Creation of a fosmid clone library

Hypothesizing that DNA uptake and DNA catabolism for nutrients are mutually inclusive events, we set out to identify genes conferring the DNA uptake characteristic of the naturally competent Bp strain 1026b by screening for functional DNA uptake in Bp strain K96243 and Bc strain K56-2 or DNA catabolism in Bc K56-2. This was achieved by a novel experimental approach that combined the use of a low-copy broad-host-range fosmid clone library containing ~50 Kbp chromosomal DNA fragments of strain 1026b (Fig 2A) with engineered recipient strains that contained chromosomally integrated counter-selection markers, which enabled positive selection of bacteria harboring fosmid clones bestowing the ability for DNA uptake (Fig 2B). Alternatively, the Bc K56-2 pool was selected on minimal medium containing purified salmon sperm DNA as a sole carbon source to screen for DNA catabolism (Fig 2B). Approximately 20,000 Escherichia coli clones were initially created, representing more than 20-fold coverage of the Burkholderia species genomes. This library was mobilized into Bp strain K96243 and B. cenocepacia (Bc) strain K56-2.

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Fig 2. Library production and counter-selection scheme.

(A) Plasmid map of an in-lab created pBBR-FOSGAT and strategy for creating the fosmid library. Bp 1026b chromosomal DNA (1) was sheared (2), and approximately 50-Kbp size fragments were ligated to pBBR-FOSGAT fosmid vector DNA (3 and 4; fosmid vector indicated in red). The ligated DNA was then packaged into λ-phage particles (5) and the particles are used to infect E. coli host cells (6). (B) Counter-selection scheme to screen for fosmid clones enabling DNA uptake or DNA catabolism. (1) pheS and sacB counter-selectable markers were inserted into Bc K56-2 and Bp K96243 chromosomes through minTn7 integration. (2) The E. coli library containing fosmid pool from (A) was conjugated with Bc K56-2 and Bp K96243 containing pheS and sacB counter-selectable markers. (3) Colonies from these two Burkholderia strains were individually pooled and incubated with flp-DNA, allowing transiently expressed Flp to excise the chromosomally integrated counter-selection markers and counter-selected on media containing cPhe and sucrose. (4) Alternatively, the Bc K56-2 pool was selected on minimal medium containing purified salmon sperm DNA as a sole carbon source.

https://doi.org/10.1371/journal.pone.0189018.g002

Identification of B. pseudomallei chromosomal gene fragments required for extracellular DNA uptake

Following mobilization of the fosmid clone library to non-competent Bp K96243 and Bc K56-2 containing chromosomally-inserted Flp recombinase target (FRT)-flanked sacB and pheS counter-selection markers, several thousand colonies were obtained for both recipient strains. After pooling the respective Bp and Bc colonies (library), the Bc library was plated on M9 medium containing salmon sperm DNA as the sole carbon and energy source (Bc K56-2 only). Additionally, fosmid clones in both species conferring the ability to uptake DNA and Flp-mediated excision of the counter-selection markers (i.e., sacB and pheS on the chromosome) were identified in two steps (Fig 2B). First, the pooled colonies were incubated with a DNA fragment encoding Flp recombinase. Once taken up into bacteria by the fosmid clones encoding the DNA uptake pathway, Flp recombinase is transiently expressed and acts on the FRT sites flanking the sacB-pheS cassette leading to excision of the counter-selectable markers from the chromosome. Second, colonies resulting from excision of the counter-selection markers from Bp K96243 and Bc K56-2 were selected by plating on sucrose and cPhe containing agar plates (Fig 2B).

Counter-selection using the entire library yielded 20–30 large and ~300 smaller colonies with Bp K96243 and 10–20 colonies with Bc K56-2. No colonies were obtained after plating of the negative controls (Bp K96243 and Bc K56-2 containing the counter-selectable markers without fosmid library). Additionally, hundreds of colonies were obtained after plating of Bc K56-2 on agar plates containing 0.1% salmon sperm DNA. Presumably, since wildtype Bc K56-2 is unable to grow on DNA as a sole carbon source (Fig 1B), these Bc K56-2 colonies contained fosmids that allowed growth on DNA as a sole carbon source. We next sequenced, characterized, and validated the functionality of several fosmid clones that confers DNA uptake and/or DNA catabolism.

Several distinct B. pseudomallei genetic regions are required for DNA uptake and/or DNA catabolism

We attempted to isolate fosmids clones from Bp and Bc and transform them into E. coli DH5α for identification. Between 10–20 colonies (both large and small) were processed from each of the selection method above, however, only a small number of fosmid clones were able to replicate in E. coli. Sequencing the fosmid vector-chromsomal DNA junction allowed for the identification of insert size and gene content (Fig 3A and S1 Table). Three unique inserts were identified in fosmids isolated from Bc (i.e., two from the counter-selection scheme, Bc3 and Bc6; and one from the selection on DNA as carbon source scheme Bc17). One unique insert was identified in fosmids isolated from Bp from the counter-selection scheme (Bp1; Fig 3A). The observed fosmid sizes, Bc3 ~40.1 kb, Bc6 ~49.7 kb Bc17 ~42.2 kb and Bp1 ~46.1 kb, are in the expected range based on the capacity of the phage DNA packaging capacity (~50 kb). Interestingly, the genomic regions from Bp 1026b in the fosmids are nearly identical to genomic regions already in the genome of Bp K96243, yet 1026b is naturally transformable but K96243 is not (Fig 3B).

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Fig 3. Gene content of four fosmid clones conferring natural competency and/or DNA catabolism.

(A) The fosmid backbone is indicated in black and the red region depicts the extent of Bp 1026b genomic DNA inserted in each fosmid. Gene products with known predicted functions are indicated by gene names and those with unknown functions are labeled with gene identifications. (B) Synteny map comparing fosmid regions of Bp K96243 and 1026b. Red regions indicate the high level of similarity between fosmid regions in strain K96243 (non-competent) versus 1026b (competent) aligned using Artemis webACT. Identical regions are indicated in red, non-identical regions in white, and blue indicates a region that is inverted in the two strains.

https://doi.org/10.1371/journal.pone.0189018.g003

Genes of special interest found in various fosmid clones are summarized in Table 1. At an initial glance, genes of interest on Bc3 that may be involved in DNA uptake and/or DNA catabolism include BP1026B_I2578, a predicted permease, and BP1026B_I2563-2562 that encode components of ABC transporters. Several hypothetical proteins of unknown function are also present and could be involved in conferring natural competency.

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Table 1. Characterization of selected genes from fosmids.

https://doi.org/10.1371/journal.pone.0189018.t001

Genes of interest on Bc6 include BP1026B_I2371 (encodes a protein with 13 transmembrane helices and is predicted to transport nucleobases, nucleosides, nucleotides and/or nucleic acids from one side of a membrane to another), BP1026B_I2369 (encodes a putative lysine decarboxylase; annotated as DNA-processing protein A or DprA in Bp K96243 which loads the recombinase RecA onto ssDNA), and BP1026B_I2363 (encodes a putative membrane protein of unknown function).

The fosmid Bc17 was selected for in Bc K56-2 growing on salmon sperm DNA. Genes of interest on this fosmid include BP1026B_II2056 (a transcriptional regulator that influence catabolic pathways), BP1026B_II2062 (a hypothetical protein showing 44% identity at the amino acid level to a B. melitensis predicted lysine decarboxylase modeled to the DprA family), BP1026B_II2080 (a pilJ homolog), and BP1026B_II2082 (encode a signal sensor/response regulator and a putative methyl accepting transducer protein).

Fosmid Bp1, counter-selected in Bp K96243, contains two genes of unknown function, BP1026B_I0820 and BP1026B_I0809. BP1026B_I0804 showed high identity to known competence protein, ComE, in Gram negatives. The Bp ComE protein has 56% homology and 38% identity at the amino acid level to the Neisseria meningitidis ComEA competence protein and 74% similarity and 56% identity to the Ralstonia solanacearum ComEA protein.

We attempted to narrow down the potential candidate genes for DNA uptake and/or DNA catabolism using several available mutants. Characterization of approximately 200 genes on the 4 fosmid clones would be overwhelming. Therefore, we selected 12 available mutant strains from the 1026b::T24 insertion mutant library to test. Mutant strains of genes BP1026B_I2371, BP1026B_I2056, BP1026B_II2080, and BP1026B_I0804 exhibited defects in both the ability to grow on DNA and uptake gfp-DNA, indicating their involvement in competency and DNA catabolism (Table 1 and S1 Fig). In contrast, BP1026B_II2062 mutant strain is only defective in its ability to grow on DNA, suggesting its sole involvement in DNA catabolism (Table 1 and S1 Fig). These individual genes will be of particular interest for future investigation, which is beyond the scope of this initial study. However, we further characterize these four fosmid clones here for DNA uptake and DNA catabolism capability.

Distinct B. pseudomallei chromosomal regions play differential roles in DNA uptake and DNA catabolism

Fosmids Bc3, Bc6, Bc17 and Bp1 were introduced into non-naturally competent Burkholderia species, Bc K56-2, Bp K96243, and Bm ATCC23344, along with the empty fosmid vector as a control. Following incubation with gfp-DNA, non-naturally competent bacteria containing the fosmids, and the empty fosmid vector were visualized under fluorescent microscopy to assess the bacterial populations that were able to uptake and express gfp-DNA. Fig 4A shows the overlay of the green channel and the DIC channel. At all levels of fluorescence excitation, there was near zero fluorescence detected above background for all the empty vector controls. As seen in the representative images, many green fluorescent bacteria populate the fosmid containing cultures. Fluorescent bacteria were counted from random images (experiments carried out in duplicate) and divided by the total number of bacteria to obtain an average percentage of fluorescent bacteria (Fig 4B). Although varied percentages of GFP-positive bacteria were observed in different species/strains, all four fosmids conferred the ability to uptake DNA in all bacteria tested.

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Fig 4. Confirmation of the ability of four fosmid clones to individually confer natural competency or growth on DNA.

(A) gfp-DNA uptake assay to assess natural competency. Individual fluorescent bacteria are visible in the representative images (green fluorescence and DIC overlay). The percentages of cells that fluoresce following gfp-DNA uptake are shown in (B). Numbers are from 3 representative images from duplicate experiments. Error bars represent the SEM. Asterisks indicate the fosmid clone gave rise to significant higher %GFP positive comparing to the corresponding empty vector control in three fields (**, P<0.005 based on unpaired t-test). (C) Growth of various fosmid-containing strains in 1x M9 with 0.25% DNA done in triplicate. Error bars represent the SEM. Asterisks indicate the fosmid clone gave rise to significant higher growth in DNA comparing to the corresponding empty vector control (*, P<0.05 based on unpaired t-test; **, P<0.005 based on unpaired t-test).

https://doi.org/10.1371/journal.pone.0189018.g004

To observe any link between DNA uptake and DNA catabolism, the same cultures used for the gfp-DNA incubation were grown on minimal media containing purified salmon sperm DNA as a sole carbon source. Bc17 fosmid was the only clone that enabled all three species to exhibit significant growth on DNA as a sole carbon source, indicating at least some linkage of DNA uptake to DNA catabolism (Fig 4C). Bc6 fosmid aided moderate levels of growth in Bp K96243 and Bm ATCC23344 when comparing to their empty vector controls (Fig 4C). In contrast, Bc3 fosmid failed to enable growth in any of the three species on DNA; and although significant, Bp1 fosmid only facilitated light growth of Bm ATCC23344 in DNA (Fig 4C).

Exploitation of fosmid clones to genetically manipulate non-naturally competent select agent Burkholderia species

Natural transformation has previously been exploited for genetic manipulation of B. pseudomallei and B. thailandensis strains [11, 12]. We reasoned that the fosmids identified in this study could be exploited for chromosomal allelic-replacement of non-naturally competent B. pseudomallei and B. mallei. To test this notion, we assessed efficacy of λ-Red mediated mutation of the vacJ gene [13, 14] in the non-naturally competent Bm and Bp that harbored the fosmid candidates, using the non-antibiotic tellurite resistance marker [15] (Fig 5). Bc was not tested due to the lack of genetic tools for λ-Red recombination. Using Bp and Bm strains, tens to hundreds of distinct tellurite resistant colonies were obtained when expression of the λ-Red system was induced by addition of rhamnose and incubation with vacJ’-kilA-telA-telB-‘vacJ DNA. All fosmid clones gave rise to tranformation in both strains. All tellurite resistant colonies tested by PCR yielded the expected mutants (Fig 5E). In the absence of these fosmid clones, λ-red recombineering does not work in non-naturally competent B. pseudomallei K96243 and B. mallei ATCC23344 [16]. These data and analysis of the genomes suggested that although competency genes do exist in both strains, adding certain components may shift the balance to increase or optimize one of the several steps of the DNA uptake process to make it now more efficient (i.e., competency induction, DNA binding, DNA translocation, DNA fragmentation, DNA protection, and/or DNA recombination).

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Fig 5. Allelic-replacement in B. mallei strain ATCC23344 and B. pseudomallei K96243 containing fosmids by natural transformation.

(A) λ-Red plasmid pKaKa2 and individual fosmid clones were co-transformed into B. mallei ATCC23344 and B. pseudomallei K96243. (B) PCR products were generated containing the tellurite resistance cassette (kilA-telA-telB) flanked with 45-bp homologies to the vacJ gene. (C) Various numbers of distinct colonies were obtained. PCR was performed for the kilA-vacJ junction (D) or the telA gene (E) and all were positive. Two gels were shown here as representative results; “-” denotes negative control using wildtype B. mallei chromosomal DNA as template for kilA-vacJ junction PCR, and “+” denotes positive control using pwFRT-tel as template for telA PCR.

https://doi.org/10.1371/journal.pone.0189018.g005

Strains, growth conditions, and media

All manipulations of select agent bacteria were performed in the CDC approved bio-containment facility at the University of Hawaii at Manoa, John A. Burns School of Medicine. 1026b::T24 insertion mutant library was obtained from Colorado State University and University of Washington. Derivatives of Escherichia coli strain EPMax10B (BioRad), E1345 and E1869 were routinely used for cloning or plasmid mobilization into Bp and Bc as described previously [15, 17]. Luria-Bertani (LB) medium (Difco) or 1x M9 minimal medium supplemented with 20 mM glucose (MG) was used to culture E. coli and Burkholderia strains. Selection of gat gene in E. coli and Bp strains was performed as previously described [17].

Plasmid construction

The plasmid pCC2FOS was obtained from Epicentre in the CopyControl™ HTP Fosmid Library Production Kit. pCC2FOS was digested with NruI and the cat-cosN fragment was ligated to the SmaI digested rep-mob fragment of pBBR-Gm to produce the broad-host-range plasmid pBBR-FOS. The cat gene was partially deleted by digestion with SspI and ScaI and inserting the EcoRV-XhoI digested P_S12-gat cassette from pwFRT-P_S12-gat [17] to produce the non-antibiotic-based broad-host-range fosmid vector pBBR-FOSGAT. Deletion of the cat gene, was verified by patching transformants containing pBBR-FOSGAT on LB-chloramphenicol 25 μg/ml.

The mini-Tn7-ara-sacBm-pheS-FRT vector was created by digesting the plasmid mini-Tn7-bar-sacBm-pheS-FRT with EcoRV and XhoI, blunt-ended, and ligated with the arabinose operon digested from pKaKa2 [16] and blunt-ended. The mini-Tn7-dhfr-sacBm-pheS-FRT vector was created in the same manner by sub-cloning the EcoRV-XhoI fragment containing the dhfr gene from pwFRT-P_CS12-dhfr [18].

Strain construction

Insertion of mini-Tn7-ara-sacBm-pheS-FRT into the chromosome of Bp strain K96243 and mini-Tn7-dhfr-sacBm-pheS-FRT into the chromosome of Bc strain K56-2 was carried out as previously described [17], selected on MA40 media for ara selection or LB + trimethoprim 100 μg/ml for dhfr selection, and insertions were verified by PCR. Sensitivity of both strains to 0.1% chlorinated phenylalanine (cPhe) and 15% sucrose was verified by patching.

Fosmid library construction

Genomic DNA (gDNA) was isolated from naturally competent Bp 1026b using phenol-chloroform extraction. The gDNA was pipetted 100 times with a P200 pipette tip to shear the DNA. To determine proper shearing, 1 μg of sheared gDNA was analyzed on a 0.5% agarose gel with a λ DNA-Monocut Mix DNA size ladder (New England BioLabs). Five μg of the sheared gDNA was end repaired using the End-Repair Enzyme Mix according to the CopyControl™ HTP Fosmid Library Production Kit. Following end repair, the gDNA was size selected on a 0.5% agarose gel run at 30 kV overnight. Fragments approximately 35–42 kb in size were excised and eluted from the gel. The pBBR-FOSGAT was digested with SmaI overnight. The linearized plasmid was dephosphorylated with calf intestinal phosphatase (NEB) for 45 min and then gel purified. A 10:1 molar ratio of plasmid to sheared gDNA was mixed and ligated overnight using T4 DNA ligase (NEB). The ligation was packaged into phage heads following the CopyControl™ HTP Fosmid Library Production Kit manual. Briefly, 25 μl of MaxPlax Packaging Extracts was mixed with the ligation reaction and incubated at 30°C for 2 h. A second 25 μl aliquot of the MaxPlax Packaging Extracts was added and incubated at 30°C for another 2 h. The reaction was stopped by addition of chloroform and dilution buffer to 1 ml and stored at 4°C. Overnight culture of E. coli cloning strain E1869 was used to inoculate 50 ml of LB broth containing 10 mM MgSO₄ and 0.2% maltose. The culture was shaken at 37°C to an OD₆₀₀ of ~1. 100 μl of bacteria was mixed with 10 μl of the packaged phage and allowed to infect for 1 h at 37°C. The infection mixture was washed twice with 1x M9 then plated on MG + 0.3% GS + 1 mM leucine. Approximately 20,000 colonies were obtained, which represented a fosmid library with more than 20x coverage of the genome according to the following equation: N = ln (1-P) / ln (1-f). Where N is the number of colonies needed for reasonable coverage, P the probability of total coverage (99%), f the proportion of the genome contained in a single clone (40,000 kb/ 7.2 Mb). The resulting number of colonies that would give us 99% probability of obtaining a fosmid library that covers the entire genome is ~860. The ~20,000 colonies were pooled and grown in MG + 0.3% GS + 1 mM leucine. The fosmid pool was transferred from E. coli into non-competent Bp K96243 and Bc K56-2 via tri-parental mating with non-antibiotic based helper plasmid, pMKY. The plasmid pMKY is a pRK2013-based helper plasmid that has all antibiotic markers deleted (replaced by the Pseudomonas aeruginosa PAO1 asd gene) and maintained in the E. coli Δasd host via asd complementation. The asd gene encodes for aspartate semialdehyde dehydrogenase, which is essential for bacterial cell wall synthesis. Library selection in Bc K56-2 transformants were selected on MG + 0.5% GS (v/v) while Bp K96243 transformants were selected on MG + 0.3% GS (v/v). Several thousand colonies were obtained from each conjugation.

Identification of competent fosmid clones: Flp recombinase-mediated marker excision and counter-selection

Bp and Bc colonies growing on the glyphosate selection plates were pooled separately and inoculated at a 100-fold dilution into liquid MG + 0.3% GS or MG + 0.5% GS, respectively. The flp gene was amplified from pCD13SK-flp-oriT-asd_Ec [16]. The resultant ~2.6 kb fragment encoding Flp and its regulatory sequence was gel purified. After growth in MG + GS media at 37°C with shaking overnight, 2 ml of bacterial culture were concentrated 100-fold by centrifugation and incubated with 2 μg of flp DNA. The bacterial cell pellet and flp DNA were gently mixed and incubated at room temperature for 30 min. The cell-DNA mixture was then added to 3 ml of MG + GS media and allowed to recover with shaking at 37°C overnight to allow for Flp expression and excision of the chromosomally located counter-selection markers flanked by FRT sites. Bc K56-2 incubated cultures were plated on MG + 0.5% GS + 0.1% cPhe (w/v) + 15% sucrose (w/v). Bp K96243 and flp DNA incubated cultures were plated on MG + 0.3% GS + 0.1% cPhe (w/v) + 15% sucrose (w/v).

Identification of DNA catabolism clone

Bc K56-2 containing the fosmid library were plated on M9 minimal agar medium containing 0.1% (w/v) purified salmon sperm DNA. Salmon sperm DNA was purchased from MPBiomedicals (Cat. #02101501; MW ~6,000,000). The salmon sperm DNA was prepared by sonicating in ten 20 sec bursts with a Kontes KT40 sonicator at maximum power using probe model ASI followed by five phenol/chloroform extractions and ethanol precipitation.

Recovery of fosmids, sequencing and insertion determination

Fosmid DNA was isolated from Bp and Bc colonies growing on cPhe + sucrose by resuspension in 100 μl of water and heating at 100°C for 10 min to lyse all the bacteria. Cell debris was removed by centrifugation at 14,000 rpm for 5 min. Highly competent DH5α cells were prepared as previously described [18] and 40 μl aliquots of bacteria were added to 10 μl of the boil-prepped lysate in a 0.2-cm electroporation cuvette to transform the fosmids into E. coli. The recovery mixture was plated on MG + 0.3% GS + 1 mM thiamine. Colonies visible after 2 days were grown in liquid media, plasmids were isolated and the gat gene was verified by PCR to ensure presence of the fosmid backbone. Positive gat transformants were grown in 150 ml MG + 0.3% GS media for 48 h and plasmids isolated using the QIAGEN Plasmid Midi Kit according to the instructions for low copy plasmids. The oligonucleotides FOSSEQDN2 (5’- AAGTTGGGTAACGCCAGGG -3’) and FOSSEQUP2 (5’- CTGAATAAGTGATAATAAG -3’) were used to determine fosmid backbone-chromosomal DNA junction sequences. Several hundred bases of sequences were obtained for each clone and those sequences were analyzed by BLAST searches for the presence of Bp DNA.

Verification of DNA uptake ability

Four selected fosmids were reintroduced into parental non-competent wild-type Bp and Bc strains by electroporation, selected on GS media, then tested for natural competency using a previously developed natural competency assay [16]. In this assay, gfp-DNA is amplified by PCR and 250 ng of the fragment is incubated for 30 min at room temperature with colonies from a plate (scraped from a plate after 4 days growth, adjusted to an OD₆₀₀ of 1.5, and concentrated by centrifugation at 10,000g). After 45 min recovery in LB broth with shaking, the bacteria are embedded in LB + 0.5% agarose on a coverslip and observed for green fluorescence. Alternatively, select agent strains were fixed in 1% paraformaldehyde (PFA) in 1x phosphate buffered saline (PBS) for 45 min before fluorescent microscopy. Additionally, to correlate gfp-DNA uptake with DNA uptake and DNA use as a carbon source, the fosmid containing strains were grown in the appropriate concentration of liquid GS media overnight for fosmid maintenance. One ml of culture was then washed twice with 1x M9 to remove all carbon sources and the cell pellet resuspended in 100 μl of 1x M9. Suspended cultures were diluted 100-fold into 1x M9 media containing 0.25% (w/v) salmon sperm DNA. Growth was recorded at 72 h post-inoculation.

λ-Red recombination in non-naturally competent select agent Burkholderia containing competency-providing fosmids

The λ-Red fosmid pKaKa2 was first transformed into Bp K96243 and Bm ATCC23344 with selection on MA40 media. Transformants were grown in MA40 and then each of the four competency-providing fosmids were electroporated into the strains carrying pKaKa2 and transformants were selected on MA40 + 0.3% GS. λ-Red recombineering was carried out as previously described [16]. Briefly, the tellurite resistance cassette was amplified from pwFRT-P_CS12-tel [18] with oligos that incorporated 50 bp of DNA homologous to the two ends of the Bm and Bp vacJ gene (the first PCR used O-1327; 5’- CATCTGCGGCATCGGGCGCGGCGGCACAGTGAACGCCGCGCAAGGCGATTAAGTTGGGTA -3’ and O-1329; 5’- GGCTGTAACCGATGTAAGTGTCGGGTCAGTGCAGCCGGATGCTCGTATGTTGTGTGGAAT -3’. Underlined regions are regions of homology to vacJ and the 3’ regions are homologous to the tel cassette. The product was then amplified using O-1328; 5’-CATCTGCGGCATCGGG-3’ and O-1339; 5’-GGCTGTAACCGATGTA-3’ which anneal to the bolded regions indicated above in the O 1327 and O 1328 sequences to create full-length PCR products. λ-Red gene expression induced with 0.2% rhamnose (w/v) and the bacteria incubated with the tellurite selectable marker DNA flanked with 50 bp of homology to vacJ. One μg of DNA was then incubated with the two strains containing each of the four fosmids for a total of seven incubations and plated on LB + tellurite 20 μg/ml to select for recombinants (we did not include allelic-replacement using Bp1 in B. pseudomallei K9243, since Bp1 initially was positively selected in strain K96243). Transformants were then patched on LB + tellurite 20 μg/ml. Several colonies from each clone was verified by PCR for both the kilA-vacJ junction and the telA gene, using primers indicated in Fig 5B.