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Brazilian Archives of Biology and Technology

Print version ISSN 1516-8913On-line version ISSN 1678-4324

Braz. arch. biol. technol. vol.44 no.3 Curitiba Sept. 2001

https://doi.org/10.1590/S1516-89132001000300004 

Purification and Properties of Asparaginase from the Testa of Immature Seeds of Pea (Pisum sativum L.)

 

Eliana P. Chagas and Ladaslav Sodek*
Departamento de Fisiologia Vegetal, Instituto de Biologia, Universidade Estadual de Campinas, Caixa Postal 6109, CEP 13087-970, Campinas - SP, Brazil

 

 

ABSTRACT

A K+-dependent asparaginase (E.C. 3.5.1.1.) was purified 1328-fold from the testas of immature pea seeds (Pisum sativum L., var. Bolero) and characterized. Antibodies raised against purified asparaginase cross-reacted with the putative asparaginase band in Western blot analyses of semi-purified extracts. However, for crude extracts of pea testas, a cross-reaction was obtained with at least four protein bands, one of which was asparaginase protein. Affinity-purified antibodies to the four strongest bands of crude extracts were fairly specific for the bands from which they were purified, suggesting a mixture of specific antibodies. The Mr of asparaginase was 69,000 by Sephacryl S200 chromatography and also by mobility on native PAGE relative to BSA. There was no evidence for dissociation into subunits on SDS-PAGE, suggesting a monomeric protein of Mr 69,000. Other properties include an apparent Km of 2.4 mM, pI between 4.5 and 5, and competitive inhibition by aspartate and glycine.

Key words: Pisum sativum, asparaginase, purification, properties

 

 

INTRODUCTION

Asparagine predominates in the transport of nitrogen in many legumes studied so far and constitutes an important source of reduced nitrogen for developing seeds (Sieciechowicz et al., 1988). In developing pea seeds, it is initially metabolized in the seed coats (Murray & Kennedy, 1980; Murray & Cordova-Edwards, 1984) giving rise to ammonia, alanine and glutamine in the endosperm fluid. As the cotyledons start growing, the cotyledons themselves develop a capacity for metabolizing asparagine (Atkins et al., 1975). Indeed, isolated pea and soybean cotyledons grow in culture with asparagine as sole source of nitrogen (Thompson et al., 1977; Lea et al., 1979; Haga & Sodek, 1987).

There are two known routes for asparagine catabolism. The first, catalysed by asparagine transaminase, involves the transamination of the amino group to form 2-oxosuccinamic acid and appears to be important in green leaves where it may play a role in photorespiration (Atkins et al., 1983; Murray et al., 1987; Joy, 1988). The second route involves the release of ammonia from the amide group in a reaction catalysed by asparaginase. This enzyme was first detected in the developing seeds of Lupinus albus (Atkins et al., 1975). Two forms of the enzyme have been identified. A K+-independent form found in L. arboreus (Lough et al., 1992a; Chang & Farnden, 1995) and L. polyphyllus (Lea et al., 1978) and a K+-dependent form found in Pisum sativum and several other legume species, including other Lupinus species (Sodek et al., 1980). Work with antibodies to the K+-independent form from L. polyphyllus revealed no cross-reaction with either pea ASNase or a number of varieties of Lupinus containing the K+-dependent enzyme, suggesting that the two forms of ASNase are immunologically distinct (Lea et al., 1984).

The K+-independent form has been more thoroughly studied, perhaps in view of its greater stability. It was first purified from L. polyphyllus (Lea et al., 1978) where it was shown to have a Mr of 72,000 with subunits of 38,000. It was later purified from L. arboreus which revealed a Mr of 75,000 (Chang & Farnden, 1995). A cDNA clone for a truncated asparaginase protein of Mr 32,775 has been isolated from this species (Lough et al., 1992b) and subsequently the complete genomic sequence was obtained (Dickson et al., 1992). The K+-dependent ASNase has been partially purified from pea leaves (Sieciechowicz & Ireland, 1989) and the seed coat of immature pea seeds (Sodek & Lea, 1993). However, purification sufficient for raising antibodies has never been achieved nor is there any information available as to its subunit composition.

The aim of this work was to purify ASNase sufficiently to raise antibodies and extend the characterization of this enzyme.

 

MATERIALS AND METHODS

Plant material: Pea plants (Pisum sativum L. cv. Bolero) were cultivated in field plots during the winter (May-August). Immature seeds were harvested when endosperm fluid was still present, before the rapid growth phase of the cotyledons. Isolated testas were stored frozen at -20oC.

Tissue extraction: Frozen testas were ground in a chilled mortar with 50 mM Tris-HCl pH 8.0 buffer containing 50 mM KCl, 1 mM dithiothreitol, 1 mM PMSF and 10% glycerol. The extract was centrifuged at 10,000 x g for 20 min and the supernatant used for purification or enzyme assay after desalting on a Sephadex G25 column.

Enzyme assay: Asparaginase (ASNase) (EC 3.5.1.1) was assayed by the ammonia-diffusion and phenol-hypochlorite method described previously (Sodek & Lea, 1993).

Purification procedure: The purification of ASNase was based on that described by Sodek & Lea (1993). Column dimensions were: Sephadex LH20 2.8 x 19 cm; DEAE-Sephacel 1.3 x 5.3 cm; Phenyl Sepharose 10 mL; Sephacryl S-200 2.6 x 83 cm; FPLC-Mono Q 0.5 x 5 cm.

Kinetic studies: Km was determined from double reciprocal plots (Lineweaver-Burke) and inhibitor constants (Ki) from secondary plots of slope from Lineweaver-Burke plots against inhibitor concentration.

Molecular weight: Estimates of molecular weight were made using the same Sephacryl S-200 column used during purification. The column was calibrated with blue dextran (2,000,000 g/mol), catalase (232,000 g/mol), b-amylase (200,000 g/mol), alcohol dehydrogenase (150,000 g/mol), BSA (67,000 g/mol), carbonic anhydrase (29,000 g/mol), chymotypsinogen (25,000 g/mol), ribonuclease A (13,700 g/mol) and cytochrome c (12,000 g/mol). For SDS-PAGE the standard protein mixture contained BSA (67,000 g/mol), ovalbumin (43,000 g/mol) chymotrypsinogen (25,000 g/mol) and ribonuclease A (13,700 g/mol).

Polyacrylamide gel electrophoresis: Native and SDS-PAGE were carried out using the Midget system (Hoeffer Sci. Inst.) with 10 and 13% acrylamide gels, respectively. After electrophoresis, proteins were detected by silver staining (Oakley et al., 1980). Other details are as described previously (Sodek & Lea, 1993).

Antibody preparation and western blot analysis: The most active fractions obtained after the FPLC MonoQ purification step were pooled, dialysed against distilled water, lyophilized and taken up in phosphate buffer saline (PBS) solution. An aliquot (containing 50 m g of protein) was emulsified with Freund’s complete adjuvant and injected subcutaneously into a rabbit. A second application, prepared with incomplete adjuvant was injected 3 weeks later. After 6 weeks, a blood sample was taken from the rabbit and the IgG fraction purified from the serum using ammonium sulphate precipitation followed by Protein-A Sepharose affinity chromatography, as described previously (Sodek & Lea, 1993).

After electrophoresis, the proteins were transferred electrophoretically to a nitrocellulose membrane (Biotrace NT, Gelman), according to Towbin et al (1979), using the LKB-Pharmacia horizontal Multiphor Nova Blot system. A constant current of 0.8 mA/cm2 was applied for 3 hr. Immunoprobing of the membrane was carried out as described previously (Sodek & Lea, 1993).

In some Western blot analyses, antibodies were first purified by affinity to proteins of a primary blot, using a technique adapted from Buckeridge & Reid (1994). After electro-transfer of proteins from a crude extract, the nitrocellulose membrane was divided into 3 parts. The first was probed and developed as usual to identify the position of the reacting proteins. The second was then sliced to isolate the regions containing each one of the reacting proteins. The cut pieces, after blocking with casein, were incubated separately overnight with the crude antibody, washed 3 times with Tris buffer saline containing Tween and finally placed overnight in 5 mL of 0.1 M glycine, pH 2.5, to dissociate the antibody from the membrane. After adjusting the pH to 7, the antibody was used to probe (overnight) the third part of the membrane, which was developed by the usual techniques.

 

RESULTS

Purification of asparaginase. Asparaginase was purified from the testas of immature seeds of Pisum sativum L. An over 1000-fold purification was acheived (Table 1). The plant material used as a source of the enzyme presented an average activity of 7 mmol NH4+/h.g tissue (s.d.=2.2, n=6). K+ ions were included in both the extraction and assay buffers, in view of its known necessity for activity. Ca2+ ions were also included in the extraction buffer although preliminary tests indicated that they had no effect on activity whether present during extraction or in the assay. Nor did EGTA have any effect when included in the assay. Nevertheless, Ca2+ was used in the extraction buffer because it appeared to improve the recovery of activity during purification, especially at later stages.

 

 

A single activity peak was obtained during all purification steps involving chromatography, except for Sephacryl S-200 where a small fraction of the total activity (about 4%) eluted ahead of the main peak. This fraction was discarded in the purification procedure described in Table 1. The purification step which produced the highest relative gain in specific activity was the treatment with ethanol (after its subsequent removal on Sephadex LH20). All purification steps produced an increase in specific activity despite the instability of the enzyme which diminished recovery. In fact, final recovery of activity was only 1%.

Electrophoretic behaviour. After some of the purification steps, fractions with asparaginase activity were analysed by native and SDS-PAGE. Following chromatography on Mono-Q, the last purification step, where all activity eluted as a single peak, native PAGE of the peak fractions revealed the presence of two distinct protein bands (denominated B1 & B2) with mobilities corresponding to Mr 85,000 and 69,000 (relative to BSA monomer and dimer) (Figure 1). Clearly, band B1 was present only in the leading fractions of the activity peak whereas band B2 was present in all the activity peak fractions. Furthermore, this band was strongest in the fraction containing the highest activity. This suggested that asparaginase activity was associated with the band B2 (Mr 69,000), but not with band B1.

 

 

Despite the apparent difference in molecular weight of the two proteins, B1 and B2, identified by native PAGE, it was not possible to separate them by molecular sieve chromatography (Sephacryl S-200), as used in the penultimate purification step. Although two peaks of activity were obtained from this column (figure 2), the first, with only 4% of the total activity, produced a slow-moving band, corresponding to a molecular weight of about 200,000, when analysed by native PAGE (Fig.2 lanes 19, 20). In any case, this activity was discarded during purification and would not be present in the extract used for Mono-Q chromatography that produced the B1 band. On the other hand, both the B1 & B2 proteins were present in the main activity peak of the Sephacryl column, as revealed by native PAGE analysis of the peak fractions (lanes 29-36). However, both proteins were present in all the activity peak fractions without any indication of separation suggesting similarity in their molecular weights; therefore other physical properties must determine their separation by native PAGE.

 

 

In order to confirm that ASNase activity was indeed associated with band B2 rather than B1, activity of the enzyme was determined directly in the gel after electrophoresis. For this purpose, a fraction with high activity eluted from the Phenyl-Sepharose column was applied to a native gel and, after electrophoresis, activity determined in gel slices by a semi-quantitative assay (Sodek & Lea, 1993). The formation of aspartic acid in the assay, as analysed by TLC, was intense for slices taken from the region of the BSA monomer (Mr 67,000; used as a marker), which corresponded therefore, to the B2 band (Mr 69,000) (data not shown).

The B1 & B2 proteins, obtained by chromatography on Mono-Q, were also submitted to SDS-PAGE analysis. From Figure 3 it may be seen that the B1 protein dissociated into subunits of about Mr 18,000, whereas the B2 (Mr 69,000) protein apparently did not dissociate since only one band was seen in the same position as in native gels.

 

 

Properties of asparaginase. Partially purified ASNase revealed Michaelis and Menten kinetics with an apparent Km of 2.4 mM. The enzyme was inhibited competitively by Gly and Asp (Ki = 7.7 mM and 11 mM, respectively). Information on the pI value was obtained after isoelectric focalization in the Rotorfor™ (Pharmacia) system, where ASNase activity was found in fractions corresponding to a pH of 4.5 to 5.0.

Western blots. Western blots using crude extracts and a partially purified fraction (Phenyl-Sepharose step) revealed six and two bands, respectively, when probed with the antibody produced against purified asparaginase (Figure 4). The four strong bands of the six identified in the crude extract by the antibody (Fig.4 -A) are denominated B1 (two closely-running bands), B2 (putative ASNase band), and B3. Two weak band were seen, one running between B2 and B3 and the other near the top of the gel. The two bands obtained with the partially purified fraction (Fig.4 -B), according to this nomenclature, correspond to B1 and B2.

 

 

Since the antibody reacted with proteins other than those running in the position of ASNase when using crude extracts, further tests were performed in order to determine whether these additional bands resulted from poor antibody specificity or to the presence of other forms of ASNase in the crude extracts. Here, the Western blot system was used to "purify" the antibody through its affinity for each of these protein bands. When the antibody that attached itself to each band of the blots was dissociated from the complex and used as a probe in a separate Western blot of the crude extract, a certain degree of specificity for each antibody was observed (fig. 5). Thus, antibody taken from the two B1 bands reacted most strongly with the same bands in the second blot, as did the B2 and B3 bands. There was, however, a weak reaction with other bands in all cases except for the antibody removed from the B3 band where no trace of reaction with the other bands could be observed.

 

 

DISCUSSION

Asparaginase was purified from the testas of immature seeds of Pisum sativum L., essentially as described by Sodek & Lea (1993). An over 1000-fold purification was achieved with a specific activity of 1328 mmol.h-1.mg-1 protein (Table 1). Although the purification factor was far superior to that obtained by Sodek & Lea (1993), the specific activity was only marginally improved. The high instability of the enzyme would appear to be responsible for this discrepancy. Indeed, final recovery of activity was only 1%.

The asparaginase from immature pea seeds has previously been characterized as being potassium-dependent (Sodek et al., 1980). The Km was 2.4 mM, somewhat lower than that reported by Sodek et al (1980), using a different assay, but nevertheless in the general range for K+-dependent ASNases, that is, 2.5 - 4.9 mM from pea leaf (Sieciechowicz & Ireland, 1989) and 2.7 mM from winged bean seeds (Chapleo & Hall, 1989). It is noteworthy that the Km of K+-independent ASNases are significantly higher (Chang & Farnden, 1995; Lea et al., 1978), in the range 6 to 12 mM. The ASNase from L. albus, with a Km of the order 10 - 12 mM (Atkins et al., 1975), would appear to be an exception, since this enzyme was later reported to be K+-dependent (Sodek et al., 1980). Some caution is necessary when comparing Kms however, in view of the findings of Sieciechowicz & Ireland (1989) that higher Kms may result from inactivation of the enzyme during assays at lower concentrations of Asn. Stabilizing the enzyme during assay by the addition of 10% glycerol avoids this problem and leads to lower Km values.

Competitive inhibition by aspartate, one of the reaction products, suggests that the reaction mechanism (Cleland, 1963) involves an ordered liberation of products from the catalytic site, with aspartate leaving last. Kinetic data for ammonium as inhibitor, which might confirm this finding, was not possible due to the assay being based on ammonium formation. The competitive inhibition observed with glycine was also reported for the K+-independent ASNase from L. arboreus (Chang & Farnden, 1995).

The Mr of 69.000 was in agreement with that found for the pea testa ASNase by Sodek et al (1980), though Sodek & Lea (1993) subsequently reported a lower value (61,000 Da). The K+-dependent ASNase from pea leaves was reported to have a Mr of 58,000 (Sieciechowicz & Ireland, 1989). In any case, the Mr of the K+-dependent enzyme from pea appears to be marginally lower than the K+-independent enzyme from Lupinus species, reported as 71,000 for L. polyphyllus (Sodek & Lea, 1993), and 75,000 for L. arboreus (Chang & Farnden, 1995).

Although the subunit structure for the K+-independent enzyme of L. arboreus (Lough et al., 1992a) and L. polyphyllus (Sodek & Lea, 1993) was characterized as 2 subunits with a Mr of 35-36 kDa, no comparable data are available for the K+-dependent ASNase. In this study, there was no evidence for the dissociation of the enzyme into subunits. Rather, the SDS-PAGE data suggest the enzyme to be composed of a single polypeptide of 69,000 Da.

Another novel feature of this study was the identification of a high MW ASNase (ca. Mr 200,000). This enzyme was not further characterized, and in any case it represented only a very small fraction of total ASNase activity.

The pI value of 4.5 - 5.0 inferred from the isoelectric focusing experiment for ASNase is close to the value of 5.2 calculated from the cloned gene of Arabidopsis thaliana by Casado et al (1995) and the value of 4.5 for K+-independent ASNase from L. arboreus (Lough et al., 1992a).

Attempts to obtain the N-terminal sequence of the purified protein were unsuccessful, suggesting a possible blocked N-terminal.

The antibody raised against the purified ASNase showed poor specificity when used as a probe in Western blot analysis of crude extracts. As well as the ASNase band itself, several others cross-reacted with the antibody. Since the protein doublet denominated B1 was difficult to separate from the ASNase protein, it is not surprising that antibodies for this protein were present in the preparation. Attempts to purify the antibody by stripping them off their respective proteins from the blots and using them separately as probes in identical blots of the crude extracts resulted in a preferential if not specific reaction with the original proteins. This suggests that the antibody preparation is a mixture of specific antibodies rather than the crude extract being composed of several forms of the ASNase protein. However, there is no explanation for the origin of the highly specific antibody to band B3, since this protein was absent from the preparation used to generate the antibody. The antibody would have to be used with caution as a probe for ASNase protein.

 

ACKNOWLEDGEMENTS

This work received financial support from FAPESP. EPC thanks CAPES for a scholarship.

 

 

RESUMO

Uma asparaginase dependente do K+ (E.C. 3.5.1.1.) foi purificada 1328 vezes a partir de testas de sementes imaturas de ervilha (Pisum sativum L., var. Bolero) e caracterizada. Anticorpos obtidos a partir da asparaginase purificada, usados como sonda em ensaios tipo "Western blot", reagiram com a banda da asparaginase de extratos semi-purificados. Entretanto, em ensaios realizados com extratos brutos de testas de ervilha, uma reação foi obtida com pelo menos 4 proteínas, entre elas a da asparaginase. O uso de anticorpos purificados por afinidade pelas 4 bandas mais evidentes do extrato bruto demonstraram um alto grau de especificidade para com as bandas de proteína das quais foram purificadas, indicando uma mistura de anticorpos específicos. A posição de eluição da atividade de asparaginase em Sephacryl S-200, bem como a sua mobilidade em PAGE não-denaturante relativo à BSA, sugere uma proteína de Mr 69.000. Em análise realizada por SDS-PAGE não foi obtida nenhuma evidência para a dissociação da proteína em subunidades, sugerindo que a proteína seja monomérica com Mr 69.000. Outras propriedades incluem um Km apparente de 2,4 mM, pI entre 4,5 e 5, e inibição competitiva pelo aspartato e pela glicina.

 

 

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Received: December 13, 1999;
Revised: August 25, 2000;
Accepted: November 22, 2000

 

 

* Author for correspondence

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