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High efficiency direct shoot organogenesis from leaf segments of Aerva lanata (L.) Juss. ex Schult by using Thidiazuron.

1. Introduction

Aerva lanata (L.) Juss. ex Schult., a medicinal herb belonging to the family Amaranthaceae, is commonly called Polpala. It is endowed with various chemical compounds such as flavonoids, alkaloids, steroids, polysaccharides, tannins, phenolic compounds, and saponins [1,2], which have contributed to its diverse uses in folklore medicine. Leaf extract of A. lanata is very effective in curing the urinary risk factors associated with calcium oxalate urolithiasis [3]. In addition to the traditional uses, the plant is reported for a number of pharmacological activities, namely, anthelminthic, demulcent, anti-inflammatory, diuretic, expectorant, hepatoprotective and nephroprotective, antidiabetic, antihyperglycemic, antimicrobial, cytotoxic, hypoglycemic, antihyperlipidemic, antiparasitic, and anthelminthic activities [4]. The bioactive active compounds responsible for the above pharmacological activities are [beta]-carboline, [beta]-sitosterol, palmitic acid, alpha amyrin, aervin, methyl aervine, and aervoside [5, 6].

The requirement of this medicinal herb is presently met from the natural populations. However, extensive utilization of this plant poses a potential threat for its existence [7]. Further, seed dormancy and seasonal availability prompted the evaluation of alternative approaches to generate the required propagation for in vitro studies, genetic transformation and commercial production of A. lanata. In vitro regeneration provides an alternative mean for large scale multiplication. Plants have been successfully regenerated through micropropagation, indirect or direct regeneration [8]. There are few reports on in vitro regeneration of A. lanata, which are also restricted to adventitious plantlet formation from shoot tip and nodal segments [7]. Direct shoot organogenesis from leaf segments represent a promising tool for mass propagation as well as genetic transformation system. To date, there is no report of direct organogenesis from leaf explants for A. lanata. Therefore, in the present study, an attempt has been made to develop an efficient direct regeneration system using leaf segments for A. lanata.

2. Materials and Methods

2.1. Establishment of Aseptic Mother Plants. Seeds of A. lanata were collected from basins of river Cauvery during January, 2012 and the plants were raised in the medicinal plant garden of Jamal Mohamed college, Tiruchirappalli, India. Nodal segments from ex vitro mother plants were used as initial explants. They were washed in running tap water for 10 min, soaked in 5% (v/v) teepol for 2 min, surface sterilized with 0.2% mercuric chloride for 10 min, and rinsed 3 times with sterile distilled water. After that, they blotted using sterilized Whatman filter paper and allowed to dry naturally. Then they were cut into small pieces of explants (0.5 cm in size) and inoculated on to MS basal media [9] supplemented with 1.0 mg [L.sup.-1] 6-benzylamino purine BAP and 0.5 mg [L.sup.-1] NAA. The polarity of the shoots was maintained during inoculation.

2.2. Culture Condition. The pH of media was adjusted 5.7 [+ or -] 0.1 before autoclaving at 121[degrees]C and 104 kPa for 15 min. All experiments were performed with semi solid media gelled with 0.8% agar powder (Himedia, Mumbai, India). Cultures were maintained at 25 [+ or -] 2[degrees]C, 16 h photoperiod under 40 [micro]mol [m.sup.-2] [s.sup.-1] light intensity provided by white fluorescent tubes and a relative humidity at 55-65%.

2.3. Influence of TDZ on Organogenesis. To study the role of TDZ on shoot organogenesis, young leaves were sectioned (approximately 0.5 x 0.5 cm) from 20 days old in vitro raised plants and incubated on MS medium supplemented with 0.25-2.0 mg [L.sup.-1] TDZ for a specific period. The frequency of shoot regeneration and the number of shoots per leaf explants were recorded after 49 days of culture (starting from the initial day of inoculation).

2.4. Influence on In Vitro Flowering. To test the influence on in vitro flowering, shootlets from 4 weeks culture were transferred to MS basal medium containing 1.0 mg [L.sup.-1] TDZ alone or in combination with 0-1.0 mg [L.sup.-1] indole-3-acetic acid (IAA) or NAA.

2.5. Rooting and Establishment of Plantlets. For root development, 25 mm regenerated shoots were excised and cultured on half strength MS medium containing 0.5-2.0 mg [L.sup.-1] IBA for 7 days, plantlets to pots filled with soil: perlite: vermiculate (1:1:1; v/v/v) mixture and acclimatized for 2 weeks under higher humidity before transferring to garden pots [10].

2.6. Histological Investigations. The origin of the adventitious shoots was studied using histological analysis. Standard procedures were followed for histological studies [11]. The samples were fixed for 24 h in FAA (70% ethanol: formalin: acetic acid = 90:5:5; v/v/v), dehydrated in a graded ethanol series, and embedded in paraffin (58[degrees]C). Sections (~10 [micro]m thick) were stained with toluene blue O. The prepared slides were examined through a light microscope (Leica, Switzerland), and all images were photographed using digital camera (Nikon, Japan).

2.7. Experimental Design and Statistical Analysis. All experiments were conducted using a completely randomized design and each experiment consisted of five explants per culture tube and 15 replicate tubes per treatment. Percentage of shoots producing roots and the numbers of roots formed per shoot were recorded 3 weeks after inoculation in IBA media. Data were subjected to a one way ANOVA followed by statistical significance test. The significant differences among the mean [+ or -] standard error were carried out using Duncan's multiple range tests and significance level of P < 0.05. (IBM SPSS ver. 19).

3. Results and Discussion

Since there is no previous information on shoot development from leaf segments of A. lanata, there has been a new report. The effect of TDZ including concentration and duration of treatment on shoot development was initially investigated. Leaf explants were cultured on MS basal medium alone or containing various concentrations of TDZ for the induction of shoots regeneration. Leaf explants cultured in all TDZ concentrations except those in basal medium that enlarged considerably and turned green within 14 days of culture (Figures 1(a) and 1(b)). All the explants in basal medium turned brown and died within two weeks of culture. Sporadic shoot formation was observed when basal medium was enriched with TDZ (Figure 1(c)). After 28 days, more adventitious shoots were observed on leaf explants cultured on media containing 1.0 mg [L.sup.-1] TDZ compared to the other TDZ concentrations, with an average of 23.6 [+ or -] 0.16 shoots per leaf explants and frequency of shoot regeneration of 90%. Increasing the concentration of TDZ above 1.0 mg [L.sup.-1] resulted in a marked reduction in shoot formation in leaf explants. In the present study, low concentrations (0.25-1.0 mg [L.sup.-1]) of TDZ had a significant effect on the percentage of shoot bud regeneration from leaf segments, and higher concentration exhibited inhibitory effect (Table 1). Similar results were also reported in other plants including Saussurea involucrata [12] and Solanum aculeatissimum [13].

Consistent subculturing of the in vitro raised plants culture after every 4 weeks on fresh MS medium containing 1.0 mg [L.sup.-1] TDZ led improved shoot proliferation response (Figure 1(f)). Subculture times longer or shorter than 4 weeks resulted in a decline in number of shoot bud induction. Similar results were also recorded for the medicinal plant S. involucrata [12], where large number of de novo shoots was regenerated in response to TDZ exposure and 4 weeks subculture.

It was obvious that the supplementation of TDZ in the culture media was important for direct organogenesis in A. lanata. Thinh [14] suggested that TDZ either increases the levels of nucleoside or the accumulation and synthesis of purine cytokinins as well as promoting the conversion of adenine to adenosine. Laloue and Pethe [15] proposed that TDZ influences the metabolism of endogenous auxins: thus altering the auxin, cytokinin ratio within the tissue, and eventually stimulating regeneration. This suggestion was also proved by several other workers [16,17].

TDZ has been demonstrated to be effective in inducing flowering in vitro for several plant species 18,19]. An interesting feature found in the present study was that the treatment of leaf explants on TDZ in combination with NAA has a positive effective on flowering in vitro (Figure 2(a)). Although 1.0 mg [L.sup.-1] TDZ with 0.5 mg [L.sup.-1] NAA achieved the highest ratio of flowering (data not shown) (Figure 2(b)), it was not suited for multiple shoot formation. Meanwhile, TDZ alone or in combination with IAA failed to induce floral bud formation. In vitro flowering was also observed in Arachis hypogea on MS medium containing cytokinins with NAA [20] and in Withania somnifera on MS medium containing cytokinins with IAA [21].

The success of micropropagation relies on the rooting percentage and survival of plantlets upon transfer to the field condition. Regenerated shoots larger than 25 mm were selected and transferred to IBA media for rooting (Figure 2(c)). The maximum frequency of rooting (86.6%) with highest number of (11.7 [+ or -] 0.15) roots per shoot was obtained in IBA at 1 mg [L.sup.-1] after 28 days (Figures 2(d) and 3). Shoots induced by TDZ and subsequently rooted in IBA has been also reported in Cyamopsis tetragonoloba [22]. More than 200 plantlets with 4 to 5 fully expanded roots were successfully hardened off inside in the growth chamber within a period of 4 weeks (Figures 2(e) and 2(f)). Thereafter these plantlets were transferred to soil and were maintained in a shade house with a survival rate of 92.0%. Regenerated plants grew well and phenotypically similar to the parental stock.

Histological analysis provided morphological details of the process of organogenesis from the leaf explants of A. lanata. One week after culture initiation, epidermal cells of the explants exhibited continuous cell division leading to formation of numerous dome shaped meristematic protrusions with high cytoplasmic content and prominent nuclei (Figures 1(d) and 1(e)). At later stages of development, adventitious shoot formation and shoots were formed directly from these meristematic protrusions. Similar observation has also been reported for Saintpaulia ionantha [23], Chirita spp. [24], and Titanotrichum oldhamii [25].

4. Conclusion

This is the first report of direct organogenesis from leaf explants in A. lanata. According to the present study, TDZ is an efficient growth regulator for promoting shoot proliferation and adventitious shoot regeneration from leaf explants of A. lanata. However, along with NAA, it significantly influence in vitro flowering. Shoot proliferation rate was higher on MS medium containing 1.0 mg [L.sup.-1] TDZ and efficient rooting was observed on half strength MS medium containing 1.0 mg [L.sup.-1] IBA.

Abbreviations

MS:     Murashige and Skoog
TDZ:    Thidiazuron
BAP:    6-Benzylamino purine
NAA:    [alpha]-Naphthalene acetic acid
IBA:    Indole-3-butyric acid
IAA:    Indole-3-acetic acid.


http://dx.doi.org/10.1155/2014/652919

Conflict of Interests

The authors declare that they have no conflict of interests.

Acknowledgments

The authors thank DST, Government of India, for providing facilities through FIST program. They also thank University Grants Commission, New Delhi, for its support through "College with potential for excellence" programme.

References

[1] S. Chandra and M. S. Sastry, "Chemical constituents of Aerva lanata," Fitoterapia, vol. 61, no. 2, p. 188, 1990.

[2] G. G. Zapesochnaya, L. N. Pervykh, and V. A. Kurkin, "A study of the herb Aerva lanata. III. Alkaloids," Chemistry of Natural Compounds, vol. 27, no. 3, pp. 336-340, 1991.

[3] M. S. Surya, M. Ashiq, and K. Jayachandran, "In vitro production of vanillin from suspension culture of Aerva lanata (L.) Juss. Ex Shultes," Indian Journal of Life Science, vol. 2, no. 1, pp. 9-15, 2012.

[4] M. Yamunadevi, E. G. Wesely, and M. Johnson, "A Chromatographic study on the Glycosides of Aerva lanata L," Chinese Journal of Natural Medicines, vol. 9, no. 3, pp. 210-214, 2011.

[5] L. Rajanna, C. Nagaveni, and M. Ramakrishnan, "In vitro shoot multiplication of a seasonal and vulnerable medicinal plant-Aerva lanata L," International Journal of Botany, vol. 7, no. 3, pp. 255-259, 2011.

[6] R. Rajesh, K. Chitra, and P. M. Paarakh, "Aerva lanata (Linn.) Juss. ex Schult.--an overview," Indian Journal of Natural Products and Resources, vol. 2, no. 1, pp. 5-9, 2011.

[7] A. R. Sahu, S. C. Rath, and J. Panigrahi, "In vitro propagation of Aerva lanata (L.) Juss. ex Schult. through organogenesis," Indian Journal of Biotechnology, vol. 12, pp. 260-264, 2013.

[8] S. Parveen, A. Shahzad, and M. Anis, "Enhanced shoot organogenesis in Cassia angustifolia Vahl.--a difficult to root drought resistant medicinal shrub," Journal of Plant Biochemistry and Biotechnolgy, vol. 21, no. 2, pp. 213-219, 2012.

[9] T. Murashige, F. Skoog, and Skoog, "A revised medium for rapid growth and bioassay with tobacco tissue cultures," Physiology of Plant, vol. 15, pp. 473-497, 1962.

[10] C. Soundar Raju, K. Kathiravan, A. Aslam, and A. Shajahan, "An efficient regeneration system via somatic embryogenesis in mango ginger (Curcuma amada Roxb.)," Plant Cell Tissue and Organ Culture, vol. 112, pp. 387-393, 2013.

[11] M. Nakano, T. Nomizu, K. Mizunashi et al., "Somaclonal variation in Tricyrtis hirta plants regenerated from 1-year-old embryogenic callus cultures," Scientia Horticulturae, vol. 110, no. 4, pp. 366-371, 2006.

[12] B. Guo, R. Amanda, Stiles, and C. Z. Liu, "Thidiazuron enhances shoot organogenesis from leaf explants of Saussurea involucrata Kar. et Kir," In Vitro Cellular and Developmental Biology, vol. 48, no. 6, pp. 609-612, 2012.

[13] B. K. Ghimire, C. Y. Yu, and I.-M. Chung, "Direct shoot organogenesis and assessment of genetic stability in regenerants of Solanum aculeatissimum Jacq," Plant Cell, Tissue and Organ Culture, vol. 108, no. 3, pp. 455-464, 2012.

[14] N. T. Thinh, Cryopreservation of germplasm of vegetatively propagated tropical monocots by vitrification [Doctoral dissertation], Kobe University, 1997.

[15] M. Laloue and C. Pethe, "Dynamics of cytokinin metabolism in tobacco cells," in Plant Growth Substances, P. E. Wareing, Ed., pp. 185-195, Academic, London, UK, 1982.

[16] F. J. C. Bespalhok and K. Hattori, "Friable embryogenic callus and somatic embryo formation from cotyledon explants of African marigold (Tagetes erecta L.)," Plant Cell Reports, vol. 17, no. 11, pp. 870-875, 1998.

[17] P. K. Saxena, K. A. Malik, and R. Gill, "Induction by thidiazuron ofsomatic embryogenesis in intact seedlings of peanut," Planta, vol. 187, no. 3, pp. 421-424, 1992.

[18] R. Gill and P. K. Saxena, "Somatic embryogenesis in Nicotiana tabacum L.: induction by thidiazuron of direct embryo differentiation from cultured leaf discs," Plant Cell Reports, vol. 12, no. 3, pp. 154-159, 1993.

[19] C.-S. Lin and W.-C. Chang, "Micropropagation of Bambusa edulis through nodal explants of field-grown culms and flowering of regenerated plantlets," Plant Cell Reports, vol. 17, no. 8, pp. 617-620, 1998.

[20] C.-S. Lin, C.-C. Lin, and W.-C. Chang, "In vitro flowering of Bambusa edulis and subsequent plantlet survival," Plant Cell, Tissue and Organ Culture, vol. 72, pp. 71-78, 2003.

[21] S. B. Narasimhulu and G. M. Reddy, "In vitro flowering and pod formation from cotyledons of groundnut (Arachis hypogaea L.)," Theoretical and Applied Genetics, vol. 69, no. 1, pp. 87-91, 1984.

[22] K. V.Saritha and C. V.Naidu, "In vitro flowering of Withania somnifera Dunal.--an important antitumor medicinal plant," Plant Science, vol. 172, no. 4, pp. 847-851, 2007

[23] N. Ahmad and M. Anis, "Rapid plant regeneration protocol for cluster bean (Cyamopsis tetragonoloba L. Taub.)," Journal of Horticultural Science and Biotechnology, vol. 82, no. 4, pp. 585-589, 2007

[24] S. Ohki, "Scanning electron microscopy of shoot differentiation in vitro from leaf explants of the African violet," Plant Cell, Tissue and Organ Culture, vol. 36, no. 2, pp. 157-162, 1994.

[25] M. Nakano, H. Takagi, S. Sugawara et al., "Adventitious shoot regeneration and micropropagation of Chirita flavimaculata W. T. Wang, C. eburnea Hance, and C. speciosa Kurz," Propagation of Ornamental Plants, vol. 9, no. 4, pp. 216-222, 2009.

K. Varutharaju, C. Soundar Raju, C. Thilip, A. Aslam, and A. Shajahan

Plant Molecular Biology Laboratory, Department of Botany, Jamal Mohamed College, Tiruchirappalli 620 020, India

Correspondence should be addressed to A. Shajahan; shajahan.jmc@gmail.com

Received 27 August 2013; Accepted 22 October 2013; Published 4 February 2014

Academic Editors: M. Cresti and S. Rodriguez-Couto

TABLE 1: Effect of TDZ on shoot regeneration from leaf
explants of A. lanata.

TDZ (mg       Percentage of       Mean number of
[L.sup.-1])    responding         shoot/explants
              explants (%)      (mean [+ or -] SE)

0.0                 0                0.0 (f)
0.25               50         8.7 [+ or -] 0.15 (d)
0.5                70         15.6 [+ or -] 0.16 (b)
1.0                90         23.6 [+ or -] 0.16 (a)
1.5                60         11.7 [+ or -] 0.15 (c)
2.0                40         6.7 [+ or -] 0.15 (e)

Data represented mean, mean [+ or -] SE (standard error)
of three replicates, each with 15 cultures.

Means having the same letter in a column were not
significantly different by Duncan's multiple range
test (P < 0.05).
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Title Annotation:Research Article
Author:Varutharaju, K.; Raju, C. Soundar; Thilip, C.; Aslam, A.; Shajahan, A.
Publication:The Scientific World Journal
Article Type:Report
Date:Jan 1, 2014
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