Cytokinin preconditioning enhances multiple shoot regeneration in Pongamia pinnata (L.) Pierre - a potential, non-edible tree seed oil source for biodiesel
Srinivas Belide*1· Ramgopal Rao Sajjalaguddam1 · Anitha Paladugu1
1Department of Biotechnology, Sreenidhi Institute of Science and Technology, Yamnampet, Andhra Pradesh, India
*Corresponding author: firstname.lastname@example.org
Financial support: Sreenidhi Institute of Science and Technology and Technical Education Quality Improvement Program (TEQIP) - World Bank.
Keywords: benzyladenine, cotyledonary node, multiple shoot induction, scanning electron microscopy, thidiazuron.
An efficient, highly reproducible protocol for multiple shoot induction and plant regeneration of Pongamia pinnata has been successfully developed using cotyledonary node explants. This study also demonstrates that preconditioning of explant stimulates production of multiple shoots from cotyledonary nodes of P. pinnata. The highest direct shoot regeneration (90%) with an average of 18.4 ± 3.1 shoots/explant were obtained when cotyledonary node explants were excised from seedlings germinated on Murashige and Skoog (MS) media supplemented with benzyladenine (BA) 1 mg l-1, and subsequently cultured on MS media with 1 mgl-1 thidiazuron (TDZ). Scanning electron microscope observations of cotyledonary node (CN) explants excised from pre-conditioned and normal seedlings, revealed larger buds with rapid development in BA-preconditioned CN explants. The addition of adenine sulphate significantly increased the average number of shoots per explant. The highest direct shoot regeneration (93%) with an average of 32.2 ± 0.93 shoots/explant was obtained from BA-preconditioned CN when cultured on MS media supplemented with 1 mg l-1 TDZ and 200 mg l-1 adenine sulphate (ADS). Repeated shoot proliferation was observed from BA preconditioned CN explants up to 3 cycles with an average of 15 shoots/explant/cycle when cultured on MS media supplemented with 1 mg l-1 TDZ and 150 mg l-1 L-glutamine, thus producing 45 shoots/CN explant. Shoots were elongated on hormone free MS media and rooted on ½ MS media supplemented with 1 mg l-1 of IBA. Rooted shoots were successfully acclimatized and established in soil with 80% success. The highly regenerative system developed in this investigation for this important tree could be a useful tool for genetic transformation.
Pongamia pinnata (L.) Pierre (Syn. Pongamia glabra Vent.) is a multipurpose legume tree indigenous to the Indian subcontinent, south East Asia and one of the non-edible oil yielding tree with high potential for seed yield (~20,000 seeds/tree). All parts of this plant have been traditionally used as crude drugs for the treatment of tumors, piles, skin diseases, wounds and ulcers. Its extracts possess significant antidiarrhoeal (Shoba and Thomas, 2001), antiplasmodial (Simonsen et al. 2001) and anti-inflammatory (Srinivasan et al. 2001) activities. The seed is source of oil (30-40% w/w) and other number of bioactive compounds such as Pongamol and Karanjin, which makes the oil non suitable for edible purpose. Recently, P. pinnata has been recognized as a viable source of oil for the production of biodiesel and proved its potential (Karmee and Chadha, 2005; Meher et al. 2006). The composition of the seed oil and the properties of Pongamia fatty acid methyl esters (FAMEs) meet North American and European industry standards (Azam et al. 2005), however the pour point (2.1ºC) and cloud point (8.3ºC) are satisfactory for tropical regions of the world. Besides the advantage of not being a food crop, Pongamia can be grown on low agriculturally productive lands not suitable for food crops, particularly lands with high levels of salt, low soil fertility and little water. In addition, through its ability to capture and convert nitrogen from the air, and phosphorus through mycorrhizal interactions on its roots this legume tree enriches soils with low nitrogen levels and eliminates the need for nitrogen fertilizer (Scott et al. 2008).
Despite the multipurpose utility of Pongamia, attempts have never been made to improve the plant either by horticultural or biotechnological approaches and there is crucial need to develop quality planting material with enhanced seed yield, oil content and fatty acid composition. Genetic engineering and plant transformation technology can be applied to change the fatty acid profile, silence the genes responsible for the production of toxic Pongamol and Karanjin in seeds etc. demands efficient regeneration system, preferably from explants amicable for Agrobacterium mediated transformation. Commercial scale planting of Pongamia is also hampered by several factors like low viability of seeds and susceptibility to Rhizoctonia hiemalis (Edwards and Naithani, 1999).
Protocols for micropropgation in P. pinnata using mature tree derived axillary meristems were reported (Sujatha and Hazra, 2007). However, use of seedling explants is advantageous for transformation and or micropropagation, due to easy planning of experiments, reduction in contamination during tissue culture and reduction in labor and maintenance costs. The objective of the study was to induce multiple shoots and regenerate whole plant from cotyledonary node (CN). We also examined the effects of benzyladenine (BA) pre-conditioning, addition of adenine sulphate (ADS) and L-glutamine (L-g) in the regeneration and proliferation response. Scanning electron microscopy (SEM) observations were made in order to clearly establish the beneficial effect of BA preconditioning at the pre-explant stage in relation to multiple shoot induction from cotyledonary node.
Seeds were collected from mature pods of locally grown Karanja (P. pinnata L. Pierre) plant. After their removal from pods, seeds of uniform size and shape were selected, washed thoroughly under tap water for 10-15 min followed by a 1 min rinse in 70% ethanol. Seeds were surface sterilized with 0.25% mercuric chloride (HgCl2) solution for 6 min. After rinsing with sterile distilled water for four to five times, seeds were inoculated in 50 ml test tubes containing 15 ml of Murashige and Skoog medium (MS) (Murashige and Skoog, 1962) and MS medium supplemented with 1 mg-1 of BA. All the seeds were incubated at 25 ± 2ºC in dark for 10-12 days for germination.
Cotyledonary node (0.5-1.0 cm) consisting of 2-4 mm of epicotyl and hypcotyl tissues with one or two intact cotyledons attached or trimmed to half of its original size is used in this study were excised both from axenic seedlings (10-12 cm) grown in dark on MS and MS+BA media. CN explants excised from seedlings grown on MS and MS+BA media were cultured on MS media supplemented with different growth hormones such as thidiazuron (TDZ) (0.5-3 mg l-1), benzyladenine (0.5-3 mg l-1) and with or without addition of adenine sulphate (ADS) and L-glutamine. All the media were adjusted to pH 5.8 before addition of (0.8%) agar (HiMedia India Ltd.), dispensed in to baby food jars (5.7 x 10.2 cm) in 40 ml aliquots and sterilized at 121ºC for 20 min. All the cultures were incubated in a culture room maintained at 25 ± 2ºC under 16/8 hrs light/dark regime, 45 µ mol m-2 s-1 irradiance level provided by cool white fluorescent tubes (Philips, Mumbai, India) with 55-60% relative humidity (RH). CN explants were sub cultured on to fresh media for every two weeks and the results were scored after four weeks of culture.
Multiple shoots (1.5-2 cm) originating from in and around of preconditioned CN region were separated and sub cultured on to fresh MS media without any hormones for shoot elongation. The remaining portion of the CN explant along with shoot buds (< 1 cm) was transferred again on to fresh MS media supplemented with TDZ and used repeatedly up to 2-3 cycles. CN isolated from normal seedlings were used for 1 or 2 times for the induction of multiple shoots.
Elongated, well developed shoots (3-5 cm long) with 3-5 leaves were excised and transferred individually on to ½ MS medium supplemented with different concentrations of indole acetic acid (0.5-3 mg l-1) and indole butyric acid (0.5-3 mg l-1) for rooting. In vitro rooted shoots were washed thoroughly in running tap water before being transplanted into plastic pots containing sterilized soil and vermiculite (1:1). Plants were covered with transparent polyethylene bags to maintain adequate moisture and transferred to the plant growth chamber (Pooja Labs, Bombay) and maintained at 24 ± 2ºC with 70-80% relative humidity. After 2-3 weeks the plantlets were transferred to pots containing normal garden soil until they were transplanted to field.
Scanning electron microscopy (SEM)
Preconditioned and normal cotyledonary nodes after 7 days of culture on MS media supplemented with 1 mg l-1 of TDZ, were fixed in glutaraldehyde (2.5%) in 0.05 M phosphate buffer (pH 7.2) for 24 hrs at 4ºC followed by 2% aqueous osmium tetroxide in 0.05 M phosphate buffer (pH 7.2) for 2 hrs. After fixation, samples were dehydrated in a series of graded alcohol and dried to critical point with electron microscopy critical point drying (CPD) unit. Dried samples were mounted over the stubs with double sided conductivity tape. A thin layer of gold was applied over the sample using an automated sputter coater (JEOL JFC-1600) for about 3 min. Mounted samples were scanned using a scanning electron microscope (JOEL-JSM 5600, Japan) at an accelerated voltage of 6 kV and the images were captured at various magnifications at RUSKA Labs, College of Veterinary Science, ANGR Agriculture University, Rajendranagar, Hyderabad.
Data collection and statistical analysis
Data on percentage of shoot regeneration were obtained after two and four weeks of culture. The average number of shoots/explant was collected from 28 day old cultures. In scoring number of shoots, each shoot consisted of apical meristem and leaves whose length from the base to meristem was at least 3-4 mm was considered and smaller shoots were not counted. A completely randomized design was used in all experiments. Analysis of variance and mean separation were carried out using Duncans Multiple Range Test (DMRT) and the significance was determined at the 5% level using MSTATC statistical software.
Pongamia seed has high oil content (approx. 40%) and can grow on malnourished soils; its FAMEs as biodiesel are environmentally safe, non-toxic and biodegradable. Because of the advantages offered by Pongamia, it is fast becoming the focus of a number of biodiesel research programs. Some of the other advantages of Pongamia are: a higher recovery and quality of oil than other crops, no direct competition with food crops as it is a non-edible source of fuel, and no direct competition with existing farmland. As a legume it is also able to fix its own nitrogen from the soil, minimizing the need for added fertilizers. By using genetic engineering and plant transformation technology, it may be possible to alter the seed oil content by seed specific expression of genes involved in fatty acid synthesis for wider applications. CN have been used in the development of regeneration and transformation protocols in trees (Aslam et al. 2009). It is well documented that TDZ has been shown to be several folds more effective in enhancing in vitro adventitious shoot initiation and proliferation (Cuenca et al. 2000; Sriskandarajah et al. 2001). The effect of TDZ on P. pinnata shoot regeneration from seedling explants has hardly been exploited. In the present study, in addition to BA preconditioning, the effectiveness of amino purine cytokinin BA and TDZ was tested for the development of reliable protocol for regeneration using CN in P. pinnata.
Influence of BA on seed germination of P. pinnata
Radicle emergence was observed in seeds after 3 days of culture on MS media or MS media supplemented with 1 mg l-1 BA. In dark grown seedlings, etiolation was observed and the seedling attained ~10 cm with in 10 days of culture. This suggested that BA at 1 mg l-1 does not restrict the germination of Pongamia seeds and the frequency of germination was 80-85%. Further increase in the concentration of BA (2-3 mg l-1) did not affect the seed germination significantly, but shoot appeared to be developmentally suppressed (Data not shown).
Effect of BA and TDZ on multiple shoot induction from normal and preconditioned CN explants
CN explants excised from seedlings grown on MS media, when cultured on MS supplemented with BA (0.5-3 mg l-1) or TDZ (0.5-3 mg l-1) resulted into multiple shoot formation with in 2-3 weeks. Among different BA (0.5-3 mg l-1) and TDZ (0.5-3 mg l-1) concentration tested, BA at 1 mg l-1 and TDZ at 1 mg l-1 induced multiple shoots in 59% and 64% of the cultures respectively (Table 1). Any further increase in BA (> 1 mg l-1) and TDZ (> 1 mg l-1) concentrations led to decrease in number of shoot buds/explant and large percentage of shoots were weak, hyperhydrated with reduced number of leaves in contrast to the development of normal shoots obtained on MS with 1 mg l-1 BA or 1 mg l-1 TDZ. The optimal medium supplements for multiple shoot formation was either 1 mg l-1 BA (7.3 + 0.92 shoots/explant) or 1 mg l-1 of TDZ (8.6 + 0.29 shoots/explant). Callus formation was also observed from the cut surfaces of CN explants cultured on shoot induction media supplemented with higher concentration of TDZ (3 mg l-1). However, no shoot formation was observed when callus cultured on various combinations and concentrations of TDZ, BA and KN (Data not presented). Without the addition of BA or TDZ no shoot formation was observed in normal and preconditioned CN explants.
Preconditioned CN explants when cultured on MS+BA (0.5-3 mg l-1) resulted in multiple shoot formation within two weeks of culture (Figure 1a). Of all the BA concentrations tested, maximum (85%) frequency of shoot induction was observed on MS medium supplemented with 1 mg l-1 BA producing up to 12.3 ± 2.1 shoots per explant (Figure 1b). In Vigna angularies, BA was also found to be most effective in inducing adventitious shoot formation from CN explants when used in both seed germination medium and shoot induction medium (Avenido and Hattori, 2000). Addition of BA (1 mg l-1) during seed germination was reported to be sufficient enough for efficient induction of shoots from CN of Mungbean (Avenido and Hattori, 2001). Histological observation in this study revealed bigger and more advanced shoots in pre-conditioned explants over control. In the present study, the effect of adding BA at 1 mg l-1 during seed germination (pre-conditioning of the explant) proved to be beneficial for early multiple shoot induction from cotyledonary node. Bigger and developmentally more advanced buds with leaf primordia were observed (Figure 2a) in BA treated explants over that of control (Figure 2b). In addition to advancing the process of regeneration, percentage of shoot induction was consistently higher when BA was used during seed germination in all treatments tested when compared to MS basal media. Although there is a report on multiple shoot induction from CN explants of Pongamia using BA (Sugla et al. 2007), the present study highlights the significance of BA preconditioning of CN explant which resulted into two fold increase in number of shoots/explant.
Preconditioned CN when cultured on MS media supplemented with different concentration of TDZ (0.5-3 mg l-1) resulted in enhanced multiple shoot regeneration when compared with normal CN cultured on MS+BA or TDZ and preconditioned CN cultured on MS+BA. Of all the TDZ concentrations tested, maximum (90%) frequency of shoot induction was observed on MS medium supplemented with 1 mg l-1 TDZ forming up to ~20 shoots per explant (Table 1). The most efficient treatment combination in terms of the proportion of shoot-producing explants and productivity per explant was reported in BA preconditioning followed by shoot induction with1 mg l-1 of TDZ. A similar culture system has been reported from CN explants in Chestnut (San José et al. 2001). TDZ at different concentrations, in either BA-preconditioned or normal CN induced more shoots/explant compared to BA indicating TDZ is more effective than BA in P. pinnata. Sujatha and Hazra (2007) also reported the effectiveness of TDZ in induction of multiple shoots from mature tree derived axillary meristems of P. pinnata.
Effect of adenine sulphate and L-glutamine
The regeneration protocol described above used normal and BA-preconditioned CN explants. BA-preconditioned explants were found to be me more responsive over normal CN explants to BA or TDZ. Although the number of explants producing shoots reached up to 90% with an average of 20 shoots per explant, however, once shoots had reached 0.5-1 cm, further development of these shoots was poor. The addition of ADS (100-200 mg l-1) to preconditioned CN explants cultured on MS medium supplemented with TDZ further increased number of shoots per explant significantly from 20 to 32 (Table 2 and Figure 1c); however there was no significant improvement in percentage of shoot regeneration. Among all the ADS concentrations tested, the optimal ADS concentration was found to be 200 mg l-1 and further increase in ADS concentration led to decrease in number of shoots/explant. It has been demonstrated that adenine, adenosine and adenylic acid have cytokinin activity and are added to the culture media to improve growth or to reinforce the response. The benefits of adenine are often only noticed when it is associated with ammonium nitrate or cytokinins such as BAP or kinetin (Van Standen et al. 2008). Our results suggest that TDZ, in combination with ADS, improves the process of organogenesis. Adenine sulphate has been used for in vitro multiplication of Carica papaya (Schmildt et al. 2007). Addition of L-glutamine to the regeneration medium did not show any significant improvement in either percentage of shoot regeneration or number of shoots/explant; however shoot development with broad leaves with more vigor was observed. Repeated shoot proliferation was also observed from BA preconditioned CN explants when cultured on MS supplemented with 1 mg l-1 TDZ and 150 mg l-1 L-glutamine (Figure 1d), up to 2-3 cycles with an average of 15 shoots from explants. The enhancement of growth rate by L-glutamine could be explained on the basis that L-glutamine provided a readily available source of nitrogen, the implication being that the formation of necessary carbon skeleton or the reduction of nitrate to ammonia is a limiting factor in the cells (Gamborg, 1970). These results are in agreement with the findings of Selvaraj at al. (2007), who studied the effect of L-glutamine on efficient shoot regeneration from cotyledons of cucumber via organogenesis.
Elongation, rooting and hardening
CN explants along with the induced shoots were subsequently transferred to plant growth regulator free media for shoot elongation (Figure 1e and Figure 1f). After 2-3 weeks, elongated shoots were excised and transferred to rooting media. CN explants cultured on MS+1 mg l-1 of TDZ and 150 mg l-1 L-glutamine were used for up to 2-3 cycles after harvesting the shoots for every 2-3 weeks. Isolated single shoots were treated with different concentration of IAA and IBA on ½ MS medium for root induction. Root initiation was observed with in 2 weeks of culture but complete root development that were suitable for hardening took 3-4 weeks. IBA and IAA showed difference in root induction response. While IBA at 1 mg l-1showed the best rooting response (64.5%) on ½ MS media with an average of 5.3 roots/shoot, indole-3-acetic acid (IAA) at the same concentration (1 mg/l) induced 3.9 roots/shoot with a frequency of 43.9% (Table 3 and Figure 1g). Similar rooting response in Pongamia was reported by Sugla et al. (2007) with 1 mg l-1 indole-3-butyric acid (IBA). There was no significant difference observed in rooting response of shoots regenerated from pre-conditioned and normal explants.
Plantlets with well-developed roots were successfully acclimatized (Figure 1h and Figure 1i) and eventually transferred to field. Eighty five percent of the plantlets transferred to sterilized soil and vermiculite survived, while 80% of the plants transferred to soil survived. The entire procedure starting from seed germination, multiple shoot induction to establishment of plant under greenhouse conditions took approximately 14 weeks.
We have been successful in developing an in vitro regeneration system from CN explants of potential biofuel plant of P. pinnata. In the present study we report a major improvement in number of shoots/explant and also highlight the repeated proliferation of shoots from BA-preconditioned CN explant up to 3 cycles with an average of 15 shoots/CN/cycle, producing ~45 shoots/CN. The ability of the treated explant to form multiple shoots is a prerequisite for efficient genetic transformation. This simple and efficient regeneration system can be adapted for mass propagation of elite varieties and for future genetic transformation studies in this economically important plant.
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