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J Biol Chem, Vol. 275, Issue 11, 7713-7722, March 17, 2000

The Antiactivator TraM Interferes with the Autoinducer-dependent Binding of TraR to DNA by Interacting with the C-terminal Region of the Quorum-sensing Activator^*

Zhao-Qing Luo^§, Yinping Qin^§, and Stephen K. Farrand^¶

From the Departments of  Crop Sciences and ^¶ Microbiology, University of Illinois at Urbana-Champaign, Urbana, Illinois 61801

	ABSTRACT

TOP ABSTRACT INTRODUCTION EXPERIMENTAL PROCEDURES RESULTS DISCUSSION REFERENCES

Conjugal transfer of Agrobacterium tumefaciens Ti plasmids is regulated by quorum sensing via the transcriptional activator TraR and the acyl-homoserine lactone Agrobacterium autoinducer (AAI). Unique to this system, the activity of TraR is negatively modulated by an antiactivator called TraM. Analyses from yeast two-hybrid studies suggest that TraM directly interacts with the activator, but the conditions under which these components interact and the region of TraR responsible for this interaction are not known. Induction of traM in a strain in which TraR was activating transcription of a reporter system led to rapid cessation of gene expression. As assessed by a genetic assay that measures AAI-dependent DNA binding, TraM inhibited TraR function before and after the transcription factor had bound to its DNA recognition site. Consistent with this observation, in gel retardation assays, purified TraM abolished the DNA binding activity of TraR in a concentration-dependent manner. Such inhibition occurred independent of the order of addition of the reactants. As assessed by far Western analyses TraM interacts with TraR by directly binding the activator. TraM in its native form interacted with native TraR and also with heat-treated TraR but only when SDS was included with the denatured protein. TraM interacted with TraR on blots prepared with total lysates of cells grown in the presence and absence of AAI. Far Western analysis of N- and C-terminal deletion mutants localized a domain of TraR contributing to TraM binding to the C-terminal portion of the activator protein. Random mutagenesis by hydroxylamine treatment and error-prone polymerase chain reaction identified several residues in this region of TraR important for interacting with TraM as well as for transcriptional activation or/and DNA binding. We conclude that TraM inhibits TraR by binding to the activator at a domain within or close to the helix-turn-helix motif located at the C terminus of the protein.

	INTRODUCTION

TOP ABSTRACT INTRODUCTION EXPERIMENTAL PROCEDURES RESULTS DISCUSSION REFERENCES

Many bacteria control the expression of certain gene sets by quorum sensing, a regulatory strategy that ties gene expression to the size of the bacterial population. Quorum sensing is dependent upon a diffusible signal molecule called the autoinducer, which in Gram-negative bacteria often is an acylated homoserine lactone (acyl-HSL¹). The signal, which the bacteria produce themselves, accumulates in the environment as the cells grow (1, 2). At a certain threshold concentration that corresponds to a critical cell density, the autoinducer interacts with its cognate receptor, resulting in expression of the target genes.

In Agrobacterium tumefaciens, the transcriptional activator TraR and its ligand Agrobacterium autoinducer (AAI,¹ N-3-oxooctanoyl-L-homoserine lactone) regulate in a quorum-dependent manner the expression of the three operons responsible for conjugal transfer of the Ti plasmids (3-6). This system, in turn, is controlled by a hierarchical cascade in which the expression of traR itself is regulated by opines, metabolites produced by the plant tumors induced by the bacteria (4, 7, 8). In the nopaline-type Ti plasmid pTiC58, traR is part of the arc operon, a group of five genes that is regulated by AccR, the repressor that responds to agrocinopines A and B (8, 9).

Purified TraR from the octopine-type Ti plasmid pTiR10 binds specifically to a cis-acting recognition site, the 18-base pair tra box, adjacent to promoters of genes regulated by quorum sensing (10). That such activity was dependent upon growth of the cells with AAI suggested that the signal is required for TraR to bind DNA. Consistent with this, in a genetic assay that measures DNA binding, TraR from the nopaline-type Ti plasmid pTiC58 bound the tra box only when the cells were cultured with AAI (11).

In addition to opine regulation, transcriptional activation by TraR is negatively modulated by the product of traM (12, 13), a component critical for quorum sensing but not for TraR-mediated autoinduction of the tra and trb operons (14). All identified traM genes encode an 11.2-kDa protein with a highly hydrophobic region located at the C terminus. Null mutations in traM result in constitutive conjugation even at low population density (14).

Addition of excess exogenous AAI does not overcome the inhibitory effect of TraM on TraR function under normal conditions (12, 15). Rather, inhibition of TraR activity by TraM is dependent upon the relative levels of these two proteins (12). In addition, TraM does not directly affect expression of traR or the tra and trb genes (12). These observations led Hwang et al. (12) to propose that TraM exerts its effect by directly interacting with TraR. Genetic analyses using the yeast two-hybrid system are consistent with this model (16).

Taken together, these results indicate that TraM functions as an antiactivator, a class of regulatory proteins that exert their inhibitory effect by interacting with and deactivating their corresponding transcription factor. However, several aspects concerning the interactions between TraM and TraR remain to be determined. First, there is no physical evidence supporting the hypothesis that these two proteins interact with each other. Second, it is not known whether TraM exerts its inhibitory effect before TraR binds DNA or if it can actively interfere with transcriptional initiation. Third, the direct consequence on TraR upon interaction with TraM remains obscure. Finally, it is not clear what role, if any, AAI plays in the interaction between TraR and TraM. In this paper, we have combined genetic analyses with biochemical tests to assess the influence of TraM on TraR activity and to analyze interactions between TraR and this antiactivator. We show that TraM negatively influences the DNA binding activity of TraR and that the antiactivator exerts its influence irrespective of whether TraR has bound to its target DNA site. Furthermore, by far Western analysis, we show that TraM binds TraR and that binding is independent of AAI. Finally, using a combination of genetic and biochemical analyses, we show that TraM binds the C terminus of TraR and that amino acid residues of TraR involved in interacting with TraM are critical for DNA binding and perhaps also for transcriptional activation.

	EXPERIMENTAL PROCEDURES

TOP ABSTRACT INTRODUCTION EXPERIMENTAL PROCEDURES RESULTS DISCUSSION REFERENCES

Bacterial Strains and Growth Conditions

Unless otherwise specified, Escherichia coli strains DH5, BL21(DE3)(pLysS) (Novagen), and their derivatives were grown at 37 °C in L broth (LB), on L agar plates, or in A medium (17). A. tumefaciens strain NT1 and its derivatives were grown at 28 °C in LB, MG/L (18), or ABM minimal medium (19). Plasmids were maintained by including the appropriate antibiotics in the media at concentrations specified previously (20). When necessary, cell growth was monitored by Klett colorimetry (red filter) or by measuring optical density at 600 nm (OD 600) using a Spectronic 20. To induce expression from P_BAD or P_trc, arabinose or IPTG was added at a final concentration of 0.4% or 200 µM, respectively. Unless otherwise specified, synthetic AAI, prepared as described previously (21), was added to a final concentration of 25 nM. X-Gal was included in agar medium at 40 µg/ml to monitor for the production of -galactosidase.

Plasmid Construction

Plasmids that allow independent induction of TraR and TraM were constructed by cloning the open reading frames of these two genes into expression vectors pKK38-I (22) and pDLB4 (20) to generate pKKTR2-I and pDLB4-M. Expression of these two genes is inducible by IPTG and arabinose, respectively. Precise deletions were constructed by PCR using Pfu DNA polymerase (Stratagene) and traR cloned in pZLQR (11) as template. For N-terminal deletions, primer 5'-attcGAATTCAGATCAGCTTTCTTCT-3' that contains the native translational stop codon (underlined antiparallel strand) was coupled with N-terminal primers containing an in-frame ATG as part of an NdeI site to amplify fragments coding for versions of TraR initiating at successively later positions. For C-terminal deletions, primer 5'-atcgcgCATATGCAGCACTGGCTGGAC-3' that contains the native ATG (italicized) in the form of an NdeI site (underlined) was coupled with C-terminal primers containing a TGA stop codon placed to give versions of TraR terminating at successively earlier positions. In all cases, PCR products were cloned into the expression vector pZLQ (11) as NdeI/EcoRI fragments, and the constructs were confirmed by DNA sequence analysis.

To reconstitute the N terminus of TraM-insensitive mutants of TraRN2-4, mutated regions of pZLQ derivatives were isolated by digesting with NotI, a restriction enzyme that recognizes two sites, one located in the middle of traR and the other in the vector distal to the 3' end of the gene. The recovered DNA fragments were cloned into a vector harboring the 5' end through the NotI site of wild-type traR. Clones with the 3' mutant half of traR inserted in the correct orientation were identified by restriction analysis. A similar strategy was used to place the 3'-half of several C-terminal deletion and missense mutants of traR into traRN2-4.

Mutagenesis

The N-terminal deletion mutant traRN2-4 (11) was subjected to chemical and error-prone PCR-mediated random mutagenesis according to previously described protocols (23, 24). PCR products were cloned into pZLQ as NdeI/EcoRI fragments.

Random 5' deletion mutagenesis of traR was carried out on pDLR1, a derivative of pDSK519 (25) carrying a copy of traR downstream from several restriction sites suitable for conducting ExoIII-mediated unidirectional digestion (26). Deletions were produced using the Erase-a-Base system (Promega) following the manufacturer's instructions.

Protein Purification

Native active TraR was purified from E. coli BL21(DE3)(pLysS) harboring pETR, a derivative of pET17-b (Novagen) containing traR, the expression of which is under the control of the T7 promoter. This strain was grown at 28 °C in 1 liter of A medium (17) containing 100 nM AAI, 200 µg/ml ampicillin, and 34 µg/ml chloramphenicol. When the OD₆₀₀ of the culture reached 0.3-0.4, expression of TraR was induced by adding IPTG to a final concentration of 200 µM. Cells were harvested following overnight induction and were stored at 80 °C. Approximately 4 g of cells were thawed, resuspended in 20 ml of TEDGT buffer (50 mM Tris-HCl, pH 7.9, 0.5 mM EDTA, 0.15 mM NaCl, 1 mM dithiothreitol, 5% glycerol, and 0.05% Tween 20) containing 10 units/ml DNase, and were broken by two passages through a French press at 10,000 pounds/square inch. Active TraR was purified from the lysate essentially as described by Zhu and Winans (10). Samples first were chromatographed on a heparin-Sepharose affinity column (Amersham Pharmacia Biotech, 16 mm × 20 cm). TraR was eluted from the column with 100 ml of a linear gradient of NaCl, from 0.15 to 1.0 M in TEDGT buffer. Fractions containing TraR, as detected by anti-TraR antibodies raised against affinity-purified His-tagged activator protein, were pooled and desalted by ultrafiltration (Amicon). The protein was further purified by fast protein liquid chromatography using a Mono-S column (HR 5/5, Amersham Pharmacia Biotech). TraR was eluted from the column with 30 ml of a linear gradient of NaCl from 0.15 to 1 M in TEDGT buffer. (His)₆-TraM was purified from BL21(DE3)(pLysS, pMA2) (16) according to the protocol of the Ni²⁺ resin manufacturer (Novagen). The two proteins were better than 95% pure as assessed by SDS-PAGE followed by staining with Coomassie Brilliant Blue. Protein concentration was determined by the Bradford method using the Coomassie Plus Protein Assay Reagent (Pierce). Purified TraR and (His)₆-TraM were stored at 20 °C in TEDGT buffer containing 50% glycerol.

In Vivo Assay of TraM Activities

E. coli strain DH5(pPBL1, pKKTR2-I, pDBL4-M) was constructed to analyze the effect of TraM on AAI-dependent DNA binding activity of TraR. Plasmid pPBL1 reports the AAI-dependent repressor activity of TraR (11), and pKKTR2-I and pDLB4-M harbor traR and traM inducible by IPTG and arabinose, respectively. An overnight culture was diluted 1:200 into fresh A medium, and the culture was incubated at 37 °C for 1 h. Synthetic AAI was added after taking the first sample (t₀), and the culture was incubated as above. After the OD₆₀₀ of the culture reached about 0.05, the culture was divided into the necessary number of subcultures, and inducers for traR and traM expression were added at appropriate times. Cultures were incubated as before; growth was monitored, and samples were taken at different time intervals following addition of the inducers.

A. tumefaciens strain NT1(pRKLH4I41, pDLB4-M) was used to examine the effect of TraM on activation of transcription by TraR. Plasmid pRKLH4I41 contains a copy of constitutively expressed wild-type traR and a traG::lacZ fusion, the expression of which is dependent upon TraR and exogenous AAI (11). An overnight culture of this strain was diluted 1:50 into ABM medium, and the new culture was incubated at 28 °C with shaking. When the culture density reached an OD₆₀₀ of about 0.05 (It₀), a sample was removed, and synthetic AAI was added to a final concentration of 25 nM. The culture was divided into the appropriate number of subcultures; incubation was continued as above, and arabinose was added at the indicated times to induce expression of traM from pDLB4-M. Samples were withdrawn at set time intervals, and the expression level of the traG::lacZ reporter was determined.

Gel Retardation Assays

The 251-base pair traA-traC intergenic region of pTiC58 (27) was amplified from pZLB251 (11) by PCR using primers 5'-GGGTGATCAGAACGTCGTTCGTCGGGAGCGGTGAGG-3' and 5'-TCACCCGGGTCGCATCTCCCTGGAAATCCTGCGGC-3'. This region contains the entire TraR-AAI dependent divergent tra promoter system (27, 28). Purified PCR product was labeled at the 3' ends with digoxigenin-11-ddUTP and terminal transferase using protocols provided by the supplier (Roche Molecular Biochemicals). For the DNA binding reaction, purified TraR was incubated with the digoxigenin-3'-end-labeled DNA fragment (2 ng) in a buffer containing 10 mM Tris-HCl, pH 7.9, 1 mM EDTA, 1 mM dithiothreitol, 60 mM KCl, 30 µg/ml salmon sperm DNA, 20 µg/ml BSA, 0.05% Tween 20, and 10% glycerol in a total volume of 20 µl. Reactions were incubated at room temperature for 20 min. After adding 5 µl of loading buffer, the samples were subjected to electrophoresis at 4 °C on a native 6% polyacrylamide gel in 0.25× TBE buffer (1× TBE: 89 mM Tris-HCl, 89 mM boric acid, 2 mM EDTA, pH 8.0). Following electrophoresis, DNA and protein-DNA complexes were electroblotted onto positively charged nitrocellulose membranes and visualized by chemiluminescence detection as described by the manufacturer's protocols (Roche Molecular Biochemicals).

Three approaches were used to test the effect of TraM on the DNA binding activity of TraR. As described above, all reactions were performed in a volume of 20 µl. In the first, labeled DNA was added to reaction mixtures containing 1 pmol of TraR (final concentration of 50 nM) and 10-240 pmol of TraM (final concentration of 1-12 µM TraM) and incubated for 20 min. In the second, DNA was added to reaction mixtures containing 100 pmol of TraM (final concentration of 5 µM) and 0.5 pmol of TraR (final concentration of 25 nM) that had been coincubated for 1-20 min. In the third, 100 pmol of TraM (final concentration of 5 µM) was added to reaction mixtures in which 0.5 pmol of TraR (final concentration of 25 nM) and DNA had been coincubated for 1-20 min. All reactions were incubated at room temperature for an additional 20 min, subjected to electrophoresis, and analyzed by electroblotting and chemiluminescence as described above.

Western Blots

Immunoblots were carried out using murine anti-(His)₆-TraR antibodies. To prepare cell lysates for such assays, overnight cultures in MG/L medium (18) were diluted 1:15 into fresh MG/L, and the cultures were incubated at the appropriate temperature with shaking. When the OD₆₀₀ of the culture reached about 0.3, IPTG was added; incubation was continued, and cells were harvested when the OD₆₀₀ reached about 1.0. When needed, AAI was added at the same time as IPTG. Cells were resuspended in one-tenth of the culture volume of SDS loading buffer (29), and the cell suspension was boiled for 5 min. Cell debris was removed by centrifugation (10 min, 4 °C) in an Eppendorf microcentrifuge (Centrifuge 5402), and 18 µl of supernatant was loaded onto a 15% SDS-PAGE gel. Following electrophoresis, proteins were electroblotted onto nitrocellulose membranes. After 1 h blocking using PBS buffer (29) containing 5% non-fat milk, membranes were incubated for 2 h in the same buffer containing anti-TraR antibodies. Antibody-protein complexes were visualized using alkaline phosphatase-coupled anti-murine second antibody (Sigma) and 5-bromo-4-chloro-3-indolyl phosphate p-toluidine salt and nitro blue tetrazolium chloride (Life Technologies, Inc.) as substrates.

Far Western Analysis

Dot Blots-- All incubations and reactions were conducted at room temperature. Native or heat-denatured (95 °C, 5 min) TraR in TEDGT buffer was spotted onto nitrocellulose membranes, and the samples were allowed to dry in air. After blocking for 30 min using PBS buffer (29) containing 5% nonfat milk, the membranes were incubated for 30 min in blocking buffer containing native or heat-denatured (His)₆-TraM at a final concentration of 45 nM. Following three washes with PBS buffer (1 ml/cm², 10 min each), the membranes were incubated for 2 h in blocking buffer containing anti-TraM antibodies (16). Reacting complexes were detected as described above for Western blots.

Gel Blots-- Purified (His)₆-TraM, TraR, or cell lysates containing TraR or its mutant derivatives were resolved by electrophoresis in 15% SDS-PAGE gels, and the proteins were electrophoretically transferred to nitrocellulose membranes. To analyze TraR and its derivatives present in cell lysates, samples for electrophoresis were prepared as described for Western blots. In some cases, following electroblotting the membranes were incubated in HYB buffer (30) for 16 h at 4 °C in an attempt to allow renaturation of the proteins. The membranes were incubated with TraM or TraR, the respective antisera, and processed all as described for the dot blots.

-Galactosidase Assay

-Galactosidase activity, expressed as units/ml culture or as units/10⁹ colony-forming units (cfu) was measured as described previously (12, 17).

DNA Sequence Analysis

Mutations were identified by double strand DNA sequence analysis conducted by the Genetic Engineering Facility at the University of Illinois.

	RESULTS

TOP ABSTRACT INTRODUCTION EXPERIMENTAL PROCEDURES RESULTS DISCUSSION REFERENCES

TraM Abolishes the Repressor and Activator Activities of TraR-- By using a genetic assay that measures gene repression as an indicator of AAI-dependent DNA binding ability of TraR (11), we examined the characteristics and in vivo kinetics of TraM inhibition of TraR activity. With the reporter strain DH5(pPBL1, pKKTR2-I, pDLB4-M), expression of traR is inducible by IPTG, whereas expression of traM is inducible by arabinose. In a subculture to which no inducer was added, the reporter gene expressed constitutively, leading to the accumulation of -galactosidase (Fig. 1, panel A). When only traR was induced, the expression of the reporter was strongly repressed (Fig. 1, panel A). However, when traR and traM were induced simultaneously or when traM was induced before traR, no repression was observed (Fig. 1, panel A). Moreover, in a culture in which traR had been induced previously, induction of traM led to the derepression of the reporter gene within 30 min (Fig. 1, panel A). Induction of traM alone had no effect on the expression of the reporter gene, indicating that the antiactivator has no repressor activity of its own (Fig. 1, panel A). The ability of TraM to abolish repression by TraR suggested that in an activation assay induction of TraM would prevent further expression of genes activated by TraR. Such was the case; in a strain that contains a traG::lacZ reporter fusion, and a plasmid coding for constitutively expressed traR and traM expressed from P_BAD, the antiactivator significantly inhibited the TraR-dependent expression of the reporter gene within 1 h after induction by addition of arabinose (Fig. 1, panel B).

View larger version (15K): [in this window] [in a new window]   Fig. 1.   TraM inhibits DNA binding and activation by TraR. Panel A, TraM inhibits repression by TraR. The reporter strain E. coli DH5(pPBL1, pKKTR2-I, pDLB4-M) was grown in A medium supplemented with AAI (25 nM) as described under "Experimental Procedures." At T0 (~106 cfu/ml) the culture was split into five subcultures; IPTG (100 µM) was added to two subcultures to induce expression of traR (, ) and arabinose (0.4%) was added to two additional subcultures to induce expression of traM (×, ). The fifth subculture () received no inducers. The cultures were incubated, and growth was followed turbidimetrically at 600 nm (). After incubation for 8 h arabinose was added to one culture previously induced with IPTG (), and IPTG was added to one culture previously induced with arabinose (×). Incubation was continued; samples were removed at the indicated times, and the cells were assayed for -galactosidase activity as described under "Experimental Procedures." Panel B, TraM inhibits activation by TraR. The reporter strain A. tumefaciens NT1(pRKLH4I41, pDLB4-M) was grown in ABM medium to a density of about 107 cfu/ml. At T0 the culture was divided into two subcultures (, ); AAI was added to one (), and incubation of both was continued. At 0- (), 2- (×), and 4-h () time points a subculture supplemented with arabinose (0.4%) to induce TraM expression was established from the culture containing AAI, and all of the cultures were incubated in parallel. Samples were removed at the indicated times from all cultures, and the cells were assayed for -galactosidase activity.

TraM Interferes with DNA Binding by TraR-- Results from these in vivo tests predicted that TraM could abolish binding between TraR and its DNA recognition site. We examined this hypothesis by determining the effect of TraM on the DNA binding activity of TraR using a gel retardation assay. As shown in Fig. 2, panel A, when mixed with target DNA, TraR caused a retardation in the mobility of the DNA probe presumably by forming a protein-DNA complex. Addition of TraM to the binding reactions prevented the activator from forming these complexes. Moreover, the inhibitory effect of TraM on the formation of such complexes was dependent upon the relative amounts of these two proteins. Under our experimental conditions, a ratio of TraM to TraR of 20:1 detectably reduced the formation of TraR-DNA complexes (Fig. 2, panel A). As the ratio was increased to 80:1, TraR-DNA complexes became undetectable (Fig. 2, panel A). In reactions in which labeled DNA was added into mixtures containing TraR and TraM that had been coincubated for 1-20 min, no detectable TraR-DNA complex was observed (Fig. 2, panel B). Furthermore, similar to observations made in our in vivo analysis in which TraM relieved repression of the reporter gene (Fig. 1, panel A), addition of TraM to reactions in which TraR and DNA had been coincubated for periods ranging from 1 to 20 min disrupted the TraR-DNA complexes (Fig. 2, panel B). Incubation of TraM alone with the same DNA probe gave no complexes detectable by gel retardation analysis (data not shown).

View larger version (20K): [in this window] [in a new window]   Fig. 2.   TraM interferes with TraR-DNA interactions. TraR with or without TraM was mixed with labeled target DNA, and the complexes were detected by gel retardation analysis as described under "Experimental Procedures." Panel A, TraM inhibits interaction between TraR and DNA in a concentration-dependent fashion. TraR (50 nM) was mixed with (His)6-TraM at concentrations of 1, 2, 4, 8, and 12 µM and before the addition of labeled target DNA. The lane labeled () contains TraR and DNA but no TraM. Panel B, order of addition has no effect on TraM inhibition of TraR-DNA complexes. TraR (25 nM) was mixed with (His)6-TraM (10 µM) (TraR + TraM) or with labeled target DNA (TraR + DNA) and incubated for 1-20 min. Labeled DNA or (His)6-TraM was added to the two mixtures, respectively, and samples were incubated for 20 min and subjected to gel retardation analysis. The lane labeled  contains TraR and DNA but no TraM. The lane labeled + contains a mixture of TraR, DNA, and TraM in which the DNA was added right after mixing TraR and TraM.

TraM Interacts with TraR by Direct Binding-- We employed far Western analysis to assess the capacity of TraM to bind TraR in vitro. Blocked nitrocellulose membranes onto which solutions with decreasing amounts of purified active TraR had been spotted were incubated with TraM protein and then with anti-TraM antiserum. Under such conditions, TraM strongly bound to TraR on these dot blots but not to BSA or to any protein species in lysates of A. tumefaciens NT1 (Fig. 3 panels I and II, and data not shown). The intensity of binding varied with the amount of TraR loaded on the filter (Fig. 3, panel II). Under the conditions tested TraM routinely gave a positive signal with spots containing as little as 15 fmol of native TraR. Identical blots probed with a control solution lacking TraM gave no detectable signal when challenged with the anti-TraM antibodies, indicating that the signal was not due to cross-recognition of TraR by anti-TraM antibodies (data not shown). Similar results were obtained when TraR was used to detect TraM fixed on the membrane (data not shown). As interactions between proteins often require that the partners be properly folded, we tested preparations of TraR, TraM, or both proteins that had been denatured by heat treatment. Heat-denatured TraM failed to bind at detectable levels to blots containing heat-denatured TraR (Fig. 3, panel I, D). However, heat-denatured TraR was bound, although poorly, by native TraM (Fig. 3, panel I, C). Interaction between heat-denatured TraM and native TraR also was detectable, but the signal was very weak (Fig. 3, panel I, B). Incubating membranes spotted with heat-denatured TraR under conditions that could allow protein renaturation (30) did not restore binding by native TraM (data not shown).

View larger version (60K): [in this window] [in a new window]   Fig. 3.   TraM binds filter-bound TraR. Panel I, TraM binds native but not denatured TraR. Solutions of purified active TraR in its native (rows A and B) and heat-denatured (rows C and D) forms were spotted onto nitrocellulose filter strips to give loads of 1, 50; 2, 40; 3, 30; 4, 20; 5, 10; and 6, 5 pmol. Bovine serum albumin (BSA, 29 pmol) was spotted onto the membranes in the last position. The filters were incubated with a solution of purified (His)6-TraM (A and C) or purified heat-denatured (His)6-TraM (B and D). Panel II, TraM binds heat-denatured TraR in the presence of SDS. Solutions of purified active TraR (rows A) and native TraR heat-denatured in the presence of SDS (rows B) were spotted in triplicate onto nitrocellulose filter strips to give loads of 1, 1; 2, 0.5; 3, 0.25; 4, 0.125; 5, 0.06; 6, 0.03; 7, 0.015; and 8, 0.0075 pmol. Filters were incubated with a solution of purified (His)6-TraM. Following incubation with the probe antiactivator, the filters were washed, blocked, and incubated with anti-TraM antiserum all as described under "Experimental Procedures." TraR-TraM-anti-TraM complexes were detected immuno-enzymatically also as described under "Experimental Procedures."

To develop an assay suitable for examining the interaction between TraM and mutants of TraR that cannot be purified in active form by current procedures (see "Experimental Procedures"), we assessed the capacity of TraM to bind to TraR transferred to nitrocellulose membranes following SDS-PAGE. TraM gave a detectable signal with as little as 0.1 pmol (26 ng) of TraR by this SDS-PAGE-based far Western analysis (Fig. 4, panel B). However, no comparable signals were detected when TraR was used as the challenging protein to detect similarly resolved TraM (data not shown). Furthermore, TraM binds to TraR present in lysates of cells following electrophoresis and electroblotting (Fig. 4, panel C). No signal was detected from the cell lysate of a control strain that does not express TraR (Fig. 4, panel C).

View larger version (27K): [in this window] [in a new window]   Fig. 4.   TraM binds specifically to TraR present in lysates of A. tumefaciens. Samples containing 100, 10, 1, and 0.1 pmol of purified active TraR were subjected to SDS-PAGE on two gels in parallel as described under "Experimental Procedures." One gel was stained with Coomassie Blue (panel A), whereas the proteins on the second gel were transferred to a nitrocellulose membrane (panel B). Similarly, equal loadings of total proteins in lysates from the traR+ strain NT1(pZLQR) grown with (lane 2) or without (lane 3) AAI and from the traR strain NT1(pZLQ) (lane 4) were separated by electrophoresis, and the proteins were transferred to a nitrocellulose filter (panel C). Filters in panels B and C were blocked, incubated with (His)6-TraM, and then with anti-TraM antiserum. TraR-TraM-anti-TraM complexes were detected immuno-enzymatically all as described under "Experimental Procedures." Lanes 1, contain protein standards of known molecular sizes in kilodaltons as indicated to the left of panel A.

Native TraM interacts strongly with heat-denatured TraR following SDS-PAGE, but only weakly when examined by dot blot analysis (Fig. 4 and Fig. 3, panel I, C). However, when SDS was included in the TEDGT buffer at 0.1%, whether before or after denaturation, heat-treated TraR dot-spotted to membranes was bound by TraM at levels even higher than that of native TraR (compare rows A and B of Fig. 3, panel II).

Interaction between TraM and TraR Does Not Require AAI-- As active TraR is tightly associated with AAI (10), it was unclear whether binding this acyl-HSL signal molecule is a prerequisite for interaction with TraM. The ability of TraM to bind TraR in cell lysates provided us with a simple and reliable way to dissect the interactions between these two proteins without the need to purify the activator. We tested for dependence of TraM binding on the autoinducer by probing for TraR present in cells grown with or without AAI. TraR present in lysates of both cultures interacted with TraM with indistinguishable intensities using both dot blot and gel blot analyses (Fig. 4, panel C, and data not shown).

TraM Binds to the C-terminal Region of TraR-- We localized the domain of TraR to which TraM binds by subjecting a series of N- and C-terminal deletion mutants of the activator to far Western analysis. Deletion mutants of TraR lacking as few as 4 amino acids from the N terminus no longer repress or activate appropriate reporter fusions (11). Furthermore, these mutants are recessive to the wild-type TraR (i.e. they do not affect the function of the wild-type protein) (11). However, some of these mutants block the effect of TraM in a strain in which the activity of wild-type TraR is inhibited by the antiactivator (16). When examined by far Western analysis, N-terminal deletion mutants of TraR lacking 4-104 residues are bound by TraM (Fig. 5, panel A). These mutants all exerted dominant interfering activity (Table I and Ref. 16). Again, no signal was detected in a strain containing the empty expression vector or when the filter was not challenged with TraM protein (Fig. 5, panel A, and data not shown).

View larger version (29K): [in this window] [in a new window]   Fig. 5.   Interaction between TraM and N-terminal deletion mutants of TraR. Equal amounts of protein from total lysates of A. tumefaciens harboring plasmids coding for wild-type and N-terminal deletion mutants of traR were subjected to SDS-PAGE, and the separated proteins were transferred to nitrocellulose membranes. The membranes were blocked and reacted with (His)6-TraM, and the complexes formed were detected using anti-TraM antiserum all as described under "Experimental Procedures." Panel A, lanes contain lysates from cells expressing the following: lane 2, wild-type TraR; lane 3, TraRN2-4; lane 4, TraRN2-9; lane 5, TraRN2-49; lane 6, TraRN2-69; lane 7, TraRN2-89; lane 8, TraRN2-104; lane 9, vector control. Panel B, lanes contain lysates from cells expressing the following: lane 2, wild-type TraR; lane 3, TraRN2-89; and the N-terminal protected mutants as follows: lane 4, TraRN41 (1-130); lane 5, TraRN68 (1-141). Lanes 1 contain protein standards of known molecular sizes in kilodaltons as indicated to the left of each panel.

N-terminal deletion mutants of TraR shortened for more than 104 amino acids failed to give any measurable phenotypes (Ref. 16 and data not shown). Furthermore, we were unable to detect proteins encoded by these mutants by either Western or far Western analysis (data not shown), suggesting that these mutant proteins are unstable. Thus, we designed a genetic screen to isolate mutants of TraR with large N-terminal deletions that still interact with TraM. A clone coding for traR was treated with ExoIII as described under "Experimental Procedures," and the subsequent ligation products were introduced into the reporter strain NT1(pRMLH4I41) (16). Among a number of candidates, we identified two mutants with relatively long 5' deletions that exhibited dominant interfering activity against wild-type TraM encoded by pRMLH4I41 (16). Sequence analysis revealed that these mutants, traRN41 and traRN68 (Table I), code for derivatives of the activator that retain the C-terminal 104 and 93 amino acids of TraR, respectively. However, the N termini of the two mutants contain, respectively, an 18- and 21-residue oligopeptide encoded by the cloning region of the vector. Like other deletion mutants that lack more than eight N-terminal amino acids, neither protein reacted with our anti-TraR antiserum in Western analysis (Ref. 11 and data not shown). However, when assessed by far Western analysis, both mutants produced detectable proteins of the anticipated sizes when probed with TraM and challenged with our anti-TraM antiserum (Fig. 5, panel B).

We also subjected a series of C-terminal deletion mutants of TraR to far Western analysis. Interactions between these mutants and TraM cannot be assessed genetically as most exert a strong dominant-negative effect on the activity of wild-type TraR (11). All such mutants encode a stable polypeptide detectable by anti-TraR antibodies (Fig. 6, panel A). TraR mutants lacking as few as 2 or as many as 20 amino acids from the C terminus gave a very weak but detectable signal. Deletions removing 25 or more amino acids resulted in polypeptides that no longer are bound by TraM at detectable levels (Fig. 6, panel B).

View larger version (29K): [in this window] [in a new window]   Fig. 6.   Interaction between TraM and C-terminal deletion mutants of TraR. Equal amounts of protein from total lysates of A. tumefaciens harboring plasmids coding for wild-type and C-terminal deletion mutants of traR were subjected to SDS-PAGE, and the separated proteins were transferred to nitrocellulose membranes. The membranes were blocked, reacted with anti-TraR antiserum (panel A) or (His)6-TraM and anti-TraM antiserum (panel B), and the complexes formed were detected as described under "Experimental Procedures." Lanes contain lysates from cells expressing the following: lane 2, wild-type TraR; lane 3, TraRC-2; lane 4, TraRC-8; lane 5, TraRC-13; lane 6, TraRC-20; lane 7, TraRC-25; lane 8, TraRC-30; lane 9, TraRC-35; lane 10, TraRC-45. Lanes 1 contain protein standards of known molecular sizes in kilodaltons as indicated to the left of each panel.

We assessed the biological consequence of these deletion mutations by transferring the C-terminal portions of some of these mutants into TraRN2-4. All but one of these C-terminal deletion derivatives of TraRN2-4 conferred a dominant interfering activity consistent with the signals observed from the far Western analysis. For example, C-terminal deletions of up to 20 residues exerted a weak but detectable dominant interfering activity and bound TraM at very low but detectable levels (Table I and Fig. 6, panel B). However, TraRN2-4/C-25, while showing weak dominant interference (Table I), did not detectably bind the antiactivator (Fig. 6, panel B). TraRN2-4/C-30, on the other hand, exhibited no dominant interfering activity and did not bind TraM at a detectable level (Table I and Fig. 6, panel B).

Substitution Mutations in the C Terminus of TraR Affect Binding by TraM-- To identify residues of TraR that are critical for interaction with TraM, we first tested four previously isolated TraR substitution mutants for their ability to bind the antiactivator. Two of these mutants, which were isolated in a screen for alleles of TraR that maintain activator activity but no longer are inhibited by TraM, contain leucine or serine substitutions for the proline at position 176 (Ref. 16; Table I). As assessed by far Western analysis, although detectable, the ability of TraM to bind to these two mutants was severely reduced (Fig. 7). The two additional mutants, traR111 and traR112, were identified as being unable to either repress or activate appropriate reporter constructs (11). These mutants produce proteins with substitutions in or near the putative helix-turn-helix (H-T-H) motif located in the C terminus (Ref. 11; Table I). TraM no longer bound TraR111 (Fig. 7). However, the antiactivator interacted with TraR112 at a level indistinguishable from that of the wild-type protein (Fig. 7).

View larger version (35K): [in this window] [in a new window]   Fig. 7.   Interaction between TraM and substitution mutants of TraR. Equal amounts of protein from total lysates of A. tumefaciens harboring plasmids coding for wild-type traR, substitution mutants of traRN2-4 (panel A), and substitution mutants of wild-type traR (panels B and C) were blocked, reacted with (His)6-TraM and anti-TraM antiserum (panels A and C) or with anti-TraR antiserum (panel B), and the complexes formed were detected as described under "Experimental Procedures." Lanes contain lysates from cells expressing the following: lane 2, NTraR/TraR; lane 3, NTraR26/TraR26; lane 4, NTraR28/TraR28; lane 5, NTraR111/TraR111; lane 6, NTraR112/TraR112; lane 7, NTraR11/TraR11; lane 8, NTraR171/TraR171; lane 9, NTraR91/TraR91; lane 10, vector control. Lanes 1 contain protein standards of known molecular sizes in kilodaltons as indicated to the left of each panel.

That TraR111 fails to bind TraM suggests that the antiactivator interacts with residues of TraR that are important for DNA binding and/or activator activity. Mutants of TraR with such phenotypes certainly will escape any genetic screen based on the protein maintaining its activator activity. Thus, we designed a more unbiased screen for TraM-insensitive mutants of TraR by searching for variants of traRN2-4 that fail to exert dominant interfering activity in strain NT1(pRMLH4I41). DNA was mutagenized by hydroxylamine treatment or by error-prone PCR and was introduced into this reporter strain. Following incubation, white colonies appearing on agar medium supplemented with AAI and X-gal were selected as harboring mutants of TraRN2-4 that no longer are able to interfere with TraM. All hydroxylamine-induced mutants were recloned into a fresh vector to avoid any effect derived from mutations in the cloning vehicle.

Eleven independent mutants that completely or partially lost dominant interfering activity but encode polypeptides with sizes indistinguishable from that of traRN2-4 were obtained from the screen. Sequence analysis identified one frameshift, three early termination mutations, and seven missense mutations, all affecting the C terminus of the protein (Fig. 8 and data not shown). Since we already had analyzed a series of C-terminal deletion mutants, we retained only the missense mutants for further studies. The seven mutants fell into two classes. In one, represented by three independent mutants, leucine at position 182 is changed to phenylalanine (L182F) (Fig. 8). In the second, represented by four independent mutants, alanine at position 195 within the putative H-T-H motif is changed into either threonine (A195T) or valine (A195V) (Fig. 8). Each of the seven mutants produced a stable protein of the expected size as judged by Coomassie Blue staining and Western analysis with anti-TraR antiserum (data not shown). However, all seven mutants failed to exert dominant interfering activity against TraM-mediated inhibition of TraR activity at levels comparable to that of the parent, TraRN2-4 (Table I). When subjected to far Western analysis, these seven mutants showed a greatly decreased ability to interact with TraM (Fig. 7, panel A).

View larger version (7K): [in this window] [in a new window]   Fig. 8.   Structure of TraR and location of the TraM binding region as defined by deletion and substitution mutations. TraR is depicted as a two-domain protein with an N-terminal AAI binding region and a C-terminal DNA recognition domain containing a helix-turn-helix motif depicted as the shaded box. The region of TraR from position 142 to the C terminus bound by TraM is shown in expanded form and includes the locations and allele names for the substitution mutations that affect (below the map) or fail to affect (above the map) interaction with the antiactivator.

Since TraRN2-4, the parent of these mutants, lacks both activator and repressor activities, we could not determine how these substitution mutations affect the activity of wild-type TraR. Thus, we replaced the N-terminal portion of these mutants with that of wild-type TraR to generate full size TraR proteins harboring the substitution mutations at leucine 182 and alanine 195. All such derivatives failed to induce expression of a traG::lacZ reporter in the presence of AAI (Table I). These mutants also were unable to repress expression of the reporter in pPBL1 (11) (Table I). Furthermore, in a manner similar to other alleles of TraR bearing mutations near or within the helix-turn-helix motif (11), these mutants exerted a strongly dominant-negative effect over the wild-type activator (data not shown). When assessed by far Western analysis, like their parents, these mutants interacted with TraM at severely decreased levels (Fig. 7, panel C).

	DISCUSSION

TOP ABSTRACT INTRODUCTION EXPERIMENTAL PROCEDURES RESULTS DISCUSSION REFERENCES

Consistent with yeast two-hybrid studies (16), our analyses using far Western blots demonstrate that TraM can bind TraR. TraM apparently binds specifically and selectively to TraR; the antiactivator did not bind detectably to any other proteins present in lysates of A. tumefaciens. Moreover, as indicated by the observation that TraM can prevent TraR from forming complexes with its DNA recognition site in vitro, the antiactivator can bind the activator in solution. The fact that binding, as measured by far Western analysis, correlates well with the biological activity of TraR mutants in vivo validates the far Western assay as a method useful for assessing interaction between pure preparations of TraM and TraR.

Functional TraR exists in dimer form and dimerization is dependent upon binding AAI.² Given that purified TraM binds efficiently to TraR present in lysates of cells not exposed to AAI, we conclude that the antiactivator can bind the inactive, monomer form of the activator. This conclusion also is consistent with our two-hybrid analysis; yeast strains expressing the TraM-bait and TraR-prey fusions display strong interaction phenotypes in the absence of AAI (16). However, as shown by dot blot far Western analysis using purified proteins (Fig. 3), TraM also binds the transcriptionally active, dimer form of the activator.

Although independent of the multimeric nature of TraR, the interaction between TraM and the activator is dependent upon the secondary structure of the two proteins. TraM must be in its native form. Thus, when denatured by heating, TraM failed to bind TraR, and binding could not be restored by simple renaturation protocols. Similarly, TraM bound heat-denatured TraR with considerably less affinity. However, if heated in the presence of SDS, or if treated with SDS after heating, denatured TraR was bound strongly by TraM. These observations suggest that denaturation by heating results in the occlusion of one or more sites of TraR required for recognition and/or binding by TraM. On the other hand, these sites must be available when the activator is associated with SDS. Although it is clear that heat-denatured TraR is not strongly bound by the antiactivator, it remains to be determined if TraM can interact with naturally misfolded TraR.

Two lines of evidence indicate that TraM interacts with a domain located within the C terminus of TraR. First, N-terminal deletion derivatives lacking as many as 141 amino acids still were bound by TraM (Fig. 5). However, removing as few as two amino acids from the C terminus of TraR greatly decreased interaction with TraM, and removing 25 or more residues completely abolished binding by the antiactivator in vitro (Fig. 6). Binding activity correlated well with the in vivo activity. N-terminal deletions extending up to 141 amino acids had little or no effect on dominant interfering activity (Table I). However, deleting as few as two residues from the C terminus of TraRN2-4 led to almost complete loss of this activity in vivo. These results are consistent with our yeast two-hybrid analyses in which prey plasmid fusions containing as few as 50 C-terminal amino acids of TraR gave positive interaction phenotypes in strains expressing TraM as the bait fusion (16). These correlations between in vitro and in vivo activities also support our hypothesis that the dominant interfering activity exhibited by N-terminal deletion mutants of TraR results from the titration of available TraM thereby allowing the coexpressed wild-type activator to initiate transcription (16). Interestingly, while mutants deleted for 2-20 C-terminal residues still showed weak binding by TraM, deleting 25 residues from the C terminus of TraR abolished binding by the antiactivator as measured by far Western analysis (Fig. 6). This result suggests that interaction between TraM and TraR involves recognition of one portion of the activator followed by more stable binding to another region of the protein.

Second, all substitution mutations in TraR isolated by virtue of an altered interaction with TraM map to the C-terminal region of the activator. The single substitution at leucine 182 and the two independent substitutions at alanine 195 almost completely abolished TraM binding as measured by far Western analysis (Fig. 7). Furthermore, these mutations strongly decreased the dominant interfering activity of the parent protein, TraRN2-4 (Table I). The two independent substitutions at proline 176 of TraR decreased but did not abolish binding by TraM. This observation is consistent with our yeast two-hybrid analysis in which the P176S mutant of TraR gave a detectable although considerably diminished interaction phenotype when tested with wild-type TraM (16). Similarly, the two substitution mutations at position 176 resulted in a substantial but not complete loss of dominant interfering activity when inserted into the TraRN2-4 polypeptide (Table I). All three of these residues are conserved in TraR of the octopine-type Ti plasmid, pTiR10, which also is inhibited by TraM (13), but not in most other members of the LuxR family (data not shown).

Two additional substitution mutants, traR111 and traR112, present an informative contrast. TraR111, with substitutions at residues 213 and 215, is not detectably bound by TraM (Fig. 7). Furthermore, when inserted into the TraRN2-4 polypeptide, the TraR111 substitutions resulted in the complete loss of dominant interfering activity (Table I). On the other hand, TraM bound to TraR112 in a manner indistinguishable from that of wild-type TraR (Fig. 7). When the TraR112 substitutions were inserted into the TraRN2-4 polypeptide, the resulting protein retained dominant interfering activity (Table I). Both alleles were isolated in a screen for mutants that abolished transcriptional activation by TraR (11). Moreover, as assessed in a repressor assay, neither mutant binds to its cis-acting promoter recognition element (11). Although both alleles contain two substitutions, in each both alterations are located within the C-terminal portion of the protein and map near or within the H-T-H domain (Fig. 8). Significantly, these residues also are conserved in TraR of pTiR10.

Residues identified as essential for binding TraM also are important for TraR activity. Thus, alterations at residue 176 decrease activator and repressor functions, whereas those at positions 182 and 195 completely abolish these activities (Table I). Similarly, the two substitutions in TraR111 at positions 213 and 215 result in the loss of activator and repressor activity. This correlation explains our earlier failure to isolate TraR mutants other than traR26 and traR28 that are unable to interact with TraM. The screen we used required that TraR retains activator function (16). Our alternative strategy, screening mutants of TraRN2-4 for loss of dominant interfering activity, circumvented this problem. However, not all residues important for DNA binding are required for TraM binding. Thus, the two substitutions in TraR112, while abolishing DNA binding and concomitant transcriptional activation, have virtually no effect on interaction with TraM (Table I and Fig. 7).

We showed by two-hybrid analysis that a fragment of TraR encompassing residues 121-185 interacts with TraM (16). Similarly, a C-terminal fragment comprised of residues 185-234 also interacted with TraM. Combined with the data reported here, we conclude that TraM interacts with TraR within a region extending from somewhere between residue 142 and 176 to the end of the protein (Fig. 8). We also propose that residues at positions 182 and 195 and at positions 213 and/or 215 are critical for binding the antiactivator. Furthermore, based on weakened binding to the C-terminal deletion mutants, we propose that the far C terminus may be required for stable binding by TraM but not necessarily for initial recognition. TraM in its interaction with TraR continues a trend in which antiactivators such as MecA (31) and anti- factors such as AsiA (32) and FlgM (33) bind to the C-terminal domain of their respective target proteins.

In the absence of the acyl-HSL the LuxR-like activators are thought to exist in a conformation in which the N-terminal region occludes the DNA binding domain located in the C-terminal portion of the protein (1). Interaction with the autoinducer is believed to alter this conformation, allowing dimerization with concomitant exposure of the DNA binding domain. The fact that TraM can bind to the monomer form of TraR and that residues near the H-T-H motif are important for such binding suggests that this C-terminal region of the activator is surface-exposed even in the absence of AAI. Thus, although binding AAI may result in a conformational change to the protein, the inability of TraR to bind DNA in the absence of the acyl-HSL signal probably is not due simply to occlusion of the H-T-H domain by the N-terminal portion of the protein. In this regard, TraM might serve as a useful reagent for experimentally probing the structure of TraR.

Our gel retardation studies indicate that TraM can prevent free, dimerized TraR from binding its target DNA (Fig. 2). TraM also can disrupt preformed TraR-DNA complexes. However, we cannot conclude from these studies that the antiactivator interacts directly with the activator bound to its target promoter site. It also is possible that TraM interacts only with free TraR, but in doing so drives the equilibrium between free and DNA-bound activator toward the unbound form. No matter the mechanism, our in vivo studies (Fig. 1) are consistent with these conclusions and clearly show that induction of TraM can rapidly and efficiently inhibit TraR-mediated transcription of target genes. Since the antiactivator inhibits repression by TraR as well as transcriptional activation, we propose that, in vivo, interaction with TraM interferes with the ability of the activator to bind its DNA target sites.

The antiactivator most likely plays two roles in the regulation of Ti plasmid conjugal transfer. First, as we have proposed (12), TraM serves to prevent TraR from initiating transcription of the tra regulon in the absence of the opine signal. Thus, as assessed by both repression and activation assays (Fig. 1) when induced prior to traR, TraM prevents the activator from productively interacting with its target DNA. This role is consistent with the observation that a traM mutant of an otherwise wild-type Ti plasmid no longer requires opines for induction of transfer (12). This, in turn, supports our previous conclusion that in the absence of the conjugal opines traR is expressed at a level which, without TraM, is sufficient to activate conjugation (12, 14). Second, induction of traM under conditions in which TraR is interacting with its target DNA leads to an almost immediate cessation of TraR activity (Fig. 1). This observation suggests that TraM down-regulates transcription initiated by TraR and may serve to control the level of expression of the tra regulon in a negative fashion under inducing conditions. Such a role also is consistent with the observation that TraR activates expression of traM and that traM mutants are hyperconjugal (12). Thus, the antiactivator is responsible for ensuring that conjugation is regulated in a quorum-dependent manner and that expression of the tra regulon in response to opine availability is maintained at a suitable level.

	ACKNOWLEDGEMENT

We thank Ping Gao for supplying some of the C-terminal deletion mutants.

	FOOTNOTES

^* This work was supported by Grant R01-GM52465 from the National Institutes of Health (to S. K. F.).The costs of publication of this article were defrayed in part by the payment of page charges. The article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

^§ Both authors contributed equally to this work.

To whom correspondence should be addressed: Dept. of Crop Sciences, University of Illinois at Urbana-Champaign, 240 Edward R. Madigan Laboratory, 1201 West Gregory Dr., Urbana, IL 61801. Tel.: 217-333-1524; Fax: 217-244-7830; E-mail: stephenf@uiuc.edu.

² Y. Qin, A. Smyth, Z.-Q. Luo, and S. K. Farrand, manuscript in preparation.

	ABBREVIATIONS

The abbreviations used are: acyl-HSL, acyl-homoserine lactone; AAI, Agrobacterium autoinducer; BSA, bovine serum albumin; H-T-H, helix-turn-helix; His₆, hexahistidine; IPTG, isopropyl--D-thiogalactopyranoside; PAGE, polyacrylamide gel electrophoresis; PCR, polymerase chain reaction; X-gal, 5-bromo-4-chloro-3-indolyl--D-galactopyranoside; cfu, colony-forming units.

	REFERENCES

TOP ABSTRACT INTRODUCTION EXPERIMENTAL PROCEDURES RESULTS DISCUSSION REFERENCES

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