- Research article
- Open Access
Escherichia coli genes that reduce the lethal effects of stress
© Han et al; licensee BioMed Central Ltd. 2010
- Received: 3 July 2009
- Accepted: 4 February 2010
- Published: 4 February 2010
The continuing emergence of antimicrobial resistance requires the development of new compounds and/or enhancers of existing compounds. Genes that protect against the lethal effects of antibiotic stress are potential targets of enhancers. To distinguish such genes from those involved in drug uptake and efflux, a new susceptibility screen is required.
Transposon (Tn5)-mediated mutagenesis was used to create a library of Escherichia coli mutants that was screened for hypersensitivity to the lethal action of quinolones and counter-screened to have wild-type bacteriostatic susceptibility. Mutants with this novel "hyperlethal" phenotype were found. The phenotype was transferable to other E. coli strains by P1-mediated transduction, and for a subset of the mutants the phenotype was complemented by the corresponding wild-type gene cloned into a plasmid. Thus, the inactivation of these genes was responsible for hyperlethality. Nucleotide sequence analysis identified 14 genes, mostly of unknown function, as potential factors protecting from lethal effects of stress. The 14 mutants were killed more readily than wild-type cells by mitomycin C and hydrogen peroxide; nine were also more readily killed by UV irradiation, and several exhibited increased susceptibility to killing by sodium dodecyl sulfate. No mutant was more readily killed by high temperature.
A new screening strategy identified a diverse set of E. coli genes involved in the response to lethal antimicrobial and environmental stress, with some genes being involved in the response to multiple stressors. The gene set, which differed from sets previously identified with bacteriostatic assays, provides an entry point for obtaining small-molecule enhancers that will affect multiple antimicrobial agents.
- Sodium Dodecyl Sulfate
- Nalidixic Acid
- Lethal Effect
- Yersinia Enterocolitica
The emergence of antimicrobial resistance is severely limiting treatment options for many important infectious diseases [1, 2]. Traditionally the problem of antimicrobial resistance has been approached by developing new compounds having increased potency. Unfortunately, development of new compounds is not keeping pace with the emergence of antibiotic-resistant pathogens. Consequently, new strategies are needed to preserve existing agents. One approach is to seek compounds that will enhance the activity of distinct antimicrobial classes by blocking resistance mechanisms. For example, β-lactamase inhibitors extended the utility of β-lactams when delivered as combinations such as Augmentin (amoxicillin-clavulanic acid) , and inhibitors of efflux pumps produced synergistic inhibition of growth against tetracycline-resistant Escherichia coli when used in combination with doxycycline . The conventional strategy has been to identify genes whose inactivation increases the ability of compounds to block bacterial growth (decreases in minimal inhibitory concentration, MIC) . Since some compounds kill bacteria by processes that are distinct from bacteriostatic action [6, 7] and since deficiencies in repair of lethal damage may not affect bacterial growth, the possibility exists that genes involved in bacterial survival are distinct from those that protect from growth inhibition. Finding genes whose products protect from the lethal effects of stress requires screening procedures that differ from those used for bacteriostatic effects.
In the present work, we used the prototype quinolone, nalidixic acid, as a probe for screening genes whose products protect E. coli from lethal effects of stress. Nalidixic acid was chosen as the initial screening agent because bacteriostatic and lethal action are distinct events that are sensitive to different drug concentrations (for review see ). Mutants of E. coli, obtained by Tn5-mediated insertional mutagenesis, were screened for those that had the same bacteriostatic susceptibility to nalidixic acid as the wild-type strain while exhibiting greater sensitivity to the lethal action of the drug. We call this new phenotype hyperlethality. With this phenotype we could eliminate from consideration mutants with altered drug uptake, efflux, and target interactions, since these properties affect bacteriostatic activity. The decreased survival of the mutants was expected in some cases to arise from disruption of genes involved in protecting from lethal stress. The hyperlethal mutants were then examined by measuring the lethal action of several other antimicrobial and environmental stresses. This work defined a novel bactericidal phenotype and identified a diverse set of poorly characterized bacterial stress-response genes as a new source of potential targets for antimicrobial enhancement.
Bacterial strains and growth conditions
Bacterial strains were derivatives of E. coli K-12. Strain AB1157 (isolate KD1045)  was used to construct the Tn5-insertion library. Strain DM4100  was used to confirm the hyperlethal phenotype following P1-mediated transduction, which was carried out according to a standard procedure . In this method P1 phage lysates were prepared using the insertion mutants as donors, and the lysates were then used to infect strain DM4100 at a multiplicity of infection of 0.2. Transductants were recovered by growth on LB plates containing 25 μg/ml of kanamycin and 0.01 M sodium citrate. Kanamycin-resistant transductants were tested for the hyperlethal phenotype with nalidixic acid. Bacterial cells were grown at 37°C either in LB broth or on LB agar plates .
All chemicals were from Sigma-Aldrich Corp. (St Louis, MO, USA). Stock solutions of nalidixic acid were prepared by dissolving in 0.1 N NaOH to yield a final concentration of 10 mg/ml. Other antibiotics were dissolved in distilled water except for tetracycline and mitomycin C, which were dissolved in 50% and 70% ethanol, respectively. Mitomycin C was freshly prepared before use; other antimicrobials were stored as concentrated stock solutions at -80°C.
Library construction and screening
Bacteriophage lambda Tn5-tac was prepared from E. coli BD1527  according to a standard procedure , and Tn5 hopping was carried out with strain AB1157 as follows: recipient cells were grown to mid-log phase (OD600 = 0.3 ~0.5), recovered by centrifugation (6,000 × g, 5 min), and resuspended in ice-cold LB liquid medium containing 0.01 M magnesium sulfate. Cells were then infected with lambda Tn5-tac at a multiplicity of infection of about 1 and incubated for 15 min at 37°C. After incubation, fresh LB medium was added, and the cells were incubated for 2 hr at 37°C for expression of kanamycin resistance. Cells were then plated on LB-agar plates containing 25 μg/ml of kanamycin. After incubation overnight at 37°C, kanamycin-resistant colonies were tested individually for nalidixic acid susceptibility (MIC) and lethality as described below. Mutants that were more readily killed by treatment with nalidixic acid at 20 μg/ml or 50 μg/ml for 2 hr but had MICs close to wild-type levels were considered to have a hyperlethal phenotype; they were selected for further analysis.
Determination of antimicrobial susceptibility and lethality
Antimicrobial susceptibiltiy (MIC99) was defined as the minimal concentration of antimicrobial agents that inhibited growth of 99% of the input cells. MIC99 was measured by applying 10 μl of serial dilutions of mid-log phase cultures (OD600 = 0.3 ~0.5) in triplicate to LB agar plates containing various concentrations of antimicrobials. Colonies were counted after overnight incubation at 37°C. The fraction of colonies recovered (relative to the CFU per ml on drug-free plates) was plotted against drug concentration, and MIC99 was determined by interpolation.
To measure lethality, cells were grown in LB liquid medium to mid-log phase (OD600 = 0.3 ~0.5) at 37°C with shaking. Cells were split into 1-ml aliquots in test tubes, and various concentrations of antimicrobial agents (2 × MIC99 to 30 × MIC99) were added. After incubation for 2 hr with shaking, cells were diluted in LB liquid medium, which eliminated drug carryover, and 10 μl of aliquots from the dilutions were spotted in triplicate on drug-free LB agar plates. Colonies were counted after overnight incubation at 37°C. Lethality was expressed as percent of control relative to the CFU per ml at the time of drug addition. The dose that reduced CFU by 90% was taken as LD90.
For screening the mutant library, kanamycin-resistant colonies were manually replica-plated with toothpicks to a series of plates containing various concentrations of nalidixic acid and incubated overnight. Colonies exhibiting the same bacteriostatic susceptibility as the parental strain were saved for lethality measurement. Survival for each colony was measured in liquid medium after a 2-hr incubation in nalidixic acid at 20 μg/ml and 50 μg/ml as described in the previous paragraph. Colonies that exhibited decreased survival relative to the parental strain were then retested for MIC and survival as described in the previous paragraphs. Strains confirmed to have a hyperlethal phenotype were further characterized as described below.
Identification of gene insertion sites
Asymmetric PCR, modified from that described previously [14–16], was used to amplify E. coli genomic sequences near the ends of Tn5 that inserted into the genome. One primer, either Tn5R10 (5' GGG ATC CCC TAC TTG TGT AT 3') or Tn5F4568 (5' AGA ATT CCT CCC GAG ATC TG 3') was complementary to the sequence at an end of Tn5; the other primer contained a 6-nucleotide random sequence followed by TGGC (Ran5-29: 5' GTT CTA CAC GAG TCA CTG CAG NNN NNN TGG C 3'). The randomized primer binds any GCCA in the genome. However, since PCR preferentially amplifies short fragments, combination of the two primers should amplify the sequences between one Tn5 end and the first few GCCA sequence elements. For the first 5 cycles of PCR, the annealing temperature was high (58°C); consequently, the primer that was complementary to the sequence at the Tn5 end preferentially bound to the substrate, which caused one strand of the substrate to be asymmetrically amplified. This high-temperature annealing was followed by a cycle using low annealing temperature (30°C) to allow the randomized primer to bind the strand that had already been amplified. Then one high-temperature (58°C) and one moderate-temperature (44°C) cycle were alternated 12 times to amplify the sequence between the two primers. For all amplification cycles, the annealing time was 1 min, while the denaturation (94°C) and extension (72°C) times were 15 sec and 2 min, respectively. The nucleotide sequence was then determined for PCR products that exhibited single bands following agarose gel electrophoresis. In some cases, the products of the first PCR were further amplified with repeated alternation of one high annealing temperature (58°C) cycle and one moderate annealing temperature (44°C) cycle in which the randomized primer was replaced with primer Fix5-29-2 (5' CTA CAC GAG TCA CTG CAG 3'), a primer sequence that was identical to 18 of the 21 5' terminal nucleotides of the randomized primer. DNA sequences obtained were used as query probes to search the E. coli K-12 genome sequence database for identifying transposon insertion sites.
Lethality of environmental stresses
The susceptibility of bacterial cells to UV irradiation was tested by applying serial dilutions of mid-log phase (OD600 = 0.3 ~0.5) cultures to agar plates that were irradiated with an Ultraviolet Crosslinker CL-1000 (UVP) at a dose of 2000 μJ/cm2 in a dark room. The plates were then covered with aluminium foil and incubated overnight at 37°C. For other stressors, mid-log phase cells were treated with 2 mM H2O2 (cells were resuspended in 0.9% saline before treatment), 10% sodium dodecyl sulfate (SDS), or high temperature (52°C) for 15 min. Serial dilutions were then prepared, and 10-μl of aliquots from the dilutions were spotted in triplicate on plates and incubated at 37°C overnight. The sensitivity of cells to the lethal effects of these stressors was expressed as percent survival of treated cells relative to that of untreated cells determined at the time of treatment (LD90 could not be used because many of the mutant-stressor combinations did not reduce survival sufficiently).
Complementation of hyperlethality by cloned genes
All DNA manipulations were carried out according to procedures described previously . The emrK and ycjU genes with their promoter regions were amplified by PCR using chromosomal DNA isolated from DM4100 as templates and cloned into pBR322. The primers used were 5'-TAG GAA TTC ATC TCC CTT CTC CCT GTA GT-3' and 5'-TAA GTC GAC ATT CTT TGT GCC AAC CTG-3' for emrK, and 5'-TGC GAA TTC CTG CTG ACC CAA AGT TAT-3' and 5'-TAG CTG CAG TCA CCT CTT TGG CGA TT-3' for ycjU. Plasmids containing wild-type ycjW, yrbB, and ybcM were from the ASKA library . The plasmids were placed in the corresponding mutant strains, as well as in the wild-type strain DM4100, by electroporation. The strains harboring the plasmids were then tested for nalidixic acid lethality. For ycjW, yrbB, and ybcM, the expression was induced by adding 1 mM of IPTG 2 hr before nalidixic acid treatment.
Screening for mutants exhibiting hyperlethality to nalidixic acid
Properties of genes that reduce the lethal effects of stress.
MIC99 of Nal (μg/ml)a
Site of insertion
Functional annotation of disrupted genes
4.5 ± 0.3
3.1 ± 0.1
4.6 ± 0.3
4.2 ± 0.6
Predicted lyase containing HEAT-repeat
4.6 ± 0.4
RfbX lipopolysaccharide PST transporter
4.8 ± 0.2
4.7 ± 0.1
Permease (major facilitator superfamily (MFS) of transporters)
3.7 ± 0.3
3.3 ± 0.2
3.0 ± 0.2
Predicted NTP-binding protein
5.3 ± 0.3
ARAC-type regulatory protein
3.4 ± 0.1
Putative LACI-type transcriptional regulator
4.1 ± 0.5
4.0 ± 0.6
Putative membrane fusion protein
4.4 ± 0.6
Putative multidrug MFS transporter
To identify the genes inactivated by Tn5 insertion, asymmetric PCR was used to amplify the sequences near the ends of Tn5 using a protocol modified from previously published reports [14–16]. Nucleotide sequence determination of the PCR products then identified 14 different genes (Table 1). Only one of these genes (ycjU, also called pgmB) appeared in the list of genes identified previously as being involved in affecting the bacteriostatic action of quinolones . The ycjU mutation caused cells to be only slightly more susceptible to nalidixic acid than the wild-type strain in our bacteriostatic measurement (Table 1, MIC99 4.1 μg/ml vs. 4.5 μg/ml). Thus, ycjU may not belong in the set previously identified as having a low MIC . The two-fold drop in LD90, from 59 μg/ml to 31 μg/ml (Fig. 1), qualified it as a gene with a hyperlethal phenotype.
Mutant susceptibility to other antimicrobial agents and environmental stressors
To determine whether the hyperlethal phenotype was restricted to quinolones, we examined the response of the mutants to a variety of other stresses. When tetracycline was tested, we found that, except for two strains TL24 (ykfM::Tn5) and TL26 (ybcM::Tn5), the mutants were more readily killed (LD90 was about half the wild-type value, Fig. 1). Increased lethality was not observed for the β-lactam ampicillin (Fig. 1). Thus, increased killing of the mutants by antimicrobial agents was not restricted to quinolones, but it was also not universal.
The effect of hydrogen peroxide was also examined, since it has recently been implicated in the lethal action of multiple antibiotics [6, 7]. After treatment with 2 mM H2O2 for 15 min, all mutants showed decreased survival compared to wild-type strain DM4100 (for many mutants survival was 20 to 30% that of the wild-type strain, Fig. 2). We also examined the effects of two other environmental stresses, exposure to high temperature and to the ionic detergent sodium dodecyl sulfate (SDS). When the set of mutants was exposed to high temperature (52°C), no substantial difference among the mutants was observed for heat-induced death (Fig. 2). With 10% SDS, the effect of the mutations on survival varied. Some mutants (yadC, ybdA, yfbQ, ykfM, yrbB, ybcM, and emrK) were less susceptible to killing than wild-type E. coli, while ycdO, yibA, and rfbC mutants were more readily killed (Fig. 2).
In summary, 14 mutant genes were associated with hyperlethality to nalidixic acid and were more readily killed by mitomycin C and peroxide; 9 were more readily killed by UV irradiation. Only 3 of the mutants were more readily killed by SDS, none by high temperature. Below we consider what has been reported previously about the diverse set of genes identified by our screening procedure. None of that information leads to an expectation of hyperlethality to nalidixic acid.
Putative function of genes exhibiting hyperlethality to nalidixic acid
Eight of the mutant genes (yadC, rfbX, rfbC, ycdO, yrbB, ybdA, emrK, and emrY) were annotated in Genbank as outer membrane proteins or proteins whose function is related to the outer membrane. The MIC99s of these mutants for nalidixic acid were in the same range as that of the wild-type strain; consequently, hyperlethality caused by these mutations was unlikely to be due to increased accumulation of drug. Since the genes were involved in protecting from the effects of nalidixic acid, mitomycin C, and hydrogen peroxide, it is likely that protection from UV irradiation also occurred at the level of downstream effects of irradiation rather than through screening cells from UV light.
The yadC mutant, which was among the more sensitive to DNA damaging agents, was considerably less sensitive than the wild-type strain to SDS. YadC is a fimbrial-like protein whose amino acid sequence suggests that it may contain β-barrel structure(s) . In E. coli, pili are adherence factors that could, in principle, protect some cells in a population from antimicrobial treatment. However, we detected no difference with respect to cellular aggregation when the yadC mutant and the wild-type strain, growing exponentially, were examined by light microscopy (not shown). Thus, the hyperlethal phenotype of the mutant was not likely to be due to lack of cellular self-association. yadC is induced immediately after exposure to the biocide polyhexamethylene biguanide , which is consistent with its involvement in a cellular response to stress.
The two rfb mutants were strikingly different in their response to UV: the rfbX mutant showed little effect, while the rfbC mutant was one of the most susceptible (Fig. 2). RfbX, also known as WzxB, is a member of the polysaccharide transporter (PST) family , and hydropathy analysis suggests that RfbX has 12 transmembrane segments . rfbC encodes dTDP-4-dehydrorhamnose 3,5-epimerase . Although the rfb genes are thought to be involved in O-antigen biosynthesis in enteric bacteria, such as Salmonella, Shigella, Klebsiella, and some serovars of E. coli , that feature may be irrelevant to the current work, since E. coli K-12 does not normally express a functional O-antigen due to defects in the rfb gene cluster [25, 26]. The fact that rfbX is induced when treated with polyhexamethylene biguanide  suggests that it may be involved in a cellular stress response.
The ycdO mutant was the most readily killed by UV irradiation (Fig. 2). YcdO is a monomeric, membrane-associated protein that contains a type I signal peptide and is transported to the periplasm with high efficiency . Since YcdO is induced at low pH due to phosphorylation of the CpxR component of the CpxAR two-component response regulator [28–30], it may be involved in bacterial envelope stress responses mediated by the CpxAR pathway.
YrbB(MlaB) is predicted to be a nucleotide-binding protein that contains a STAS domain . YrbB is a component of an ABC transport system that maintains lipid asymmetry in the Gram-negative outer membrane by preventing surface exposure of phospholipids . Although the YrbB mutant is more sensitive than the wild-type strain to the presence of EDTA-SDS, it does not show hypersusceptibility to erythromycin, rifampicin, bacitracin, or novobiocin . These data indicate that the yrbB mutation does not change the permeablility to most compounds, which is consistent with our finding that the yrbB mutation did not change the bacteriostatic effects of nalidixic acid.
ybdA, emrK, and emrY are postulated to encode efflux pumps, although MIC determinations with nalidixic acid showed no evidence that the mutations affected efflux (Table 1). The YbdA protein is a member of the major facilitator superfamily (MFS) of transporters , while EmrK and EmrY show sequence similarity to members of the EmrAB-TolC drug efflux system. The two emr mutants were exceptionally sensitive to mitomycin C (Fig. 1), UV irradiation, and H2O2 (Fig. 2). The ybdA and emrK mutants were among the least susceptible to the lethal effects of SDS (Fig. 2), as expected of efflux mutants. Perhaps the ErmK, ErmY, and YbdA proteins normally pump out toxic metabolites induced by DNA damage.
Two genes,ybcM and ycjW, are predicted to be involved in cell regulation. YbcM is a putative DNA-binding transcriptional regulator that is induced by the biocide polyhexamethylene biguanide ; in Yersinia enterocolitica a homolog of ybcM is induced by low temperature . These properties are consistent with YbcM being involved in bacterial stress responses. YcjW is a putative LacI-type transcriptional regulator. Although the biological role of YcjW is unknown, ycjW transcripts accumulate in a strain harboring wild-type relA but not in a relA mutant after treatment with 4-azaleucine, an inhibitor that interferes with translation . These data suggest that YcjW may be involved in the bacterial stringent response.
Three other genes, ycjU, yibA, and yfbQ, encode putative cytosolic proteins of unknown function. The ycjU mutant is among the most sensitive to UV irradiation (Fig. 2). YcjU has been annotated in sequence data bases as a putative β-phosphoglucomutase that belongs to the superfamily of haloacid dehalogenase (HAD)-like hydrolases. In vitro, YcjU hydrolyzes small phosphodonors , which suggest that the protein is likely to have other physiological roles. The yibA mutant was among the most sensitive to UV irradiation and H2O2 (Fig. 2). YibA is a predicted lyase containing a HEAT-repeat, which forms a rod-like helical structure in proteins. Transcription profiling experiments suggested that yibA may belong to the σ32 regulon , whose genes are expressed in E. coli in response to heat shock. Thus, the role of YibA in antimicrobial susceptibility may be exerted through alternative sigma factor-regulated stress responses. However, the yibA mutant was not particularly sensitive to high temperature. A third mutant, in yfbQ, was the most sensitive to mitomycin C. The only information available refers to the gene product as a potential aminotransferase.
Reactive oxygen species-mediated response to lethal antimicrobials
Although no clear metabolic connection exists among the genes we identified, some guidance can be gained from the recent proposal that lethal antimicrobials share a common cell death pathway involving a reactive oxygen cascade [6, 7]. The lethal activity of a variety of antimicrobials, including the fluoroquinolone norfloxacin, is accompanied by an increase in hydroxyl radical, and lethal activity is greatly reduced by treating E. coli cells with agents that block the accumulation of hydroxyl radical . The idea emerged that lethal antimicrobials act in part by generating a signal that causes an accumulation of superoxide, which reacts with iron-sulfur clusters to release peroxide and iron. Peroxide and iron then form highly toxic hydroxyl radicals through the Fenton reaction. Superoxide can also be converted to peroxide by superoxide dismutase and by spontaneous dismutation. The resulting increase in peroxide would contribute to the formation of hydroxyl radical. In support of this idea, we found that deletion of both superoxide dismutase genes reduced the lethality of norfloxacin . As expected, a deficiency of catalase, which converts peroxide to water, led to an increase in the lethality of norfloxacin . Mutations in genes that normally protect from the accumulation of reactive oxygen species would be recovered by our screen for hyperlethality to nalidixic acid. Such mutants are expected to also be more readily killed by other DNA damaging agents, such as mitomycin C, peroxide, and UV irradiation, as seen for 9 of the 14 of the genes we identified.
Complementation of hyperlethality by cloned genes
The present work described a novel screening process for identifying genes involved in protecting E. coli from quinolone-mediated death due to events occurring after formation of quinolone-gyrase-DNA complexes. Using this screen we identified 14 poorly characterized genes. Scattered evidence suggests that many of these genes are linked to protective stress responses, which is supported by our finding that mutations in these putative protective genes resulted in decreased survival following treatment with several stressors. The diverse set of genes described may serve as potential targets for future screening of small-molecule antimicrobial potentiators.
This work was supported by National Natural Science Foundation of China (Grant No. 30860012) and Natural Science Foundation of Yunnan Province of China (Grant No. 2005C0007R) to T.L, NIH grants AI35257 and AI 073491 to K.D, and NIH grant AI068014 to XZ.
- Levy SB: Antibiotic resistance-the problem intensifies. Adv Drug Deliv Rev. 2005, 57 (10): 1446-1450. 10.1016/j.addr.2005.04.001.View ArticlePubMedGoogle Scholar
- Levy SB, Marshall B: Antibacterial resistance worldwide: causes, challenges and responses. Nat Med. 2004, 10 (12 Suppl): S122-129. 10.1038/nm1145.View ArticlePubMedGoogle Scholar
- Buynak JD: Understanding the longevity of the beta-lactam antibiotics and of antibiotic/beta-lactamase inhibitor combinations. Biochem Pharmacol. 2006, 71 (7): 930-940. 10.1016/j.bcp.2005.11.012.View ArticlePubMedGoogle Scholar
- Nelson ML, Levy SB: Reversal of tetracycline resistance mediated by different bacterial tetracycline resistance determinants by an inhibitor of the Tet(B) antiport protein. Antimicrobial agents and chemotherapy. 1999, 43 (7): 1719-1724.PubMed CentralPubMedGoogle Scholar
- Tamae C, Liu A, Kim K, Sitz D, Hong J, Becket E, Bui A, Solaimani P, Tran KP, Yang H: Determination of antibiotic hypersensitivity among 4,000 single-gene-knockout mutants of Escherichia coli. Journal of bacteriology. 2008, 190 (17): 5981-5988. 10.1128/JB.01982-07.PubMed CentralView ArticlePubMedGoogle Scholar
- Kohanski MA, Dwyer DJ, Hayete B, Lawrence CA, Collins JJ: A common mechanism of cellular death induced by bactericidal antibiotics. Cell. 2007, 130 (5): 797-810. 10.1016/j.cell.2007.06.049.View ArticlePubMedGoogle Scholar
- Dwyer DJ, Kohanski MA, Hayete B, Collins JJ: Gyrase inhibitors induce an oxidative damage cellular death pathway in Escherichia coli. Mol Syst Biol. 2007, 3: 91-10.1038/msb4100135.PubMed CentralView ArticlePubMedGoogle Scholar
- Drlica K, Malik M, Kerns RJ, Zhao X: Quinolone-mediated bacterial death. Antimicrobial agents and chemotherapy. 2008, 52 (2): 385-392. 10.1128/AAC.01617-06.PubMed CentralView ArticlePubMedGoogle Scholar
- Bachmann BJ: Pedigrees of some mutant strains of Escherichia coli K-12. Bacteriol Rev. 1972, 36 (4): 525-557.PubMed CentralPubMedGoogle Scholar
- Sternglanz R, DiNardo S, Voelkel KA, Nishimura Y, Hirota Y, Becherer K, Zumstein L, Wang JC: Mutations in the gene coding for Escherichia coli DNA topoisomerase I affect transcription and transposition. Proceedings of the National Academy of Sciences of the United States of America. 1981, 78 (5): 2747-2751. 10.1073/pnas.78.5.2747.PubMed CentralView ArticlePubMedGoogle Scholar
- Miller J: Experiments in Molecular Genetics. 1972, Cold Spring Harbor, New York: Cold Spring Harbor Laboratory PressGoogle Scholar
- Chow WY, Berg DE: Tn5tac1, a derivative of transposon Tn5 that generates conditional mutations. Proceedings of the National Academy of Sciences of the United States of America. 1988, 85 (17): 6468-6472. 10.1073/pnas.85.17.6468.PubMed CentralView ArticlePubMedGoogle Scholar
- Sambrook J, Russel DW: Molecular Cloning: A Laboratory Manual. 2001, Cold Spring Harbor, New York: Cold Spring Harbor Laboratory Press, 3Google Scholar
- Liu YG, Mitsukawa N, Oosumi T, Whittier RF: Efficient isolation and mapping of Arabidopsis thaliana T-DNA insert junctions by thermal asymmetric interlaced PCR. Plant J. 1995, 8 (3): 457-463. 10.1046/j.1365-313X.1995.08030457.x.View ArticlePubMedGoogle Scholar
- Liu YG, Mitsukawa N, Whittier RF: Rapid sequencing of unpurified PCR products by thermal asymmetric PCR cycle sequencing using unlabeled sequencing primers. Nucleic acids research. 1993, 21 (14): 3333-3334. 10.1093/nar/21.14.3333.PubMed CentralView ArticlePubMedGoogle Scholar
- Liu YG, Whittier RF: Thermal asymmetric interlaced PCR: automatable amplification and sequencing of insert end fragments from P1 and YAC clones for chromosome walking. Genomics. 1995, 25 (3): 674-681. 10.1016/0888-7543(95)80010-J.View ArticlePubMedGoogle Scholar
- Kitagawa M, Ara T, Arifuzzaman M, Ioka-Nakamichi T, Inamoto E, Toyonaga H, Mori H: Complete set of ORF clones of Escherichia coli ASKA library (A Complete Set of E. coli K-12 ORF Archive): Unique Resources for Biological Research. DNA Res. 2005, 12 (5): 291-299. 10.1093/dnares/dsi012.View ArticlePubMedGoogle Scholar
- Mizuno T: Compilation of all genes encoding two-component phosphotransfer signal transducers in the genome of Escherichia coli. DNA Res. 1997, 4 (2): 161-168. 10.1093/dnares/4.2.161.View ArticlePubMedGoogle Scholar
- Zhai Y, Saier MH: The beta-barrel finder (BBF) program, allowing identification of outer membrane beta-barrel proteins encoded within prokaryotic genomes. Protein Sci. 2002, 11 (9): 2196-2207. 10.1110/ps.0209002.PubMed CentralView ArticlePubMedGoogle Scholar
- Allen MJ, White GF, Morby AP: The response of Escherichia coli to exposure to the biocide polyhexamethylene biguanide. Microbiology (Reading, England). 2006, 152 (Pt 4): 989-1000.View ArticleGoogle Scholar
- Paulsen IT, Beness AM, Saier MH: Computer-based analyses of the protein constituents of transport systems catalysing export of complex carbohydrates in bacteria. Microbiology (Reading, England). 1997, 143 (Pt 8): 2685-2699.View ArticleGoogle Scholar
- Liu D, Cole RA, Reeves PR: An O-antigen processing function for Wzx (RfbX): a promising candidate for O-unit flippase. Journal of bacteriology. 1996, 178 (7): 2102-2107.PubMed CentralPubMedGoogle Scholar
- Yao Z, Valvano MA: Genetic analysis of the O-specific lipopolysaccharide biosynthesis region (rfb) of Escherichia coli K-12 W3110: identification of genes that confer group 6 specificity to Shigella flexneri serotypes Y and 4a. Journal of bacteriology. 1994, 176 (13): 4133-4143.PubMed CentralPubMedGoogle Scholar
- Schnaitman CA, Klena JD: Genetics of lipopolysaccharide biosynthesis in enteric bacteria. Microbiological reviews. 1993, 57 (3): 655-682.PubMed CentralPubMedGoogle Scholar
- Liu D, Reeves PR: Escherichia coli K12 regains its O antigen. Microbiology (Reading, England). 1994, 140 (Pt 1): 49-57.View ArticleGoogle Scholar
- Stevenson G, Neal B, Liu D, Hobbs M, Packer NH, Batley M, Redmond JW, Lindquist L, Reeves P: Structure of the O antigen of Escherichia coli K-12 and the sequence of its rfb gene cluster. Journal of bacteriology. 1994, 176 (13): 4144-4156.PubMed CentralPubMedGoogle Scholar
- Sturm A, Schierhorn A, Lindenstrauss U, Lilie H, Bruser T: YcdB from Escherichia coli reveals a novel class of Tat-dependently translocated hemoproteins. The Journal of biological chemistry. 2006, 281 (20): 13972-13978. 10.1074/jbc.M511891200.View ArticlePubMedGoogle Scholar
- Stancik LM, Stancik DM, Schmidt B, Barnhart DM, Yoncheva YN, Slonczewski JL: pH-dependent expression of periplasmic proteins and amino acid catabolism in Escherichia coli. Journal of bacteriology. 2002, 184 (15): 4246-4258. 10.1128/JB.184.15.4246-4258.2002.PubMed CentralView ArticlePubMedGoogle Scholar
- Maurer LM, Yohannes E, Bondurant SS, Radmacher M, Slonczewski JL: pH regulates genes for flagellar motility, catabolism, and oxidative stress in Escherichia coli K-12. Journal of bacteriology. 2005, 187 (1): 304-319. 10.1128/JB.187.1.304-319.2005.PubMed CentralView ArticlePubMedGoogle Scholar
- Cao J, Woodhall MR, Alvarez J, Cartron ML, Andrews SC: EfeUOB (YcdNOB) is a tripartite, acid-induced and CpxAR-regulated, low-pH Fe2+ transporter that is cryptic in Escherichia coli K-12 but functional in E. coli O157:H7. Molecular microbiology. 2007, 65 (4): 857-875. 10.1111/j.1365-2958.2007.05802.x.View ArticlePubMedGoogle Scholar
- Aravind L, Koonin EV: The STAS domain - a link between anion transporters and antisigma-factor antagonists. Curr Biol. 2000, 10 (2): R53-55. 10.1016/S0960-9822(00)00335-3.View ArticlePubMedGoogle Scholar
- Malinverni JC, Silhavy TJ: An ABC transport system that maintains lipid asymmetry in the gram-negative outer membrane. Proceedings of the National Academy of Sciences of the United States of America. 2009, 106 (19): 8009-8014. 10.1073/pnas.0903229106.PubMed CentralView ArticlePubMedGoogle Scholar
- Pao SS, Paulsen IT, Saier MH: Major facilitator superfamily. Microbiol Mol Biol Rev. 1998, 62 (1): 1-34.PubMed CentralPubMedGoogle Scholar
- Bresolin G, Neuhaus K, Scherer S, Fuchs TM: Transcriptional analysis of long-term adaptation of Yersinia enterocolitica to low-temperature growth. Journal of bacteriology. 2006, 188 (8): 2945-2958. 10.1128/JB.188.8.2945-2958.2006.PubMed CentralView ArticlePubMedGoogle Scholar
- Sabina J, Dover N, Templeton LJ, Smulski DR, Soll D, LaRossa RA: Interfering with different steps of protein synthesis explored by transcriptional profiling of Escherichia coli K-12. Journal of bacteriology. 2003, 185 (20): 6158-6170. 10.1128/JB.185.20.6158-6170.2003.PubMed CentralView ArticlePubMedGoogle Scholar
- Kuznetsova E, Proudfoot M, Gonzalez CF, Brown G, Omelchenko MV, Borozan I, Carmel L, Wolf YI, Mori H, Savchenko AV: Genome-wide analysis of substrate specificities of the Escherichia coli haloacid dehalogenase-like phosphatase family. The Journal of biological chemistry. 2006, 281 (47): 36149-36161. 10.1074/jbc.M605449200.View ArticlePubMedGoogle Scholar
- Zhao K, Liu M, Burgess RR: The Global Transcriptional Response of Escherichia coli to Induced σ32 Protein Involves σ32 Regulon Activation Followed by Inactivation and Degradation of σ32 in vivo. The Journal of biological chemistry. 2005, 280 (18): 17758-17768. 10.1074/jbc.M500393200.View ArticlePubMedGoogle Scholar
- Wang X, Zhao X: Contribution of oxidative damage to antimicrobial lethality. Antimicrobial agents and chemotherapy. 2009, 53 (4): 1395-1402. 10.1128/AAC.01087-08.PubMed CentralView ArticlePubMedGoogle Scholar
- Malik M, Capecci J, Drlica K: Lon protease is essential for paradoxical survival of Escherichia coli exposed to high concentrations of quinolone. Antimicrobial agents and chemotherapy. 2009, 53 (7): 3103-3105. 10.1128/AAC.00019-09.PubMed CentralView ArticlePubMedGoogle Scholar
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