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Items: 1 to 50 of 88

1.

Cytochrome bcc-aa3 Oxidase Supercomplexes in the Aerobic Respiratory Chain of Streptomyces coelicolor A3(2).

Falke D, Fischer M, Biefel B, Ihling C, Hammerschmidt C, Reinefeld K, Haase A, Sinz A, Sawers RG.

J Mol Microbiol Biotechnol. 2019 Mar 12;28(6):255-268. doi: 10.1159/000496390. [Epub ahead of print]

PMID:
30861513
2.

Activity of Spore-Specific Respiratory Nitrate Reductase 1 of Streptomyces coelicolor A3(2) Requires a Functional Cytochrome bcc-aa 3 Oxidase Supercomplex.

Falke D, Biefel B, Haase A, Franke S, Fischer M, Sawers RG.

J Bacteriol. 2019 May 8;201(11). pii: e00104-19. doi: 10.1128/JB.00104-19. Print 2019 Jun 1.

PMID:
30858301
3.

Insights Into the Redox Sensitivity of Chloroflexi Hup-Hydrogenase Derived From Studies in Escherichia coli: Merits and Pitfalls of Heterologous [NiFe]-Hydrogenase Synthesis.

Dragomirova N, Rothe P, Schwoch S, Hartwig S, Pinske C, Sawers RG.

Front Microbiol. 2018 Nov 21;9:2837. doi: 10.3389/fmicb.2018.02837. eCollection 2018.

4.

The Extended C-Terminal α-Helix of the HypC Chaperone Restricts Recognition of Large Subunit Precursors by the Hyp-Scaffold Machinery during [NiFe]-Hydrogenase Maturation in Escherichia coli.

Thomas C, Waclawek M, Nutschan K, Pinske C, Sawers RG.

J Mol Microbiol Biotechnol. 2018;28(2):87-97. doi: 10.1159/000489929. Epub 2018 Jul 11.

5.

Cytochrome bd Oxidase Has an Important Role in Sustaining Growth and Development of Streptomyces coelicolor A3(2) under Oxygen-Limiting Conditions.

Fischer M, Falke D, Naujoks C, Sawers RG.

J Bacteriol. 2018 Jul 25;200(16). pii: e00239-18. doi: 10.1128/JB.00239-18. Print 2018 Aug 15.

6.

Organohalide respiratory chains: composition, topology and key enzymes.

Schubert T, Adrian L, Sawers RG, Diekert G.

FEMS Microbiol Ecol. 2018 Apr 1;94(4). doi: 10.1093/femsec/fiy035. Review.

PMID:
29718172
7.

o-Phthalate derived from plastics' plasticizers and a bacterium's solution to its anaerobic degradation.

Sawers RG.

Mol Microbiol. 2018 Jun;108(6):595-600. doi: 10.1111/mmi.13975. Epub 2018 May 9.

PMID:
29679505
8.

The C-terminal Six Amino Acids of the FNT Channel FocA Are Required for Formate Translocation But Not Homopentamer Integrity.

Hunger D, Röcker M, Falke D, Lilie H, Sawers RG.

Front Microbiol. 2017 Aug 22;8:1616. doi: 10.3389/fmicb.2017.01616. eCollection 2017.

9.

A H2 -oxidizing, 1,2,3-trichlorobenzene-reducing multienzyme complex isolated from the obligately organohalide-respiring bacterium Dehalococcoides mccartyi strain CBDB1.

Hartwig S, Dragomirova N, Kublik A, Türkowsky D, von Bergen M, Lechner U, Adrian L, Sawers RG.

Environ Microbiol Rep. 2017 Oct;9(5):618-625. doi: 10.1111/1758-2229.12560. Epub 2017 Jul 13.

PMID:
28631290
10.

Analysis of HypD Disulfide Redox Chemistry via Optimization of Fourier Transformed ac Voltammetric Data.

Adamson H, Robinson M, Bond PS, Soboh B, Gillow K, Simonov AN, Elton DM, Bond AM, Sawers RG, Gavaghan DJ, Parkin A.

Anal Chem. 2017 Feb 7;89(3):1565-1573. doi: 10.1021/acs.analchem.6b03589. Epub 2017 Jan 19.

11.

Dormancy: Illuminating How a Microbial Sleeping Beauty Awakens.

Sawers RG.

Curr Biol. 2016 Nov 7;26(21):R1139-R1141. doi: 10.1016/j.cub.2016.08.039.

12.

Anaerobic Formate and Hydrogen Metabolism.

Pinske C, Sawers RG.

EcoSal Plus. 2016 Oct;7(1). doi: 10.1128/ecosalplus.ESP-0011-2016. Review.

PMID:
27735784
13.

Phosphate and oxygen limitation induce respiratory nitrate reductase 3 synthesis in stationary-phase mycelium of Streptomyces coelicolor A3(2).

Falke D, Fischer M, Sawers RG.

Microbiology. 2016 Sep;162(9):1689-1697. doi: 10.1099/mic.0.000349. Epub 2016 Aug 5.

PMID:
27499000
14.

Oxygen and Nitrate Respiration in Streptomyces coelicolor A3(2).

Sawers RG, Falke D, Fischer M.

Adv Microb Physiol. 2016;68:1-40. doi: 10.1016/bs.ampbs.2016.02.004. Epub 2016 Mar 10. Review.

PMID:
27134020
15.

The glycyl-radical enzyme 2-ketobutyrate formate-lyase, TdcE, interacts specifically with the formate-translocating FNT-channel protein FocA.

Falke D, Doberenz C, Hunger D, Sawers RG.

Biochem Biophys Rep. 2016 Apr 16;6:185-189. doi: 10.1016/j.bbrep.2016.04.005. eCollection 2016 Jul.

16.

Little red floaters: gas vesicles in an enterobacterium.

Sawers RG.

Environ Microbiol. 2016 Apr;18(4):1091-3. doi: 10.1111/1462-2920.13245. Epub 2016 Mar 17. No abstract available.

PMID:
26992018
17.

Identification of a multi-protein reductive dehalogenase complex in Dehalococcoides mccartyi strain CBDB1 suggests a protein-dependent respiratory electron transport chain obviating quinone involvement.

Kublik A, Deobald D, Hartwig S, Schiffmann CL, Andrades A, von Bergen M, Sawers RG, Adrian L.

Environ Microbiol. 2016 Sep;18(9):3044-56. doi: 10.1111/1462-2920.13200. Epub 2016 Feb 16.

PMID:
26718631
18.

Heterologous complementation studies in Escherichia coli with the Hyp accessory protein machinery from Chloroflexi provide insight into [NiFe]-hydrogenase large subunit recognition by the HypC protein family.

Hartwig S, Thomas C, Krumova N, Quitzke V, Türkowsky D, Jehmlich N, Adrian L, Sawers RG.

Microbiology. 2015 Nov;161(11):2204-19. doi: 10.1099/mic.0.000177. Epub 2015 Sep 11.

PMID:
26364315
19.

Identification of an Isothiocyanate on the HypEF Complex Suggests a Route for Efficient Cyanyl-Group Channeling during [NiFe]-Hydrogenase Cofactor Generation.

Stripp ST, Lindenstrauss U, Sawers RG, Soboh B.

PLoS One. 2015 Jul 17;10(7):e0133118. doi: 10.1371/journal.pone.0133118. eCollection 2015.

20.

Coordination of Synthesis and Assembly of a Modular Membrane-Associated [NiFe]-Hydrogenase Is Determined by Cleavage of the C-Terminal Peptide.

Thomas C, Muhr E, Sawers RG.

J Bacteriol. 2015 Sep;197(18):2989-98. doi: 10.1128/JB.00437-15. Epub 2015 Jul 13.

21.

Chromogenic assessment of the three molybdo-selenoprotein formate dehydrogenases in Escherichia coli.

Hartwig S, Pinske C, Sawers RG.

Biochem Biophys Rep. 2015 Mar 30;1:62-67. doi: 10.1016/j.bbrep.2015.03.006. eCollection 2015 May.

22.

SlyD-dependent nickel delivery limits maturation of [NiFe]-hydrogenases in late-stationary phase Escherichia coli cells.

Pinske C, Sargent F, Sawers RG.

Metallomics. 2015 Apr;7(4):683-90. doi: 10.1039/c5mt00019j.

PMID:
25620052
23.

Of mothballs and old yellow enzymes.

Sawers RG.

Mol Microbiol. 2015 Jan;95(2):157-61. doi: 10.1111/mmi.12874. Epub 2014 Dec 19.

24.

The importance of iron in the biosynthesis and assembly of [NiFe]-hydrogenases.

Pinske C, Sawers RG.

Biomol Concepts. 2014 Mar;5(1):55-70. doi: 10.1515/bmc-2014-0001. Review.

PMID:
25372742
25.

Physiology and bioenergetics of [NiFe]-hydrogenase 2-catalyzed H2-consuming and H2-producing reactions in Escherichia coli.

Pinske C, Jaroschinsky M, Linek S, Kelly CL, Sargent F, Sawers RG.

J Bacteriol. 2015 Jan;197(2):296-306. doi: 10.1128/JB.02335-14. Epub 2014 Nov 3.

26.

Mapping cell envelope and periplasm protein interactions of Escherichia coli respiratory formate dehydrogenases by chemical cross-linking and mass spectrometry.

Zorn M, Ihling CH, Golbik R, Sawers RG, Sinz A.

J Proteome Res. 2014 Dec 5;13(12):5524-35. doi: 10.1021/pr5004906. Epub 2014 Oct 3.

PMID:
25251153
27.

Oxygen-dependent control of respiratory nitrate reduction in mycelium of Streptomyces coelicolor A3(2).

Fischer M, Falke D, Pawlik T, Sawers RG.

J Bacteriol. 2014 Dec;196(23):4152-62. doi: 10.1128/JB.02202-14. Epub 2014 Sep 15.

28.

The influence of oxygen on [NiFe]-hydrogenase cofactor biosynthesis and how ligation of carbon monoxide precedes cyanation.

Stripp ST, Lindenstrauss U, Granich C, Sawers RG, Soboh B.

PLoS One. 2014 Sep 11;9(9):e107488. doi: 10.1371/journal.pone.0107488. eCollection 2014.

29.

Pyruvate formate-lyase interacts directly with the formate channel FocA to regulate formate translocation.

Doberenz C, Zorn M, Falke D, Nannemann D, Hunger D, Beyer L, Ihling CH, Meiler J, Sinz A, Sawers RG.

J Mol Biol. 2014 Jul 29;426(15):2827-39. doi: 10.1016/j.jmb.2014.05.023. Epub 2014 Jun 2.

30.

Identification of key residues in the formate channel FocA that control import and export of formate.

Hunger D, Doberenz C, Sawers RG.

Biol Chem. 2014 Jul;395(7-8):813-25. doi: 10.1515/hsz-2014-0154.

PMID:
24659605
31.

Hydrogen-oxidizing hydrogenases 1 and 2 of Escherichia coli regulate the onset of hydrogen evolution and ATPase activity, respectively, during glucose fermentation at alkaline pH.

Poladyan A, Trchounian K, Sawers RG, Trchounian A.

FEMS Microbiol Lett. 2013 Nov;348(2):143-8. doi: 10.1111/1574-6968.12281. Epub 2013 Oct 10.

32.

A respiratory nitrate reductase active exclusively in resting spores of the obligate aerobe Streptomyces coelicolor A3(2).

Fischer M, Falke D, Sawers RG.

Mol Microbiol. 2013 Sep;89(6):1259-73. doi: 10.1111/mmi.12344. Epub 2013 Aug 14.

33.

The [NiFe]-hydrogenase accessory chaperones HypC and HybG of Escherichia coli are iron- and carbon dioxide-binding proteins.

Soboh B, Stripp ST, Bielak C, Lindenstrauß U, Braussemann M, Javaid M, Hallensleben M, Granich C, Herzberg M, Heberle J, Sawers RG.

FEBS Lett. 2013 Aug 19;587(16):2512-6. doi: 10.1016/j.febslet.2013.06.055. Epub 2013 Jul 10.

34.

A universally applicable and rapid method for measuring the growth of streptomyces and other filamentous microorganisms by methylene blue adsorption-desorption.

Fischer M, Sawers RG.

Appl Environ Microbiol. 2013 Jul;79(14):4499-502. doi: 10.1128/AEM.00778-13. Epub 2013 May 10.

35.

Selective selC-independent selenocysteine incorporation into formate dehydrogenases.

Zorn M, Ihling CH, Golbik R, Sawers RG, Sinz A.

PLoS One. 2013 Apr 25;8(4):e61913. doi: 10.1371/journal.pone.0061913. Print 2013.

36.

HypD is the scaffold protein for Fe-(CN)2CO cofactor assembly in [NiFe]-hydrogenase maturation.

Stripp ST, Soboh B, Lindenstrauss U, Braussemann M, Herzberg M, Nies DH, Sawers RG, Heberle J.

Biochemistry. 2013 May 14;52(19):3289-96. doi: 10.1021/bi400302v. Epub 2013 May 2.

PMID:
23597401
37.

Levels of control exerted by the Isc iron-sulfur cluster system on biosynthesis of the formate hydrogenlyase complex.

Pinske C, Jaroschinsky M, Sawers RG.

Microbiology. 2013 Jun;159(Pt 6):1179-89. doi: 10.1099/mic.0.066142-0. Epub 2013 Apr 4.

PMID:
23558265
38.

Staphylococcus aureus and Pseudomonas aeruginosa express and secrete human surfactant proteins.

Bräuer L, Schicht M, Worlitzsch D, Bensel T, Sawers RG, Paulsen F.

PLoS One. 2013;8(1):e53705. doi: 10.1371/journal.pone.0053705. Epub 2013 Jan 22.

39.

Coordination of FocA and pyruvate formate-lyase synthesis in Escherichia coli demonstrates preferential translocation of formate over other mixed-acid fermentation products.

Beyer L, Doberenz C, Falke D, Hunger D, Suppmann B, Sawers RG.

J Bacteriol. 2013 Apr;195(7):1428-35. doi: 10.1128/JB.02166-12. Epub 2013 Jan 18.

40.

Contribution of hydrogenase 2 to stationary phase H2 production by Escherichia coli during fermentation of glycerol.

Trchounian K, Soboh B, Sawers RG, Trchounian A.

Cell Biochem Biophys. 2013 May;66(1):103-8. doi: 10.1007/s12013-012-9458-7.

PMID:
23090790
41.

Evidence for an oxygen-sensitive iron-sulfur cluster in an immature large subunit species of Escherichia coli [NiFe]-hydrogenase 2.

Soboh B, Kuhns M, Braussemann M, Waclawek M, Muhr E, Pierik AJ, Sawers RG.

Biochem Biophys Res Commun. 2012 Jul 20;424(1):158-63. doi: 10.1016/j.bbrc.2012.06.096. Epub 2012 Jun 23.

PMID:
22735263
42.

Terminal reduction reactions of nitrate and sulfate assimilation in Streptomyces coelicolor A3(2): identification of genes encoding nitrite and sulfite reductases.

Fischer M, Schmidt C, Falke D, Sawers RG.

Res Microbiol. 2012 Jun;163(5):340-8. doi: 10.1016/j.resmic.2012.05.004. Epub 2012 Jun 1.

PMID:
22659143
43.

Aconitase B is required for optimal growth of Xanthomonas campestris pv. vesicatoria in pepper plants.

Kirchberg J, Büttner D, Thiemer B, Sawers RG.

PLoS One. 2012;7(4):e34941. doi: 10.1371/journal.pone.0034941. Epub 2012 Apr 6.

44.
45.

Analysis of hydrogenase 1 levels reveals an intimate link between carbon and hydrogen metabolism in Escherichia coli K-12.

Pinske C, McDowall JS, Sargent F, Sawers RG.

Microbiology. 2012 Mar;158(Pt 3):856-68. doi: 10.1099/mic.0.056622-0. Epub 2012 Jan 12.

PMID:
22241049
46.

Structure of hydrogenase maturation protein HypF with reaction intermediates shows two active sites.

Petkun S, Shi R, Li Y, Asinas A, Munger C, Zhang L, Waclawek M, Soboh B, Sawers RG, Cygler M.

Structure. 2011 Dec 7;19(12):1773-83. doi: 10.1016/j.str.2011.09.023.

47.

Characterization of Escherichia coli [NiFe]-hydrogenase distribution during fermentative growth at different pHs.

Trchounian K, Pinske C, Sawers RG, Trchounian A.

Cell Biochem Biophys. 2012 Apr;62(3):433-40. doi: 10.1007/s12013-011-9325-y.

PMID:
22095389
48.

A-type carrier protein ErpA is essential for formation of an active formate-nitrate respiratory pathway in Escherichia coli K-12.

Pinske C, Sawers RG.

J Bacteriol. 2012 Jan;194(2):346-53. doi: 10.1128/JB.06024-11. Epub 2011 Nov 11.

49.

Dependence on the F0F1-ATP synthase for the activities of the hydrogen-oxidizing hydrogenases 1 and 2 during glucose and glycerol fermentation at high and low pH in Escherichia coli.

Trchounian K, Pinske C, Sawers RG, Trchounian A.

J Bioenerg Biomembr. 2011 Dec;43(6):645-50. doi: 10.1007/s10863-011-9397-9. Epub 2011 Nov 12.

PMID:
22081210
50.

Metabolic deficiences revealed in the biotechnologically important model bacterium Escherichia coli BL21(DE3).

Pinske C, Bönn M, Krüger S, Lindenstrauss U, Sawers RG.

PLoS One. 2011;6(8):e22830. doi: 10.1371/journal.pone.0022830. Epub 2011 Aug 3.

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