Update of thermotolerant genes essential for survival at a critical high temperature in Escherichia coli.

Previous screening of a single-gene knockout library consisting of 3,908 disrupted-mutant strains allowed us to identify 51 thermotolerant genes that are essential for survival at a critical high temperature (CHT) in Escherichia coli [Murata M, Fujimoto H, Nishimura K, Charoensuk K, Nagamitsu H, Raina S, Kosaka T, Oshima T, Ogasawara N, Yamada M (2011) PLoS ONE 6: e20063]. In this study, we identified another 21 thermotolerant genes. E. coli thus has 72 thermotolerant genes in total. The genes are classified into 8 groups: genes for energy metabolism, outer membrane organization, DNA double-strand break repair, tRNA modification, protein quality control, translation control, cell division and transporters. This classification and physiological analysis indicate the existence of fundamental strategies for survival at a CHT, which seems to exclude most of the heat shock responses.

Introduction

Like general essential genes that are imperative for growth, there are genes, called thermotolerant genes, that are indispensable for survival at a critical high temperature (CHT), a level close to that causing cell death [1, 2]. To understand the molecular mechanisms supporting survival at a CHT in Escherichia coli, genome-wide screening with a single-gene knockout library has been performed, and 51 thermotolerant genes essential for growth at 47°C have been identified [1]. Genes for which expression is affected by exposure to a CHT have also been identified [1]. Unexpectedly, the former contents are not consistent with the latter except for dnaJ and dnaK, indicating that a specific set of non-heat shock genes is required for the organism to survive under such a severe condition. More than half of the mutants of thermotolerant genes are sensitive to H2O2, suggesting that the mechanism of thermotolerance partially overlaps with that of oxidative stress resistance. Interestingly, gene sets for a lipopolysaccharide biosynthesis system for outer membrane organization and for a sulfur-relay system for tRNA modification are included, and they would have been acquired by horizontal gene transfer.

Here, we update thermotolerant genes in E. coli and discuss the possible thermotolerant mechanisms for survival at a CHT. Notably, we obtained evidence that ATP synthesis by oxidative phosphorylation is essential at a CHT but not at temperatures below the CHT.

Materials and methods

Materials

Oligonucleotide primers for polymerase chain reaction (PCR) were purchased from FASMAC Co, Ltd (Atsugi, Japan). Other chemicals were all of analytical grade.

Bacterial strains and growth conditions

The strains used in this study were derivatives of E. coli K-12. BW25113 (rrnB3, ΔlacZ4787, hsdR514, Δ(araBAD)567, Δ(rhaBAD)568, rph-1) [1] and mutants of BW25113 in the Keio collection as a single-gene knockout library [3] were grown on plates or in liquid of modified Luria-Bertani (LB) medium (1% Bactotryptone, 0.5% yeast extract, and 0.5% NaCl) at various temperatures as described previously [1].

Effects of glucose and MgCl2 and sensitivity to H2O2

To examine the effects of supplements, glucose (0.5% (w/v)) or MgCl2 (20 mM) was added to the LB liquid culture as described in detail previously [1]. The experiments were performed three times, and the results were confirmed to be reproducible.

RT-PCR analysis

Cultures were grown in LB medium at 37°C until the exponential phase, and then the temperature was up-shifted to 46°C and incubation was continued for 8 min. Total RNA was immediately prepared from the heat-stressed cells by the hot phenol method [1, 4]. RT-PCR analysis was performed using a One-Step RNA PCR kit (AMV) (TAKARA BIO Inc, Otsu, Japan) to examine the expression of immediate downstream genes of disrupted genes as described in detail previously [1, 5]. The primer set used for each gene is shown in S1 Table. After the completion of PCR, the products were analyzed by 1.2% agarose gel electrophoresis and stained with ethidium bromide.

DNA manipulation

Recombinant plasmids for expression of thermotolerant genes, atpA, gntK, lpxL, fimG, yccM, yraN, cydD and nhaA, were constructed, generating pUC-atpA, pUC-gntK, pUC-lpxL, pUC-fimG, pUC-yccM, pUC-yraN, pUC-cydD and pUC-nhaA, respectively. The DNA fragment of each gene, including the sequence from 40-bp upstream from the translation initiation codon to the stop codon, was amplified and inserted into pUC19 by In-Fusion cloning (Clontech, USA). Amplification of the DNA fragment was performed by PCR using a specific primer set for each gene (S2 Table) and the genomic DNA of BW25113 as a template [6]. The DNA fragment of pUC19 [7] was also amplified by PCR using two primers, 5'-ACTCTTCCTTTTTCAATATTATTGAAGCA-3' and 5'-CTGTCAGACCAAGTTTACTCATATATAC-3', and pUC19 DNA as a template. The primer set for each thermotolerant gene and that for pUC19 shared 15 overlapping sequences that were required for In-Fusion cloning. Each gene inserted into the vector was designated to be transcribed from the lac promoter on the plasmid.

Complementation test

pUC-atpA, pUC-gntK, pUC-lpxL, pUC-fimG, pUC-yccM, pUC-yraN, pUC-cydD and pUC-nhaA DNAs were introduced into BW25113atpA::kan, BW25113gntK::kan, BW25113lpxL::kan, BW25113fimG::kan, BW25113yccM::kan, BW25113yraN::kan, BW25113cydD::kan and BW25113nhaA::kan cells, respectively. The empty plasmid DNA of pUC19 was also introduced into each of these mutant strains and BW25113, which were used as controls. These transformants were grown in LB medium at 37°C or 45°C for appropriate times. The experiments were performed three times, and the results were confirmed to be reproducible.

Results and discussion

Identification of new thermotolerant genes

In a previous study, three successive screening steps were performed in a single-gene knockout library [3], and eventually 51 mutant strains that were sensitive to a CHT were found and reported [1]. In the screening process, 26 strains that exhibited relatively slow growth at 30°C on plates at the 1st screening, which was examined at least twice for confirmation, were removed from further screenings by a spotting test and liquid culture. In this study, the 26 mutants were subjected to the 2nd and 3rd screenings of spotting and liquid culturing tests at a CHT as described previously [1] and careful growth experiments in liquid culture at 30°C, 37°C, 39°C, 44°C, 45°C and 46°C. All of the mutants were found to be significantly sensitive to a temperature of 46°C and some were even sensitive to 44°C (S1 Fig and Table 1). However, 5 of those mutants, atpB, atpC, atpE, atpF and atpH, that encode constituents in the complex of the F1Fo-type ATP synthase showed little growth even at low temperatures, 30°C, 37°C and 39°C. Thus, out of the corresponding 26 genes, the 5 genes for the ATP synthase were excluded and 21 genes have become new thermotolerant genes in E. coli. In addition, the effects of supplements on cell growth of the sensitive mutants at a CHT were examined under the same conditions as those used previously [1] (S2 Fig and Table 1). Their sensitivity to H2O2 at 30°C was also tested because about 60% of disrupted mutants of thermotolerant genes are sensitive to H2O2 [1] (S2 Fig and Table 1). Moreover, according to the gene organization in the local region including the disrupted gene (S3 Fig), a possible polar effect of insertion of the aph cassette [3] was examined by RT-PCR with a specific primer set for each gene (S1 Table), but none of the mutants showed an obvious polar effect (S3 and S4 Figs), suggesting that the thermosensitive phenotype in the 21 mutants is due to disruption of the targeted gene. Furthermore, functional complementation was performed on 8 thermotolerant genes selected from five categories that are shown below (S5 Fig). As a result, all of the genes cloned on the plasmid were able to almost completely or partially complement the corresponding gene-knockout mutant. Notably, it was found that introduction of the empty vector, pUC19, and pUC-lpxL caused a negative and a positive effect, respectively, on growth at 37°C in BW25113 lpxL::kan. Similar but slightly weaker effects were found in the complementation of mutations of yraN, yccM and nhaA. It is likely that these mutations are sensitive to the presence of pUC19 and that each plasmid clone of these genes not only complements the corresponding mutation but also gives resistance to the vector. The mechanism of the growth influence by pUC19, however, is not obvious.

Table 1

Thermotolerant genes identified in this study.

Classification	Sub-classification	Gene	Function	30°Ca	37°Cb	44°Cc	45°Cd	46°Ce	Glcf	Mg2+g	H2O2h
Energy metabolism (Group A)	Oxidative phosphorylation	atpA	F1 sector of membrane-bound ATP synthase, alpha subunit					-
	Oxidative phosphorylation	atpD	F1 sector of membrane-bound ATP synthase, beta subunit					-	+	++	S
	Oxidative phosphorylation	atpG	F1 sector of membrane-bound ATP synthase, gamma subunit					-
	Oxidative phosphorylation	nuoC	NADH:ubiquinone oxidoreductase, chain C, D					-
	Pentose phosphate pathway	gntK	Gluconate kinase 2					-		+	S
	Pentose phosphate pathway	phnN	Ribose 1,5-bisphosphokinase					-
	Ubiquinone/menaquinone biosynthesis	ubiE	Ubiquinone/menaquinone biosynthesis C-methyltransferase UbiE					-
	Ubiquinone biosynthesis	ubiH	2-octaprenyl-6-methoxyphenol hydroxylase			-	-	-			S
	Ubiquinone biosynthesis	ubiX	Flavin prenyltransferase UbiX					-
	Amino acid metabolism	dapF	Diaminopimelate epimerase			-	-	-
	Amino acid metabolism	trpB	Tryptophan synthase, beta chain					-	+		S
	Vitamin B6 metabolism	pdxH	Pyridoxin/pyridoxamine 5'-phosphate oxidase				-	-	+		S
Outer membrane biosynthesis (Group B)	Lipopolysaccharide biosynthesis	lpxL	Lipid A biosynthesis lauroyltransferase				-	-		++	S
	Secretion system	fimG	Minor component of type I fimbriae					-		++	S
DNA repair (Group C)	Putative endonuclease	yraN	Predicted Mrr Cat superfamily					-		++	S
tRNA modification (Group D)	tRNA modification	yccM	Sulfur relay system, 4Fe-4S membrane protein				-	-		+
Others	ABC transporter	cydD	ATP-binding/membrane protein CydD					-	++	++	S
	Sodium-proton antiporter	nhaA	Na+:H+ antiporter, NhaA family					-	+	++	S
	Hypothetical protein	yjiY	Putative transporter, Carbon starvation protein CstA superfamily					-			S
	Hypothetical protein	ydgH	Uncharacterized deacetylase					-		++	S
	Hypothetical protein	yaiS	DUF1471 family periplasmic protein					-			S

a to e“-” means very weak growth at indicated temperatures.

f According to the data in S2 Fig, ratios of growth in the presence of glucose to that in the absence of glucose at 46°C were estimated.

“++” and “+” represent more than 2.0 and 1.5–2.0, respectively.

gAccording to the data in S2 Fig, ratios of growth in the presence of MgCl2 to that in the absence of MgCl2 at 46°C were estimated.

“++” and “+” represent more than 2.0 and 1.5–2.0, respectively.

hAccording to the data in S2 Fig, ratios of growth in the presence of H2O2 to that in the absence of H2O2 at 30°C were estimated.

“S” represents less than 0.5.

Next, the 21 genes corresponding to the 21 thermosensitive mutants were classified on the basis of their functions by using public databases including the KEGG pathway database. Interestingly, most of the 21 thermotolerant genes were found to be classified into categories defined in a previous study: energy metabolism, outer membrane stabilization and tRNA modification (Table 1). It is noteworthy that this study allowed us to find lacking pieces in the following system or pathway. Six genes that are involved in the sulfur-relay system for tRNA modification are included in the previous list of thermotolerant genes [1], and yccM as the last one in the sulfur-relay system was newly identified. Similarly, lpxL, which encodes KDO2-lipid IV(A) lauroyltransferase, is a new thermotolerant gene in the lipopolysaccharide biosynthesis pathway.

The functions of the newly identified thermotolerant genes are summarized in Table 1. Most of them were categorized into group A, including genes for components or their synthesis in the respiratory chain and in the complex of the F1Fo-type ATP synthase and for enzymes involved in the pentose phosphate pathway, the biosynthesis of lysine or phenylalanine/tyrosine/tryptophan and the metabolism of vitamin B6. The remaining genes were members of groups B, C and D. It is noteworthy that disruption of fimG for the outer membrane component in type 1 fimbriae, but not disruption of genes for its other components, causes thermosensitivity, suggesting the importance of outer membrane stability. As noticed previously, the growth of mutants that belong to group B or C was partially improved by the addition of Mg2+. Examination of the effect of H2O2 on growth showed that 14 mutants are sensitive to H2O2, being 67% of 21 newly identified thermotolerant genes (Table 1). This ratio is consistent with that of 51 previously identified ones, suggesting that the mechanism of thermotolerance partially overlaps with that of oxidative stress resistance in E. coli, as reported previously [1]. Additionally, DNA chip analysis [1] indicate that none of 21 newly identified thermotolerant genes are not up-regulated when cells are transiently exposed to a CHT, like most of previously identified thermotolerant genes.

Notably, functions of the members of group A suggest that ATP synthesis by substrate-level phosphorylation can support cell survival at temperatures up to 46°C but that ATP synthesis by oxidative phosphorylation is essential at a CHT. On the other hand, mutations of genes for subunits interacting with the membrane in the complex of the ATP synthase were found to be very sensitive even to low temperatures compared to other subunits of the complex. Presumably, mutations for the membrane-interacting subunits cause H+ leakage in the membrane, resulting in diminishment of membrane potential, which reduces cell survival of the organism. In addition, the dependence of oxidative phosphorylation at a CHT seems consistent with the essentiality of aceE, aceF, lpd, lipA and ackA at a CHT [1], which are mapped in the pyruvate metabolism pathway from pyruvate to acetyl CoA [8-11] that functions as energy metabolism for production of ATP. Therefore, these findings allow us to speculate that a metabolic flow at a CHT is toward the TCA cycle and increase in respiratory activity.

Possible mechanisms for survival at a CHT

In total, 72 thermotolerant genes were found in E. coli (Table 2). Intriguingly, thermotolerant genes in E. coli include only a small number of heat shock genes and are mostly genes responsible for functions to stabilize the membrane or to assist fundamental metabolism [1]. These functions are essential for survival in a 2–3°C range close to the CHT in E. coli. Genes categorized as genes responsible for energy metabolism seem to contribute to the synthesis of ATP, which may be required for repairing damage of macromolecules, protein, DNA or RNA. Many genes responsible for outer membrane stabilization and tRNA modification are involved in modification and stabilization of the structure of LPS and tRNA, respectively. Genes responsible for translation control or cell division may avoid or overcome accidents in translation or the cell division process at a CHT. On the other hand, the involvement of genes in DNA double-strand break repair and chaperone/proteinase suggests accumulation of reactive oxygen species (ROS) at a CHT, being consistent with evidence that a higher temperature results in accumulation of more oxidative stress [12] and the finding that mutants of all members in both groups exhibited sensitivity to H2O2 [1] and Table 1.

Table 2

List of thermotolerant genes in E. coli.

Classificationa	Gene	Definition	Function
Energy Metabolism (Group A)	aceE	Pyruvate metabolism	Pyruvate dehydrogenase compenent E1 decarboxylase component E1
	aceF	Pyruvate metabolism	Pyruvate dehydrogenase, dihydrolipoyltransacetylase compenent E2
	lpd	Pyruvate metabolism	Lipoamide dehydrogenase, E3 component, subunit of three comlexes
	lipA	Pyruvate mechanism	Liponate synthase
	ackA	Pyruvate metabolism	Acetate kinase A and propionate kinase 2
	rpe	Pentose phosphate pathway	D-ribulose-5-phosphate 3-epimerase
	cydB	Respiratory chain	Cytochrome d ubiquinol oxidase subunit II
	yhcB	Respiratory chain	Cytochrome d ubiquinol oxidase subunit III
	atpAb	Oxidative phosphorylation	F1 sector of membrane-bound ATP synthase, alpha subunit
	atpD	Oxidative phosphorylation	F1 sector of membrane-bound ATP synthase, beta subunit
	atpG	Oxidative phosphorylation	F1 sector of membrane-bound ATP synthase, gamma subunit
	nuoC	Oxidative phosphorylation	NADH:ubiquinone oxidoreductase, chain C, D
	gntK	Pentose phosphate pathway	Gluconate kinase 2
	phnN	Pentose phosphate pathway	Ribose 1,5-bisphosphokinase
	ubiE	Ubiquinone/menaquinone biosynthesis	Ubiquinone/menaquinone biosynthesis C-methyltransferase UbiE
	ubiH	Ubiquinone biosynthesis	2-octaprenyl-6-methoxyphenol hydroxylase
	ubiX	Ubiquinone biosynthesis	Flavin prenyltransferase UbiX
	dapF	Amino acid metabolism	Diaminopimelate epimerase
	trpB	Amino acid metabolism	Tryptophan synthase, beta subunit
	pdxH	Vitamin B6 metabolism	Pyridoxine/pyridoxamine 5'-phosphate oxidase
	ybhH	Hypothetical protein	Putative isomerase
Outer membrane stabilization (Group B)	gmhB	Lipopolysaccharide biosynthesis	D,D-heptose 1,7-bisphosphate phosphatase
	lpcA (gmhA)	Lipopolysaccharide biosynthesis	D-sedoheptulose 7-phosphate isomerase
	rfaC (waaC)	Lipopolysaccharide biosynthesis	ADP-heptose:LPS heptosyl transferase I
	rfaD (waaD)	Lipopolysaccharide biosynthesis	ADP-L-glycero-D-mannoheptose-6-epimerase, NAD(P)-binding
	rfaE (gmhC)	Lipopolysaccharide biosynthesis	Fused heptose7-phosphate kinase and heptose 1-phosphate adenyltransferase
	rfaF (waaF)	Lipopolysaccharide biosynthesis	ADP-heptose:LPS heptosyltransferase II
	rfaG (waaG)	Lipopolysaccharide biosynthesis	Glucosyltransferase I
	lpxL	Lipopolysaccharide biosynthesis	Lipid A biosynthesis lauroyltransferase
	ydcL	Peptidoglycan-associated lipoprotein	Predicted lipoprotein
	yfgL	Peptidoglycan-associated lipoprotein	Protein assembly complex, lipoprotein component
	ynbE	Peptidoglycan-associated lipoprotein	Predicted lipoprotein
	nlpI	Peptidoglycan-associated lipoprotein	Conserved protein
	ycdO	Peptidoglycan-associated lipoprotein	Conserved protein
	pal	Outer membrane integrity	Tol/Pal system, peptidoglycan-associated outer membrane lipoprotein
	tolQ	Outer membrane integrity	Tol/Pal system, membrane-spanning protein
	tolR	Outer membrane integrity	Tol/Pal system, membrane-spanning protein
	yciM	Outer membrane integrity	Conserved hypothetical protein
	fimG	Secretion system	Minor component of type 1 fimbriae
DNA repair (Group C)	dnaQ	DNA replication & repair, DSBR	DNA polymerase III subunit, epsilon
	holC	DNA replication & repair, DSBR	DNA polymerase III subunit, chi
	priA	DNA replication & repair, DSBR	Primosome factor n'
	ruvA	DNA replication & repair, DSBR	Component of RuvABC resolvasome, endonuclease
	ruvC	DNA replication & repair, DSBR	Conserved protein required for cell growth
	yraN	Hypothetical protein	Predicted Mrr Cat superfamily
tRNA modification (Group D)	iscS	tRNA modification	Sulfer relay system, cysteine desulfurase
	yheL (tusB)	tRNA modification	Sulfer relay system, predicted intracellular sulfur oxidation protein
	yheM (tusC)	tRNA modification	Sulfer relay system, predicted intracellular sulfur oxidation protein
	yheN (tusD)	tRNA modification	Sulfer relay system, predicted intracellular sulfur oxidation protein
	yhhP (tusA)	tRNA modification	Sulfer relay system, conserved protein required for cell growth
	yccM	tRNA modification	Sulfur relay system, 4Fe-4S membrane protein
	miaA	tRNA modification	Delta(2)-isopentenylpyrophosphate tRNA-adenosine transferase
	trmU	tRNA modification	tRNA (5-methylaminomethyl-2-thiouridylate)-methyltransferase
	truA	tRNA modification	Pseudouridine synthase A
Chaperone /protease (Group E)	dnaJ	Chaperone system	Chaperone Hsp40, co-chaperone with DnaK
	dnaK	Chaperone system	Chaperone Hsp70, co-chaperone with DnaJ
	degP	Chaperone system	Chaperone/serine endoprotease
	rseA	Chaperone regulator	Anti-sigma factor
Translational control (Group F)	rpmJ	Translational control	50S ribosomal subunit L36, related to secY expression
	rpsF	Translational control	30S ribosomal subunit S6, modified with glutamic acid or phosphate
	dksA	Translational control	DNA-binding transcriptional regulator or rRNA transcription
	smpB	Translational control	Component of trans-translation process
Cell division (Group G)	xerC	Related to cell division	Site-specific tyrosine recombinase for chromosome dimmer resolution
	dedD	Related to cell division	Membrane-anchored periplasmic protein involved in separation
	envC	Related to cell division	Regulator of cell wall hydrolases responsible for cell separation
Transporter (Group H)	zntA	Membrane transport	Zinc/cadmium/mercury/lead-exporting ATPase
	ybgH	Membrane transport	Predicted proton-dependent oligopeptide transporter, POT family
	cydD	Membrane transport	ATP-binding/permease protein CydD
	nhaA	Membrane transport	Na+/H+ antiporter, NhaA family
	yjiY	Hypothetical protein	Putative transporter, carbon starvation protein CstA superfamily
Others	yaiS	Hypothetical protein	Uncharacterized deacetylase
	ydgH	Hypothetical protein	DUF1471 family periplasmic protein

aA new group of transporter (Group H) is added. Transporters were classified in others in previous paper [1].

bThermotolerant genes identified in this study are shown by bold letters.

Taken together, we propose a model of intracellular problems at a CHT and their protection mechanisms as shown in Fig 1. Under conditions at high temperatures close to a CHT, membrane fluidity may dramatically increase, causing leakage of electrons from the respiratory chain to generate ROS that give rise to oxidative damages to macromolecules. DNA double-strand breaks and protein denaturation by oxidative modifications seem to occur in the cytoplasm or periplasm because the corresponding genes become indispensable at a CHT. As protection mechanisms against these problems as thermotolerant mechanisms, LPS and membrane proteins may strengthen the membrane structure to prevent membrane fluidity. However, ROS scavenging genes were not found as thermotolerant genes. This may be due to the existence of homologues that can perform the same function in E. coli. Notably, overexpression of sodA for superoxide dismutase or katE for catalase significantly increased the number of viable and culturable cells at a CHT [12]. Similarly, overexpression of catalase and superoxide dismutase genes increased the degree of thermotolerance in Saccharomyces cerevisiae [13]. Notably, the generation of ROS might be enhanced by an increase in respiratory activity, as speculated above, for oxidative phosphorylation at a CHT. In addition to membrane stabilization and scavenging of ROS, there are protection mechanisms of stabilization of tRNA by modification and repair of DNA double-strand breaks or denatured proteins in E. coli. Moreover, there are other trouble-shooting mechanisms in translation or cell division at a CHT.

Fig 1

A model of intracellular problems at a CHT and their protection mechanisms.

At a CHT, the level of ROS is increased as described in the text, resulting in damage of macromolecules. There are various possible protection mechanisms as thermotolerant mechanisms, such as stabilization of the membrane to protect electron leakage from the respiratory chain, scavenging ROS, and stabilization of tRNA by modification and repair of DNA double-strand breaks or denatured proteins. Abbreviations used are: OM, outer membrane; IM, inner membrane; O2•-, superoxide radical anion; H2O2, hydrogen peroxide; •OH, hydroxyl radical.

Since the screening in this study was performed with a single-gene knockout library covering all non-essential genes in E. coli, knowledge of physiological functions of the 72 thermotolerant genes will be very beneficial for the genetic conversion of non-thermotolerant to thermotolerant bacteria.

Growth of thermosensitive mutants in LB liquid culture at different temperatures.

Each of the 26 thermosensitive mutant strains (open circles) and the parental strain, BW25113 (closed circles), were grown in 30 ml LB medium at 30°C, 37°C, 39°C, 44°C, 45°C and 46°C. At the times indicated, turbidity at OD600 was measured. A, group A; B, group B; C, group C; D, group D; E, group E.

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Effects of addition of glucose and MgCl2 and sensitivity to H2O2.

Thermosensitive mutant strains are shown by gene names. Growth conditions are described in Materials and Methods. Black and white columns represent turbidity under the conditions with and without supplements (0.5% glucose (A) or 20 mM MgCl2 (B)) or 0.5 mM H2O2 (C).

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Gene organizations around genes having either an essential gene or a thermotolerant gene as a just downstream gene.

Gene organizations around 19 thermotolerant genes that may have either an essential gene or a thermotolerant gene as a just downstream gene are depicted. Black boxes represent 19 identified thermotolerant genes. Grey boxes represent possible essential or thermotolerant genes. The direction of boxes shows the direction of transcription.

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Testing of possible polar effects by aph insertion.

Total RNA was prepared from cells cultured at 37°C (a) and 46°C (b) and subjected to RT-PCR as described in Materials and Methods. RT-PCR was performed with primers specific for a just downstream gene of each thermotolerant gene to amplify about 500-bp DNA fragments. After RT reaction, PCR was performed for 15, 20, 25 and 30 cycles and each PCR product was electrophoresed on 1.2% agarose gel, followed by staining with ethidium bromide. Arrowheads indicate amplified products by RT-PCR.

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Complementation experiments with plasmid clones of representative thermotolerant genes.

Transformants with plasmid clones (open circles), BW25113atpA::kan (pUC-atpA), BW25113gntK::kan (pUC-gntK), BW25113lpxL::kan (pUC-lpxL), BW25113fimG::kan (pUC-fimG), BW25113yccM::kan (pUC-yccM), BW25113yraN::kan (pUC-yraN), BW25113cydD::kan (pUC-cydD) and BW25113nhaA::kan (pUCNHAA), and transformants with an empty vector (closed circles), BW25113atpA::kan (pUC19), BW25113gntK::kan (pUC19), BW25113lpxL::kan (pUC19), BW25113fimG::kan (pUC19), BW25113yccM::kan (pUC19), BW25113yraN::kan (pUC19), BW25113cydD::kan (pUC19) and BW25113nhaA::kan (pUC19), and BW25113 (pUC19) (open triangles) were grown in 30 ml LB medium at 37°C (at left side) and 45°C (at right side), except that cells in the BW25113lpxL::kan background and its control cells were examined at 37°C (at left side) and 43°C (at right side) because of the negative effect of pUC19 (see related description in the text). At the times indicated, turbidity at OD600 was measured.

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RT-PCR primers used in this study.

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Primers for gene cloning for complementation experiments.

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