Difference between revisions of "Paper"

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==Ute Wünn==
+
* strongly repressed in response to glucose starvation in M9 medium {{PubMed|23033921}}: [[hupA]] [[cycC]]  
<pubmed> 16855235 18487328 </pubmed>
 
und [http://onlinelibrary.wiley.com/doi/10.1002/pmic.201000812/pdf dieser Review]
 
  
==Ev Dannies==
+
==not yet in SubtiWiki==  
 +
<pubmed>31239381  31237868
 +
  31235516
 +
    31134210    31197963 31160399 31066113
 +
    31199835  31217292 </pubmed>
  
<pubmed> 20534550 20435731 </pubmed>
+
==POTM 2018==
 +
<pubmed>     </pubmed>
  
==Jan Gerwig==
+
== für Master-Seminar ==
 
+
<pubmed>   24529384    20431016    24097941    22773139    21127214</pubmed>
<pubmed>8811173 16761951 </pubmed>
 
 
 
==Leonie Rempeters==
 
 
 
<pubmed> 14981237 15522087 14991003 </pubmed>
 
 
 
+ Manuskript Newman et al.
 
 
 
==Stefanie Großhennig==
 
 
 
==not yet in SubtiWiki==
 
* [[trigger enzymes]] zu control of transcription factors (SW + Liste)
 
* Regulators of core metabolism alle auch zu transcription factors and their control (in Liste schon gemacht)
 
 
 
===sonst===
 
 
 
* [[xynP]] in Excel-Liste zu transporters/ other und membrane proteins
 
* [[yhfU]] in Excel-Liste zu transporters/ other
 
* [[xynB]] raus aus membrane proteins
 
* [[metA]], [[ytnA]], [[hprT]] raus aus cell envelope stress proteins
 
* [[bcaP]] zu utilization of amino acids
 
* [[yqaF]]-[[yqdA]]-[[yqaG]]-[[yqaH]]-[[yqaI]]-[[yqaJ]]-[[yqaK]]-[[yqaL]]-[[yqaM]]-[[yqaN]] zu SknR regulon
 
* [[sfp/2]] zu miscellaneous metabolic pathways, biofilm formation, biosynthesis of antibacterial compounds, pseudogenes
 

Latest revision as of 10:09, 6 April 2020

  • strongly repressed in response to glucose starvation in M9 medium PubMed: hupA cycC

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)

Björn Richts, Jonathan Rosenberg, Fabian M Commichau
##Title##
Front Mol Biosci: 2019, 6;32
[PubMed:31134210] [WorldCat.org] [DOI] (P e)

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)


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)