Growth characteristics and dynamics of protein synthesis in callus cultures from Glycine wightii (Wight & Arn.) Verdc.

Características do crescimento e dinâmica da síntese de proteínas em cultura de calos de Glycine wightii (Wight & Arn.) Verdc.

CIÊNCIAS AGRÁRIAS

Growth characteristics and dynamics of protein synthesis in callus cultures from Glycine wightii (Wight & Arn.) Verdc.

Características do crescimento e dinâmica da síntese de proteínas em cultura de calos de Glycine wightii (Wight & Arn.) Verdc.

André Luis Coelho da Silva^I; Cecília Sulzbacher Caruso^II; Renato de Azevedo Moreira^III; Ana Cecília Góes Horta^IV

^IEngenheiro Agrônomo, Dr., Grupo de Biofísica Molecular e Espectroscopia /USP-IFSC, Cx. P. 369 13560-970, São Carlos, SP, Brasil [e-mail]

^IIDra.,USP-IFSC, Cx. P. 369 13560-970 São Carlos, SP, Brasil

^IIIProfessor Titular, Dr., LABLEC-DBBM/UFC, Cx. P. 6020 60451-970 Fortaleza, CE Brasil

^IVProfessora Adjunto, Dra., LABLEC-DBBM/UFC, Cx. P. 6020 60451-970 Fortaleza, CE Brasil

ABSTRACT

Cotyledon explants were first cultured on MS medium supplemented with 4.52 M 2,4-D and 0.46 mM kinetin. The development of the calli was followed (0, 4, 8, 12, 16, 20, 24, 28 and 32 days after) and the growth curve was determined, based in fresh and dry weight. The growth curve presented sigmoidal form with four distinct phases. The highest growth percentage was observed at the exponential phase and the lowest at the stationary phase. These results indicated that cotyledon callus subculture should be performed 20 days after inoculation. The calli obtained after a period of 28 days were freeze dried, macerated and submitted to extraction with buffers of different pH values (2.6; 4.0; 6.0; 8.0 and 10.0) and the proteins in the extracts were determined by Bradford method. The pH 8.0 buffer was the most efficient to extract the largest amount of protein. The amino acid analyses calli showed a high content of aspartic acid and low content of metionin. The dynamics of protein synthesis in calli was followed by SDS-PAGE electrophoresis.

Index terms:Glycine,Leguminosae, callogenesis, SDS-PAGE.

RESUMO

Explantes cotiledonários foram primeiramente cultivados em meio MS suplementado com 2,4-D 4,52 mM e cinetina 0,46 mM. O desenvolvimento dos calos foi acompanhado (0, 4, 8, 12, 16, 20, 24, 28 até 32 dias após o subcultivo) e uma curva de crescimento foi determinada com base nos pesos fresco e seco dos calos. A curva de crescimento apresentou um padrão sigmoidal com quatro fases distintas. A maior porcentagem de crescimento foi observada na fase exponencial e a menor na fase estacionária. Estes resultados indicam que o subcultivo dos calos pode ser realizado 20 dias após a inoculação. Os calos obtidos após um período de 28 dias foram liofilizados, macerados e submetidos à extração de proteínas solúveis, utilizando tampões com diferentes valores de pH (2,6; 4,0; 6,0; 8,0 e 10,0) e o teor protéico dos extratos foi determinado pelo método de Bradford. O tampão pH 8,0 foi o mais eficiente na extração de proteínas solúveis dos calos. A análise de aminoácidos mostrou que os calos apresentam um alto teor de ácido aspártico/asparaina em um baixo teor de metionina. A dinâmica da síntese de proteínas nos calos foi acompanhada por ensaios eletroforéticos (SDS-PAGE).

Termos para indexação: Glycine, Leguminosae, calogênese, SDS-PAGE.

INTRODUCTION

Glycine wightii is an important climbing vine-like perennial, belonging to the family Leguminosae, sub-family Papilionoideae, genus Glycine and sun-genus Bracteata. This species is indigenous to Africa an in Brazil is commonly called "perennial soybean" (FIGUEIREDO, 2000).

The techniques of plant tissue culture possess an enormous potential for the plant improvement and can also be used as a tool for studing protein synthesis. Tissue culture, inclusive of in vitro cells, tissues and organs, is a convenient and effective means in breeding genetics, physiology and biochemistry of legumes and it can also contribute to production of biomass and metabolites.

In vitro culture of glycine species has been reported from cotyledons and hypocotyls (PANDEY & BANSAL, 1992), leaves (HAMMATT et al., 1987). Although the in vitro tissue culture has been reports for different dicotyledonous and monocotyledonous species, the number of reports dealing with dynamics of proteins synthesis in callus culture is still low (PODDER et al., 1993, SAARE-SURMINSKI et al., 1999; SERRA et al., 2000). Callus and cell culture could not only be an alternate continuo source of proteins, but could also be an useful and important model system to study their regulation and biosynthesis (PODDER et al., 1993) and in biochemistry studies (SERRA et al., 2000).

The objective of the present work was investigate the growth characteriscs of the callus cultrure from Glycine wightii and to follow the dynamics of the proteins synthesis during this growth. The interest in the present study is based on the fact that plant tissue and cell cultures could be a useful and important tool to study biochemical em physiological parameters associated with the cell growth and dynamics, such as, intracellular levels of proteins.

MATERIAL AND METHODS

Plant material

Glycine wightii (Wight & Arn.) Verdc. madure seeds were collected from plants growing in the city of São Carlos-SP (Brazil). The botanical identification was carried out at the Department of Botanic, Federal University of Viçosa (UFV).

Germination conditions seeds

The seeds were pretreated by imersion in concentrated sulfuric acid (98%) for 20 minutes and washed exhaustively in running tap water. The seeds were sterilized with 2-2.5 % NaClO for 15 min. After washing several times with sterile water, they were placed between two sheets of filter paper Whatman 3 M moistened sterile destilled water and kept in Petri dishes, in the dark. The seedlings were harvested with 7 days old.

Callus induction and maintenance

Segments (18 + 2 mm) were taken from cotyledons of the seedlings and placed on solidified medium consisted of MS salts (MURASHIGE & SKOOG, 1962) to supplemented with 4.52 mM 2,4-D, 0.46 mM kinetin and 3% sucrose (SILVA et al., 2003). The medium was adjusted to pH 5.8 with 1 N NaOH, autoclaved and dispensed in 100 x 15 mm petri dishes (25 ml medium for dish).The cultures were incubated at 28 + 2 ºC in the dark. After 4 weeks, the developed calli of cotyledons were separated from explants and transferred to fresh medium of same composition. The calli were subcultured for an additional 4 weeks.

Callus growth determination

Cotyledon callus stocks established previously were used to determine the growth curves. Pieces of friable callus (similar size) were inoculated in the MS medium supplemented with 4.52 mM 2,4-D, 0.46 mM kinetin and 3% sucrose . The culture was incubated at 28 + 2 ºC in the dark. The development was monitored at 4 days intervals up to 32 days and a growth curve was determined based in fresh and dry weigh of the calli.

Protein content determination

The calli from cotyledon obtained after 28 days were lyophilized, macerated and submitted to extraction with 0.1 M glycine-HCl pH 2.6, 0.1 M NaOAc pH 4.0, 0.1 M NaOAc pH 6.0, 0.1 M Tris-HCl pH 8.0 and 0.1 M Na-borate pH 10.0 buffers, all containing 0.15 M NaCl. The samples were sonicated for 1 hour and clarified by centrifugation at 12.000 x g for 20 min at 4 ºC. The clear supernatants were used for determination of soluble protein content. The protein content in the different fractions was performed according to Bradford (1976), using bovine serum albumine (BSA) as standard.

Dynamic of proteins synthesis

The proteins synthesis in calli during the growth curve was followed by measurement of protein content (BRADFORD, 1976) and by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) as described by Laemmli (1970). The samples (10 mg of callus powder) were dissolved in 1 ml of 0.1 M Tris-HCl pH 8, 2% sodium dodecyl sulfate (SDS) buffer with 1% b-mercaptoetanol and incubated at 100 ºC for 10 min. Silver staining was performed as described by Blum et al. (1987). The identification of the components of the storage proteins in the total extracts from G. wightii seeds was made using a protein marker extracted from soybean (Glycine max). The approximate molecular weights of the b-coglycinin subunits corresponded to 76, 72 and 53 kDa for a', a and b-subunits and those of the glycinin subunits to 45 and 38 kDa for the acidic, and 22 kDa for the basic subunits, as previously described by Shuttuck-Edidens & Beachy (1985).

Amino acid composition

Amino acid analysis was performed after hydrolysis at 110 ºC of callus samples (in sealed glass tubes under N2) for 20 h in 6 M HCl. After hydrolysis, HCl was removed by evaporation and the residue was analyzed, in a BIOCHROM 20 (Pharmacia) amino acid analyzer. Tryptophan was determined according to the method described by Pintér-Szakács & Molnár-Perl (1990).

Data analysis

For callus growth and protein, the experiments were carried out at least two time with 5 replicates. Five plates (5 explants / plate) were used every 4 days during the culture period to measure the growth callus and protein contents. Means standard error were applied to analyze the data.

RESULTS AND DISCUSSION

Growth curves of cotyledon calli were plot based on fresh and dry weights (Figure 1). Cotyledon calli presented sigmoid growth curves with lag, exponential, linear and stationary phases. The adaptive period (lag phase), in which the fresh and dry weight of calli increases slowly, occured up to 4th day for cotyledon calli . According to Sragg & Allan (1993), the lag phase is considered an energy producer period. The fast growth phases (exponential and linear phases) occurred between 4th and 16th day. The exponential or biosynthetic phase is the period of maximum celular division and greatest growth rate of the calli, while the linear phase is the period in which the cells grow but the cellular division decreases (SCRAGG & ALLAN, 1993). The stationary phase of cotyledon calli occurred between the 16th and 32nd day. In this phase, the rate of cellular division is gradually reduced and then remain constant. According to Smith (2000), in the stationary phase occurs deprivement of nutrients in culture medium and a reduction of the O2 amounts inside the cells.

Figure 2 shows the influence of pH in the solubility of calli proteins. The protein content from Glycine wightii is 150 mg.g^-1 seeds powder (VISWANATHAN et al., 2001). It was found a maximum (soluble) protein content at pH 8.0 (39.1 mgProtein.g^-1 cotyledon calli powder) and a minimum content at pH 4.0 (9.0 mgProtein.g^-1 cotyledon calli ). Gupta & Srivastava (1998) studing the calli from Zizyphus mauritiana, also observed that the cotyledon calli had a higher protein content (28.7 mgProtein.g^-1 callus powder).

The protein content was analyzed during the growth callus (Figure 3). The results showed that between the 0 and 12th day of culture there was a decrease in the protein content. This reduction possibly occurred due to an adaptation period of calli in the culture medium. The increase in the protein levels between 12th and 16th day of culture could be related to mitotic activity during the exponential and linear growth phases. Gutmann et al. (1996) also observed an increment in the protein levels in the cells of Larix leptoeuropaea during the first 2 weeks of culture, followed by a decrease of this content during the following weeks. The cell cycle is carried out by thesynthesis of several new proteins that bring on morphological and biochemical changes in the cell during the mitotic activity. The decrease of the protein levels during to stationary phase correlates with the physiological stress related to diminishing nutrition in the medium, ageing and cell degeneration. Lal et al. (1992) also observed an increase in the protein level during the growth phase of the sugarcane callus and a decrease during the celular differentiation phase.

In cotyledon different days of the growth curves, SDS-PAGE analysis of the proteins extracts revealed some little change for the bands protein. Despite the differences observed, the protein patterns obtained from cotyledon calli powder electrophoresis (Figure 4-A2) were similar to proteins obtained from soybean and G. wightii seeds powder (Figure 4-A1), with predominance of bands with molecular mass characteristc of b-coglycinin (subunits corresponded to 76, 72 and 53 kDa for a', a and b-subunits) and those of the glycinin (subunits to 45 and 38 kDa for the acidic, and 22 kDa for the basic subunits), the main reserve proteins of soybean (BROOKS & MORR, 1985). In particular, some protein bands started to disappear between 0 and 12th day in both cultures (Figures 4-A1). This reduction may have occurred due to the decrease of soluble protein during that period. Between the 12th and 28th day of the callus culture, it was observed that protein bands with molecular weights between 94 and 20 kDa reappeared, suggesting a "de novo" synthesis process. In addition, other protein bands (between 20 and 45 kDa) were preserved during the growth of the cotyledon calli (Fig. 4-A2).

The data on amino acid content of the cotyledon calli powder revealed that such as soybean seeds powder, calli proteins are well balanced in the essential amino acids, except slightly limiting in cystine, methionine and tryptophan are the conspicuous limiting amino acids (Table 1). These results are comparable to data reported for G. wightii seeds flour (VISWANATHAN et al., 2001) and other soybean cultivars (VASCONCELOS et al., 1997). Cotyledon calli flour showed a high percentage of aspartic acid/asparagines. Others amino acids showed similar values.

CONCLUSION

Our results suggest thatcallus culture provides an interesting model system to investigate the dinamic of protein biosynthesis, thus providing a clue to their physiological functions. Moreover, by knowing which proteins are being synthesized in callus culture obtained from different explants and stages of growth and can lead to identifying the role of these proteins.

ACKNOWLEDGMENTS

This work was supported by grants from the Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq).

(Recebido para publicação em 4 de novembro de 2004 e aprovado em 26 de setembro de 2005)

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Publication Dates

• Publication in this collection
  18 Aug 2008
• Date of issue
  Dec 2005

History

• Accepted
  26 Sept 2005
• Received
  04 Nov 2004