
• REIS, É. S. et al Teor e composição química do óleo essencial de Melissa officinalis L. in vitro sob influência do meio de cultura. Acta Scientiarum. Agronomy, v. 31, p. 331-335, 2009.
• SÁ, R. D.; SOARES, L. A. L.; RANDAU, K. P. Óleo essencial de Chenopodium ambrosioides L.: estado da arte. Revista de Ciências Farmacêuticas Básica e Aplicada, v. 36, n. 2, p. 267-276, 2015.
• SILVA, G. M. et al Effect of chemical and physical factors in in vitro propagation and volatile fraction analysis of Aloysia triphylla (L'Herit) Britton. Acta Horticulturae, n. 1155, p. 309-316, 2017.
• TAIZ, L.; ZEIGER, E. Fisiologia vegetal 4. ed. Porto Alegre: Artmed, 2009. 819 p.
• TORRES, A. C.; CALDAS, L. S.; BUSO, J. A. Cultura de tecidos e transformação genética de plantas Brasília: Embrapa-SPI: Embrapa-CNPH, 1998.
• VERISSIMO, L. F. et al Herbs of interest to the Brazilian Federal Government: female reproductive and developmental toxicity studies. Revista Brasileira de Farmacognosia, v. 21, p. 1163-1171, 2011.
• VILLA, F. et al Micropropagação de duas espécies frutíferas, em meio de cultura DSD1, modificado com fontes de boro e zinco. Ciencia e Agrotecnologia, v. 33, p. 468-472, 2009.
• VILLA, F. et al Multiplicação in vitro de porta-enxerto de videira em variações do meio MS. Acta Scientiarum. Agronomy, v. 28, n. 3, 2006.

Publication Dates

• Publication in this collection
  Oct-Dec 2018

History

• Received
  26 Feb 2016
• Accepted
  18 Nov 2017