Difference between revisions of "Paper"
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==POTM 2018== | ==POTM 2018== |
Revision as of 16:38, 12 July 2019
not yet in SubtiWiki
Nikolai P Radzinski, Marina Besprozvannaya, Eric L McLean, Anusha Talwalkar, Briana M Burton
DNA-Membrane Anchor Facilitates Efficient Chromosome Translocation at a Distance in Bacillus subtilis.
mBio: 2019, 10(3);
[PubMed:31239381]
[WorldCat.org]
[DOI]
(I e)
Katherine R Hummels, Daniel B Kearns
Suppressor mutations in ribosomal proteins and FliY restore Bacillus subtilis swarming motility in the absence of EF-P.
PLoS Genet: 2019, 15(6);e1008179
[PubMed:31237868]
[WorldCat.org]
[DOI]
(I e)
Bentley Shuster, Mark Khemmani, Yusei Nakaya, Gudrun Holland, Keito Iwamoto, Kimihiro Abe, Daisuke Imamura, Nina Maryn, Adam Driks, Tsutomu Sato, Patrick Eichenberger
Expansion of the Spore Surface Polysaccharide Layer in Bacillus subtilis by Deletion of Genes Encoding Glycosyltransferases and Glucose Modification Enzymes.
J Bacteriol: 2019, 201(19);
[PubMed:31235516]
[WorldCat.org]
[DOI]
(I e)
Sofia Arnaouteli, D A Matoz-Fernandez, Michael Porter, Margarita Kalamara, James Abbott, Cait E MacPhee, Fordyce A Davidson, Nicola R Stanley-Wall
##Title##
Proc Natl Acad Sci U S A: 2019, 116(27);13553-13562
[PubMed:31217292]
[WorldCat.org]
[DOI]
(I p)
Cameron V Sayer, Bidisha Barat, David L Popham
Identification of L-Valine-initiated-germination-active genes in Bacillus subtilis using Tn-seq.
PLoS One: 2019, 14(6);e0218220
[PubMed:31199835]
[WorldCat.org]
[DOI]
(I e)
Seoungjun Lee, Ling Juan Wu, Jeff Errington
Microfluidic time-lapse analysis and reevaluation of the Bacillus subtilis cell cycle.
Microbiologyopen: 2019, 8(10);e876
[PubMed:31197963]
[WorldCat.org]
[DOI]
(I p)
Emily E Brown, Allyssa K Miller, Inna V Krieger, Ryan M Otto, James C Sacchettini, Jennifer K Herman
##Title##
J Bacteriol: 2019, 201(16);
[PubMed:31160399]
[WorldCat.org]
[DOI]
(I e)
Cordelia A Weiss, Jakob A Hoberg, Kuanqing Liu, Benjamin P Tu, Wade C Winkler
Single-Cell Microscopy Reveals That Levels of Cyclic di-GMP Vary among Bacillus subtilis Subpopulations.
J Bacteriol: 2019, 201(16);
[PubMed:31138629]
[WorldCat.org]
[DOI]
(I e)
Björn Richts, Jonathan Rosenberg, Fabian M Commichau
##Title##
Front Mol Biosci: 2019, 6;32
[PubMed:31134210]
[WorldCat.org]
[DOI]
(P e)
Michael F Dion, Mrinal Kapoor, Yingjie Sun, Sean Wilson, Joel Ryan, Antoine Vigouroux, Sven van Teeffelen, Rudolf Oldenbourg, Ethan C Garner
Bacillus subtilis cell diameter is determined by the opposing actions of two distinct cell wall synthetic systems.
Nat Microbiol: 2019, 4(8);1294-1305
[PubMed:31086310]
[WorldCat.org]
[DOI]
(I p)
Natalí B Rasetto, Antonela Lavatelli, Natalia Martin, María Cecilia Mansilla
Unravelling the lipoyl-relay of exogenous lipoate utilization in Bacillus subtilis.
Mol Microbiol: 2019, 112(1);302-316
[PubMed:31066113]
[WorldCat.org]
[DOI]
(I p)
Aude Trinquier, Jonathan E Ulmer, Laetitia Gilet, Sabine Figaro, Philippe Hammann, Lauriane Kuhn, Frédérique Braun, Ciarán Condon
tRNA Maturation Defects Lead to Inhibition of rRNA Processing via Synthesis of pppGpp.
Mol Cell: 2019, 74(6);1227-1238.e3
[PubMed:31003868]
[WorldCat.org]
[DOI]
(I p)
Takahiro Seki, Takuya Furumi, Michihiro Hashimoto, Hiroshi Hara, Satoshi Matsuoka
Activation of extracytoplasmic function sigma factors upon removal of glucolipids and reduction of phosphatidylglycerol content in Bacillus subtilis cells lacking lipoteichoic acid.
Genes Genet Syst: 2019, 94(2);71-80
[PubMed:30971625]
[WorldCat.org]
[DOI]
(I p)
Daniel F Rojas-Tapias, John D Helmann
Identification of Novel Spx Regulatory Pathways in Bacillus subtilis Uncovers a Close Relationship between the CtsR and Spx Regulons.
J Bacteriol: 2019, 201(13);
[PubMed:30962353]
[WorldCat.org]
[DOI]
(I e)
Saurabh Bhattacharya, Amit K Baidya, Ritesh Ranjan Pal, Gideon Mamou, Yair E Gatt, Hanah Margalit, Ilan Rosenshine, Sigal Ben-Yehuda
A Ubiquitous Platform for Bacterial Nanotube Biogenesis.
Cell Rep: 2019, 27(2);334-342.e10
[PubMed:30929979]
[WorldCat.org]
[DOI]
(I p)
POTM 2018
für Master-Seminar
Laura Hobley, Sok Ho Kim, Yukari Maezato, Susan Wyllie, Alan H Fairlamb, Nicola R Stanley-Wall, Anthony J Michael
Norspermidine is not a self-produced trigger for biofilm disassembly.
Cell: 2014, 156(4);844-54
[PubMed:24529384]
[WorldCat.org]
[DOI]
(I p)
Sara A Leiman, Janine M May, Matthew D Lebar, Daniel Kahne, Roberto Kolter, Richard Losick
D-amino acids indirectly inhibit biofilm formation in Bacillus subtilis by interfering with protein synthesis.
J Bacteriol: 2013, 195(23);5391-5
[PubMed:24097941]
[WorldCat.org]
[DOI]
(I p)
Tobias J Erb, Patrick Kiefer, Bodo Hattendorf, Detlef Günther, Julia A Vorholt
GFAJ-1 is an arsenate-resistant, phosphate-dependent organism.
Science: 2012, 337(6093);467-70
[PubMed:22773139]
[WorldCat.org]
[DOI]
(I p)
Felisa Wolfe-Simon, Jodi Switzer Blum, Thomas R Kulp, Gwyneth W Gordon, Shelley E Hoeft, Jennifer Pett-Ridge, John F Stolz, Samuel M Webb, Peter K Weber, Paul C W Davies, Ariel D Anbar, Ronald S Oremland
A bacterium that can grow by using arsenic instead of phosphorus.
Science: 2011, 332(6034);1163-6
[PubMed:21127214]
[WorldCat.org]
[DOI]
(I p)
Ilana Kolodkin-Gal, Diego Romero, Shugeng Cao, Jon Clardy, Roberto Kolter, Richard Losick
D-amino acids trigger biofilm disassembly.
Science: 2010, 328(5978);627-9
[PubMed:20431016]
[WorldCat.org]
[DOI]
(I p)