Literature DB >> 3132711

Extracellular control of spore formation in Bacillus subtilis.

A D Grossman1, R Losick.   

Abstract

Spore formation in the Gram-positive bacterium Bacillus subtilis has been classically viewed as an example of unicellular differentiation that occurs in response to nutritional starvation. We present evidence that B. subtilis produces an extracellular factor(s) that is required, in addition to starvation conditions, for efficient sporulation. This factor is secreted and accumulates in a cell density-dependent fashion such that cells at a low density sporulate poorly under conditions in which cells at a high density sporulate efficiently. Conditioned medium (sterile filtrate) from cells grown to a high density contains this extracellular differentiation factor (EDF-A) and stimulates spore formation of cells at low density under normal starvation conditions. EDF-A is heat-resistant, protease-sensitive, and dialyzable, indicating that it is at least in part an oligopeptide. Production of EDF-A is reduced or eliminated in spoOA and spoOB mutants, which are defective in many processes associated with the end of vegetative growth. Mutations in abrB, which suppress many of the pleiotropic phenotypes of spoOA mutants, restore production of EDF-A.

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Year:  1988        PMID: 3132711      PMCID: PMC280430          DOI: 10.1073/pnas.85.12.4369

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  24 in total

1.  Genetic analysis of Bacillus subtilis spo mutations generated by Tn917-mediated insertional mutagenesis.

Authors:  K Sandman; R Losick; P Youngman
Journal:  Genetics       Date:  1987-12       Impact factor: 4.562

2.  Cell interactions in myxobacterial growth and development.

Authors:  M Dworkin; D Kaiser
Journal:  Science       Date:  1985-10-04       Impact factor: 47.728

3.  Identification of the promoter for a spore coat protein gene in Bacillus subtilis and studies on the regulation of its induction at a late stage of sporulation.

Authors:  K Sandman; L Kroos; S Cutting; P Youngman; R Losick
Journal:  J Mol Biol       Date:  1988-04-05       Impact factor: 5.469

4.  Initiation of antibiotic production by the stringent response of Bacillus subtilis Marburg.

Authors:  K Ochi; S Ohsawa
Journal:  J Gen Microbiol       Date:  1984-10

5.  Enzyme changes during Bacillus subtilis sporulation caused by deprivation of guanine nucleotides.

Authors:  N Vasantha; E Freese
Journal:  J Bacteriol       Date:  1980-12       Impact factor: 3.490

Review 6.  Genetic transformation.

Authors:  H O Smith; D B Danner; R A Deich
Journal:  Annu Rev Biochem       Date:  1981       Impact factor: 23.643

Review 7.  The peptide antibiotics of Bacillus: chemistry, biogenesis, and possible functions.

Authors:  E Katz; A L Demain
Journal:  Bacteriol Rev       Date:  1977-06

8.  The role of manganese in growth and sporulation of Bacillus subtilis.

Authors:  N Vasantha; E Freese
Journal:  J Gen Microbiol       Date:  1979-06

9.  Commitment to sporulation in Bacillus subtilis and its relationship to development of actinomycin resistance.

Authors:  J M Sterlini; J Mandelstam
Journal:  Biochem J       Date:  1969-06       Impact factor: 3.857

10.  Regulation of expression of genes coding for small, acid-soluble proteins of Bacillus subtilis spores: studies using lacZ gene fusions.

Authors:  J M Mason; R H Hackett; P Setlow
Journal:  J Bacteriol       Date:  1988-01       Impact factor: 3.490

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  67 in total

1.  Providencia stuartii genes activated by cell-to-cell signaling and identification of a gene required for production or activity of an extracellular factor.

Authors:  P N Rather; X Ding; R R Baca-DeLancey; S Siddiqui
Journal:  J Bacteriol       Date:  1999-12       Impact factor: 3.490

Review 2.  Mob psychology.

Authors:  Stephen C Winans; Bonnie L Bassler
Journal:  J Bacteriol       Date:  2002-02       Impact factor: 3.490

3.  Control of a family of phosphatase regulatory genes (phr) by the alternate sigma factor sigma-H of Bacillus subtilis.

Authors:  R S McQuade; N Comella; A D Grossman
Journal:  J Bacteriol       Date:  2001-08       Impact factor: 3.490

4.  Global analysis of the general stress response of Bacillus subtilis.

Authors:  A Petersohn; M Brigulla; S Haas; J D Hoheisel; U Völker; M Hecker
Journal:  J Bacteriol       Date:  2001-10       Impact factor: 3.490

Review 5.  PAS domains: internal sensors of oxygen, redox potential, and light.

Authors:  B L Taylor; I B Zhulin
Journal:  Microbiol Mol Biol Rev       Date:  1999-06       Impact factor: 11.056

6.  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

7.  The extracytoplasmic function sigma factor SigY is important for efficient maintenance of the Spβ prophage that encodes sublancin in Bacillus subtilis.

Authors:  Rebecca Mendez; Alba Gutierrez; Jasmin Reyes; Leticia Márquez-Magaña
Journal:  DNA Cell Biol       Date:  2012-03-08       Impact factor: 3.311

8.  Novel roles of the master transcription factors Spo0A and sigmaB for survival and sporulation of Bacillus subtilis at low growth temperature.

Authors:  Marcelo B Méndez; Lelia M Orsaria; Valeria Philippe; María Eugenia Pedrido; Roberto R Grau
Journal:  J Bacteriol       Date:  2004-02       Impact factor: 3.490

9.  Differential action and differential expression of DNA polymerase I during Escherichia coli colony development.

Authors:  J A Shapiro
Journal:  J Bacteriol       Date:  1992-11       Impact factor: 3.490

10.  Effects of phosphorelay perturbations on architecture, sporulation, and spore resistance in biofilms of Bacillus subtilis.

Authors:  Jan-Willem Veening; Oscar P Kuipers; Stanley Brul; Klaas J Hellingwerf; Remco Kort
Journal:  J Bacteriol       Date:  2006-04       Impact factor: 3.490

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