Identification of in vivo HSP90-interacting proteins reveals modularity of HSP90 complexes is dependent on the environment in psychrophilic bacteria

Abstract

Heat shock protein 90 (HSP90) is a conserved molecular chaperone that functions as part of complexes in which different client proteins target it to diverse sets of substrates. In this paper, HSP90 complexes were investigated in γ-proteobacteria from mild (Shewanella oneidensis) and cold environments (Shewanella frigidimarina and Psychrobacter frigidicola), to determine changes in HSP90 interactions with client proteins in response to the adaptation to cold environments. HSP90 participation in cold adaptation was determined using the specific inhibitor 17-allylamino-geldanamycin. Then, HSP90 was immunoprecipitated from bacterial cultures, and the proteins in HSP90 complexes were analyzed by two-dimensional gel electrophoresis and identified by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry. According to HSP90-associated protein analysis, only 15 common proteins were found in both species from the same genus, S. oneidensis and S. frigidimarina, whereas a significant higher number of common proteins were found in both psychrophilic species S. frigidimarina and P. frigidicola 21 (p < 0.001). Only two HSP90-interacting proteins, the chaperone proteins DnaK and GroEL, were common to the three species. Interestingly, some proteins related to energy metabolism (isocitrate lyase, succinyl-CoA synthetase, alcohol dehydrogenase, NAD(+) synthase, and malate dehydrogenase) and some translation factors only interacted with HSP90 in psychrophilic bacteria. We can conclude that HSP90 and HSP90-associated proteins might take part in the mechanism of adaptation to cold environments, and interestingly, organisms living in similar environments conserve similar potential HSP90 interactors in opposition to phylogenetically closely related organisms of the same genus but from different environments.

Introduction

Molecular chaperones are essential components of the quality control machinery present in the cell (Hartl and Hayer-Hartl 2002). They optimize bacterial physiological responses, directing client proteins, facilitating developmental signaling, and, as heat shock proteins (HSPs), are indispensable for survival in unpredictable environments. HSPs have been identified and characterized from various Bacteria and Archaea, and, like most organisms, they generally possess more than one set of HSPs (Laksanalamai and Robb 2004). Many microorganisms from extreme environments have been well characterized, and increasing access to genomic sequence data has recently allowed the analysis of the protein families related to stress responses. According to these data, HSPs appear to be ubiquitous in extremophiles (Laksanalamai and Robb 2004).

Environmentally sensitive chaperone functions would have different potential consequences for the evolution of populations and lineages under selection in changing environments (Rutherford 2003). In this work, we propose that such changes might influence the common adaptation pattern of different microbial species to a particular environment, leading to positive covariation and explaining the long-term stability of population and community abundance in the absence of compensatory dynamics or competition.

Among HSPs, HSP90 is a key component of this machinery. It is a ubiquitous molecular chaperone that is found in Eubacteria and all branches of Eukarya (Zhao et al. 2005) and have been found in a variety of organisms suggesting that it is ancient and conserved (Chen et al. 2006). HSP90 typically functions as a part of large complexes, which include other client proteins essential in posttranslational control (Chen et al. 2006). It is thought that HSP90 target to its client proteins to different sets of substrates (Zuehlke and Johnson 2009). The prokaryote HSP90 homolog, also known as high temperature protein G (HTPG), exists in most bacterial species, and it has evolved into three lineages via two gene duplication events. Hsp90/htpG genes, like most bacterial genes, have only one exon. Their proteins are 588–681 amino acids long. This subfamily of proteins is the shortest in the HSP90 family, with a molecular mass ranging from 66.7 to 78.0 kDa (Chen et al. 2006). HSP90 implication in temperature adaptation seems to be a controversial subject. Although htpG gene is not completely essential neither in Escherichia coli nor in Bacillus subtilis (Bardwell and Craig 1988; Versteeg et al. 1999), it has been found to be abundant in normal growth conditions. In both cases, the htpG deletion mutant is viable but grows poorly at high temperatures. In the absence of HSP90, recovery of cells from a heat shock is retarded, and this delay can be eliminated by overproduction of HSP90 (Versteeg et al. 1999). In B. subtilis, htpG gene is induced about 10-fold upon a sudden temperature increase at the level of both transcription and translation (Versteeg et al. 2003). Regarding cold acclimation, very few bacterial species have been studied until now, but it is known that HSP90 is essential for thermal stress management in cyanobacteria (Tanaka and Nakamoto 1999) and contributes significantly to the ability of cyanobacteria to acclimate to cold temperatures (Hossain and Nakamoto 2002).

The HSP90 because of its interaction with essential proteins, its ubiquity, and its high degree of conservation provides an interesting tool for adaptation and evolution studies. With the aim of determining whether HSP90 and its interacting proteins take part in the mechanism of adaptation to cold environments, we compared HSP90-associated proteins in two species from distant bacterial genera (Shewanella frigidimarina and Psychrobacter frigidicola) from a similar Antarctic cold environment and in two bacterial species of the same genus (Shewanella oneidensis and S. frigidimarina) and from different environments (mesophilic and psychrophilic bacteria, respectively).

gamma-Proteobacteria represent a collection of microorganisms that form a taxonomic group based on 16S rRNA comparisons, but they are diverse in their habitats, lifestyles, and metabolic preferences (Mrázek et al. 2006). In this group, the genus Shewanella comprises more than 20 species inhabiting a wide range of environments including spoiled food (Jorgensen and Huss 1989; Shewan 1971), oil field wastes (Deppe et al. 2005), redox interfaces in marine and freshwater, cold water, and sediments of the deep sea and mesophilic ones all around the planet. S. oneidensis has been the most studied species in the genus as it is unique among known bacteria in its capacity to use a wide range of terminal electron acceptors in respiration including heavy metals, which makes it an attractive candidate for bioremediation (Heidelberg et al. 2002; Lovley et al. 2004). Several Shewanella species have been found in Antarctic Continental shelf sediments (Bozal et al. 2002; Brinkmeyer et al. 2003) as well as in sea-ice microbial communities (adapted to grow at temperatures below 4°C). Some of these are cultivated strains, while others are as yet uncultivated and exemplify psychrophilic Antarctic strains identified only by sequence analysis of 16S rRNA. Among them, as counterparts of the mesophilic bacterium S. oneidensis, a psychrophilic species from this genus has been considered in this study: S. frigidimarina, a bacterial species that was originally isolated from the Antarctic coastal sites (Bowman et al. 1997, 2003).

Further, the genus Psychrobacter includes species that were primarily isolated from cold to warm, slightly to highly saline ecosystems ranging from glacial ice to sea-ice to chilled meat and fish to clinical samples. Among these bacteria, we have compared a bacterial species: P. frigidicola, isolated from the same Antarctic cold environment (Bowman et al. 1996).

Due to the potential importance of HSP90 and its client proteins, this paper has focused on HSP90-associated proteins from the mesophilic bacterium S. oneidensis and from the psychrophilic bacteria S. frigidimarina and P. frigidicola in order to elucidate the changes of HSP90-interacting network in dependence of environment. Firstly, the participation of HSP90 in cold acclimation was studied in cultures of S. oneidensis and S. frigidimarina using the specific HSP90 inhibitor 17-allylamino-17-demethoxy-geldanamycin (17AGG; Prodromou et al. 1997; Stebbins et al. 1997). Secondly, HSP90 was immunoprecipitated from bacterial cultures of S. oneidensis, S. frigidimarina, and P. frigidicola with a specific anti-HSP90 antibody. HSP90 immunoprecipitates were subjected to two-dimensional gel electrophoresis (2-DGE). Finally, proteins were identified from individual gels by peptide mass fingerprinting using matrix-assisted laser desorption/ionization time-of-flight (MALDI-TOF) mass spectrometry (MS).

Materials and methods

Bacterial strains and growth conditions

Microorganisms included in this study were purchased from culture collections (ATCC®). Broth cultures of S. oneidensis (MR-1, 700550™), S. frigidimarina (ACAM591, 700753™), P. frigidicola (ACAM304, 700361™), E. coli (DH5a, 53868™), B. subtilis (NCIB3610, 6051™), Salmonella bongori (CIP82.33, 43975™), and Burkholderia fungorum (CCUG31961T, BAA463™) were prepared as follows: 500-μl aliquots of mid-exponential grown cultures were transferred to 500-ml Erlenmeyer flasks containing 100 ml fresh, temperature-equilibrated medium (Marine broth 2216 for psychrophilic species and Luria–Bertani for mesophilic species). Four biological replicates were grown from each bacterial species. The flasks were incubated aerobically with agitation at 150 rpm, at 12°C or 30°C for psychrophilic or mesophilic bacteria, respectively, until an absorbance (OD₆₀₀) of 0.3 had been attained. The cells were then harvested by centrifugation (10,000×g, 15 min, 4°C), rinsed in PBS, and stored at −20°C until use. Cultures of S. oneidensis and S. frigidimarina for viability assays were prepared in multiwell plates with their corresponding culture conditions.

All general chemicals were purchased from Sigma unless stated otherwise in parenthesis. The chemicals used in isoelectric focusing (IEF) and in sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) were purchased from GE Healthcare.

MTT assay

A colorimetric assay based on 3-(4, 5-dimethylthiazol-2-yl)-2, 5-diphenyl tetrazolium bromide (MTT) was used for detection of bacterial viability in the presence of 17AGG. MTT is a yellow tetrazolium salt that is converted into blue formazan by dehydrogenases of live cells. The amount of blue formazan formation is proportional to the number of live bacteria in the sample, so the MTT assay can be used satisfactorily to quantify the viability of the bacteria within appropriate cell concentrations (Abate et al. 2004). The assay was performed by incubating bacterial cultures of 10⁵ bacteria/ml in the presence of 17AGG 10 μM for 24 h and then with 0.2 mg/ml sterile MTT during 1.5 h in an incubator at 12°C or 30°C. After the incubation period, bacteria were lysed with an equal volume of 10 mM HCl, 10% SDS in the incubator overnight. Values are given in absorbances (test 595 nm, reference 690 nm).

Amino acid sequence alignment of HSP90 and comparative phylogenetic analysis of bacterial species

The multiple protein alignments of HSP90/HTPG sequences were carried out using the ClustalW program. The HSP90 phylogenetic tree was established from 15 sequence alignments using neighbor-joining and parsimonia methods. The tree was drawn using the MEGA program (Tamura et al. 2007).

Preparation of cell extracts and protein determination

Bacteria from each biological replicate (four in total) were obtained from the individual cultures. The cells were harvested, washed, and lysed in buffer A (20 mM Tris–HCl, pH 7.6; 140 mM potassium chloride; 2 mM benzamidine; 1 mM EDTA; 10 μg/ml pepstatin A, leupeptin, and antipain), using a French Press at 4°C. Cell debris was removed by centrifugation at 11,000×g for 10 min to obtain a supernatant, and the protein extracts were processed using a 2-D Clean-Up kit (GE Healthcare, Spain). The pellet was frozen and stored at −80°C. The protein content was determined in cell extracts using the Bio-Rad protein assay based on the Bradford method using different dilutions of BSA as the standard. The samples were adjusted to a protein concentration of 5–10 mg/ml. All steps were carried out at 4°C.

Immunoprecipitation of HSP90

Cell extracts were immunoprecipitated with the monoclonal anti-HSP90 antibody (clone AC88, Calbiochem, San Diego, CA, USA) in order to study the HSP90-associated proteins, as previously described (Cid et al. 2004, 2007a), with some modifications. Firstly, HSP90 was immunoprecipitated in each sample (100 μg) with 1 μg of antibody for 4 h at 4°C in buffer A. Protein G-Sepharose (25 μl of 50% slurry) was then added for 1 h at 4°C and centrifuged. The immunoprecipitation was developed in stringent conditions to minimize unspecific complexes. The immunoprecipitates were washed in 1 ml of cold buffer with 0.5 M lithium chloride, then washed two times in 1 mL of cold buffer without lithium chloride, and subjected to SDS-PAGE followed by silver staining or immunoblotting. Further, immunoprecipitations were carried out for 2-DGE followed by protein identification MALDI-TOF MS peptide mass fingerprinting. HSP90 was immunoprecipitated from each sample (1,200 μg) with 4 μg of the antibody and 100 μl of protein G-Sepharose as described above. In all experiments, negative controls omitting the antibody were run in parallel.

Western blot

Western blotting was used to detect HSP90 in the cell extracts. Cell extracts (100 μg of protein) were subjected to immunoprecipitation with the monoclonal anti-HSP90 antibody and followed by SDS-PAGE using 5–12% discontinuous acrylamide (2.6% C) gels. The gels were electroblotted onto polyvinylidene difluoride membranes (GE Healthcare) which were individually incubated for 1 h with monoclonal anti-HSP90 antibody, washed and then incubated after at room temperature for 1 h with peroxidase-conjugated goat anti-species IgG antibody (Bio-Rad, USA), developed with ECL reagent (GE Healthcare, Spain), and exposed to film (Hyperfilm, GE Healthcare, Spain).

Two-dimensional gel electrophoresis

Horizontal slab gel IEF was combined with SDS-PAGE for 2-DGE by using the Multiphor II apparatus for the first dimension and standard vertical slab gel electrophoresis for the second dimension, according to the manufacturer’s instructions. Immunoprecipitated samples were prepared in 7 M urea/2 M thiourea and 5% β-mercaptoethanol, centrifuged and applied to pH gradient strips for IEF. Carrier ampholyte urea IEF was carried out using immobilized pH 3–10 and 3–11 non-linear gradient strips (18 and 24 cm, respectively).

After the first dimension, the IEF strips were processed for the second dimension in SDS-PAGE carried out on 12% acrylamide (2.6% crosslinking) gels (1.0 mm thick) with IEF strips being used as the stacking gels. The spots resolved by 2-DGE from the preparative gels were stained with Coomassie blue or with MALDI-MS compatible silver reagent for peptide mass fingerprinting analysis and protein identification.

Protein identification by peptide mass fingerprinting

Protein spots were excised manually from the Coomassie or silver-stained 2-DGE gels, de-stained, and then digested automatically using a Proteineer DP protein digestion station (Bruker-Daltonics, Bremen, Germany). The identification protocol used was based on the method previously described in (Cid et al. 2007b) with minor variations. An aliquot of the above digestion solution was mixed with an aliquot of α-cyano-4-hydroxycinnamic acid (Bruker-Daltonics) in 33% aqueous acetonitrile and 0.1% trifluoroacetic acid. This mixture was deposited onto a MALDI probe (600 μm AnchorChip for Bruker-Daltonics) and allowed to dry at room temperature. MALDI-TOF MS (/MS) data were obtained using an Ultraflex TOF–TOF mass spectrometer equipped with a LIFT-MS/MS device (Bruker-Daltonics) and a 4,800 MALDI-TOF–TOF mass spectrometer (Applied Biosystems). Spectra were acquired in the positive-ion mode at 50 Hz laser frequency, and 100 to 1,500 individual spectra were averaged. When available, for fragment ion analysis in the tandem time-of-flight (TOF/TOF) mode, precursors were accelerated to 8 kV and selected in a timed ion gate. Spectral data were analyzed through MS BioTools program (Bruker-Daltonics) or ProteinPilot software (Applied Biosystems) to search the NCBInr database using the Mascot database search algorithm (Matrix Science, London, UK; Cid et al. 2010).

Results

HSP90 inhibition reduces the bacterial viability at cold temperature

With the aim of determining whether HSP90 and its client proteins take part in the mechanism of adaptation to cold environments, we studied the viability of S. oneidensis and S. frigidimarina in the presence of the specific HSP90 inhibitor 17AGG at 12°C and 30°C. The doses of 17AGG used in the present study were previously determined by a set of dose–response experiments in which the effects of 17AGG were examined using cultures of S. oneidensis (Fig. 1a). Since the calculated IC50 was 7.7 μM, a dose of 10 μM was chosen for further experiments. Then, the viability of S. oneidensis and S. frigidimarina in the presence of 17AGG was evaluated with a MTT colorimetric assay. Decreased MTT activity is considered to be an index of bacterial damage. As a linear relationship between MTT OD values and concentration of bacteria was found at cell concentrations ranging from 10⁴ to 10⁶ bacteria/ml (data not shown), the assay of living metabolically active bacteria was performed by incubating cultures of 10⁵ bacteria/ml with MTT. 17AGG very significantly induced lower MTT activity values on both Shewanella species as compared with their corresponding control cultures. In S. oneidensis, a significant difference can be found in MTT activity values between cultures treated with 17AGG and control at 12°C or 30°C (p < 0.01; Fig. 1b), and similar significance was obtained for S. frigidimarina at 30°C, but HSP90 inhibition was even higher for treated cultures of S. frigidimarina at 12°C (p < 0.001; Fig. 1c). Considering their percentages with respect to their corresponding control cultures, both Shewanella species at 30°C treated with 17AGG grew less than did their corresponding control cultures (73% S. oneidensis (p < 0.05) and 71% S. frigidimarina (p < 0.01)) and very poorly at 12°C (51% S. oneidensis (p < 0.05) and 41% S. frigidimarina (p < 0.001); Fig. 1d). The comparison in these two bacterial species also demonstrated a significant difference in MTT values in each species at 12°C and 30°C (p < 0.01 for S. oneidensis and p < 0.001 for S. frigidimarina) and between both species at 12°C (p < 0.05; Fig. 1d). All these experiments inhibiting HSP90 demonstrate the participation of this protein in cell viability and in cold adaptation in the psychrophilic bacteria S. frigidimarina.

Fig. 1.

S. oneidensis and S. frigidimarina viability after exposure to HSP90 specific inhibitor 17AGG. a Dose–response experiments of 17AGG in S. oneidensis cultures at 12°C. Values are given in absorbances (test 595 nm, reference 690 nm). The calculated IC50 was 7.7 μM. 17AGG decreased MTT activity in S. oneidensis (b) and S. frigidimarina (c) at 12°C and 30°C. Data represent the mean ± SEM of three experiments run in duplicate. Statistical differences were studied by Student’s t test (*p < 0.05; **p < 0.01; ***p < 0.001, compared to the corresponding control). d MTT activity in cultures of S. oneidensis and S. frigidimarina treated with 17AGG. Statistical differences were studied by one-sample t test (*p < 0.05; **p < 0.01; ***p < 0.001), compared to the corresponding control as 100%, and comparison between percentages were done by Student’s t test

Comparative phylogenetic analysis of HSP90 from Shewanella and Psychrobacter

To establish the homology of HSP90 in the species compared, we used a final data set of 15 available sequences (12 from the genus Shewanella and three from the genus Psychrobacter) and 673 sites. HSP90 amino acid sequences were deduced from DNA sequence data from publicly available genomes by conducting a TBLASTN. HSP90 sequences were obtained from the NCBI database and UniProt Knowledgebase. The phylogenetic analysis of HSP90 for comparison of the bacteria is shown in Fig. 2. HSP90 protein comparisons showed that sequences belonging to each genus can be clearly distinguished. Further, a comparative view of the unrooted HSP90 tree shows the expected separate grouping of Shewanella and Psychrobacter (Fig. 2).

Fig. 2.

Phylogenetic tree from HSP90. Phylogenetic tree derived from HSP90 sequences, using the neighbor-joining method

Immunoprecipitation of HSP90

The immunoprecipitation of HSP90 was achieved with monoclonal anti-HSP90 antibody that was raised against a conserved epitope shown to react with HSP90 in multiple species, including the prokaryote HSP90 homolog HTPG (Lopatin et al. 2000; Riehl et al. 1985). Western blot analysis was carried out to confirm that the anti-HSP90 antibody used specifically recognizes this protein in several bacterial genera and to determine whether the antibody is able to immunoprecipitate the protein. The bacterial genera analyzed were S. oneidensis, S. frigidimarina, and P. frigidicola (Fig. 3). Other bacterial genera were used as controls: E. coli, B. subtilis, S. bongori, and B. fungorum (not shown). Immunoprecipitated HSP90 (Fig. 3a) was identified by Western blot analysis (Fig. 3b) and excised from silver-stained SDS-PAGE and subjected to MALDI-TOF MS peptide mass fingerprinting in order to corroborate their identity. In all genera, the immunoprecipitated and blotted protein was identified as the prokaryote HSP90 homolog HSP90/HTPG. The results shown in Fig. 3 demonstrate that the antibody had immunoprecipitated the HSP90/HTPG protein in cell extracts, which was detected with an apparent molecular weight between 72 and 74 kDa.

Fig. 3.

Determination of antibody reaction to HSP90 using cell extracts. a Silver-stained gel of HSP90 immunoprecipitates from cell extracts of S. frigidimarina (1), S. oneidensis (2), and P. frigidicola (3) and a control without cell extract (c). b Western blot for HSP90 in cell extracts from the same immunoprecipitates incubated with anti-HSP90 monoclonal antibody. The positions of relative molecular weight standards (in thousands) are also indicated. Three different cultures were assayed in all experiments; the figures are representative results

Study of proteins in HSP90 complexes in S. oneidensis, S. frigidimarina, and P. frigidicola

We have selected three HSP90 γ-proteobacteria for comparative analysis. These include S. oneidensis, S. frigidimarina, and P. frigidicola. In addition to these psychrophilic species, S. oneidensis was selected as mesophilic bacterium to compare with S. frigidimarina because both would share the same genetic background but are adapted to different environments. With the aim of identifying the proteins that interact with HSP90 in these compared species, immunoprecipitations of HSP90 complexes were carried out from the individual species under the conditions described above. Isolated complexes were separated on SDS-PAGE and were silver-stained. At first glance, it could be observed that the protein pattern in HSP90 immunoprecipitates was more similar in the psychrophilic species than in either of the Shewanella species (Fig. 3). Therefore, 2-DGE experiments followed by image analysis of HSP90 immunoprecipitates were developed to elucidate the number and identity of common spots in the three species in at least three out of four replicates of 2-DGE gels. The most abundant spots were then isolated from gels and identified by MALDI-TOF MS peptide mass fingerprinting. Figure 4 summarizes the methodological strategy to identify the HSP90-associated proteins in the three bacterial species compared, S. oneidensis, S. frigidimarina, and P. frigidicola.

Fig. 4.

Summary of the overall experimental strategy. Schematic representation of the experimental design followed to identify HSP90-interacting proteins in the three compared bacterial species

HSP90-interacting proteins in S. oneidensis and S. frigidimarina

The 2-DGE analysis of HSP90 immunoprecipitates in S. oneidensis and S. frigidimarina detected 132 total spots, 66 in each bacterial species (Fig. 5a, b). The most intense spots in image analysis (30 in S. oneidensis and 35 in S. frigidimarina) were identified by MALDI-TOF MS peptide mass fingerprinting (Tables 1 and 2). In S. frigidimarina, 15 spots (24%) were common to S. oneidensis (Fig. 6). These spots were identified as chaperone proteins DnaK and GroEL; ribosomal proteins S1, S4, L1, and L5; flavocytochrome C fumarate reductase; outer membrane porin; single-strand binding protein; protein kinase; methylcitrate synthase; universal stress protein; and three hypothetical proteins. The rest of HSP90-associated proteins identified by MALDI-TOF MS were not common in these species, taking into account their similarity in BLAST analysis.

Fig. 5.

2-DGE gels of HSP90-interacting proteins. Cell extracts were obtained from S. oneidensis, S. frigidimarina, and P. frigidicola and separately subjected to immunoprecipitation with monoclonal anti-HSP90 antibody. Conditions for growth and immunoprecipitation are given in “Materials and methods” section. HSP90 immunoprecipitates from the three species were resolved by 2-DGE gels following image analysis. Numbered spots marked with circles corresponded to common proteins identified by MALDI-TOF MS and described in Tables 1, 2, and 3. The figure is a representative of four 2-DGE experiments of S. oneidensis (red circles; a), S. frigidimarina (green circles; b), and P. frigidicola (blue circles; c)

Table 1.

Identification of HSP90-interacting proteins in S. oneidensis

Identified in S. oneidensis
Spot number	Theoretical/apparent M w (kDa)	Theoretical/apparent pI	Name/accession number	Protein scorea	Common in S. oneidensis and S. frigidimarina	Common in S. oneidensis and P. frigidicola
1	155/150	5.6/4.5	PK/NP_717078	66	+
2	69/70	4.8/4.9	DnaK/NP_716751	137	+	+
3	60/64	6.7/6.7	FR/1D4C_A	195	+
4	61/60	4.9/6	S1/NP_717992	129	+
5	57/57	4.8/5.2	GroEL/NP_716337	142	+	+
6	42/42	6.2/6.5	MCS/NP_715984	71	+
7	40/40	4.7/5.8	Porin/NP_719427	322	+
8	29/38	6.5/6.4	HypSO4719/NP_720235	167	+
9	26/35	5.9/6.2	SSB/NP_719558	155	+
10	25/35	9.6/6.5	L1/NP_715861	168	+
11	28/29	5.5/4.5	HypSO3578/NP_719123	84	+
12	27/30	8.5/5.3	HypSO2746/NP_718330	130	+
13	23/23	10.1/6	S4/NP_715895	79	+
14	18/18	10.1/5	S5/YP_961580	131	+
15	16/12	5.3/4.2	Usp/NP_719222	107	+
90	72/72	5.3/5.3	HTPG/NP_717622	163	+	+
135	105/110	5.7/5.8	GDH/NP_716412	216
136	115/120	6.1/6.3	SRR/NP_718130	90
137	62/60	5.0/5.2	UCP/NP_716619	116
138	58/61	6.4/5.7	TR/NP_718048	123
139	52/58	5.2/5.3	AP/NP_719845	225
140	50/47	5.3/5.3	hslU/NP_719692	98
141	44/42	5.1/5.2	EF-T/YP_732335	188
142	39/40	5.2/5.2	O-FMN/NP_718946	189
143	39/41	5.1/5.2	HPD/NP_717569	205
144	28/30	5.4/5.9	HypSO3184/NP_718740	120
145	22/23	5.0/4.3	AHR/YP_734504	250
146	17/15	5.8/6.1	FUR/YP_869355	176
147	29/20	7.9/8.5	Flagellin/NP_718793	210
148	16/14	5.5/5.8	NDK/NP_717870	451
Total, 30					16	3

PK protein kinase, DnaK chaperone protein DnaK, FR chain A, crystal structure of the uncomplexed form of the flavocytochrome C fumarate reductase, S1 30S ribosomal protein S1, GroEL chaperone protein GroEL, MCS methylcitrate synthase, Porin outer membrane porin, HypSO4719 hypothetical protein SO4719, SSB putative single-strand binding protein, L1 50S ribosomal protein L1, HypSO3578 hypothetical protein SO3578, HypSO2746 hypothetical protein SO2746, S4 30S ribosomal protein S4, S5 30S ribosomal protein S5, Usp universal stress protein, HTPG high temperature protein G, GDH glycine dehydrogenase, SRR sensor histidine kinase/response regulator, UCP urease domain-containing protein, TR transporter, AP agglutination protein, hslU ATP-dependent protease ATP-binding subunit, EF-T elongation factor Tu, O-FMN oxidoreductase FMN-binding, HPD 4-hydroxyphenylpyruvate dioxygenase, HypSO3184 hypothetical protein SO3184, AHR alkyl hydroperoxide reductase/thiol specific antioxidant/mal allergen, FUR ferric uptake regulator, NDK nucleoside diphosphate kinase

^aProtein scores greater than 66 were significant (p < 0.05) in the Mascot database search algorithm (Matrix Science, UK)

Table 2.

Identification of HSP90-interacting proteins in S. frigidimarina

Identified in S. frigidimarina
Spot number	Theoretical/apparent M w (kDa)	Theoretical/apparent pI	Name/accession number	Protein scorea	Common in S. frigidimarina and S. oneidensis	Common in S. frigidimarina and P. frigidicola
1	150/150	5.3/4.5	PK/YP_752088	100	+
2	69/70	4.7/4.9	DnaK/YP_749660	72	+	+
3	63/65	6.3/6.7	FR/YP_752356	83	+
4	61/60	4.9/6	S1/YP_750807	78	+
5	57/57	4.8/5.3	GroEL/YP_752326	125	+	+
6	41/42	6.1/6.5	MCS/YP_750544	171	+
7	40/40	4.7/5.8	Porin/YP_749202	178	+
8	30/38	8.3/6.4	STS/YP_752581	125	+
9	26/35	5.9/6.2	SSB/YP_752376	99	+
10	25/35	9.3/6.5	L1/YP_748839	89	+
11	26/29	5.6/4.5	HypSfri0668/YP_749366	82	+
12	27/30	6.4/5.3	HypSfri1464/YP_750154	93	+
13	25/23	9.4/6	S4/YP_748839	62	+
14	18/20	10.1/5	S5/YP_748866	110	+
15	16/12	5.3/4.2	Usp/YP_749629	91	+
16	145/160	5.6/4.7	Rne/YP_734533	86		+
17	156/110	5.9/5.6	RNApol/YP_732331	115		+
18	96/100	6.0/5.6	IF2/YP_749681	155		+
19	50/75	9.3/8	PolyA/YP_001762154	109		+
20	77/80	5.0/5.6	EF-G/YP_748846	133		+
21	53/65	5.3/6	NADsyn/YP_752467	97		+
22	59/60	5.5/5.3	ICL/YP_751815	150		+
23	35/40	5.1/5.3	MDH/YP_751848	94		+
24	30/40	5.2/6	MinD/YP_750424	227		+
25	41/39	5.4/5.4	SCoA/YP_751025	95		+
26	40/38	5.2/6.2	ADH/YP_752100	134		+
27	26/30	10.0/6.3	S3/YP_748855	152		+
28	20/25	4.6/6	Pcryo/YP_749290	192		+
29	30/24	5.0/4.9	TerD/ABI70595	134		+
30	23/20	9.9/8.6	L3/YP_748849	142		+
31	20/20	8.5/6.3	IF3/YP_001366423	129		+
32	28/18	4.8/5.3	LysM/YP_738353	189		+
33	14/18	11.0/10	S11/YP_748872	157		+
34	10/17	11.0/10	L27/YP_751764	128		+
90	72/72	5.1/5.3	HTPG/YP_750227	109	+	+
Total, 35					16	22

PK protein kinase, DnaK chaperone protein DnaK, FR chain A, crystal structure of the uncomplexed form of the flavocytochrome C fumarate reductase, S1 30S ribosomal protein S1, GroEL chaperone protein GroEL, MCS methylcitrate synthase, Porin outer membrane porin, STS putative sulfate transport system substrate-binding protein, SSB putative single-strand binding protein, L1 50S ribosomal protein L1, HypSfri0668 hypothetical protein Sfri0668, HypSfri1464 hypothetical protein Sfri1464, S4 30S ribosomal protein S4, S5 30S ribosomal protein S5, Usp universal stress protein, Rne ribonuclease, Rne/Rng family, RNApol DNA-directed RNA polymerase, subunit beta-prime, IF2 translation initiation factor IF2, polyA poly (A) polymerase, EF-G elongation factor G, NADsyn NAD (+) synthase (glutamine-hydrolyzing), ICL isocitrate lyase and phosphorylmutase, MDH malate dehydrogenase, MinD septum site-determining MinD, SCoA succinyl-CoA synthetase, ADH alcohol dehydrogenase GroES-like protein, S3 ribosomal protein S3, Pcryo hypothetical protein Pcryo_1853, TerD probable tellurium resistance TerD, L3 ribosomal protein L3, IF3 translation initiation factor IF3, LysM peptidoglycan-binding LysM, S11 30S ribosomal protein S11, L27 50S ribosomal protein L27, HTPG high temperature protein G

^aProtein scores greater than 62 were significant (p < 0.05) in the Mascot database search algorithm (Matrix Science, UK)

Fig. 6.

Distribution of HSP90-interacting proteins. The relative protein abundance of HSP90-associated proteins detected in 2-DGE gels was compared between S. frigidimarina and either S. oneidensis or P. frigidicola, considering the common or different number of spots in number (a) and in percentage (b). In b, the total percentages of spots in S. frigidimarina are also represented. Statistical differences were compared by Student’s t test (n.s. not significant)

HSP90-interacting proteins in S. frigidimarina and P. frigidicola

In the 2-DGE experiments of HSP90 immunoprecipitates in S. frigidimarina and P. frigidicola, 122 total spots were detected, 66 and 56 spots, respectively (Fig. 5b, c). The most intense spots in image analysis (35 in S. frigidimarina and 30 in P. frigidicola) were identified by MALDI-TOF MS peptide mass fingerprinting (Tables 2 and 3), and 21 (34%) of these were found in S. frigidimarina and common to P. frigidicola (Fig. 6). The common HSP90-associated proteins were identified by MALDI-TOF MS peptide mass fingerprinting as chaperone proteins DnaK and GroEL; ribosomal proteins L3, L27, S3, and S11; translation initiation factors IF2 and IF3; Rne; RNApol; PolyA; EF-G; NADsyn; ICL; MDH; MinD; SCoA; ADH; Pcryo; TerD; and LysM. Only two of these HSP90-associated proteins (DnaK and GroEL) were found to be common to all three bacterial species. The rest of HSP90-associated proteins identified by MALDI-TOF MS were not common in these species, taking into account their similarity in BLAST analysis.

Table 3.

Identification of HSP90-interacting proteins in P. frigidicola

Identified in P. frigidicola
Spot number	Theoretical/apparent M w (kDa)	Theoretical/apparent pI	Name/accession number	Protein scorea	Common in P. frigidicola and S. oneidensis	Common in P. frigidicola and S. frigidimarina
2	70/70	4.5/4.9	DnaK/AAZ19979	135	+	+
5	58/59	4.8/5.2	GroEL/Q4FU94	103	+	+
16	160/160	5.4/4.7	Rne/YP_579550	178		+
17	155/110	5.9/5.6	RNApol/Q1Q8Q0	150		+
18	100/100	6.0/5.5	IF2/YP_263377	105		+
19	84/75	9.6/8	PolyA/YP_579391	145		+
20	79/80	4.9/5.6	EF-G/YP_265177	119		+
21	61/65	5.3/6	NADsyn/YP_001280772	120		+
22	59/60	5.1/5.3	ICL/YP_581121	96		+
23	35/40	4.9/4.9	MDH/YP_581305	157		+
24	30/40	5.1/6	MinD/YP_581352	169		+
25	42/39	4.7/5.3	SCoA/ZP_00146840	122		+
26	39/39	5.2/6	ADH/YP_581659	103		+
27	27/30	10.2/6.3	S3/ZP_01272929	173		+
28	25/25	8.8/6	Pcryo/YP_581114	126		+
29	20/24	4.4/4.9	TerD/YP_264050	100		+
30	22/20	9.9/8.6	L3/YP_263786	84		+
31	19/20	8.5/6.3	IF3/YP_265380	184		+
32	18/18	5.9/5.8	LysM/YP_579785	73		+
33	14/18	11.0/10	S11/YP_263809	116		+
34	9/17	10.7/10	L27/YP_264854	109		+
90	74/74	4.7/5.2	HTPG/YP_581259	106	+	+
335	51/50	4.5/5.9	TF/YP_581494	112
336	33/33	5.3/5.0	UP/YP_264782	86
337	35/35	6.1/6.8	UP/YP_580621	126
338	28/28	5.3/5.3	TRR/YP_001279607	83
339	31/29	5.3/5.6	EDR/YP_001280155	79
340	24/27	5.2/4.9	AK/YP_001279708	72
341	23/26	8.6/7.1	RMTE/YP_001279439	117
342	23/24	9.5/9.7	DsbA/YP_579397	89
Total, 30					3	22

DnaK chaperone protein DnaK, GroEL chaperone protein GroEL, Rne ribonuclease, Rne/Rng family, RNApol DNA-directed RNA polymerase, subunit beta-prime, IF2 translation initiation factor IF2, polyA poly (A) polymerase, EF-G elongation factor G, NADsyn NAD (+) synthase (glutamine-hydrolyzing), ICL isocitrate lyase and phosphorylmutase, MDH malate dehydrogenase, MinD septum-site determining MinD, SCoA succinyl-CoA synthetase, ADH alcohol dehydrogenase GroES-like protein, S3 ribosomal protein S3, Pcryo hypothetical protein Pcryo_1853, TerD probable tellurium resistance TerD, L3 ribosomal protein L3, IF3 translation initiation factor IF3, LysM peptidoglycan-binding LysM, S11 30S ribosomal protein S11, L27 50S ribosomal protein L27, HTPG high temperature protein G, TF trigger factor, UP uncharacterized protein, TRR two-component response regulator, EDR exodeoxyribonuclease III, AK adenylate kinase, RMTE ribosomal RNA large subunit methyltransferase E, DsbA oxidoreductase DSBA

^aProtein scores greater than 72 were significant (p < 0.05) in the Mascot database search algorithm (Matrix Science, UK)

Two independent laboratories validated the identification by MALDI-TOF MS peptide mass fingerprinting to corroborate the identities of the proteins shown in Tables 1, 2, and 3. The score included in these tables was the lowest score registered for each protein identification. Taken together, the results described here demonstrate that a significantly (p = 0.0006) higher number of common HSP90-associated proteins are found in S. frigidimarina common to P. frigidicola compared to S. oneidensis (Fig. 6). The total number of common spots in S. oneidensis and S. frigidimarina was not significantly different (p = 0.501) from that in S. frigidimarina and P. frigidicola.

Regarding the position of the proteins in the 2-DGE gels (Fig. 5), it has been suggested that there is a shift in the average isoelectric point of the proteome toward basic values as the optimum growth temperature changes to minimize protein aggregation with variable growth temperature. In extremophiles, most proteins appear to be acidic, with the pI ranging from 4 to 6 (Fig. 5 and Tables 1, 2, and 3). However, a small number of HSP90-interacting proteins appear to be very basic proteins with pIs of more than 8. This suggests a possible alternative role for these proteins, as exemplified by the nucleotide binding proteins found in the HSP15 from E. coli (Kawashima et al. 2000). Nevertheless, when they occur in extremophiles, basic proteins are always accompanied by at least one paralog with an acidic pI (Fig. 5). In this case, the greater coincidence in protein positions in 2-DGE gels in psychrophilic species as compared to both the Shewanella species (Fig. 5a, b) may be a result of the same shift in the isoelectric point due to a cold environment. In order to confirm this, we attempted to identify most of the HSP90 co-immunoprecipitated proteins in silver-stained 2-DGE gels from S. oneidensis, but those proteins related to energy metabolism and protein synthesis that had been found in psychrophilic species did not co-immunoprecipitate with HSP90 in S. oneidensis (Table 1). Following identification, spot migration in the 2-DGE gels was reexamined and the following discrepancies were noted. Spots 10, 13, 14, 27, and 28; four ribosomal proteins, L1, S4, S5, and S3; and hypothetical protein Pcryo_1853 focused at a lower pI in the 2-DGE gels (Fig. 5); three proteins had molecular weights inconsistent with their predicted molecular weight; spot 16 migrated more slowly (was larger) than expected for Rne in S. frigidimarina while spots 17 and 19 in P. frigidicola migrated more quickly (were smaller) than expected for RNApol and PolyA, respectively. These differences in mass and pI may be due to posttranslational modifications, truncated or degraded forms, aberrant migration, and/or errors in determining masses from the gels. In addition, errors in genome annotation can result in mismatches between predicted and observed molecular weight.

Interaction of DnaK and GroEL with HSP90

To demonstrate that client proteins really interact physically with HSP90, we investigated the effect of the specific inhibitor 17AGG on HSP90 complexes. The addition of the inhibitor to HSP90 immunoprecipitates resulted in the loss of several proteins in HSP90 complexes. In these complexes, the loss of DnaK and GroEL was very evident when they were detected by 2-DGE in HSP90 immunoprecipitates incubated with 17AGG (Fig. 7a).

Fig. 7.

Interaction of DnaK and GroEL with HSP90. a Effect of the specific HSP90 inhibitor 17AGG. HSP90 immunoprecipitates were incubated without (−) and with (+) 17AGG and after labeled with Cy3 (control, in green) and Cy5 (in red), respectively. The immunoprecipitates were combined and analyzed by 2-DGE as in Fig. 5. Gels were scanned with a Typhoon Imager. The codetected spots corresponding to DnaK and GroEL in S. oneidensis, S. frigidimarina, and P. frigidicola are represented. Similar results were obtained in three separated experiments. b Western blot analysis with anti-DnaK antibodies (top) or anti-GroEL antibodies (bottom) of HSP90 immunoprecipitates. c Western blot analysis with anti-HSP90 in DnaK and GroEL immunoprecipitates. Line C control of unspecific binding to the beads. MW are indicated. The figure is a representative of three different experiments

The interaction between DnaK or GroEL and HSP90 was also confirmed by Western blot analysis with anti-DnaK or anti-GroEL antibodies in HSP90 immunoprecipitates (Fig. 7b) and by Western blot analysis with anti-HSP90 antibodies in DnaK or GroEL immunoprecipitates (Fig. 7c).

Global HSP90 interaction network

The global HSP90 interaction network deduced from the experimental data obtained from the study of S. oneidensis, S. frigidimarina, and P. frigidicola is represented in Fig. 8. It shows the proteins associated with HSP90 in each bacterial species; a color code differentiates their cellular function.

Fig. 8.

Overview of the HSP90 interaction data. Network overview showing the proteins that interact with HSP90 in S. oneidensis, S. frigidimarina, and P. frigidicola. HSP90-interacting proteins are colored according to cellular processes. Shaded circles around groups of proteins indicate the main groups of HSP90-interacting proteins found in psycrophilic bacteria: proteins related to energy metabolism (shaded in blue) and protein synthesis (shaded in pink)

Discussion

As the induction of HSPs is a universal response and HSP90-interacting proteins have been described to participate in critical cell functions (Chen et al. 2006), we have investigated HSP90 and HSP90-associated proteins to elucidate their participation in bacterial viability and cold adaptation. Although most of previous studies in other bacterial species had been carried out with htpG mutants (Bardwell and Craig 1988; Hossain and Nakamoto 2002; Tanaka and Nakamoto 1999; Versteeg et al. 1999), we have chosen a different strategy using the specific HSP90 inhibitor 17AGG, as the amino-terminal domain of approximately 200 amino acid residues which contains the geldanamycin/nucleotide binding site (Prodromou et al. 1997; Stebbins et al. 1997) is conserved in Shewanella. The relative growing of S. oneidensis and S. frigidimarina in the presence of 17AGG indicates that HTPG is not completely essential for normal growth, as previously observed for E. coli (Bardwell and Craig 1988) and B. subtilis (Versteeg et al. 1999) in thermal stress, but this protein plays an important role especially in cold acclimation, according with the significant differences obtained in cultures of S. frigidimarina at 12°C compared to its control (P < 0.001; Fig. 1). This interesting role of HSP90 could be an effect of its interaction with other client proteins, which might be determined by temperature.

An amino acid sequence alignment of HSP90 for comparison of bacterial species and their subsequent phylogenetic analysis was undertaken, which demonstrated that Shewanella species showed similar HSP90 sequences, with regard to both their DNA and protein sequences and a clear difference between the genus Shewanella and Psychrobacter. Nevertheless, preliminary assays to compare HSP90 co-immunoprecipitated proteins among S. oneidensis, S. frigidimarina, and P. frigidicola using SDS-PAGE demonstrated considerable analogy in the protein pattern between S. frigidimarina and P. frigidicola.

In order to elucidate the HSP90-associated proteins common to both psychrophilic bacteria, we analyzed HSP90 immunoprecipitates performed with specific antibodies using a widely tested methodology (Cid et al. 2004, 2007a). In our studies, we used an anti-HSP90 monoclonal antibody that was raised against a conserved epitope shown to react with HSP90 in multiple species, including the prokaryote HSP90 homolog HTPG (Lopatin et al. 2000; Riehl et al. 1985). The antibody also recognized the protein in the bacterial species studied, as was demonstrated by Western blot and MALDI-TOF MS analysis.

Several 1-DGE experiments using immunoprecipitated samples confirmed that HSP90 complexes from psychrophilic species had in common more proteins than had species from the same genus. We endeavored to compare these three species which represent either the same genus or the same environment. An experimental approach using 2-DGE demonstrated that the number of common proteins in HSP90 complexes in both psychrophilic bacteria is very significantly higher than the number of common proteins associated to HSP90 in Shewanella species, although they are closely related phylogenetically. Thus, using MALDI-TOF MS, we systematically identified those proteins that interact in vivo with HSP90 and are key determinants of protein functions at different temperatures (Strocchi et al. 2006). Proteins that interact only very transiently with HSP90 may have escaped detection in this analysis, but such proteins are not expected to be strongly dependent on the chaperone complexes for their function. Further, 2-DGE comparisons were performed between the whole extracts and their corresponding immunoprecipitates to check that the identified proteins were enriched in the precipitates.

All HSP90 interactions detected in the three bacterial species are summarized in Fig. 8. Based on our results, we have classified the common HSP90-associated proteins in the three bacterial species according to the categories below.

Chaperones

These are involved in protein folding which is an essential step to ensure functional assembly. When the temperature falls, these proteins act mainly on the regulation of cellular protein synthesis, particularly at the level of initiation of translation and also prevent the formation of mRNA secondary structures (Georlette et al. 2004). We have found two main chaperones associated with HSP90 in the three species: DnaK and GroEL. The chaperone DnaK (HSP70) has been found as a HSP90-interacting protein in the three species, which probably takes part in the mechanisms of stress tolerance through the DnaK/DnaJ system. It has also been demonstrated in other psychrophilic bacteria such as Colwellia maris that the dnaK gene is highly expressed on incubation of the cells at 18–20°C (Yamauchi et al. 2004). The chaperone GroEL (HSP60) is essential for growth and viability under many environmental conditions (Fayet et al. 1989; Houry et al. 1999). In vivo, GroEL is involved in the folding of approximately 10% of newly synthesized polypeptides (Wong and Houry 2004). Several studies have demonstrated the catalytic activity of GroEL in the folding process of soluble proteins such as malate dehydrogenase and enolase (Goulhen et al. 2004; Houry et al. 1999).

Plasma membrane and cell wall

It has been reported that adaptation to the cold reduces membrane fluidity. Some proteins associated with membrane and cell wall formation have been found to co-immunoprecipitate with HSP90 in our experiments; of these, outer membrane porin appeared in Shewanella. This porin forms hydrophilic channels through the outer membrane, and it has been reported that GroEL is able to refold a disordered porin and promote the recovery of its pore-forming activity (Goulhen et al. 2004). In psychrophiles, septum site-determining MinD and peptidoglycan-binding LysM were found. It has already been demonstrated in other psychrophilic species that inhibition of septum formation is temperature dependent (Gounot et al. 1977). In S. frigidimarina and P. frigidicola, the septum site-determining MinD has been found to bind to HSP90, also indicating a possible temperature-dependent mechanism in septum formation.

Replication and protein synthesis

It has been documented that the ability of psychrophiles to grow at low temperatures depends on adaptative changes in cellular proteins and lipids (Russell 1990). Changes in proteins are genotypic and are related to the properties of enzymes and translation systems, whereas changes in lipids are phenotypic and are important in regulating membrane fluidity and permeability. In our study, we have found some translation factors associated with HSP90 in psychrophilic species but not in S. oneidensis, such as translation initiation factor IF2, translation initiation factor IF3, and elongation factor G. It has been assessed that one of the major effects of cold temperatures on microorganisms is the inhibition of translation initiation and elongation (Broeze et al. 1978; Georlette et al. 2004). In these psychrophilic species, the association of HSP90 with these translation factors may represent a method of coping with the stress situation of cold temperatures. As a similar example, in E. coli, it has been demonstrated that expression of IF2 and IF3 is enhanced after cold shock that contributes to establishing the cold shock translational bias whereby cold shock mRNAs are preferentially translated by cold stressed cells while bulk mRNAs are discriminated against (Giuliodori et al. 2004, 2007).

Ribosomal-related proteins

Ribosomal proteins L1, S1, S4, and S5 were detected in Shewanella complexes, while other four ribosomal proteins, S3, S11, L3, and L27, were only present in complexes from psychrophilic species. Among proteins related to RNA, three proteins have been found in psychrophiles: ribonuclease, Rne/Rng family, poly (A) polymerase, and DNA-directed RNA polymerase, subunit beta-prime.

Energy metabolism

For organisms inhabiting environments at extreme temperatures, energy levels must be adjusted accordingly in order to maintain biological processes at viable levels. It has been demonstrated that in the psychrophiles, adenylate levels are invariably elevate as temperatures fall (Napolitano and Shain 2005). The stoichiometry of these changes target pivotal enzymes in cellular metabolism, and there is also evidence for compensation of enzymatic activity in some energy-related pathways (Napolitano and Shain 2005). Among the enzymes involved in carbohydrate metabolism, we have found isocitrate lyase and phosphorylmutase, succinyl-CoA synthetase, alcohol dehydrogenase, NAD (+) synthase, and malate dehydrogenase associated with HSP90 in both psychrophilic species, but not in S. oneidensis. A few crystallographic structures of cold-adapted enzymes have been elucidated. The analysis of their 3D structure, taking malate dehydrogenase as an example, revealed that better accessibility of the catalytic cavity to ligands and a decrease in conformational stability together with an increase in the flexibility of the molecular structure (Georlette et al. 2004) can be achieved by chaperone intervention. Flavocytochrome reductase and methylcitrate synthase are the only proteins in this group that are common to both Shewanella species but are not present in P. frigidicola.

Others

Several hypothetical proteins have been found associated to HSP90: Hypothetical proteins SO4719, SO3578, and SO2746 in S. oneidensis were found to be similar in BLAST analysis to three hypothetical proteins in S. frigidimarina. Further, hypothetical protein Pcryo_1853 and probable tellurium resistance TerD were located in psychrophiles.

In our study, HSP90 sequence comparisons have differentiated Shewanella and Psychrobacter as two different genera. Nevertheless, regarding the HSP90-associated proteins, a new cluster can be hypothesized (Fig. 9), which suggests that the general similarity of HSP90 interactors in psychrophilic bacteria implies that the same selective mechanisms must occur in both cold-adapted species.

Fig. 9.

HSP90-interacting protein cluster. Cluster analysis resolved with the common proteins identified by MALDI-TOF MS (see Tables 1, 2, and 3) in HSP90 immunoprecipitates from S. oneidensis, S. frigidimarina, and P. frigidicola comparing these bacterial species and showing the relationship between both psychrophilic species

In conclusion, although general mechanisms of adaptation to cold environments are well-known in bacteria, they have traditionally been studied in cold shock experiments (Polissi et al. 2003), but not in long-term adaptation. From our results, it seems that in the genus Shewanella, this adaptation is achieved through a chaperone system that involves DnaK and GroEL proteins, but in psychrophilic bacteria, other proteins—i.e., proteins associated to HSP90—with main functions such as energy metabolism and protein synthesis may contribute to the mechanism of adaptation to cold environments. This hypothesis leads to the contention that complex stress response networks should not only be determined by transcriptome or proteome analysis alone since they are also modulated by the environment of the bacteria. The protein interactions and assemblies that we have identified provide the first experimental study considering environmental influences with regard to protein interaction networks that should be taken into account in “systems biology” approaches and in computational interaction predictions and agree with some published theoretical works (Babu et al. 2006).

Abbreviations

HSP90

Heat shock protein 90

HTPG

High temperature protein G

17AGG

17-Allylamino-17-demethoxy-geldanamycin

2-DGE

Two-dimensional gel electrophoresis

MALDI-TOF MS

Matrix-assisted laser desorption/ionization time-of-flight mass spectrometry