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Journal of Bacteriology, April 2005, p. 2555-2557, Vol. 187, No. 7
0021-9193/05/$08.00+0     doi:10.1128/JB.187.7.2555-2557.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.

Characteristic Thermodependence of the RadA Recombinase from the Hyperthermophilic Archaeon Desulfurococcus amylolyticus

Yury V. Kil, Eugene A. Glazunov, and Vladislav A. Lanzov^*

Division of Molecular and Radiation Biophysics, Petersburg Nuclear Physics Institute, Russian Academy of Sciences, Gatchina/St. Petersburg, Russia

Received 5 November 2004/ Accepted 29 December 2004

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The Desulfurococcus amylolyticus RadA protein (RadA_Da) promotes recombination at temperatures approaching the DNA melting point. Here, analyzing ATPase of the RadA_Da presynaptic complex, we described other distinguishing characteristics of RadA_Da. These include sensitivity to NaCl, preference for lengthy single-stranded DNA as a cofactor, protein activity at temperatures of over 100°C, and bimodal ATPase activity. These characteristics suggest that RadA_Da is a founding member of a new class of archaeal recombinases.

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RadA belongs to the RecA/RadA/Rad51 protein superfamily found in all three domains of life, the Bacteria, Archaea, and Eukarya (3, 11, 13). As homologous DNA transferases, these filamenting proteins are responsible for homologous recombination, recombination DNA repair, and other aspects of DNA metabolism (5, 8, 9). Like other members of this family, RadA polymerizes on single-stranded DNA (ssDNA) in the presence of ATP, forming a presynaptic complex (PC) which possesses the ATPase activity. PC interacts with double-stranded DNA (dsDNA) to promote homologous pairing and strand exchange, the two critical steps of recombination (4, 15).

The biochemical and recombination activities of five RadA proteins from different hyperthermophilic crenarchaeons and euryarchaeons have been described (6, 7, 10, 14, 17). One of them, RadA from Pyrobaculum islandicum (RadA_Pi), has been studied in more detail than the others. The ATPase of its PC exhibits two disparate catalytic modes, and its PC is active within a wide temperature range (from 37 to 90°C) (17).

Earlier, we described a distinguishing property of RadA protein from crenarchaeon Desulfurococcus amylolyticus (RadA_Da), namely, its ability to promote efficient strand exchange even at 95°C (6). Here, we continued the analysis of biochemical activities of RadA_Da and presented its additional characteristics, which include both expected and distinguishing properties of the protein with regard to known activities of the RecA and RadA recombinases.

ATP hydrolysis is an intrinsic property of the ternary PC (RecA/RadA/Rad51::ATP::ssDNA) formed by any member of the homologous recombinase family. The hydrolysis rate is strongest for the RecA PC (k_cat = 30 min^–1) and is reduced roughly 10 times for representatives of the RadA/Rad51 subfamily. Though ATP hydrolysis is not necessary for the initiation of recombination by the PC, it is essential for the strand exchange progression and completion (4). Since the accumulation of ADP results in PC inactivation, the ATP hydrolysis is routinely used to monitor an active state of PC.

As ATP hydrolysis catalyzed by RadA_Da was measured at temperatures around 90°C and above in the absence of ATP-regenerating system, a linear part of ATPase kinetics was observed within the limits of 1 to 4 min of the reaction (data not shown). Unless otherwise specified, the experimental conditions used in all further experiments were as follows. The reaction was carried out at 90°C in the 20-µl mixture containing TMD buffer (25 mM Tris-HCl [pH 7.5], 10 mM MgCl₂, and 1 mM dithiothreitol), 20 mM NaCl, 1 mM ATP, 15 µM RadA_Da, and 150 µM X174 ssDNA (in nucleotides [nt]). The amount of [¹⁴C]ATP hydrolyzed was measured by using a thin-layer chromatography method as described previously (6).

The 20 mM NaCl used in this mixture was found to be optimal for ATP hydrolysis catalyzed by RadA_Da (k_cat = 3.2 min^–1) (Fig. 1). This concentration is fivefold lower than that used for RadA_Pi (17). Moreover, the addition of 100 mM NaCl resulted in a 3.2-fold decrease of the monomer k_cat value. Similar results were obtained with KCl (data not shown). The data indicate a pronounced sensitivity of the RadA_Da ATP hydrolysis to monovalent cations.

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FIG. 1. The rate constant for ATP hydrolyzed by the RadADa::ATP::ssDNA PC as a function of NaCl concentration. Optimal experimental conditions (90°C, X174 ssDNA) were used; see the text for details.

Besides k_cat, two other steady-state kinetic quantitative characteristics of ATP hydrolysis were determined. These included the S₀₅ value, the substrate concentration for the half-maximal observed rate of hydrolysis, and n_H, the Hill coefficient that serves as a measure of the degree of cooperativity for binding ATP to RadA_Da during filament formation. The dependence between the rate at which ATP was hydrolyzed and the ATP concentration (data not shown) gave us an S₀₅ of 75 µM. This dependence was converted into a Hill plot, the slope of which gave an n_H of 1.2. Both the low rate constant (k_cat) and the low cooperativity (n_H), measured at optimal conditions (90°C, 20 mM NaCl, and lengthy ssDNA [see below]), characterize RadA_Da protein as a typical representative of the RadA/Rad51 subfamily (15, 18).

The effect of ssDNA chain length on k_cat is presented in Table 1. Two oligonucleotides (21 and 53 nt), four PCR fragments (from 250 to 940 bp) of human genomic DNA, dsDNA, and ssDNA of two phages were used as DNA cofactors in PC-dependent ATP hydrolysis. Different forms of M13 phage DNA were used to control the complete melting of dsDNA molecules under experimental conditions. Circular and linearized M13 ssDNA demonstrated the same ability to stimulate ATP hydrolysis as a linearized dsDNA of this phage, whereas the supercoiled dsDNA (replicative form I) was a weak cofactor due to the only partial denaturation at 90°C (Table 1). At optimal assay conditions, the RadA_Da PC was able to hydrolyze ATP efficiently with ssDNA cofactors of 940 nt and greater. This cofactor size is about 30-fold longer than that for RecA protein from Escherichia coli (RecA_Ec) (2). Thus, RadA_Da prefers lengthy ssDNA as cofactors for ATPase activity, and the same preference could probably be applied to the formation of the PC.

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TABLE 1. The rate constant of ATP hydrolysis as a function of ssDNA chain length in composition of the RadADa presynaptic complexa

As was shown before (1), a single amino acid replacement (of Cys129 with Met) alters the basic characteristics of wild-type RecA_Ec, resulting in the reduced kinetics of strand transfer, lower k_cat of DNA-dependent ATP hydrolysis, increased sensitivity to monovalent cations, and the requirement for a longer ssDNA for the PC ATPase activity. Interestingly, the features of RadA_Da addressed here repeat the alterations in properties of this RecA_Ec mutant. Therefore, the suggestion that a limited number of amino acid replacements (possibly just one) are capable of standardizing the RadA_Da characteristics listed above to make them closer to those of wild RecA_Ec cannot be excluded.

The ability of RadA_Da PC to promote recombination at 95°C encouraged us to look for the highest temperatures at which the PC can hydrolyze ATP and to determine factors which provide such thermostability. In Fig. 2A, the rate constants of PCs formed at the temperatures indicated (80 to 100°C) are compared with those of PCs formed at 80°C. Results suggest that the preformation of PCs at 80°C guarantees the conservation of at least a part of the activity up to 102°C.

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FIG. 2. Factors of the RadADa PC thermostabilization. (a) ATPase activity as a function of temperature. The PC was formed (circles) or preformed at 80°C (triangles), and its ATPase was measured at the temperatures indicated. (b) The residual ATPase activity as a function of RecADa preliminary temperature preincubation in TMD buffer with 20 mM NaCl for the times indicated. Circles, 15 µM RadADa preincubated at 90°C; triangles, 180 µM RadADa preincubated at 100°C.

Another important factor turned out to be the stable oligomer formation at high protein concentration. We used 180 µM RadA_Da as the concentration which corresponds to roughly 10,000 protein molecules per bacterium, the number reported for RecA in E. coli (12). Figure 2B shows that after boiling for 30 min (180 µM RadA_Da in TMD buffer with 20 mM NaCl), RadA_Da protein retained one-third of its original activity (this residual activity was measured at 90°C with 15 µM RadA_Da under other standard conditions). For comparison, a preincubation of 15 µM RadA_Da at 90°C for 6 min resulted in a complete inactivation of the protein. The data indicate that two factors, preliminary PC formation and high protein concentration, save, at least partially, the activity of RadA_Da protein, even at 100°C. This conclusion gives the basis of a possible mechanism of RadA_Da protein thermoresistance. RadA_Da should exist as an oligomer or polymer in vivo, even if not being used in recombination repair. This suggestion is consistent with recent observation that Rad51 homolog from hyperthermophilic archaeon Pyrococcus furiosus assembles into inactive heptameric rings before its conversion into active DNA-bound filaments (16).

Figure 3 shows the thermodependence of the RadA_Da PC ATPase, presented in coordinates of an Arrhenius plot. The graph reveals two catalytic modes of ATPase activity with the transition point at 70°C and may reflect the transition between two conformation states of the protein with different modes of functional activation. The first mode has a relatively high energy of activation (46 kcal/mol), whereas the second one has a much lower activation energy (13.9 kcal/mol). In addition, the protein is characterized by a negligible activity below 65°C. For comparison, the thermodependence of RadA_Pi is presented in the same coordinates (see the data from Fig. 6 in reference 17). The latter also exhibits a biphasic Arrhenius plot with two characteristic energies of activation and a transition point at 75°C. The difference between thermodependence of the crenarchaeal recombinases RadA_Da and RadA_Pi appears obvious. RadA_Pi belongs to a class of thermotropic proteins which maintain activity in a wide range of temperatures (37 to 90°C), whereas the activity of RadA_Da is strongly temperature dependent, being close to zero at temperatures below 65°C. Summarizing all data presented in the paper, we suggest that RadA_Da represents a new class of thermophilic recombinases.

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FIG. 3. The comparison of PC thermodependence for RadADa and RadAPi monitored by their ATPase activities. The solid thick line and the broken line show the Arrhenius plot of RadADa and RadAPi, respectively. Eact (activation energy) was calculated from the formula Eact = RT ln(kcat) for each linear part of the plot. The transition temperatures between two catalytic modes (70 and 75°C) are shown. The data for RadAPi were published earlier (17).

 
We thank Alex M. Kagansky and anonymous reviewers for critical reading of the manuscript.

This work was partially supported by a Fogarty International Research Collaboration Award (grant 2 R03 TWO1318-04).

 
* Corresponding author. Mailing address: Division of Molecular and Radiation Biophysics, Petersburg Nuclear Physics Institute, Russian Academy of Sciences, Gatchina/St. Petersburg 188300, Russia. Phone: 7-812-2473141. Fax: 7-812-2473141. E-mail: vlanzov{at}bpc.spbstu.ru.

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Journal of Bacteriology, April 2005, p. 2555-2557, Vol. 187, No. 7
0021-9193/05/$08.00+0     doi:10.1128/JB.187.7.2555-2557.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.

This Article Abstract Full Text (PDF) Alert me when this article is cited Alert me if a correction is posted Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Reprints and Permissions Copyright Information Books from ASM Press MicrobeWorld Citing Articles Citing Articles via Google Scholar Google Scholar Articles by Kil, Y. V. Articles by Lanzov, V. A. Search for Related Content PubMed PubMed Citation Articles by Kil, Y. V. Articles by Lanzov, V. A.