| Volume 1* |
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xiii | |
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xiv | |
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xv | |
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1 | (2) |
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Section 2: Key overview chapters, |
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3 | (244) |
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2.1 Stress-induced changes in transcript stability, |
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5 | (4) |
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2.2 StressChip for monitoring microbial stress response in the environment, |
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9 | (14) |
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2.3 A revolutionary paradigm of bacterial genome regulation, |
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23 | (14) |
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2.4 Role of changes in a70-driven transcription in adaptation of E. coli to conditions of stress or starvation, |
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37 | (11) |
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2.5 The distribution and spatial organization of RNA polymerase in Escherichia coli: growth rate regulation and stress responses, |
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48 | (16) |
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2.6 The ECF classification: a phylogenetic reflection of the regulatory diversity in the extracytoplasmic function a factor protein family, |
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64 | (33) |
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2.7 Toxin-antitoxin systems in bacteria and archaea, |
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97 | (11) |
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2.8 Bacterial sRNAs: regulation in stress, |
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108 | (7) |
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Timofey S. Rozhdestvensky |
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2.9 Bacterial stress responses as determinants of antimicrobial resistance, |
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115 | (22) |
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2.10 Transposable elements: a toolkit for stress and environmental adaptation in bacteria, |
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137 | (9) |
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2.11 CRISPR-Cas system: a new paradigm for bacterial stress response through genome rearrangement, |
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146 | (15) |
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2.12 The copper metallome in prokaryotic cells, |
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161 | (13) |
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2.13 Ribonucleases as modulators of bacterial stress response, |
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174 | (11) |
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2.14 Double-strand-break repair, mutagenesis, and stress, |
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185 | (11) |
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Maria Angelica Bravo Nunez |
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2.15 Sigma factor competition in Escherichia coli: kinetic and thermodynamic perspectives, |
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196 | (7) |
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Kuldeepkumar Ramnaresh Gupta |
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2.16 Iron homeostasis and iron-sulfur cluster assembly in Escherichia coli, |
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203 | (12) |
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2.17 Mechanisms underlying the antimicrobial capacity of metals, |
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215 | (10) |
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2.18 Acyl-homoserine lactone-based quorum sensing in members of the marine bacterial Roseobacter Glade: complex cell-to-cell communication controls multiple physiologies, |
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225 | (9) |
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2.19 Native and synthetic gene regulation to nitrogen limitation stress, |
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234 | (13) |
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Section 3: One-, two-, and three-component regulatory systems and stress responses, |
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247 | (54) |
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3.1 Two-component systems that control the expression of aromatic hydrocarbon degradation pathways, |
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249 | (8) |
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3.2 Cross-talk of global regulators in Streptomyces, |
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257 | (11) |
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3.3 NO-H-NOX-regulated two-component signaling, |
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268 | (9) |
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3.4 The two-component CheY system in the chemotaxis of Sinorhizobium meliloti, |
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277 | (5) |
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3.5 Stimulus perception by histidine kinases, |
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282 | (19) |
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Section 4: Sigma factors and stress responses, |
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301 | (68) |
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4.1 The extracytoplasmic function sigma factor EcfO protects Bacteroides fragilis against oxidative stress, |
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303 | (8) |
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4.2 Regulation of energy metabolism by the extracytoplasmic function (ECF) a factors of Arcobacter butzleri, |
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311 | (10) |
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Irati Martinez-Malaxetxebarria |
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4.3 Extracytoplasmic function sigma factors and stress responses in Corynebacterium pseudotuberculosis, |
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321 | (7) |
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4.4 The complex roles and regulation of stress response a factors in Streptomyces coelicolor, |
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328 | (16) |
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4.5 Proteolytic activation of extra cytoplasmic function (ECF) a factors, |
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344 | (8) |
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4.6 The ECF family sigma factor aH in Corynebacterium glutamicum controls the thiol-oxidative stress response, |
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352 | (9) |
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4.7 Posttranslational regulation of antisigma factors of RpoE: a comparison between the Escherichia coli and Pseudomonas aeruginosa systems, |
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361 | (8) |
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Section 5: Small noncoding RNAs and stress responses, |
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369 | (54) |
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5.1 Bacterial small RNAs in mixed regulatory circuits, |
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371 | (12) |
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5.2 Role of small RNAs in Pseudomonas aeruginosa virulence and adaptation, |
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383 | (10) |
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5.3 Physiological effects of posttranscriptional regulation by the small RNA SgrS during metabolic stress in Escherichia coli, |
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393 | (9) |
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5.4 Three rpoS-activating small RNAs in pathways contributing to acid resistance of Escherichia coli, |
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402 | (10) |
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5.5 Thermal stress noncoding RNAs in prokaryotes and eukaryotes: a comparative approach, |
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412 | (11) |
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Jose Luis Martinez-Guitarte |
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Section 6: Toxin-antitoxin systems and stress responses, |
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423 | (56) |
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6.1 Epigenetics mediated by restriction modification systems, |
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425 | (12) |
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6.2 Toxin-antitoxin systems as regulators of bacterial fitness and virulence, |
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437 | (9) |
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6.3 Mechanisms of stress-activated persister formation in Escherichia coli, |
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446 | (8) |
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6.4 Identification and characterization of type II toxin-antitoxin systems in the opportunistic pathogen Acinetobacter baumannii, |
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454 | (9) |
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6.5 Transcriptional control of toxin-antitoxin expression: keeping toxins under wraps until the time is right, |
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463 | (10) |
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6.6 Opposite effects of GraT toxin on stress tolerance of Pseudomonas putida, |
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473 | (6) |
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Section 7: Stringent response to stress, |
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479 | (38) |
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7.1 Preferential cellular accumulation of ppGpp or pppGpp in Escherichia coli, |
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481 | (8) |
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7.2 Global Rsh-dependent transcription profile of Brucella suis during stringent response unravels adaptation to nutrient starvation and cross-talk with other stress responses, |
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489 | (11) |
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7.3 The stringent response and antioxidant defences in Pseudomonas aeruginosa, |
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500 | (7) |
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7.4 Molecular basis of the stringent response in Vibrio cholerae, |
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507 | (10) |
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Section 8: Responses to UV irradiation, |
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517 | (34) |
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8.1 UV stress-responsive genes associated with enterobacterial integrative conjugative elements of the ICE SXT/R391 group, |
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519 | (9) |
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8.2 Altered outer membrane proteins in response to UVC radiation in Vibrio parahaemolyticus and Vibrio alginolyticus, |
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528 | (4) |
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8.3 Ultraviolet-B radiation effects on the community, physiology, and mineralization of magnetotactic bacteria, |
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532 | (13) |
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8.4 Nucleotide excision repair system and gene expression in Mycobacterium smegmatis, |
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545 | (6) |
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Section 9: SOS and double stranded repair systems and stress, |
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551 | (36) |
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9.1 The SOS response modulates bacterial pathogenesis, |
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553 | (8) |
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9.2 RNAP secondary-channel interactors in Escherichia coli: makers and breakers of genome stability, |
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561 | (9) |
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9.3 How a large gene network couples mutagenic DNA break repair to stress in Escherichia coli, |
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570 | (7) |
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Maria Angelica Bravo Ntiriez |
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9.4 Double-strand DNA break repair in mycobacteria, |
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577 | (10) |
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Section 10: Adaptation to oxidative stress, |
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587 | (60) |
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10.1 Peroxide-sensing transcriptional regulators in bacteria, |
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589 | (14) |
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10.2 Regulation of oxidative stress-related genes implicated in the establishment of opportunistic infections by Bacteroides fragilis, |
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603 | (6) |
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Regina Maria Cavalcanti Pilotto Domingues |
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10.3 Investigation into oxidative stress response of Shewanella oneidensis reveals a distinct mechanism, |
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609 | (10) |
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10.4 An omics view on the response to singlet oxygen, |
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619 | (13) |
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10.5 Regulators of oxidative stress response genes in Escherichia coli and their conservation in bacteria, |
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632 | (6) |
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10.6 Hydrogen peroxide resistance in Bifidobacterium animalis subsp. lactis and Bifidobacterium longum, |
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638 | (9) |
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Section 11: Adaptation to osmotic stress, |
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647 | (46) |
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11.1 Interstrain variation in the physiological and transcriptional responses of Pseudomonas syringae to osmotic stress, |
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649 | (8) |
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11.2 Management of osmotic stress by Bacillus subtilis: genetics and physiology, |
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657 | (20) |
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11.3 Hyperosmotic response of Streptococcus mutans: from microscopic physiology to transcriptomic profile, |
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677 | (10) |
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11.4 Defective ribosome maturation or function makes Escherichia coli cells salt-resistant, |
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687 | (6) |
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Section 12: Dessication tolerance and drought stress, |
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693 | (44) |
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12.1 Consequences of elevated salt concentrations on expression profiles in the rhizobium S. meliloti 1021 likely involved in heat and desiccation stress, |
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695 | (14) |
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12.2 Genes involved in the formation of desiccation-resistant cysts in Azotobacter vinelandii, |
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709 | (7) |
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12.3 Osmotic and desiccation tolerance in Escherichia coli 0157:H7 and Salmonella enterica requires rp oS (e), |
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716 | (9) |
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12.4 Desiccation of Salmonella enterica induces cross-tolerance to other stresses, |
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725 | (12) |
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I1 | |
| Volume 2* |
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xiii | |
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xiv | |
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xv | |
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Section 13: Heat shock responses, |
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737 | (44) |
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13.1 Heat shock response in bacteria with large genomes: lessons from rhizobia, |
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739 | (8) |
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13.2 Small heat shock proteins in bacteria, |
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747 | (7) |
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13.3 Transcriptome analysis of bacterial response to heat shock using next-generation sequencing, |
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754 | (3) |
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13.4 Comparative analyses of bacterial transcriptome reorganisation in response to temperature increase, |
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757 | (9) |
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13.5 Participation of Ser—Thr protein kinases in regulation of heat stress responses in Synechocystis, |
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766 | (15) |
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Section 14: Chaperonins and stress, |
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781 | (46) |
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14.1 GroEL/ES chaperonin: unfolding and refolding reactions, |
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783 | (8) |
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14.2 Functional comparison between the DnaK chaperone systems of Streptococcus intermedius and Escherichia coli, |
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791 | (5) |
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14.3 Coevolution analysis illuminates the evolutionary plasticity of the chaperonin system GroES/L, |
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796 | (16) |
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14.4 C1pL ATPase: a novel chaperone in bacterial stress responses, |
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812 | (8) |
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14.5 Duplicated groEL genes in Myxococcus xanthus DK1622, |
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820 | (7) |
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Section 15: Cold shock responses, |
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827 | (70) |
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15.1 Gene regulation by cold shock proteins via transcription antitermination, |
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829 | (8) |
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15.2 Metagenomic analysis of microbial cold stress proteins in polar lacustrine ecosystems, |
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837 | (8) |
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15.3 Role of two-component systems in cold tolerance of Clostridium botulinum, |
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845 | (9) |
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15.4 Cold shock CspA protein production during periodic temperature cycling in Escherichia coli, |
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854 | (5) |
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15.5 Cold shock response in Escherichia coli: a model system to study posttranscriptional regulation, |
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859 | (14) |
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15.6 New insight into cold shock proteins: RNA-binding proteins involved in stress response and virulence, |
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873 | (8) |
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15.7 Light regulation of cold stress responses in Synechocystis, |
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881 | (9) |
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15.8 Escherichia coli cold shock gene profiles in response to overexpression or deletion of CsdA, RNase R, and PNPase and relevance to low-temperature RNA metabolism, |
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890 | (7) |
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Section 16: Adaptation to acid stress, |
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897 | (56) |
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16.1 Acid-adaptive responses of Streptococcus mutans, and mechanisms of integration with oxidative stress, |
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899 | (12) |
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16.2 Acid survival mechanisms in neutralophilic bacteria, |
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911 | (16) |
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16.3 Two-component systems in sensing and adapting to acid stress in Escherichia coli, |
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927 | (8) |
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16.4 Slr1909, a novel two-component response regulator involved in acid tolerance in Synechocystis sp. PCC 6803, |
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935 | (9) |
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16.5 Comparative mass spectrometry-based proteomics to elucidate the acid stress response in Lactobacillus plantarum, |
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944 | (9) |
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Section 17: Adaptation to nitrosative stress, |
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953 | (62) |
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17.1 Transcriptional regulation by thiol-based sensors of oxidative and nitrosative stress, |
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955 | (12) |
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17.2 Haemoglobins of Mycobacterium tuberculosis and their involvement in management of environmental stress, |
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967 | (9) |
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17.3 What is it about NO that you don't understand? The role of heme and HcpR in Porphyromonas gingivalis's response to nitrate (NO3), nitrite (NO2), and nitric oxide (NO), |
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976 | (13) |
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17.4 Di-iron RICs: players in nitrosative-oxidative stress defences, |
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989 | (8) |
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17.5 The Vibrio cholerae stress response: an elaborate system geared toward overcoming host defenses during infection, |
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997 | (12) |
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17.6 Ensemble modeling enables quantitative exploration of bacterial nitric oxide stress networks, |
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1009 | (6) |
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Section 18: Adaptation to cell envelope stress, |
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1015 | (50) |
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18.1 The Cpx inner membrane stress response, |
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1017 | (8) |
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18.2 New insights into stimulus detection and signal propagation by the Cpx-envelope stress system, |
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1025 | (6) |
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18.3 Promiscuous functions of cell envelope stress-sensing systems in Klebsiella pneumoniae and Acinetobacter baumannii, |
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1031 | (12) |
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Vijaya Bharathi Srinivasan |
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18.4 Influence of BrpA and Psr on cell envelope homeostasis and virulence of Streptococcus mutans, |
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1043 | (12) |
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18.5 Modulators of the bacterial two-component systems involved in envelope stress, transport, and virulence, |
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1055 | (10) |
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Section 19: Iron homeostasis, |
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1065 | (66) |
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19.1 Iron homeostasis and environmental responses in cyanobacteria: regulatory networks involving Fur, |
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1067 | (12) |
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19.2 Interplay between 02 and iron in gene expression: environmental sensing by FNR, ArcA, and Fur in bacteria, |
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1079 | (11) |
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19.3 The iron-sulfur cluster biosynthesis regulator IscR contributes to iron homeostasis and resistance to oxidants in Pseudomonas aeruginosa, |
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1090 | (13) |
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19.4 Transcriptional analysis of iron-responsive regulatory networks in Caulobacter crescentus, |
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1103 | (6) |
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19.5 Protein-protein interactions regulate the release of iron stored in bacterioferritin, |
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1109 | (9) |
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19.6 Protein dynamics and ion traffic in bacterioferritin function: a molecular dynamics simulation study on wild-type and mutant Pseudomonas aeruginosa BfrB, |
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1118 | (13) |
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Section 20: Metal resistance, |
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1131 | (64) |
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20.1 Nickel toxicity, regulation, and resistance in bacteria, |
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1133 | (12) |
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20.2 Metabolic networks to counter Al toxicity in Pseudomonas fluorescens: a holistic view, |
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1145 | (9) |
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20.3 Genomics of the resistance to metal and oxidative stresses in cyanobacteria, |
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1154 | (11) |
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20.4 Cross-species transcriptional network analysis reveals conservation and variation in response to metal stress in cyanobacteria, |
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1165 | (6) |
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20.5 The extracytoplasmic function sigma factor-mediated response to heavy metal stress in Caulobacter crescentus, |
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1171 | (13) |
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20.6 Metal ion toxicity and oxidative stress in Streptococcus pneumoniae, |
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1184 | (11) |
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Section 21: Quorum sensing, |
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1195 | (58) |
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21.1 Quorum sensing and bacterial social interactions in biofilms: bacterial cooperation and competition, |
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1197 | (9) |
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21.2 Recent advances in bacterial quorum quenching, |
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1206 | (15) |
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21.3 LuxR-type quorum-sensing regulators that are antagonized by cognate pheromones, |
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1221 | (11) |
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21.4 Adaptation to environmental stresses in Streptococcus mutans through the production of its quorum-sensing peptide pheromone, |
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1232 | (10) |
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21.5 Quorum sensing in Bacillus cereus in relation to cysteine metabolism and the oxidative stress response, |
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1242 | (11) |
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Section 22: Chemotaxis and biofilm formation, |
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1253 | (76) |
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22.1 The flagellum as a sensor, |
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1255 | (10) |
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22.2 Flagellar motility and fitness in xanthomonads, |
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1265 | (9) |
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22.3 Understanding Listeria monocytogenes biofilms: perspectives into mechanisms of adaptation and regulation under stress conditions, |
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1274 | (5) |
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Lizziane Kretli Winkelstroter |
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Fernanda Barbosa dos Reis-Teixeira |
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Elaine Cristina Pereira De Martinis |
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22.4 Biofilm formation and environmental signals in Bordetella, |
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1279 | (8) |
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22.5 Biofilm formation by rhizobacteria in response to water-limiting conditions, |
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1287 | (8) |
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22.6 Stress conditions triggering mucoid-to-nonmucoid morphotype variation in Burkholderia, and effects on virulence and biofilm formation, |
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1295 | (9) |
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22.7 Effect of environmental conditions present in the fishery industry on the biofilm-forming ability of Staphylococcus aureus, |
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1304 | (6) |
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22.8 Biofilm development and stress response in the cholera bacterium, |
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1310 | (12) |
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22.9 Outer membrane vesicle secretion: from envelope stress to biofilm formation, |
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1322 | (7) |
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Section 23: Viable but nonculturable (VBNC) cells, |
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1329 | |
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23.1 Resuscitation of Vibrios from the viable but nonculturable state is induced by quorum-sensing molecules, |
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1331 | (7) |
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23.2 Differential resuscitative effects of pyruvate and its analogs on VBNC (viable but nonculturable) Salmonella, |
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1338 | (8) |
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23.3 Environmental persistence of Shiga toxin-producing E. coli, |
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1346 | (8) |
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23.4 Of a tenacious and versatile relic: the role of inorganic polyphosphate (poly-P) metabolism in the survival, adaptation, and virulence of Campylobacter jejuni, |
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1354 | |
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I1 | |