Literature DB >> 114234

The decrease of guanine nucleotides initiates sporulation of Bacillus subtilis.

J M Lopez, C L Marks, E Freese.   

Abstract

Massive sporulation of Bacillus subtilis normally begins when carbon, nitrogen or phosphorus sources able to support rapid growth are no longer available. Sporulation can also be induced in exponentially growing cultures, in the presence of rapidly utilizable ammonia, glucose and phosphate if growth is partially but not completely inhibited either by inhibitors of nucleotide synthesis (hadacidin, decoyinine or 6-azauracil) or by purine deprivation in purine and especially in guanine auxotrophs. All these conditions allowing sporulation result in a decrease in the intracellular concentration of guanosine di- and tri-phosphates and usually uridine di- and triphosphates while other nucleotides decrease in some but increase in other cases. A decrease of uracil nucleotides alone, in a uracil auxotroph, does not produce massive sporulation. Our results demonstrate that the partial reduction of a guanine nucleotide, probably relative to some other compound, suffices to initiate sporulation. This reduction may always play a decisive role in the initiation of sporulation, as we have observed it under all conditions so far known to produce massive sporulation.

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Year:  1979        PMID: 114234     DOI: 10.1016/0304-4165(79)90357-x

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  64 in total

1.  Analysis of tnrA alleles which result in a glucose-resistant sporulation phenotype in Bacillus subtilis.

Authors:  B S Shin; S K Choi; I Smith; S H Park
Journal:  J Bacteriol       Date:  2000-09       Impact factor: 3.490

2.  Bacillus subtilis functional genomics: global characterization of the stringent response by proteome and transcriptome analysis.

Authors:  Christine Eymann; Georg Homuth; Christian Scharf; Michael Hecker
Journal:  J Bacteriol       Date:  2002-05       Impact factor: 3.490

3.  Additional targets of the Bacillus subtilis global regulator CodY identified by chromatin immunoprecipitation and genome-wide transcript analysis.

Authors:  Virginie Molle; Yoshiko Nakaura; Robert P Shivers; Hirotake Yamaguchi; Richard Losick; Yasutaro Fujita; Abraham L Sonenshein
Journal:  J Bacteriol       Date:  2003-03       Impact factor: 3.490

4.  Complex regulation of the Bacillus subtilis aconitase gene.

Authors:  Hyun-Jin Kim; Sam-In Kim; Manoja Ratnayake-Lecamwasam; Kiyoshi Tachikawa; Abraham L Sonenshein; Mark Strauch
Journal:  J Bacteriol       Date:  2003-03       Impact factor: 3.490

5.  RelA protein is involved in induction of genetic competence in certain Bacillus subtilis strains by moderating the level of intracellular GTP.

Authors:  Takashi Inaoka; Kozo Ochi
Journal:  J Bacteriol       Date:  2002-07       Impact factor: 3.490

6.  Transcriptional regulation of Bacillus subtilis glucose starvation-inducible genes: control of gsiA by the ComP-ComA signal transduction system.

Authors:  J P Mueller; G Bukusoglu; A L Sonenshein
Journal:  J Bacteriol       Date:  1992-07       Impact factor: 3.490

7.  Biochemical characterization of ribosome assembly GTPase RbgA in Bacillus subtilis.

Authors:  David Achila; Megha Gulati; Nikhil Jain; Robert A Britton
Journal:  J Biol Chem       Date:  2012-01-20       Impact factor: 5.157

Review 8.  ppGpp conjures bacterial virulence.

Authors:  Zachary D Dalebroux; Sarah L Svensson; Erin C Gaynor; Michele S Swanson
Journal:  Microbiol Mol Biol Rev       Date:  2010-06       Impact factor: 11.056

9.  Environmental dependence of stationary-phase metabolism in Bacillus subtilis and Escherichia coli.

Authors:  Victor Chubukov; Uwe Sauer
Journal:  Appl Environ Microbiol       Date:  2014-02-28       Impact factor: 4.792

10.  Interaction of Bacillus subtilis CodY with GTP.

Authors:  Luke D Handke; Robert P Shivers; Abraham L Sonenshein
Journal:  J Bacteriol       Date:  2007-11-09       Impact factor: 3.490

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