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Brazilian Archives of Biology and Technology

Print version ISSN 1516-8913

Braz. arch. biol. technol. vol.56 no.3 Curitiba May/June 2013

http://dx.doi.org/10.1590/S1516-89132013000300010 

BIOLOGICAL AND APPLIED SCIENCES

 

Organogenesis from in vitro-derived leaf and internode explants of Hoya wightii ssp. palniensis -a vulnerable species of Western Ghats

 

 

Subbaiah Revathi LakshmiI, Jambarapu Herald Franklin BenjaminI, Tirupathi Senthil KumarII, Garimella Venkata Suryanarayana MurthyIII; Mandali Venkateswara RaoI,*

IDepartment of Plant Science
IIDepartment of Industry University Collaboration; Bharathidasan University; Tiruchirappalli 620 024; Tamil Nadu
IIIBotanical Survey of India; Southern Circle; Coimbatore-641 003; Tamil Nadu

 

 


ABSTRACT

An efficient system was developed for indirect plant regeneration from in vitro-derived leaf and internode explants of Hoya wightii ssp. palniensis. Maximum percentage of the organogenic callus was obtained on MS medium supplemented with NAA (1.0 mg/l) and 2,4-D (2.0 mg/l). The best shoot bud induction was observed on MS medium with BA (1.0 mg/l) +IBA (0.5 mg/l). The coconut water (15%) was better, resulting in a differentiation of the shoot initials in to well-developed shoots. The elongated shoots (› 3cm long) were rooted on a full strength MS basal medium, supplemented with 0.2 mg/l of IBA. Finally, the rooted plants were transferred to the soil with 80% success rate. This protocol was utilized for the in vitro propagation of this endangered plant species.

Key words: In vitro explants, organogenesis, Hoya wightii ssp. Palniensis, vulnerable plant, growth regulators


 

 

INTRODUCTION

Hoya wightii ssp. palniensis, commonly known as wax plant due to its waxy nature, belongs to the family Asclepiadaceae. It is a woody trailing herb, endemic to Pambar Shola of Western Ghats of Tamil Nadu, India. Mathew (1992) and Matthew (1996) reported an individual population of H. wightii ssp. palniensis in the ravine of Pambar Shola, Tamil Nadu, India. The genus Hoya is of horticultural importance in Europe, Australia and America. H. wightii ssp. palniensis possesses white flowers with red coronas which are borne in an umbel that can last for a week. Seed setting is very rare. Single follicle setting was observed during 2007 at Vattakanal Conservation Trust by the authors. These features limit its population to Western Ghats of Tamil Nadu, India. Imminent extinction threat of this species necessitates developing the conservation strategies and in vitro tissue culture techniques appear as a promising alternative to ensure its regeneration and conservation. Plant regeneration through organogenesis and somatic embryogenesis has been reported in other species of Hoya such as H. kerrii (Tube et al. 2007) and H. carnosa (Maraffa et al. 1981) and micropropagation of this species (Lakshmi et al. 2010).

The present study describes a protocol for the organogenesis of this species from in vitro derived leaf and internode explants since the use of in vitro derived explants will eliminate the need for disinfection. Shoot regeneration from in vitro derived explants have been reported in other plants such as Decalepis hamiltonii by Giridhar et al. (2004); Vaccinium corymbosum (Billings et al. 1988); Pyrus communis (Leblay et al. 1991); Elaegnus angustifolia (Economou and Maloupa, 1995); Pistachio vera L. cv. Siirt (Tilkat and Onay, 2009); Morus alba (Chitra and Padmaja, 2005); Phellodendron amurense (Azad et al. 2005). This is the first report on indirect organogenesis and the establishment of complete plantlets from the regenerated leaf and internode explants of H. wightii ssp. palniensis.

 

MATERIALS AND METHODS

Establishment of In Vitro Shoot Cultures

Single long apical bud of 0.5 - 1.0 cm was aseptically cultured in the conical flasks, each containing 50 ml of MS medium. To establish the shoot cultures, the apical shoot tips were cultured on the MS medium containing KN (1.0 mg/l) + IBA (0.3 mg/l), in addition to 30 g/l sucrose and 8 g/l agar. A detailed method for the optimized surface sterilization and culture initiation from mature H. wightii spp. palniensis has been reported by Lakshmi et al. (2010). Adventitious shoot buds from the initiation medium were subcultured on the fresh initiation medium every 2-3 weeks. The regenerated adventitious shoot buds from the in vitro cultures were maintained and proliferated on the initiation medium for about six months. The pH of the medium was adjusted to 5.7 using 0.1 N NaOH or 0.1 N HCl, prior to autoclaving at 121ºC for 20 min. All the cultures were placed and maintained in a growth room under a 16-h photoperiod (60 µ mol m-2s-1) with day and night temperatures of 25±2ºC.

Callus Induction from Axenic Leaf and Internode Explants

To initiate the callus induction and shoot regeneration from the axenic leaf and internode tissues, in vitro-regenerated shoots maintained for nearly six months on the culture initiation medium were used as source material. Semi mature leaf and internode were excised and abaxial sides in contact with the medium. The MS callus induction medium supplemented with 3% (w/v) sucrose at different concentrations of auxins 2,4 - D or NAA or IBA or Pic at 0.5, 1.0, 1.5, 2.0, 3.0 and 4.0 mg/l were tested in the callus induction experiment. These cultures were incubated at 25±2ºC in dark for seven days and then they were transferred to 16/8h light incubation. The cultures were observed constantly for any morphological response and after four weeks in culture, the percentage of explants showing callus induction was recorded. Each treatment contained at least 20 explants and the experiment was repeated two times.

Shoot Regeneration from Callus

The primary callus of green compact nature was then transferred to the culture bottles containing shoot regeneration medium. The MS medium supplemented with 3% sucrose and different concentrations and combinations of BA, KN or TDZ at 0.5, 1.0, 1.5 and 2.0 mg/l and auxins such as IAA, IBA and NAA at the concentrations of 0.1, 0.2, 0.5 and 1.0 mg/l were tested in the shoot regeneration experiments. The cultures were observed constantly for the percentage of explants regenerating shoots via adventitious shoot buds induction and proliferation.

Shoot Multiplication and Elongation

The adventitious shoots regenerated from the adventitious buds were used for further multiplication. GA3 (0.5 mg/l) was added to the shoot regeneration medium for shoot elongation. The shoot regeneration medium used was MS medium supplemented with BA (1.0 mg/l) + IBA(0.5 mg/l). After elongation, the clusters of apical shoots (5-10mm long) were segmented and used for proliferation and multiplication studies. Four different concentrations each of AA (25, 50, 100 and 150 mg/l), CA (5, 10, 25 and 50 mg/l), PVP (10, 25, 50 and 100 mg/l), CE (25, 50, 100 and 150 mg/l), YE (25, 50, 100 and 150 mg/l), ME (25, 50, 100 and 150 mg/l) and CW (5, 10, 15 and 25%) were added separately to shoot regeneration medium, i.e., MS+BA (1.0 mg/l)+ IBA (0.5 mg/l) and GA3 (0.5 mg/l) were added based on the response observed in previous two experiments, and they were added in this assessment along with the additives to enhance its shoot multiplication rate. For shoot proliferation and multiplication, each treatment was replicated twice and each replicate consisted of at least 20 explants. Four weeks after the culturing, the percentage of number of shoots and shoot length of newly formed shoots were recorded.

In Vitro Rooting of Shoots

Elongated shoots (› 3 cm long) harvested from the six times subculture were used for the rooting. The shoots longer than 3 cm were transferred to a rooting medium containing the MS medium with 3% sucrose and 8 g/l agar. The effects of the different concentrations of IBA, IAA and NAA (0.1, 0.2 and 0.3 mg/l) on rooting were evaluated. For rooting studies, each treatment was replicated three times, and each experiment consisted of at least 10 explants. After four weeks, the percentage of rooted shoots and the number of roots per shoot were recorded.

Acclimatization

The rooted shoots were carefully taken out of the medium and washed thoroughly in the running tap water, being careful not to damage the roots, to remove the traces of the medium attached to the roots. Then, they were planted in 3-cm paper cups containing a sterile 1:1:1 (w/w/w) red soil to sand and coconut coir mixture, enriched with a ¼ strength MS salt solution, covered with a polythene bag to maintain the high humidity, and placed in a culture room at 25±2ºC (day and night). The polythene bags were opened for 5 mins each the first two days, the length of the opening time doubled each subsequent day. Then, following four week period of acclimatization by the progressive reduction of the humidity level from 90 to 60%, the established plants were transferred to earthen pots and kept in a shade house for further growth and observation at Vattakanal Conservatory Trust, Kodaikanal as a part of reintroduction.

Experimental Design and Data Collection

All the experiments were conducted using the completely randomized block design. Significance was determined by the analysis of variance, and the least significant (P< 0.05) differences among the mean values were estimated using Duncan's new Multiple Range Test.

 

RESULTS AND DISCUSSION

A number of preliminary experiments revealed that the phytohormones were essential for the induction of callus from the leaf and internode explants and no callus was induced by the basal MS medium only. A series of attempts were made to initiate the shoots from the primary callus using the individual cytokinins. It was noticed that the KN, BA and TDZ failed to initiate the shoot buds from the callus and the callus explant died within a short period. In order to obtain the alternate source of explant for indirect shoot regeneration, axenic cultures derived by the protocol of Lakshmi et al. (2010) was used as explant. This is the first report on organogenesis of H. wightii ssp. palniensis. In general, the explants derived from the micropropagated shoots have an early and greater capacity for morphogenesis than the tissue excised from the field plants (George 1996), which is attributed to the absence of lag period between the explanting and adaptation to in vitro conditions.

The presence of smaller yet active meristematic centers of the microplants compared to relatively larger but quiescent meristems of the shoots of mature plants might be the reason for the successful regeneration of the explants from the micropropagated shoots in the present study (Amin and Jaiswal 1987).

The leaf and internode explants from the axenic shoots served as the explants for the induction of organogenic callus. The callus initiation was observed on the cut edges of leaf and internodes 15 days after the culture incubation (including initial seven days dark incubation). The induction of callus was mainly influenced by the auxin type and concentration used (Table 1). Initially (15 days), all the calli were yellow to white in color (Fig.1) with soft, friable and unorganized morphology. This callus was sub-cultured every two weeks (15d) for 60 days on to fresh medium of the same composition after which the callus showed varied nature on the different types of auxins used (Table 1). Most of the calli became yellow to green compact organogenic in nature after a total of 60 days (Fig. 1 A and B). Only green compact callus was investigated further and reported in this study.

The mean percentage of callus induction of in vitro leaf ranged from 20.0-83.6% while the internode ranged from 20 - 100% based on the concentration of auxins used (Table 1). Maximum percentage of the organogenic callus was obtained on MS medium supplemented with NAA (1.0 mg/l) and 2,4-D (2.0 mg/l). NAA supplementation on callus induction has been reported on Saintpanlia ionantha (Khan et al. 2007).

Effect of Cytokinins on Shoot Regeneration

Sixty days old organogenic callus obtained from the callus induction medium was transferred to the shoot regeneration medium containing MS basal medium supplemented with BA, KN or TDZ. For the leaf-derived callus, a higher number of responses of shoot regeneration was obtained when the culture medium was supplemented with the in vitro shoot regeneration and multiplication BA 1.0 mg/l (78%) with 8.4 shoots/explant (Table studies of many plants. It showed high cytokinin 2 and Fig. 1 C). For the internode-derived callus, activity by promoting the shoot multiplication and significant difference was detected among the growth of leaf explant of Momordica cymbalaria cytokinin media supplementation treatments, and (Nikam et al. 2009); Elaeagnus angustifolia the explant responsiveness ranged from 56.0-(Karami and Piri 2009) and from internode of 87.2% and maximum number of shoots/explant Withania somnifera (Kulkarni et al. 2000) and was obtained on MS medium fortified with BA 1.0 Piper colubrinum (Kelkar and Krishnamurthy mg/l. BA has long been used most frequently for 1998). This was reflected in the present study too.

The better effect of BA over other cytokinins for shoot bud induction has been attributed to the abilities of plant synthetic growth regulators or to the ability of BA to induce the endogenous production of Zeatin. The MS medium supplemented with KN also showed marked influence on shoot formation but the number of shoots formed was lower than on BA amended medium. This could be due to the fact that the KN was less effective than the BA in the formation of multiple shoot buds (Murashige 1974). TDZ showed least percentage of response on both the explants used (Table 2). The difference in the number of shoots formed in the leaf and internode explant could be a result of difference in the regeneration potential of different explants, which was attributed by the physiological state, age and cellular differentiation among the constituent cells (Murashige 1974). Among the explants tested, the internode explant showed high morphogenic efficiency. The efficiency of the internode callus over the leaf callus might be due to the passage of some internode components from the pre-existing axillary buds that were essential to evoke the caulogenesis. Moreover, stem internodes contained sufficient cytokinins at the time of excision for the adventitious shoot production (Douglas 1984).

Effect of Auxin on Shoot Multiplication

The effect of three different auxins (IAA, IBA and NAA) was tested on shoot multiplication in the MS basal medium containing BA (1.0 mg/l). The MS basal medium amended with BA 1.0 mg/l and IBA 0.5 mg/l showed high percentage of response 82.5 and 84% on leaf and internode explants, respectively. A superior response for the number of shoots 12.5 and 19.5 from the leaf and internode explants was observed on the MS medium incorporated with BA 1.0 mg/l + IBA (0.5 mg/l) (Fig. 1 E).

The superiority of the IBA over NAA and IAA on shoot regeneration through organogenesis has also been reported in other plants, including Ophiorrhiza prostrata (Beegum et al. 2007); Alibertia edulis (Silva et al. 2008); Ceropegia candelabrum (Beena et al. 2003) and Curcuma elongation, the shoots regenerated on MS+BA 1.0 zedoaria (Loc et al. 2005). Next to IBA, NAA mg/l+ IBA 0.5 mg/l was transferred to GA3 showed maximum numbers but the quality of supplementation at 0.5 mg/l on shoot regeneration shoots was not desirable. The NAA supplemented medium (MS+BA 1.0 mg/l +IBA 0.5 mg/l). The shoot multiplication medium resulted in basal GA3 supplementation not only increased the shoot callus formation at the concentrations used. The length, but also increased the shoot number. GA3 IAA supplementation on MS+BA 1.0 mg/l stimulates the elongation by inhibiting the action produced the least number of shoots and lower of auxins in meristematic regions (Taiz and Zeiger percentage for shoot multiplication. For the shoot 1998).

Effect of Antioxidants on Shoot Multiplication

The effect of three different antioxidants (AA, CA and PVP) was tested on shoot multiplication in the MS medium containing BA 1.0 mg/l+IBA 0.5 mg/l+GA3 0.5 mg/l. The shoot multiplication obtained from the regeneration medium containing the antioxidants showed maximum number of shoots than that on regeneration medium containing auxins and cytokinins, i.e., MS+BA 1.0 mg/l+IBA 0.5 mg/l+GA3 0.5 mg/l. MS medium incorporated with BA 1.0 mg/l+IBA 0.5 mg/l+GA3 0.5 mg/l+AA 150 mg/l was higher to that containing the CA or PVP on shoot multiplication (Table 4). The optimum concentration of the AA, CA and PVP on shoot multiplication was 150, 50 and 25 mg/l, respectively. The maximum number of shoots/explant (31.4) was obtained at 150 mg/l AA supplementation.

AA has also been shown to possess a stimulatory effect during the organogenesis by increasing the shoot multiplication rate of Salvia broussanetii (Mederos-Molina 2006), Lathyrus cicera (Sahin-Demirbag et al. 2008) and Sterculia urens (Hussain et al. 2008). From this study, it was found that the addition of ascorbic acid in the regeneration medium was beneficial for shoot multiplication. CA supplementation showed moderate and PVP supplemented medium showed least response for shoot multiplication (Table 4).

Effect of Organic Supplements on Shoot Multiplication

The role of organic supplements on shoot multiplication was examined after optimizing the synergistic effect of auxin and cytokinin. The influence of different organic supplements (CH, YE, ME and CW) was tested in MS basal medium containing 1.0 mg/l BA+ 0.5 mg/l IBA and GA30.5 mg/l for shoot multiplication. The addition of ME and CW increased the number of shoots, whereas CH and YE showed least influence over shoot multiplication (Table 4). Shoots regenerated on MS+BA 1.0 mg/l+ IBA 0.5 mg/l+GA3 0.5 mg/l+ CW or ME produced more number of shoots than shoot regeneration obtained on MS+BA 1.0 mg/l+ IBA 0.5 mg/l+GA3 0.5 mg/l+ CH or YE. MS medium supplemented with BA 1.0 mg/l+ IBA 0.5 mg/l+GA3 0.5 mg/l+ CW 15% was superior to that containing malt extract or yeast extract or casein hydrolysate on shoot regeneration and multiplication (Table 4). The higher efficiency of CW over other supplements on organogenesis has also been proved in other plants, including Ananas comosus by Atique Akbar et al. (2003), Curcuma zedoaria by Loc et al. (2005) and Sterculia urens (Hussain et al. 2008). This study showed that CW supplementation could improve the shoot multiplication in H. wightii ssp. palniensis as it was composed of many amino acids, nitrogenous compounds, inorganic supplements, organic acids, sugars and their alcohols, vitamins, growth substances (Cytokinins and auxins) and many other unknown components (George 1993). This could make CW a unique natural supplement in plant tissue culture studies. The optimum concentration of CW, ME, CH and YE on shoot multiplication was 15%, 25 mg/l, 25 mg/l and 50 mg/l respectively. The maximum number of shoots/explant (31.6) was produced at 15% CW supplementation. Malt extract supplementation produced moderate response, whereas YE and CH amended medium showed least response for shoot multiplication (Table 4).

Rooting

The shoots after multiplication were isolated and transferred on to the MS medium containing different auxins. The mean percentage of rooting ranged from 50-76, 0- 50 and 0-80% were recorded on the rooting medium, supplemented with NAA, IAA and IBA, respectively. The highest rooting response (80%) (Table 5) was obtained on the MS medium supplemented with IBA, with an average root length of 4.6cm. These observations were consistent with those reported transferred on to the MS medium containing by Salma et al. (2008), Raha and Roy (2003), different auxins. The mean percentage of rooting Neeta Mishra et al. (2003) and Atique Akbar et al. ranged from 50-76, 0-50 and 0-80% were (2003). The efficacy of the NAA at lower recorded on the rooting medium, supplemented concentrations in vitro rooting has been reported in with NAA, IAA and IBA, respectively. The various medicinal plants, e.g., Verbascum thapsus highest rooting response (80%) (Table 5) was L. (Turker et al. 2001) and Santolina canescens obtained on the MS medium supplemented with Lagasca (Casado et al. 2002).

Acclimatization of Regenerated Plants

The rooted plants with three-four fully expanded leaves and well-developed roots were transferred to the pots containing red soil, sand and coconut coir (1:1:1). Normal growth for the potted plants was observed after four weeks of transfer. After two months, they were transferred to larger pots containing the same ingredients and moved to a green house. After transplantation to soil, 70% of the rooted plantlets survived and grew to maturity when transferred to a green house (Fig. 1 G). The regenerated plants did not show visible varieties in the morphological or growth characteristics when compared to the donor plants.

 

CONCLUSION

This is the first report describing a protocol for organogenesis of H. wightii ssp. palniensis. The presence of the cytokinin BA in combination with IBA and GA3 was required for the efficient shoot multiplication and proliferation. The addition of AA and CW was useful for the improvement of shoot regeneration. The IBA favored the root induction and development. The explants derived from the micropropagated shoots showed better organogenic potential than the explants from the mature plants.

The organogenesis and plant regeneration system developed in this study could be utilized in future for the in vitro culture, transformation and secondary metabolites production experiments.

 

ACKNOWLEDGEMENTS

We acknowledge financial support from the University Grants Commission, New Delhi and Mr. R.W. Stewart and Mrs. Tanya Balcar and their team of Vattakkanal Conservation Trust, Kodaikanal for the help rendered during the reintroduction program.

 

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Received: January 27, 2011;
Revised: July 02, 2011;
Accepted: Setember 29, 2012.

 

 

* Author for correspondence: mvrao_456@yahoo.co.in

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