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Applied and Environmental Microbiology, October 2007, p. 6144-6149, Vol. 73, No. 19
0099-2240/07/$08.00+0     doi:10.1128/AEM.00413-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

Inactivation of an Iron Transporter in Lactococcus lactis Results in Resistance to Tellurite and Oxidative Stress

Mark S. Turner,^* Yu Pei Tan, and Philip M. Giffard

Infectious Diseases Program, Cells and Tissue Domain, Institute for Health and Biomedical Innovation, Queensland University of Technology, Brisbane, Australia

Received 22 February 2007/ Accepted 30 July 2007

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In Lactococcus lactis, the interactions between oxidative defense, metal metabolism, and respiratory metabolism are not fully understood. To provide an insight into these processes, we isolated and characterized mutants of L. lactis resistant to the oxidizing agent tellurite (TeO₃^2–), which generates superoxide radicals intracellularly. A collection of tellurite-resistant mutants was obtained using random transposon mutagenesis of L. lactis. These contained insertions in genes encoding a proton-coupled Mn²⁺/Fe²⁺ transport homolog (mntH), the high-affinity phosphate transport system (pstABCDEF), a putative osmoprotectant uptake system (choQ), and a homolog of the oxidative defense regulator spx (trmA). The tellurite-resistant mutants all had better survival than the wild type following aerated growth. The mntH mutant was found to be impaired in Fe²⁺ uptake, suggesting that MntH is a Fe²⁺ transporter in L. lactis. This mutant is capable of carrying out respiration but does not generate as high a final pH and does not exhibit the long lag phase in the presence of hemin and oxygen that is characteristic of wild-type L. lactis. This study suggests that tellurite-resistant mutants also have increased resistance to oxidative stress and that intracellular Fe²⁺ can heighten tellurite and oxygen toxicity.

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Lactococcus lactis interacts with oxygen in a complex fashion. When grown with aeration in conventional growth media, it produces damaging reactive oxygen species (ROS), such as H₂O₂, OH^·, and O₂^–. It can defend itself against these compounds with superoxide dismutase and peroxidases. However, the peroxidase activity is low, resulting in H₂O₂ accumulation. In the presence of iron, this is converted to the OH^· radical via the Fenton reaction. The OH^· radical is very reactive and damages a wide variety of biomolecules. While L. lactis is not an obligate anaerobe, a clear manifestation of its oxygen sensitivity is the very poor survival of aerated cells in stationary phase (2, 20). This picture is complicated by the ability of L. lactis to carry out respiration when supplied with exogenous hemin (4). Respiring cultures grow to a high optical density, acidify the medium less, and have a greatly extended survival time in stationary phase in comparison with nonrespiring aerated cultures (4). The basis for the survival in stationary phase has been examined by Rezaïki et al. (20), who found that respiring cells scavenge oxygen from the medium and so prevent the formation of ROS.

There has been significant but not extensive research into the molecular details of L. lactis oxidative stress and oxidative defense. Superoxide dismutase- and thioredoxin reductase-deficient mutants have been shown to have defective growth under aerobic conditions (22, 29). In addition, insertional mutagenesis studies aimed at identifying genes involved in thermal resistance and acid resistance revealed that mutants deficient in high-affinity phosphate transport, purine metabolism, and the stringent response are resistant to multiple stressors, including oxidative stress (3, 6, 19). These studies also identified several genes of unknown function that impact on oxidative defense. To date, the direct identification of L. lactis insertion mutants affected in oxidative defense has not been reported.

Potassium tellurite (K₂TeO₃) is used as a selective and differential agent in a number of different bacteriological media for the isolation of food-borne pathogens. In general, gram-positive bacteria are much more tellurite resistant than gram-negative bacteria. The mechanism of tellurite toxicity is not fully understood, although there is now strong evidence that it imposes oxidative stress through the generation of ROS and in particular O₂^– during intracellular reduction to tellurium (18, 26). It is likely that its oxidizing action has some similarities to paraquat, which also generates intracellular O₂^–. The aim of this study was to identify genes involved in the oxidative defense mechanisms of L. lactis. We hypothesized that L. lactis tellurite-resistant insertion mutants would also be resistant to oxidative stress. Twenty tellurite-resistant strains were isolated from a pool of random insertion mutants. The tellurite-resistant mutants were found to be resistant to oxidative stress and contained insertions in genes encoding a metal ion transporter, a phosphate uptake system, a compatible solute uptake system, and a redox regulator homolog. Moreover, it was found that the metal ion transporter mutant is defective in Fe²⁺ uptake and has altered growth properties under respiration-conducive conditions.

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Bacterial strains, chemicals, and enzymes.
L. lactis subsp. cremoris MG1363 was grown using M17 supplemented with 0.5% glucose (GM17) or 1% glucose (2x GM17) (Oxoid, Basingstoke, United Kingdom) and was incubated at 30°C or 37°C as required. L. lactis containing pGh9::ISS1 (13) was grown in the presence of 2 µg/ml erythromycin. Escherichia coli JM109 (Promega, Madison, WI) and E. coli XL1-Blue (Stratagene) were used in cloning experiments and were grown using either Luria-Bertani medium (Oxoid, Basingstoke, United Kingdom) or brain heart infusion medium (Oxoid, Basingstoke, United Kingdom) containing 300 µg/ml erythromycin at 30°C or 37°C as required. Cysteine (Sigma-Aldrich, St. Louis, MO) and potassium tellurite (K₂TeO₃) in a 3.5% solution (Oxoid) or as a powder (Sigma-Aldrich) were added to growth media as required. Restriction enzymes, DNA ligase, and Expand DNA polymerase were obtained from Roche (Indianapolis, IN).

Construction of a transposon library using pGh9::ISS1 and isolation of tellurite-resistant mutants.
A random L. lactis transposon library was prepared essentially as described by Maguin et al. (13). The library (containing 16,000 mutants) was scraped from the surface of agar plates, mixed, and stored at –80°C in 40% glycerol. An aliquot of this library was grown to log phase and spread onto GM17 agar containing 2 µg/ml erythromycin and 0.1 mM or 0.05 mM tellurite. In the middle of the plate was placed a 6-mm-diameter disk to which 10 µl cysteine (1 M) was added. Plates were incubated at 36.5°C for 2 days. Out of 3 x 10⁵ mutants plated, there were 106 colonies on the plate containing 0.1 mM tellurite (resistant mutant frequency was 3.5 x 10^–4 per mutant) and 900 colonies on the plate containing 0.05 mM tellurite (resistant mutant frequency was 3 x 10^–3 per mutant). Twenty tellurite-resistant mutants were purified by streaking onto GM17 agar containing 2 µg/ml erythromycin and 0.1 mM tellurite and incubated at 36.5°C and were the subject of further study.

Characterization of tellurite-resistant mutants.
Chromosomal DNA was obtained from tellurite-resistant mutants by standard methods (9) and the ISS1 flanking sequences were cloned in E. coli as described previously, except that cultures were grown at the permissive temperature (13). Sequencing of the ISS1 flanking regions was performed using primer ISS1-seq1 (5'-CACGATAGCTTAGATTGTAACG-3') (for EcoRI loopouts) or ISS1-seq2 (5'-GAACCGAAGAAATGGAACGCTC-3') (for HindIII loopouts). The ISS1 insertion site for 12 out of 20 mutants was determined by plasmid rescue. Inverse PCR was performed on each of the mutants (following EcoRI digestion and religation) using primers ErmUS (5'-AACGAGCTCATACACCAATCAGTGCAA-3') and ISS1-seq1. The band sizes obtained by inverse PCR for the eight uncharacterized mutants were the same as those for bands obtained from the characterized mntH or pstA insertion mutants. PCR was performed on undigested chromosomal DNA of the eight uncharacterized mutants by use of primers specific for the mntH (MntH-DS-Xho [5'-AGCCTCGAGTGCTTTTCGCGCTCGCTC-3']) or pstA (PstA-check [5'-AATTGGGTCAAGGGCTGATG-3']) genes and ISS1-seq1. These PCR products were sequenced to identify the exact ISS1 insertion site in these mutants. The sequences of the flanking genomic regions were compared to the L. lactis subsp. cremoris MG1363 genome (31) and to other genes in databases by use of BLAST programs (1). To isolate stable ISS1 mutants, the integrated plasmid was excised as described previously (13). Tellurite-resistant mutants were confirmed by growing them to late log phase, diluting the culture 1 in 100 in fresh GM17, and streaking a loopful onto GM17 agar containing 0.4 mM tellurite and 0.5 mM cysteine or GM17 agar containing 0.4 mM tellurite. Wild-type (wt) L. lactis MG1363 was also included, and the plates were incubated overnight at 37°C.

Survival after aerated growth.
Overnight nonaerated cultures of L. lactis MG1363 and the mutants grown at 30°C were diluted 1 in 1,000 in 2x GM17 and incubated at 30°C under aerated conditions. The medium was less than 1/10 of the culture tube volume, and the cultures were shaken at 230 rpm. Dilutions were carried out after 9 and 24 h of incubation, and 10-µl spots were plated onto GM17 agar to determine viable cell numbers.

Iron uptake analysis.
Measurement of Fe²⁺ uptake was performed using the colorimetric ferrozine assay (24), which can measure the bacterially mediated depletion of iron from solutions (11). Cultures of L. lactis MG1363 and the mntH mutant were harvested at late log growth phase, washed once, resuspended in 50 mM NaCl to similar densities (wt optical density at 600 nm [OD₆₀₀] = 5.45; mntH mutant OD₆₀₀ = 5.6), and kept on ice for 30 min. Cells (0.5 ml) were mixed with 0.5 ml NaCl (50 mM) and were warmed by placing in a water bath set at 30°C for 10 min. The assay was started by the addition of 10 µl of 10 mM FeSO₄·6H₂O, which was freshly prepared to minimize oxidation. To measure the effect of Mn²⁺ on iron uptake, 10 µl of 100 mM MnSO₄·H₂O (i.e., at a concentration 10 times higher than that of iron) was added 1 min prior to the addition of iron. Samples (150 µl) were taken from the assay after 30 min, and the cells were removed by centrifugation for 1 min at 18,000 x g. A portion (100 µl) of supernatant was assayed for Fe²⁺ concentration using the ferrozine assay as previously described (30). Control reaction mixtures containing no cells showed that the level of Fe²⁺ remained constant for the duration of the experiment and was not affected by the presence of other metal ions (Mn²⁺, Zn²⁺, or Mg²⁺).

Respiration growth studies.
Overnight nonaerated cultures of L. lactis MG1363 and the mntH mutant grown at 30°C were diluted 1 in 1,000 in 2x GM17 and incubated at 30°C under either aerated or respiration-conducive conditions. Cultures were grown for 20 h with shaking at 180 rpm in Erlenmeyer flasks filled to less than 1/10 flask volume either in the absence (aeration) or in the presence (respiration) of autoclaved hemin (final concentration, 10 µg/ml; Sigma) or filtered hemin precursor protoporphyrin IX (PPIX) (final concentration, 10 µg/ml; Sigma). At this point, the OD₆₀₀ values of the cultures and the pH levels of the spent supernatants were measured.

Hemin-induced toxicity assay.
Overnight nonaerated cultures of L. lactis MG1363 and the mntH mutant grown at 30°C were diluted 1 in 1,000 in 2x GM17 with or without autoclaved hemin (10 µg/ml final) and incubated at 30°C under aerated conditions. Cultures were shaken at 230 rpm in culture tubes filled to less than 1/10 total tube volume, and the OD₆₀₀ was followed during the incubation.

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Isolation and characterization of L. lactis mutants with greater resistance to tellurite.
Random insertional mutagenesis was performed on L. lactis by use of pGh9::ISS1, and tellurite-resistant mutants were selected on plates containing tellurite (0.1 or 0.05 mM) with a filter disk containing cysteine placed in the center (see Materials and Methods). Previous work has shown that cysteine significantly heightens the toxicity of tellurite to Staphylococcus aureus, and this was also found to be the case with L. lactis (reference 27 and unpublished data). Twenty mutants were isolated, and the genes which contained the integrated pGh9::ISS1 plasmids were identified by sequence comparison with genes from the L. lactis subsp. lactis MG1363 genome (31) and other bacteria (Table 1). It was found that 12 mutants had insertions in the same position in a gene encoding a protein similar to the proton-dependent transporter MntH. MntH is a member of the Cß class of the natural resistance-associated macrophage protein (Nramp) family (21), members of which have been shown to mediate the uptake of Mn²⁺ and or Fe²⁺, the latter with much lower affinity (12, 15). Five mutants had independent insertions in the pstA and pstD genes, which encode components of the Pst high-affinity phosphate transporter. One pstA mutant contained another pGh9::ISS1 located elsewhere in the chromosome, which was not identified. Two mutants had the same insertion in a gene encoding the ATPase component of a putative proline/glycine-betaine/carnitine transport system (ChoQ), which most probably functions in osmoprotection. Finally, one mutant had an insertion just upstream of the trmA gene, which was previously identified as being involved in temperature resistance in L. lactis MG1363 (3). One of each class of mutant (mntH, pstD, choQ, and trmA) was selected and stabilized by excision of the transposed plasmid (see Materials and Methods). Each of these stable mutants was confirmed as being more resistant than the wt both to a combination of tellurite and to cysteine or tellurite alone (Fig. 1).

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TABLE 1. Genes affected in the tellurite-resistant mutants and their putative functions

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FIG. 1. Growth of tellurite-resistant mutants but not wt L. lactis MG1363 on tellurite-containing agar. Log-phase-grown cells were diluted (10–2) and streaked onto GM17 agar, GM17 agar containing 0.4 mM tellurite plus 0.5 mM cysteine, or GM17 agar containing 0.4 mM tellurite. Plates were incubated overnight at 37°C. The pstD mutant grew slower on tellurite containing agars and produced pinpoint colonies after 24 h.

Tellurite-resistant mutants have improved survival following aerated growth.
Following fermentative growth under aerated conditions, L. lactis cells have severe protein and DNA damage, high spontaneous mutation frequencies, and poor survival due to oxidative stress (20). We investigated whether the tellurite-resistant mutants had improved oxidative stress resistance by measuring their survival following aerated growth. After 9 h of growth (early stationary phase), cell viability was the same for the mutants as for the wt (Fig. 2). However, 24 h after growth, the mutants showed survivals approximately 1,000-fold (mntH and trmA) and >10-fold (pstD and choQ) greater than that of the wt. This suggests that the mutants are more resistant to the toxic oxidative effects resulting from aerated growth.

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FIG. 2. Survival of wt L. lactis MG1363 and tellurite-resistant mutants following growth under aerated conditions. Overnight nonaerated cultures were diluted 1 in 1,000 in 2x GM17 and incubated at 30°C with shaking. After 9 and 24 h, viable cell numbers were determined by diluting the cultures and spotting 10 µl onto GM17 agar. Plates were incubated overnight at 30°C. This experiment was performed twice, with similar results observed each time.

mntH insertion mutagenesis impairs Fe²⁺ uptake.
It has been shown that free iron is a major contributor to mortality following the aerated growth of L. lactis due to its participation in the Fenton reaction (20). We hypothesized that the mntH mutant is more resistant to tellurite and oxidative stress because it is unable to transport iron efficiently and consequently has lower intracellular iron levels. Measurement of iron uptake by the wt and the mntH mutant was performed using the ferrozine assay to monitor iron depletion from a solution after 30 min. The removal of iron by the mntH mutant was significantly (>2-fold) lower than that by the wt (Fig. 3, left). This confirms that MntH is a major iron transporter in L. lactis. Residual iron transport activity in the mntH mutant suggests that L. lactis also contains other iron transporters. As manganese has been reported to be the major metal ion transported by MntH proteins in gram-negative bacteria (12, 15), we tested the effect of manganese addition on iron uptake by wt and mntH mutant cells. Manganese actually increased iron uptake by both strains (Fig. 3). Other metal ions, Zn²⁺ or Mg²⁺, had little or no effect (iron uptake was not affected by Zn²⁺ and was slightly inhibited by Mg²⁺; data not shown), suggesting that this effect is not a general metal ion phenomenon. The addition of a lower concentration of Mn²⁺ (the same concentration as Fe²⁺) also stimulated Fe²⁺ uptake (data not shown). This suggests that manganese is not a competitive inhibitor of iron uptake but instead stimulates iron transport at least partially independently of MntH.

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FIG. 3. Uptake of iron by L. lactis MG1363 (wt) and the mntH mutant either in the absence (left) or in the presence (right) of manganese. The total amount of Fe2+ added to the cells was 100 nmol (final concentration, 99 µM). Mn2+ was added at a 10-fold-higher concentration (990 µM) shortly before the addition of Fe2+. Fe2+ remaining in the supernatant was measured after 30 min. Triplicate iron uptake assays were performed.

The mntH mutant affects respiration and is more resistant to hemin-induced oxidative stress.
L. lactis undergoes respiration metabolism in the presence of oxygen and exogenous hemin or the hemin precursor PPIX (4). Since iron in the form of hemin is required for functional cytochrome activity and respiration, we investigated whether MntH-mediated iron transport affects respiration in L. lactis. Growth characteristics of the wt and the mntH mutant under static, aerated, and respiration (aerated plus hemin or PPIX) growth conditions were examined. No significant differences in final biomass and pH between the wt and the mntH mutant under static and aerated conditions were observed (Table 2). Under respiration conditions with exogenous hemin or PPIX, the final biomasses were similar between the two strains, but the pH for the mntH mutant was consistently lower than that for the wt (Table 2). This suggests that MntH-mediated iron transport has an effect upon respiration in L. lactis.

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TABLE 2. L. lactis MG1363 (wt) and mntH mutant growth yields and pH values under static, aerated, and respiration-conducive conditions

It has been reported that the addition of hemin to stationary-phase-exiting cultures of L. lactis results in an increase in the lag phase due to oxidative stress caused by precocious hemin uptake (7). It is most probable that the toxic effect of hemin is due to the iron component. It was hypothesized that the mntH mutant contains lower intracellular iron levels and would be more resistant to the toxic effects of hemin. Overnight cultures of the wt and the mntH mutant were diluted into growth media with or without added hemin and incubated with aeration. While the addition of hemin resulted in a significant lag phase for the wt, it had a negligible effect on the mntH mutant (Fig. 4). This suggests that iron in hemin in combination with iron transported by MntH causes significant oxidative stress. This result may also explain the lower final pH observed for the mntH mutant culture when grown under respiration conditions.

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FIG. 4. Effect of hemin on the growth of wt L. lactis MG1363 and the mntH mutant under aerobic conditions. Overnight nonaerated cultures were diluted 1 in 1,000 in 2x GM17 (broken lines) or 2x GM17 containing hemin (solid lines) and incubated at 30°C with shaking. The optical densities of the wt (squares) and the mntH mutant (triangles) were monitored for 9 h. This experiment was performed three times, with similar results observed each time.

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In this study, we set out to use tellurite resistance as a means of identifying L. lactis genes involved in redox functions and oxidative stress. It has previously been reported (2, 20) that a key manifestation of oxidative stress is L. lactis is death during stationary phase in nonrespiring aerated cultures. All tellurite-resistant insertion mutants analyzed displayed increased survival under these conditions. This demonstrates that tellurite resistance is indeed a valuable selectable phenotype for revealing genes whose products impose oxidative stress. This is consistent with the well-accepted model that tellurite toxicity is due to the production of ROS (18, 25, 26).

Of the genes identified, mntH is arguably of the most interest. MntH belongs to the very widespread Nramp family of high-affinity proton-linked divalent cation transporters. This family is found in virtually all cellular life. In bacteria, many genomes contain several genes that encode diverged Nramp members. Fully characterized Nramp examples from bacteria have been found to be most active in transporting Mn²⁺ and Fe²⁺, the latter with much lower affinity (12, 15). This has resulted in a convention of naming Nramp members found in bacteria "MntH" (H⁺-dependent manganese transporter). The nramp gene family has been subjected to extensive duplication and divergence, and there is also evidence for horizontal gene transfer (21). The bacterial mntH genes have been divided into three major classes (A, B, and C), and class C has been divided into C, Cß, and C. The L. lactis MG1363 genome contains two putative mntH genes (31). One of these encodes a class B MntH (MntA; llmg_2171) that is most closely related to MntH sequences from Thermoanaerobacter and Clostridium, so the gene is likely to have entered the L. lactis genome by horizontal transfer. The other mntH gene is the one identified in this study. It encodes a class Cß MntH. Its closest relatives are all found in lactic acid bacteria, in particular, Enterococcus, Oenococcus, and Lactobacillus brevis. Other class Cß sequences are found in a wide variety of other lactic acid bacteria. While the complexity of this family makes it difficult to trace horizontal gene transfer events and reliably determine which mntH sequences are orthologs and which are paralogs, it is clear that the MntH class Cß transporters are widely distributed in the lactic acid bacteria and have been there for a long time.

The class Cß MntH transporters encoded by lactic acid bacteria have not been studied extensively. Hayashi et al. (10) found that the L. brevis mntH gene is a marker for hop resistance in beer-brewing fermentations, and it was suggested that Mn²⁺ and Mg²⁺ uptake is used to defend against the ionophores found in hop bitter compounds. Groot et al. (8) hypothesized that the MntH proteins potentially encoded by the Lactobacillus plantarum genome contribute to the accumulation of high intracellular manganese ion compounds. However, inactivating the genes alone or in combination had no measurable effect, so the roles of these genes in L. plantarum remain obscure. In the case of L. lactis, an attempt has been made to express the class Cß MntH in E. coli, but it was apparently not functional (21). We have obtained strong evidence that the L. lactis class Cß MntH is responsible for a large proportion of iron uptake under the experimental conditions used. The tellurite resistance of the mntH mutant is consistent with the well-known ability of iron to generate ROS, in particular the hydroxyl radical, which is especially damaging to biomolecules. This has been shown to be the case for L. lactis by Rezaïki et al. (20), who demonstrated a strong correlation between free iron availability in the growth medium and oxidative damage in aerated stationary-phase cultures. The metal ion specificity of MntH in L. lactis is not yet known. It was found here that manganese, but not other metal ions, stimulated an increase in iron uptake in L. lactis in an at least partially MntH-independent manner. This suggests that manganese does not competitively inhibit iron transport by MntH, unlike what has been reported for other MntH proteins, but does not rule out Mn²⁺ as a substrate for MntH (12, 15).

It was of interest to determine the effect of mntH inactivation on respiratory metabolism. Our hypothesis was that the lesion would have little effect in cultures with exogenous hemin but a significant effect on cultures with exogenous PPIX (hemin precursor). The rationale was that iron-deficient cells would be defective in the ability to synthesize hemin from PPIX. This, however, proved not be the case. The mntH mutant is clearly capable of respiratory metabolism in the presence of either hemin or PPIX, although in both instances, a key marker for respiratory metabolism was less marked in the mutant than in the parent. Specifically, the stationary-phase pH was lower. It may be that the defective iron uptake is reducing the amount of cytochrome in the PPIX-supplemented culture, with observed respiratory metabolism accounted for by mntH-independent iron uptake. However, why there is a similar reduction of respiratory activity in the hemin-supplemented culture remains obscure. A partial answer may be inferred from our observation that hemin-induced aerated culture lag phase is eliminated in the mntH mutant. This suggests that the amount of hemin entering the cell is less in the mntH mutant. However, it is also possible that oxidative stress is additive with respect to cytoplasmic free iron and hemin and that the mntH mutant cells were at a lower oxidative stress level than the wt before the hemin was added and so were hemin resistant. This remains to be resolved.

It was concluded that the L. lactis class Cß MntH transporter is required for maximal iron uptake and that its inactivation depletes the cells of iron sufficiently to protect against oxidative stress but not sufficiently to prevent respiratory metabolism taking place in the presence of exogenous PPIX. This may be of significance to the dairy industry, as inactivation of mntH results in cells that in conventional growth media can gain the great majority of benefits of respiration with respect to biomass production but have additional resistance to oxidative stress imposed by (i) the presence of exogenous hemin in the aerated lag phase or (ii) aeration during growth in the absence of hemin.

Another gene of interest identified in the course of this study is trmA. This has previously been identified in L. lactis as a site of insertion mutations that relieve temperature sensitivity in a recA or clpP background and also has been shown to increase temperature and puromycin resistance when disrupted in a wt background (3, 6). There are eight genes in the trmA family encoded by the L. lactis MG1363 genome (31), and they have homology to the oxidative stress regulator Spx from Bacillus subtilis (16). Recent work has revealed novel roles of L. lactis TrmA homologs SpxB and TrmA in regulating peptidoglycan acetylation and lysozyme resistance (28).

The bases for the tellurite resistance of the choQ and pst mutants remain obscure. The ChoQ homolog from Listeria monocytogenes (OpuCA) is regulated by the stress-induced sigma-B system and plays a role in osmoregulation and virulence (5, 23). Insertions in genes encoding the high-affinity phosphate uptake system (PstABCDEF) have been identified in a number of searches for stress-resistant insertion mutants (3, 19). It may be that phosphate depletion induces a number of stress responses that cause cross-resistance to a range of stressors, including oxidative stress, and this has already been shown when examining H₂O₂ resistance (3, 19). It is feasible that the choQ mutant has a similar basis.

In conclusion, selection for tellurite resistance is an effective means of obtaining insertions in genes involved in oxidative stress or defense. This study has lead to the identification of a novel iron transporter and to the demonstration that several previously discovered genes contribute to oxidative stress or impede oxidative defense.

 
We thank Raquel Lo, Terry Walsh, Willa Huston, and the Bug Masters for helpful discussions on various aspects of this work.

This research was supported by grants from ARC (grant no. DP0665546) and NHMRC (grant no. 290526).

 
* Corresponding author. Present address: School of Land, Crop and Food Sciences, University of Queensland, Brisbane, QLD 4072, Australia. Phone: (61-7) 3365-1171. Fax: (61-7) 3365-1177. E-mail: m.turner2{at}uq.edu.au

Published ahead of print on 3 August 2007.

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Applied and Environmental Microbiology, October 2007, p. 6144-6149, Vol. 73, No. 19
0099-2240/07/$08.00+0     doi:10.1128/AEM.00413-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

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