evauluation of oligonucleotide microarrays and expression ...nhac-2, 5.66 (z: 6.00) ↑heat na/h...

1
Evauluation of Oligonucleotide Microarrays and Expression Analysis of Desulfovibrio vulgaris Cells in Metal-Reducing Conditions M.E. Clark 1* , Q. He 2* , Z. He 2 , L. Wu 2 , J.D. Wall 3 , T.C. Hazen 4 , K. Huang 4 , E. Alm 4 , A.P. Arkin 4 , J. Zhou 2 , and M.W. Fields 1 1 Miami University, Oxford, OH; 2 Oak Ridge National Laboratory, Oak Ridge, TN; 3 University of Missouri, Columbia, MO; 4 Lawrence Berkeley National Laboratory, Berkeley, CA Abstract Objectives: (i) Construct whole-genome microarrays for Desulfovibrio vulgaris; (ii) Determine optimal conditions for hybridization conditions; and (iii) Identify whole-genome expression patterns of D. vulgaris cells grown under metal-reducing conditions. Results: Recent studies have shown that the design characteristics of probes can significantly affect hybridization behavior, and therefore, possibly affect the dataset of genes with altered expression profiles. In order to experimentally establish the criteria for the design of gene-specific probes, an oligonucleotide array was constructed that contained perfect-match and mismatch probes. The effects of probe-target identity, continuous stretch, mismatch position, and hybridization free energy on specificity were examined. Second, in order to determine the effect of probe length on signal intensities, microarrays with different length probes were used to monitor gene expression. Based on the experimental results, a set of criteria were suggested for the design of gene-specific and group-specific probes, and these criteria should provide valuable information for the development of new software and algorithms for microarray-based studies. The whole-genome microarrays of D. vulgaris were constructed using 70mer probes. Currently, growth conditions and medium are being evaluated for transcriptomic characterization with respect to growth phase and heavy metal responsive genes. The elucidation of growth-phase dependent gene expression is essential for a general understanding of growth physiology that is also crucial for data interpretation of stress-responsive genes (e.g., chromium). We recently cultivated D. vulgaris in a defined medium and sampled biomass over time for approximately 70 h to characterize the shifts in gene expression as cells transitioned from logarithmic phase growth to stationary phase. Each respective time point during exponential phase had a similar number of ORFs (7 to 9% of the genome) that were up-expressed (>3-fold) and approximately 5.5 to 6.0% of the ORFs were down-expressed (<3-fold). Also, a majority of the predicted ORFs did not display altered expression patterns when early- and late-exponential phases were compared. As the cells entered into early stationary phase, approximately 7% of the ORFs were up-expressed, whereas 3.5% to 4% of the genome was up-expressed as the cells experienced prolonged stationary-phase. Within the first hours of stationary-phase, up-expressed ORFs included proteases, chaperonins, permeases, and hypothetical proteins. Interestingly, preliminary comparisons suggest that many of the ORFs that were up-expressed in early stationary phase also had altered expression levels in response to other cellular stresses. Preliminary data suggests that 0.05 mM Cr(VI) but not 0.01 mM Cr(VI) decreased growth in the defined medium with lactate and sulfate. In addition, D. vulgaris grew well in a defined, minimal medium designed to be analogous to FRC groundwater. We are presently analyzing microarray data to identify sub-sets of genes that respond to growth phase changes and/or stresses, as well as the determination of the optimal growth conditions in the presence of Cr(VI). NaCl T5, T7, T8 GGDEF domain protein 208701 ^ heat-shock T9 dcrA MAC-protein 208703 ^ NO 2 T5, T8, T9 sensory box/ HK 208671 ^ sensory box/ HK / RR 207606 ^ heat-shock T5, T6, T9 MAC protein 207350 ^ NO 3 T6, T8 RR 206316 T6 sensory box/ HK 206146 ^ T6 – T9 sensory box/ HK 209265 * T6, T7 sensory box/ HK / RR 209192 ^ sensory box/ HK / RR 209009 ^ O 2 T5, T6, T7 σ 54 -dependent transcript. regulator 207582 ^ heat-shock T6, T9 sensory box protein 206995 * Additional Responses Time-Point Change ORF Description ORF ID Comparison of fold changes of 21 ORFs consistently detected by PCR amplicon (circles), 70mer (squares), 60mer (up triangles) and 50mer (down triangles) arrays when S. oneidensis MR-1 cells were exposed to pH 4 for 30 min. ORFs were up-regulated above the line y = 1.0 (solid), ORFs were down-regulated below the line y = -1.0 (middle dash), and ORFs were not changed between the two lines. Average number of genes detected among 96 ORFs selected from Shewanella oneidensis MR-1 at an SNR >3.0. 500 ng of genomic DNA (A) or 10 μg of cDNA target RNA (B) was labeled with Cy-dyes and hybridized with this array. The data are represented as average with standard deviation of three slides (6 spots). 0 10 20 30 40 50 60 70 80 Helicobacter pylori J99 Synechoccus 8102 Streptooccus agalactiae 2603V/R Deinococcus radiodurans Clostridium acetobutlyicum Bacillus subtilis E. coli K-12 Oceanbacillus Bacteroides thetaiotaomicron Bdellovibrio HD100 Streptomyces ceolicolor A32 Archaeoglobus fulgidus Vibrio vulnifericans Ralstonia Caulobacter CB15 Shewanella oneidnesis Pseudomonas aeruoginosa Geobacter metallireducnes Desulfuromonas acetoxidans Geobacter sulfureducens Desulfovibrio G20 Desulfovibrio vulgaris Number of Predicted ORFs with PAS domain Z C B D N A Clostridium acetobutylicum FliA S E D N H Vibrio cholerae FliA S Z C B D N H A Pseudomonas aeruginosa PAO1 FliA S E1,2 C B D N1,2 H A Ralstonia solanacearum S E1-6 Z C B N H1, 2 A Sinorhizobium meliloti D Fusobacterium nucleatum C B N A Chlorobium tepidum TLS D H Caulobacter crescentus CB15 S D Bacteroides thetaiotaomicron D Deinococcus radiodurans FliA S E Z C B D N H A Shewanella oneidensis MR-1 FliA S E Z C B D N H A Escherichia coli K-12 ? E D N H Desulfuromonas acetoxidans ? D N H Desulfotalea psychrophila FliA ? E1-2 C B D N A Bdellovibrio bacteriovorus HD100 FliA ? Z C B D1, D2 N H A Geobacter sulfureducens PCA FliA ? Z C B D N H A Desulfovibrio desulfuricans G20 FliA ? Z C B D N H A Desulfovibrio vulgaris 28 38 24 160 140 70 54 32 40 10 100 1000 0 5 10 15 20 0 10 20 30 40 50 60 70 Cell Protein and Carbohydrate During Lactate and Sulfate Growth for D. vulgaris Time (h) 10 100 0 10 20 30 40 50 60 70 Sampling Time Points for Transcriptomic Anlayses Time (h) T1 T2 T3 T4 T5 T6 T7 T8 T9 D. vulgaris has a high number of predicted ORFs with PAS- and/or sensory domains Occurrence of Predicted σ-Factors from a Range of Different Genomes The D. vulgairs Genome Does Not Appear to Contain a Recognized σ 38 0 50 100 150 200 250 300 T2 T3 T4 T5 T6 T7 T8 T9 Number of ORFs with Altered Expression at Each Respective Sampling Point Up-Expressed Down-Expressed Time Points ORFs with Predicted PAS-Domains that have Altered Expression Levels Between Exponential- and Stationary-Growth Phases NO 2 heat 1.89 (z: 1.97) transport component of feoA 208071 NO 3 cold cold 1.94 (z: 1.61) metE, 5- methyltetrahydropteroyltri-E-hc- S-methyltransferase 208898 2.04 (z: 3.61) 2.24 (z: 4.17) flgM hypothetical protein 209462 209463 2.12 (z: 2.91) hypothetical protein 206409 NO 2 NaCl 2.07 (z: 2.61) hypothetical protein 209052 2.07 (z: 2.48) fld; flavodoxin (Fe-repressed) 208179 2.04 (z: 2.80) metK, S-adenosylmethionine synthetase 207942 NO 3 cold 1.97 (z: 2.94) metF, 5,10-mth reductase 206429 2.53 (z: 4.63) ahcY, adenosylhomocysteinase 209551 heat 2.41 (z: 3.14) katA, catalase 209629 heat NaCl co-culture-CH 4 2.47 (z: 2.95) hypothetical protein 207938 NO 2 heat 2.70 (z: 2.63) hypothetical protein 208070 heat 1.81 (z: 2.62) 2.34 (z: 3.76) carbon starvation protein A 209542 209543 2.30 (z: 4.44) flaB3, flagellin 207937 NO 2 heat 2.36 (z: 3.08) hypothetical protein 208964 NO 2 Putative FUR-box 2.99 (z: 2.25) conserved hypothetical protein 209207 NO 2 O 2 heat NaCl 3.36 (z: 2.75) hypothetical protein 208180 heat NO 2 NaCl 4.83 (z: 6.02) 3.96 (z: 3.55) feoB feoA 208068 208069 Additional Responses Change Expression Predicted Function Gene ID Up-Expression T4 versus T1 O 2 heat -2.39 (z: -4.06) lysA2 diaminopimelate dc 208063 heat -1.97 (z: -3.43) conserved hypothetical protein 206094 heat -0.54 to -2.0 ribosomal proteins 206743- 206772 heat -2.19 (z: -3.95) Na/A symporter 206150 Additional Responses Change Expression Predicted Function Gene ID Down-Expression T4 versus T1 2.11 to 2.50 hypothetical proteins 207638- 207641 2.03 (z: 3.54) metK, S- adenosylmethionine syn 207942 2.19 (z: 2.02) conserved hypothetical (PO 4 /phosphonate) 209182 NO 3 heat 2.30 (z: 2.82 universal stress protein 206465 2.27 (z: 3.15) sodB 207901 2.97 (z: 4.32) isoamylase 206369 2.50 (z: 4.28) putative, lipoprotein 206808 heat 3.21 (z: 2.90) mviN, integral membrane protein 206613 3.22(z: 5.25) 2.31 (z: 3.30 membrane proteins 206982 206983 co-culture NaCl 1.80 to 3.32 presumptive phage proteins 209131- 209137 3.25 (z: 2.12) carboxyl-terminal protease 207823 NO 3 NaCl heat co-culture 3.22 (z: 2.86 zraP,Zn-resistance 208912 heat 3.65 (z: 2.45) hypothetical protein 208851 1.20 to 3.51 presumptive phage proteins 208370- 208380 O 2 3.48 (z: 5.70) dsrC 208282 3.42 (z: 3.03) aa transport, putative 206856 3.95 (z: 6.65) sugar transferase domain 209685 3.89 (z: 7.29) integration host factor 208486 heat 3.81 (z: 2.90) tail/DNA circulation protein 208364 3.76 (z: 2.50 lysozyme 206564 3.70 (z: 2.86) hypothetical protein 208791 heat 5.66 (z: 6.00) nhaC-2, Na/H antiporter 208626 5.02 (z: 7.00) polysaccharide deacetylase 209679 4.55 (z: 3.36) hypothetical protein 207275 NO 3 heat 4.69 (z: 5.25) membrane protein 208597 NO 3 heat 5.45 (z: 4.24) cold shock domain protein 207324 NO 3 4.11 (z: 2.35) dctM, dicarboxylate transporter 208332 4.13 (z: 3.96) oxidoreductase 208628 3.98 (z: 4.04) ADP- ribosylglycohydrolase 208807 NO 2 heat NaCl 4.05 (z: 3.49) 2.47(z: 1.86) feoA feoB 208069 208068 NO 3 heat 5.72 (z: 5.71) major facilitator 209625 NO 2 heat NaCl co-culture 2.30 (z: 2.84) hspC, heat shock 207934 Additional Responses Change Expression Predicted Function Gene ID Up-Expression T5 versus T1 Survey of Down-Expressed ORFs at T5 to T9 Ribosomal Proteins and Translation: 6 SSU and 10 LSU proteins were down-expressed greater than 2-fold. These ribosomal proteins were also down-expressed in response to nitrate, nitrite, and heat. Other proteins associated with translation were also down-expressed: nusG, secE, EF-Ts, IF-1, and SecF. Biosynthesis: ribose-P-pyrophosphokinase, RNA-binding protein, ACP-reductase, ACP-synthase, ribonuclease P, gycerol-P acyl transferase, and histone-acetylation. Hypothetical and Conserved Hypotheticals: Many hypothetical or conserved hypothetical proteins were down-expressed and some were also down-expressed in response to heat, nitrite, and nitrate while others appeared to be unique to stationary-phase growth. Between 40 and 50% of the significantly down-expressed ORFs (T5-T9) were hypothetical or conserved hypothetical proteins. Sulfate Permease: Three mono-cistronic permeases. Each displayed a different pattern of expression at T5: 208981 Up-expressed; 209213 Down-expressed; 207471 unchanged. Ferritin: D. vulgaris has two predicted ferritin-like proteins: 206840 expression was unchanged at T5 but 207018 was down-expressed. heat 2.44(z: 3.88) mviN, integral membrane protein 206613 NO 2 heat NaCl co-culture 2.50 (z: 2.04) hspC, heat shock 207934 heat 3.65 (z: 2.45) hypothetical protein 208851 4.55 (z: 3.36) hypothetical protein 207275 3.03 (z: 4.34) 5- formyltetrahydrofolate cyclo-ligase 209300 2.94 (z: 1.69) GDP-mannose-4,6- dehydratase 209384 3.12 (z: 4.68) lysozyme 206564 4.17 (z: 3.02) integration host factor 208486 NO 3 NaCl heat co-culture 3.19(z: 2.66) zraP,Zn-resistance 208912 NO 2 heat NaCl co-culture 3.44(z: 4.69) 1.71(z: 2.09) feoA feoB 208069 208068 O 2 3.85 (z: 6.29) dsrC 208282 3.99 (z: 2.55) hypothetical protein 207275 4.12 (z: 3.51) sensory box/ HK / RR 209192 heat 3.80 (z: 2.16) ispD 206898 3.66 (z: 3.66) TPR domain 208077 3.56 (z: 2.66) TonB domain 208316 heat 3.17 (z: 2.17) glucokinase 206469 4.22 (z: 4.37) oxidoreductase 208628 1.60 to 3.83 presumptive phage proteins 208370- 208380 heat 4.74 (z: 3.65 nhaC-2, Na/H antiporter 208626 NO 3 heat 4.89(z: 7.23) major facilitator 209625 NO 3 heat 4.98 (z: 5.10) membrane protein 208597 4.91 (z:2.96) hypothetical protein 209014 2.04 to 4.45 presumptive phage proteins 206552- 206556 2.34 to 4.54 presumptive phage proteins 209131- 209137 3.27 to 4.25 hypothetical proteins 209138- 209141 2.30 (z: 2.33) putative DNA repair 209738 2.30 (z: 2.33) von Willebrand factor; Ankyrin 207604 NO 2 heat 5.76 (z: 6.87) cold shock domain protein 207324 3.25 (z: 2.12) carboxyl-terminal protease 207823 5.02 (z: 7.00) polysaccharide deacetylase 209679 2.48 (z: 3.28) glycosyl hydrolase 209665 2.42 (z: 2.47) glnB-3 regulatory P-II 209709 Additional Responses Change Expression Predicted Function Gene ID Up-Expression T6 versus T1 T7, T8, T8 -2.04 (z:-3.40) plasmid stabilization system family 207508 T6, T7, T8, T9 -2.29 (z: -2.19) fructose-1,6- bisphosphatase 207307 T5, T6, T7, T9 -2.29 (z: -3.31) sulfate permease 209213 T6, T9 -2.21 (z: -3.12) vacJ lipoprotein, putative 206681 T5, T6, T7 -2.55 (z: -2.16) peptidyl-prolyl cis- trans isomerase C 206915 T5, T6, T7 -2.27 (z: -2.97) UDP-3-0-acyl N- acetylglucosamine deacetylase 208427 T5, T6 -2.67 (z: -2.73) 3-dehydroquinate dehydratase (aromatic aa biosynthesis) 207124 T5, T6, T8 -2.84 (z: -3.18) GGDEF (putative adenyl cyclase) 206371 T5, T6, T7, T8, T9 -2.89 (z: -3.95) glycosyl transferase (LPS or EPS) 209502 T6 -2.94 (z: -3.28) L-lactate permease 207771 T4, T5, T6 -3.54 (z: -3.31) outer membrane protein P1 206699 T5, T6, T7, T8, T9 -3.30 (z: -4.56) conserved hypothetical protein 208347 208348 T5, T6, T7, T8, T9 -3.52 (z: -5.41) Plasmid maintenance toxin 206956 Time-Points Representative Values Predicted Function Gene ID Down-Expression T5 to T9 T7, T9 2.57 (z: 2.82) transglycosylase SLT domain protein 2 08200 T7, T8, T9 2.41 (z: 4.34) type III secretion system protein 209604 T7, T9 2.32 (z: 2.85) σ-54 dependent transcriptional regulator/ RR 209666 T7 T7 2.67 (z: 2.92) 3.01 (z: 2.16) peptidase oligopeptide ABC transporter 208072 208073 T6, T7 2.47 (z: 3.22) sensory box/ HK/ RR 209009 T5, T6, T7, T8, T9 2.94 (z: 2.50) mviN, integral membrane protein 206613 T6, T7, T8, T9 3.23 (z: 2.75) putative DNA repair 209738 T5, T6, T7, T8, T9 3.68 (z: 4.35) presumptive phage proteins 208370- 208380 T5, T6, T7, T8, T9 3.93 (z: 3.97) lysozyme 206564 T6, T7, T8 3.93(z: 4.89) TPR domain 208077 T7 3.93 (z: 4.43) epimerase/dehydrat ase 207948 T7 3.81(z: 4.00) acetyltransferase, GNAT family 209191 T5, T7, T8, T9 4.68(z: 5.47) sugar transferase domain 209685 T7, T8, T9 5.45 (z: 4.13) major facilitator 209625 T5, T6, T7, T8, T9 5.53 (z: 3.92 nhaC-2, Na/H antiporter 208626 T7, T8 5.35 (z: 10.42) aminotransferase 209678 T5, T6, T7, T8 5.31 (z: 9.37) polysaccharide deacetylase 209679 T6, T7, T8, T9 3.17 (z: 2.17) glucokinase 206469 T7, T9 3.20 (z: 3.13) polysaccharide biosynthesis protein 209285 T7, T8, T9 3.45 (z: 1.79) GDP-mannose 4,6- dehydratase 209384 T4 – T9 1.83(z: 2.28) 3.28(z: 3.69) feoA feoB 208069 208068 T5, T6, T7, T9 2.95 (z: 2.61) zraP,Zn-resistance 208912 T7 2.98(z: 2.50) aIF-2BI family 209012 T5, T6, T7, T8, T9 6.36 (z: 7.09) cold shock domain protein 207324 Time-Points Change Expression Predicted Function Gene ID Up-Expression T5 to T9 Major Conclusions:

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Page 1: Evauluation of Oligonucleotide Microarrays and Expression ...nhaC-2, 5.66 (z: 6.00) ↑heat Na/H antiporter 208626 polysaccharide 5.02 (z: 7.00) deacetylase 209679 207275 hypothetical

Evauluation of Oligonucleotide Microarrays and Expression Analysis of Desulfovibrio vulgaris Cells in Metal-Reducing ConditionsM.E. Clark1*, Q. He2*, Z. He2, L. Wu2, J.D. Wall3, T.C. Hazen4, K. Huang4, E. Alm4, A.P. Arkin4, J. Zhou2, and M.W. Fields1

1Miami University, Oxford, OH; 2Oak Ridge National Laboratory, Oak Ridge, TN; 3University of Missouri, Columbia, MO; 4Lawrence Berkeley National Laboratory, Berkeley, CA

AbstractObjectives: (i) Construct whole-genome microarrays for Desulfovibrio vulgaris; (ii) Determine optimal conditions for hybridization conditions; and (iii) Identify whole-genome expression patterns of D. vulgaris cells grown under metal-reducing conditions. Results: Recent studies have shown that the design characteristics of probes can significantly affect hybridization behavior, and therefore, possibly affect the dataset of genes with altered expression profiles. In order to experimentally establish the criteria for the design of gene-specific probes, an oligonucleotide array was constructed that contained perfect-match and mismatch probes. The effects of probe-target identity, continuous stretch, mismatch position, and hybridization free energy on specificity were examined. Second, in order to determine the effect of probe length on signal intensities, microarrays with different length probes were used to monitor gene expression. Based on the experimental results, a set of criteria were suggested for the design of gene-specific and group-specific probes, and these criteria should provide valuable information for the development of new software and algorithms for microarray-based studies.

The whole-genome microarrays of D. vulgaris were constructed using 70mer probes. Currently, growth conditions and medium are being evaluated for transcriptomic characterization with respect to growth phase and heavy metal responsive genes. The elucidation of growth-phase dependent gene expression is essential for a general understanding of growth physiology that is also crucial for data interpretation of stress-responsive genes (e.g., chromium). We recently cultivated D. vulgaris in a defined medium and sampled biomass over time for approximately 70 h to characterize the shifts in gene expression as cells transitioned from logarithmic phase growth to stationary phase. Each respective time point during exponential phase had a similar number of ORFs (7 to 9% of the genome) that were up-expressed (>3-fold) and approximately 5.5 to 6.0% of the ORFs were down-expressed (<3-fold). Also, a majority of the predicted ORFs did not display altered expression patterns when early- and late-exponential phases were compared. As the cells entered into early stationary phase, approximately 7% of the ORFs were up-expressed, whereas 3.5% to 4% of the genome was up-expressed as the cells experienced prolonged stationary-phase. Within the first hours of stationary-phase, up-expressed ORFs included proteases, chaperonins, permeases, and hypothetical proteins. Interestingly, preliminary comparisons suggest that many of the ORFs that were up-expressed in early stationary phase also had altered expression levels in response to other cellular stresses. Preliminary datasuggests that 0.05 mM Cr(VI) but not 0.01 mM Cr(VI) decreased growth in the defined medium with lactate and sulfate. In addition, D. vulgaris grew well in a defined, minimal medium designed to be analogous to FRC groundwater. We are presently analyzing microarray data to identify sub-sets of genes that respond to growth phase changes and/or stresses, as well as the determination of the optimal growth conditions in the presence of Cr(VI).

↓ NaCl↑ T5, T7, T8GGDEF domain protein208701^

↑ heat-shock↑ T9dcrA MAC-protein208703^

↑ NO2↑ T5, T8, T9sensory box/ HK208671^

↑ T6, T7, T8sensory box/ HK / RR207606^

↑ heat-shock↑ T5, T6, T9MAC protein207350^

↑ NO3↑ T6, T8RR206316 ↑ T6sensory box/ HK206146^

↑ T6 – T9sensory box/ HK209265*

↑ T6, T7sensory box/ HK / RR209192^

↑ T6, T7sensory box/ HK / RR209009^

↓ O2↓ T5, T6, T7σ54-dependent transcript. regulator207582^

↑ heat-shock↑ T6, T9sensory box protein 206995*

Additional ResponsesTime-Point ChangeORF DescriptionORF ID

Comparison of fold changes of 21 ORFs consistently detected by PCR amplicon (circles), 70mer (squares), 60mer (up triangles) and 50mer (down triangles) arrays when S. oneidensis MR-1 cells were exposed to pH 4 for 30 min. ORFs were up-regulated above the line y = 1.0 (solid), ORFs were down-regulated below the line y = -1.0 (middle dash), and ORFs were not changed between the two lines. Average number of genes detected among 96 ORFs selected

from Shewanella oneidensis MR-1 at an SNR >3.0. 500 ngof genomic DNA (A) or 10 µg of cDNA target RNA (B) was labeled with Cy-dyes and hybridized with this array. The data are represented as average with standard deviation of three slides (6 spots).

0 10 20 30 40 50 60 70 80

Helicobacter pylori J99Synechoccus 8102

Streptooccus agalactiae 2603V/RDeinococcus radiodurans

Clostridium acetobutlyicumBacillus subtilis

E. coli K-12Oceanbacillus

Bacteroides thetaiotaomicronBdellovibrio HD100

Streptomyces ceolicolor A32Archaeoglobus fulgidus

Vibrio vulnifericansRalstonia

Caulobacter CB15Shewanella oneidnesis

Pseudomonas aeruoginosaGeobacter metallireducnes

Desulfuromonas acetoxidansGeobacter sulfureducens

Desulfovibrio G20Desulfovibrio vulgaris

Number of Predicted ORFs with PAS domain

ZCBDNAClostridium acetobutylicumFliASEDNHVibrio choleraeFliASZCBDNHAPseudomonas aeruginosa PAO1FliASE1,2CBDN1,2HARalstonia solanacearum

SE1-6ZCBNH1, 2ASinorhizobium melilotiDFusobacterium nucleatum

CBNAChlorobium tepidum TLSDHCaulobacter crescentus CB15

SDBacteroides thetaiotaomicronDDeinococcus radiodurans

FliASEZCBDNHAShewanella oneidensis MR-1FliASEZCBDNHAEscherichia coli K-12

?EDNHDesulfuromonas acetoxidans?DNHDesulfotalea psychrophila

FliA?E1-2CBDNABdellovibrio bacteriovorus HD100FliA?ZCBD1, D2NHAGeobacter sulfureducens PCAFliA?ZCBDNHADesulfovibrio desulfuricans G20FliA?ZCBDNHADesulfovibrio vulgaris

28382416014070543240

10

100

1000

0

5

10

15

20

0 10 20 30 40 50 60 70

Cell Protein and Carbohydrate During Lactate and Sulfate Growth for D. vulgaris

Time (h)

10

100

0 10 20 30 40 50 60 70

Sampling Time Points for Transcriptomic Anlayses

Time (h)

T1

T2

T3

T4 T5

T6T7 T8 T9

D. vulgaris has a high number of predicted ORFs with PAS- and/or sensory domains

Occurrence of Predicted σ-Factors from a Range of Different GenomesThe D. vulgairs Genome Does Not Appear to Contain a Recognized σ38

0

50

100

150

200

250

300

T2 T3 T4 T5 T6 T7 T8 T9

Number of ORFs with Altered Expression at Each Respective Sampling Point

Up-ExpressedDown-Expressed

Time Points

ORFs with Predicted PAS-Domains that have Altered Expression Levels Between Exponential- and Stationary-Growth Phases

↑ NO2

↑ heat1.89 (z: 1.97)transport component of feoA 208071

↑ NO3

↑ cold↑ cold

1.94 (z: 1.61)metE, 5-methyltetrahydropteroyltri-E-hc-S-methyltransferase

208898

2.04 (z: 3.61)2.24 (z: 4.17)

flgM hypothetical protein

209462209463

2.12 (z: 2.91)hypothetical protein206409

↑ NO2

↑ NaCl2.07 (z: 2.61)hypothetical protein209052

2.07 (z: 2.48)fld; flavodoxin (Fe-repressed)208179

2.04 (z: 2.80)metK, S-adenosylmethioninesynthetase

207942

↑ NO3

↑ cold1.97 (z: 2.94)metF, 5,10-mth reductase206429

2.53 (z: 4.63)ahcY, adenosylhomocysteinase209551

↓ heat2.41 (z: 3.14)katA, catalase209629

↓ heat↓ NaCl↓ co-culture-CH4

2.47 (z: 2.95)hypothetical protein207938

↑ NO2

↑ heat2.70 (z: 2.63)hypothetical protein208070

↑ heat1.81 (z: 2.62)2.34 (z: 3.76)

carbon starvation protein A209542209543

2.30 (z: 4.44)flaB3, flagellin207937

↑ NO2

↓ heat2.36 (z: 3.08)hypothetical protein208964

↑ NO2

Putative FUR-box2.99 (z: 2.25)conserved hypothetical protein209207

↑ NO2

↑ O2

↑ heat↑ NaCl

3.36 (z: 2.75)hypothetical protein208180

↑ heat↑ NO2

↑ NaCl

4.83 (z: 6.02)3.96 (z: 3.55)

feoBfeoA

208068208069

Additional ResponsesChange ExpressionPredicted FunctionGene ID

Up-Expression T4 versus T1

↑ O2

↑ heat-2.39 (z: -4.06)lysA2

diaminopimelate dc208063

↑ heat-1.97 (z: -3.43)conserved hypothetical protein206094

↓ heat-0.54 to -2.0ribosomal proteins206743-206772

↓ heat-2.19 (z: -3.95)Na/A symporter 206150

Additional ResponsesChange ExpressionPredicted FunctionGene ID

Down-Expression T4 versus T1 2.11 to 2.50hypothetical proteins207638-207641

2.03 (z: 3.54)metK, S-adenosylmethionine syn

207942

2.19 (z: 2.02)conserved hypothetical (PO4/phosphonate)

209182

↑ NO3

↑ heat2.30 (z: 2.82universal stress protein2064652.27 (z: 3.15) sodB207901

2.97 (z: 4.32)isoamylase206369

2.50 (z: 4.28)putative, lipoprotein206808

↑ heat3.21 (z: 2.90)mviN, integral membrane protein

206613

3.22(z: 5.25)2.31 (z: 3.30

membrane proteins206982206983

↓ co-culture↓ NaCl

1.80 to 3.32presumptive phage proteins

209131-209137

3.25 (z: 2.12)carboxyl-terminal protease

207823

↑ NO3

↑ NaCl↑ heat↑ co-culture

3.22 (z: 2.86zraP,Zn-resistance208912

↑ heat3.65 (z: 2.45)hypothetical protein208851

1.20 to 3.51presumptive phage proteins

208370-208380

↑ O23.48 (z: 5.70)dsrC2082823.42 (z: 3.03)aa transport, putative206856

3.95 (z: 6.65)sugar transferase domain209685

3.89 (z: 7.29)integration host factor208486

↑ heat3.81 (z: 2.90)tail/DNA circulation protein

208364

3.76 (z: 2.50lysozyme2065643.70 (z: 2.86)hypothetical protein208791

↑ heat5.66 (z: 6.00)nhaC-2,Na/H antiporter

208626

5.02 (z: 7.00)polysaccharide deacetylase

209679

4.55 (z: 3.36)hypothetical protein207275

↑ NO3

↑ heat4.69 (z: 5.25)membrane protein208597

↑ NO3

↑ heat5.45 (z: 4.24)cold shock domain

protein207324

↑ NO34.11 (z: 2.35)dctM, dicarboxylatetransporter

208332

4.13 (z: 3.96)oxidoreductase208628

3.98 (z: 4.04)ADP-ribosylglycohydrolase

208807

↑ NO2

↑ heat↑ NaCl

4.05 (z: 3.49)2.47(z: 1.86)

feoAfeoB

208069208068

↑ NO3

↑ heat5.72 (z: 5.71)major facilitator 209625

↑ NO2

↑ heat↑ NaCl↑ co-culture

2.30 (z: 2.84)hspC, heat shock207934

Additional Responses

Change Expression

Predicted FunctionGene ID

Up-Expression T5 versus T1

Survey of Down-Expressed ORFs at T5 to T9Ribosomal Proteins and Translation: 6 SSU and 10 LSU proteins were down-expressed greater than 2-fold. These ribosomal proteins were also down-expressed in response to nitrate, nitrite, and heat. Other proteins associated with translation were also down-expressed: nusG, secE, EF-Ts, IF-1, and SecF.

Biosynthesis: ribose-P-pyrophosphokinase, RNA-binding protein, ACP-reductase, ACP-synthase, ribonuclease P, gycerol-P acyltransferase, and histone-acetylation.

Hypothetical and Conserved Hypotheticals: Many hypothetical or conserved hypothetical proteins were down-expressed and some were also down-expressed in response to heat, nitrite, and nitrate while others appeared to be unique to stationary-phase growth. Between 40 and 50% of the significantly down-expressed ORFs (T5-T9) were hypothetical or conserved hypothetical proteins.

Sulfate Permease: Three mono-cistronic permeases. Each displayed a different pattern of expression at T5: 208981 Up-expressed; 209213 Down-expressed; 207471 unchanged.

Ferritin: D. vulgaris has two predicted ferritin-like proteins: 206840 expression was unchanged at T5 but 207018 was down-expressed.

↑ heat2.44(z: 3.88)mviN, integral membrane protein

206613

↑ NO2

↑ heat↑ NaCl↑ co-culture

2.50 (z: 2.04)hspC, heat shock207934

↑ heat3.65 (z: 2.45)hypothetical protein208851

4.55 (z: 3.36)hypothetical protein207275

3.03 (z: 4.34)5-formyltetrahydrofolate cyclo-ligase

209300

2.94 (z: 1.69)GDP-mannose-4,6-dehydratase

209384

3.12 (z: 4.68)lysozyme206564

4.17 (z: 3.02)integration host factor208486

↑ NO3

↑ NaCl↑ heat↑ co-culture

3.19(z: 2.66)zraP,Zn-resistance208912

↑ NO2

↑ heat↑ NaCl↓ co-culture

3.44(z: 4.69)1.71(z: 2.09)

feoAfeoB

208069208068

↑ O23.85 (z: 6.29)dsrC208282

3.99 (z: 2.55) hypothetical protein207275

4.12 (z: 3.51)sensory box/ HK / RR209192

↓ heat3.80 (z: 2.16)ispD206898

3.66 (z: 3.66)TPR domain 208077

3.56 (z: 2.66)TonB domain 208316

↑ heat3.17 (z: 2.17)glucokinase206469

4.22 (z: 4.37) oxidoreductase208628

1.60 to 3.83presumptive phage proteins

208370-208380

↑ heat4.74 (z: 3.65nhaC-2,Na/H antiporter

208626

↑ NO3

↑ heat4.89(z: 7.23)major facilitator 209625

↑ NO3

↑ heat4.98 (z: 5.10)membrane protein208597

4.91 (z:2.96)hypothetical protein209014

2.04 to 4.45presumptive phage proteins

206552-206556

2.34 to 4.54presumptive phage proteins

209131-209137

3.27 to 4.25hypothetical proteins209138-209141

2.30 (z: 2.33)putative DNA repair209738

2.30 (z: 2.33)von Willebrand factor; Ankyrin

207604

↑ NO2

↑ heat5.76 (z: 6.87)cold shock domain

protein207324

3.25 (z: 2.12)carboxyl-terminal protease

207823

5.02 (z: 7.00)polysaccharide deacetylase

209679

2.48 (z: 3.28)glycosyl hydrolase209665

2.42 (z: 2.47)glnB-3 regulatory P-II209709

Additional Responses

Change Expression

Predicted FunctionGene ID

Up-Expression T6 versus T1

T7, T8, T8-2.04 (z:-3.40)plasmid stabilization system family

207508

T6, T7, T8, T9-2.29 (z: -2.19)fructose-1,6-bisphosphatase

207307

T5, T6, T7, T9-2.29 (z: -3.31)sulfate permease209213

T6, T9-2.21 (z: -3.12)vacJ lipoprotein, putative

206681

T5, T6, T7-2.55 (z: -2.16)peptidyl-prolyl cis-trans isomerase C

206915

T5, T6, T7-2.27 (z: -2.97)UDP-3-0-acyl N-acetylglucosaminedeacetylase

208427

T5, T6-2.67 (z: -2.73)3-dehydroquinate dehydratase (aromatic aa biosynthesis)

207124

T5, T6, T8-2.84 (z: -3.18)GGDEF (putative adenyl cyclase)

206371

T5, T6, T7, T8, T9-2.89 (z: -3.95)glycosyl transferase(LPS or EPS)

209502T6-2.94 (z: -3.28)L-lactate permease207771

T4, T5, T6-3.54 (z: -3.31)outer membrane protein P1

206699

T5, T6, T7, T8, T9-3.30 (z: -4.56) conserved hypothetical protein

208347208348

T5, T6, T7, T8, T9-3.52 (z: -5.41)Plasmid maintenance toxin

206956

Time-PointsRepresentative Values

Predicted FunctionGene ID

Down-Expression T5 to T9

T7, T92.57 (z: 2.82)transglycosylaseSLT domain protein

208200

T7, T8, T92.41 (z: 4.34)type III secretion system protein

209604

T7, T92.32 (z: 2.85)σ-54 dependent transcriptional regulator/ RR

209666

T7T7

2.67 (z: 2.92)3.01 (z: 2.16)

peptidaseoligopeptide ABC transporter

208072208073

T6, T72.47 (z: 3.22)sensory box/ HK/ RR

209009

T5, T6, T7, T8, T92.94 (z: 2.50)mviN, integral membrane protein

206613

T6, T7, T8, T93.23 (z: 2.75) putative DNA repair

209738

T5, T6, T7, T8, T93.68 (z: 4.35) presumptive phage proteins

208370-208380

T5, T6, T7, T8, T93.93 (z: 3.97)lysozyme206564

T6, T7, T83.93(z: 4.89)TPR domain 208077

T73.93 (z: 4.43)epimerase/dehydratase

207948

T73.81(z: 4.00)acetyltransferase, GNAT family

209191

T5, T7, T8, T94.68(z: 5.47)sugar transferasedomain

209685

T7, T8, T95.45 (z: 4.13)major facilitator 209625

T5, T6, T7, T8, T95.53 (z: 3.92nhaC-2,Na/H antiporter

208626

T7, T85.35 (z: 10.42)aminotransferase209678

T5, T6, T7, T85.31 (z: 9.37)polysaccharide deacetylase

209679

T6, T7, T8, T93.17 (z: 2.17)glucokinase206469

T7, T93.20 (z: 3.13)polysaccharide biosynthesis protein

209285

T7, T8, T93.45 (z: 1.79)GDP-mannose 4,6-dehydratase

209384

T4 – T91.83(z: 2.28)3.28(z: 3.69)

feoAfeoB

208069208068

T5, T6, T7, T92.95 (z: 2.61)zraP,Zn-resistance208912

T72.98(z: 2.50)aIF-2BI family209012

T5, T6, T7, T8, T96.36 (z: 7.09)cold shock domain protein

207324

Time-PointsChange Expression

Predicted Function

Gene ID

Up-Expression T5 to T9

Major Conclusions: