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Electronic Journal of Biotechnology

versión On-line ISSN 0717-3458

Electron. J. Biotechnol. v.10 n.3 Valparaíso jul. 2007

http://dx.doi.org/10.4067/S0717-34582007000300009 

Environmental Biotechnology
  Plant Biotechnology
Electronic Journal of Biotechnology ISSN: 0717-3458 Vol. 10 No. 3, Issue of July 15, 2007
© 2007 by Pontificia Universidad Católica de Valparaíso -- Chile Received March 24, 2006 / Accepted January 24, 2007
DOI: 10.2225/vol10-issue3-fulltext-9 How to reference this article
RESEARCH ARTICLE

Induction of in vitro roots cultures of Thypha latifolia and Scirpus americanus and study of their capacity to remove heavy metals

María del Socorro Santos-Díaz*
Centro de Investigación y Estudios de Posgrado
Facultad de Ciencias Químicas
Universidad Autónoma de San Luis Potosí
Manuel Nava 6, San Luis Potosí
CP 78210, México
Tel: 444 8262440
Fax: 444 8262372
E-mail: ssantos@uaslp.mx

María del Carmen Barrón-Cruz
Centro de Investigación y Estudios de Posgrado
Facultad de Ciencias Químicas
Universidad Autónoma de San Luis Potosí
Manuel Nava 6, San Luis Potosí
CP 78210, México
Tel: 444 8262440
Fax: 444 8262372

María Catalina Alfaro-De la Torre
Centro de Investigación y Estudios de Posgrado
Facultad de Ciencias Químicas
Universidad Autónoma de San Luis Potosí
Manuel Nava 6, San Luis Potosí
CP 78210, México
Tel: 444 8262440
Fax: 444 8262372

*Corresponding author

Financial support: We are grateful to SHIGO-CONACYT (2002-060-205) for financial support and for the scholarship to MCBC (2002-020605).

Keywords: heavy metals, in vitro root cultures, phytoremediation, Scirpus americanus, Thypha latifolia.

Abbreviations:

2,4-D: 2,4-dichlorophenoxiacetic acid
CDFs: cation diffusion facilitators
IAA: indolacetic acid
IBA: indolbutyric acid
NAA: naphtalen acetic acid

Abstract
Reprint (PDF)
Abstract
Article
References

We have established the conditions to obtain in vitro root cultures of Thypha latifolia and Scirpus americanus and have investigated their capacity to remove Pb(II), Mn(II) and Cr(III) from the culture medium. The best conditions for the in vitro culture growth were: an inoculum of 0.2 g of T. latifolia roots and 0.05 g of S. americanus roots (fresh weight), Murashige-Skoog medium and 2 mg L-1of indolacetic acid. The T. latifolia and S. americanus root cultures were cultivated onto media containing Cr (15 µg L-1), Pb (60 µg L-1) or Mn (1.8 mg L-1). Both species were able to remove Pb and Cr near to 100% and 71-100% of Mn from the medium solution during the 6-8 days of experimentation. According to metal concentrations removed from the medium containing the growing root mass, the in vitro root culture of S. americanus can be considered as an accumulator for Pb (157.73 µg g-1), Cr (55.6 µg g-1) and Mn (5000 µg g-1).

Article
Article
Materials and Methods
Results
Discussion
Figure 1
Figure 2
Figure 3
Table 1
Table 2
References

Heavy metals are toxic pollutants that have serious adverse effects on human health. They are toxic because can replace other essential metals in pigments or enzymes, disrupting the function of these molecules (Manios et al. 2003). Also because they may cause oxidative stress, especially transition metals as Fe2+/3+ and Cu+/2+ (Rivetta et al. 1997).

The removal of metals from solution using plants offers an attractive alternative, because it is solar driven and can be carried out in situ, minimizing cost and human exposure (McCutcheon and Schnoor, 2003). Plants have developed different mechanisms of tolerance to the metals and to the metal accumulation. Some plants excrete organic acids, as malate and citrate, that act as metal chelators and decrease the rhizospheric pH increasing the bioavailability of metals for phytoextraction (Pivetz, 2001). Organic acids can also inhibit metal uptake because they complex the metal outside the root (phytostabilization). For example, citrate inhibits Al and Cu uptake in some plant species (De la Fuente et al. 1997; Murphy et al. 1999). The high metal tolerance may be in part due to the highly efficient intracellular compartmentalization. The uptake of metals requires their transport across the root cell membrane to the symplast. This process involves specific membrane transporter proteins as heavy metal ATPases (HMAs), the natural resistance-associated macrophage proteins (Nramps), and cation diffusion facilitators (CDFs) (Hall and Williams, 2003). Once inside the cell, the metals could be translocated to their final destination by membrane metal transporters, and metal-binding proteins as metallothioneins (Goldsbrough, 2000). Metal chaperones are a different class of proteins that bring metals to specific targets in the cell (Himelblau et al. 1998). For the storage in the vacuole (sequestration), certain metals may be complexed by phytochelatins. These compounds are synthesized enzymatically from glutathione. Complex of metals bound by glutahione or phytochelatins are shuttled to the vacuole by an ATP-binding cassette (ABC) type transporter protein in the tonoplast. Other metal-binding molecules that are involved in the metal complexation in the vacuole are organic acids (Kramer et al. 2000) and sulphides, in the particular case of cadmium (Cobbett, 2000). Additional mechanisms of tolerance are the assimilation of metals into organic molecules by metal-modifying enzymes (e.g. selenate is metabolized to dimethylselenide) or the changes in the oxidation state of metals that reduce their toxicity (e.g. toxic Cr VI is reduced to the non toxic Cr III; Lytle et al. 1998; De Souza et al. 2000).

The plants are efficient in the removal metals from their solid or liquid environment as also the plant cell cultures do. In vitro culture of plant organs (roots and shoots) allow indefinite propagation and experimentation using tissues derived from the same plant, thus avoiding the effects of variability between individual specimens. Axenic conditions in culture prevent microbial symbiosis disguising the metal uptake characteristics of plants grown in soil. Experiments using separately cultured organs also allow the metal accumulation properties of each organ to be identified. Some examples include the removal of Sr2+ by shoots of Solanum laciniatum (Kartosentono et al. 2001), and hyper-accumulation of Cd by hairy roots of Thlaspi caerulescens (Nedelkoska and Doran, 2000). Another advantages of in vitro cultures is the facility to obtain variants with different tolerance to several biotic stresses (Ben-Hayyim, 1987; Santos-Díaz and Ochoa-Alejo, 1994).

Some plants that have potential on phytoremediation are Thypha latifolia (reed mace) and Scirpus americanus (american tule). These species are able to grow on water bodies contaminated with heavy metals formed as result of industrial and domestic effluents (Montante-Montelongo et al. 1995) or in sludge compost watered with metaliferus water (Manios et al. 2003).

This work is focused on T. latifolia and S. americanus plants growing on an artificial lake contaminated with Pb, Cr, Fe, Ni, Cu and Mn, known as Tenorio Tank. This tank has an extension of 209 ha and represent a serious problem of pollution beside to be the habitat of several species of water birds (Montante-Montelongo et al. 1995). It has been observed that the lake areas colonized by the T. latifolia and S. americanus plants shows better quality of water than those areas absent of vegetation. Therefore, it is plausible that the aquatic plants are participating on phytoremediation process. As the roots are in direct contact with water they should be the main responsible for the pollutants removal.

On the basis of this observations, the aim of this research was to develop a protocol to establish the in vitro roots cultures of T. latifolia and S. americanus and later on to investigate if they have the capacity to remove Pb(II), Mn(II) and Cr(III). Their concentrations are the most important in the water column of Tenorio Tank. Because phytoremediation and phytomining requires growth of the plants, the experiments were carried out in nutrient media under conditions supporting the root growth.

Materials and Methods

The T. latifolia and S. americanus roots were collected from plants growing on the Tenorio Tank. Segments of roots (5 to 10 cm) were washed for 3 days on a soap solution and then were rinsed with tap water. They were treated with 5% sodium hypochloride-0.2% Tween-20, during 15 min and transferred to a quarter strength concentration of Murashige-Skoog medium, ¼ MS (Murashige and Skoog, 1962) containing 10 ml L-1 Plant Preservative Mixture (PPM) for 24 hrs. The roots were transferred to liquid MS medium supplemented with 116 µM myo-inositol, 1.2 μM thiamine-HCl and 3% sucrose. The pH of the media was adjusted to 5.7 after addition of the auxins indolacetic acid (IAA), indolbutyric acid (IBA), naphtalen acetic acid (NAA) or 2,4-dichlorophenoxiacetic acid (2,4-D). The media were sterilized at 120ºC for 20 min.

The roots were cultured in 250 ml flasks on a orbital shaker operated at 130 rpm and maintained at 25ºC and photoperiod of 16 hrs light (45 µmol m-2s-1) and 8 hrs dark. Previous to the experiments of metal removal the roots were subcultured every 15 days during 2 months to have active growing cultures. The growth of the roots was measured as increased on dry weight. The roots of T. latifolia and S. americanus were placed on 50 ml flasks with 10 ml medium MS containing Cr (15 µg L-1), Pb (60 µg L-1) or Mn (1.8 mg L-1). The media of three flasks of each treatment, were collected by filtration and the removal of metals from solutions was quantified every 2 days, during 8 days. The samples were acidified with 3 µl mL-1 HNO3 0.02N, filtrated through membranes (0.22 µM pore size) and place on HDPE flasks. The metals concentration was analyzed using an Atomic Absorption Spectrophotometer (3110 Perkin Elmer with graphite furnace). The quality control of the metal analysis was performed using a reference water (Riverine SLRS-3 water; NRC-CNRC, Canada) added to the culture media to simulate the sample matrix composition. The metal recovery during the analysis varied between 85-110% of the certified concentration of the reference material.

Three replications per treatment and two independent experiments were included per analysis. In order to evaluate statistically and significant differences among mean values, an ANOVA and Tukey test were used at the significance level of 95%.

Results

To establish the in vitro root cultures 0.4 g or 0.2 g of fresh roots of T. latifolia, and 0.1 and 0.05 g of roots of S. americanus were used as inoculum. Different mass was used since S. americanus roots were more compact. The T. latifolia roots have grown faster using the higher inoculum and reached the maximum at day 9. However, after this time a rapid decrease on growth was observed. With 0.2 g of roots the growth was constant until day 6 and then it decreased gradually (Figure 1a). In the case of S. americanus roots, no growth was observed at any time tested when 0.1 g of roots was used. With 0.05 g of roots a rapid increase in dry weight was evident at 6th day decreasing slowly with time (Figure 1b). According to these results, the inoculum selected, for next experiments, were 0.2 g of T. latifolia roots and 0.05 g of S. americanus roots. The decreasing growth observed with the higher inoculum probably is due to a rapid consumption of nutrients from the culture medium and to a consequent starvation of roots.

As the auxins generally promote lateral root formation, we tested the effect of 1 mg L-1 IAA, IBA, NAA or 2,4-D. After 10 days, the growth of roots of T. latifolia onto the culture media containing NAA or IBA was lower in comparison with control medium. An increase in biomass was observed until day 4 onto the medium with 2,4-D. The IAA promoted the highest growth of roots reaching the maximum at day 8 (Figure 2a). The roots of S. americanus presented a similar behaviour. The growth of roots was lower on media with ANA and 2,4-D in comparison with control medium. The highest increase in growth was obtained again with IAA but at day 6 (Figure 2b).

Once selected the auxin promoting the most important increase of growth, we analyzed the effects of different concentration of IAA on rooting. As expected, the exogenous IAA caused abundant lateral roots formation in T. latifolia compared with control medium. The increase in radical growth was proportional to the concentration of auxin until 8 day (Figure 3a). In the case of S. americanus roots a small increase in dry weight was observed with 0.1 and 0.5 mg L-1of IAA but just until day 4. However, using higher concentration of IAA (1-2 mg L-1) an increase between 3 to 3.5 fold was observed in comparison to control medium (Figure 3b).

In summary, the optimal conditions to establish the in vitro roots culture corresponded to an inoculum of 0.2 g of T. latifolia roots and 0.05 g of S. americanus roots (fresh weight) and MS medium containing 2 mg L-1 of IAA.

To measure the Pb, Cr and Mn removalby roots the experiments were conducted over a period of 8 days. The results shown that growth of T. latifolia and S. americanus roots was essentially unaffected by the presence of Pb, Cr or Mn onto medium (Table 1). The S. americanus and T. latifolia roots removed from the culture medium about 50% of Pb at 4 hrs, period that was nominated time 0. The metal was totally captivated at day 4 by S. americanus cultures and about 95% at day 8 by T. latifolia roots. In the case of Cr its removal was slower reaching only 34% (T. latifolia) and 47% (S. americanus) at time 0. Close of 90% of metal was removed from the medium at day 4 in both cultures. On the other hand, the removal of Mn was time dependent. The T. latifolia roots were able to remove only 70% of metal at the end of the experiment while those of S. americanus removed 100% at day 8. These results indicate that both cultures have the ability to efficiently remove the metals without deleterious effect.

Table 2 shows the maximum removal of metal from the solution related to the quantity of root biomass (gram of dried weight) that has growth in the culture medium. According to these data S. americanus cultures removed between 1.5-3 fold more metals than T. latifolia roots and in a shorter time.

Discussion

The in vitro roots culture is an ideal system to study the process involved in heavy metals uptake because they can be propagated indefinitely, are very stable, and eliminate the effect of variations between individual seedlings (Pollard and Baker, 1996). Previous papers have demonstrated the effectiveness of in vitro roots cultures to remove metals (Nedelkoska and Doran, 2000). Yet, the metal concentrations in biomass grown in liquid culture are usually greater than those in soil-grown plants due to the greater bioavailability of metal ions in solution.

In this work, we selected the T. latifolia and S. americanus species since they are adapted to grow on presence of heavy metals. To initiate the in vitro culture the roots were cultivated in media with auxins because it is widely accepted that auxins have a central role in adventitious root initiation (Blakesley, 1994). In T. latifolia and S. americanus root cultures the auxin IAA promoted the highest root formation. As it is a natural endogenous hormone probably it was rapidly catabolised to a suitable level in cells under strict metabolic regulation (Vuylsteker et al. 1998). It has been described that IAA improves the number and quality of roots in several species because it stimulates the cellular division of radical primordium, promotes the synthesis of specific proteins and increases the sugar release into the phloem (Wilson, 1994). The stimulatory effect of IAA has also been described on in vitro culture of normal and hairy roots of Pueraria lobata (Liu et al. 2002) and horseradish (Nakasimada et al. 1994). The selected conditions allowed the fast growing of roots in the in vitro cultures. To our knowledge, this is the first report that describes a protocol to establish the in vitro root culture of these species.

The T. Latifolia and S. americanus root cultures were able to remove Pb and Cr near to 100% and 71-100% of Mn from the medium solution during the 6-8 days of experimentation.The mechanisms of metals removal seems to be characterized by a rapid then by a slower metal concentration decrease in the solution. The rapid decrease could be related to a sorption process at the root surface. Plant cells have an abundance of negatively charged-sites on their walls, so ion-exchange and other interactions between metals and carboxyl, sulphate, amino and other groups are likely to occur (Kratochvil and Volesky, 1998). The sorption of Pb, Mn and Zn to the root surface has been described in wetland plant (Phalaris arundinacea) by microtomography and X-ray microprobe images (Hansel et al. 2001). Adsorption and precipitation at the root surfaces seems to be the mechanism. Other mechanism of short-term removal, such a chelation and covalent binding cannot be discounted.

The slower metal concentration decreasing can be due to an absorption process that should involve transport across the biological membrane and the internalization of the metal. This response could be a critical defensive strategy of the plant, providing time for the development of intracellular mechanism of metal complexation with specific proteins or sequestration onto the vacuole. In the particular case of Thlaspi caerulescens the analysis of root cell wall fractions revealed that the hairy roots partitioned virtually all the Cd uptake by the biomass in the cell wall fraction for 7 to 10 days before allowing passage into the symplast (Nedelkoska and Doran, 2000). The mechanism of Cd hyperaccumualtion in this species seems to be related to an efficient antioxidative defense, particularly an enhanced catalase activity (Boominathan and Doran, 2003). Further studies will be required to define the specific mechanisms of tolerance to Pb, Cr and Mn in S. americanus root cultures. It will be necessary to determine if the metal removal is the result of an adsorption and/or absorption process and which molecules are participating (glutathion, glutathion S-transferase, organic acid, fitoquelatins, methalothioneins, etc.).

On the other hand, the plants have been divided in three arbitrary categories according to the ability to remove metals: normal plants, accumulators and hyperaccumulators. In the particular case for Cr, Pb and Mn metals, an accumulator concentrates more than 50 µg Cr g-1, 100 µg Pb g-1 and 2000 µg Mn g-1 dry weight while an hyperaccumulator concentrates 1000 µg g-1 of Cr and Pb, and 10,000 µg g-1 of Mn (Reeves and Baker, 2000). Considering the quantity of roots used and the metal removed from solution we have calculated the metal concentration removed per gram of tissue. Taking into account these data, the T. latifolia species correspond to the category of normal plants and S. americanus could be considered as an accumulator for Pb (157.73 µg g-1), Cr (55.6 µg g-1) and Mn (5000 µg g-1). To date there are few reports of plants that accumulate Mn but there are no known Pb hyperaccumulator plants (Lasat, 2002).

Even when the in vitro root cultures of S. americanus were not a hyperaccumulator it is an interesting model due to its tolerance to several metals. It has been described that plants able to accumulate more than one metal, present some mechanisms that includes the induction of specific enzymes or phytochelatins, and the participation of specific transporters. For example, phytochelatins complexes with Cd, Ag and Cu has been identified on Arabidopsis thaliana, Silene vulgaris, Holcus lanauts, Agrostis castelana and Thlaspi caerulescens (Cobbett, 2000; Schat et al. 2002). The enhanced tolerance to Cd, Co, Cu, Mg, Ni, Pb and Zn in transgenic tomato plants was related to an increase in 1-aminocyclopropane-1-carboxilic acid (ACC) deaminase activity (Grichko et al. 2000) and the tolerance to Cd, Co and Zn in Thlaspi goesingense is related to a CDF present in vacuoles (Hall and Williams, 2003).

The root cultures present an additional advantage to study the mechanisms of tolerance to heavy metals. It is well known that the in vitro production of secondary metabolites can be increased several times by modifying the culture conditions (Charlwood et al. 1990). This strategy could also be used to increase the metal tolerance on S. americanus root cultures. There are many examples from the literature describing plants which synthesize and accumulate secondary metabolites (glyceollins) upon treatment with metals. The mechanism proposed suggests that heavy metals induce an oxidative stress. The lipid oxidation process generate oxilipins, signaling molecules responsible for the heavy metal-induced defense response, this is, enzymes, glyceollins, proteins, transporters and/or quelators (Mithöfer et al. 2004).

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