Literature DB >> 4199504

Phenotypes of pleiotropic-negative sporulation mutants of Bacillus subtilis.

S P Brehm, S P Staal, J A Hoch.   

Abstract

The phenotypic properties of representatives of the five genetic classes of pleiotropic-negative sporulation mutants have been investigated. Protease production, alkaline and neutral proteases, was curtailed in spoA mutants, but the remainder of mutant classes produced both proteases, albeit at reduced levels. The spoA and spoB mutants plaqued phi2 and phi15 at high efficiency, but the efficiency of plating of these phages on spoE, spoF, and spoH mutants was drastically reduced. Antibiotic was produced by the spoH mutants and to a degree by some spoF mutants, but the other classes did not produce detectable activity. The spoA mutants were less responsive to catabolite repression of histidase synthesis by glucose than was the wild type. Severe catabolite repression could be induced in spoA mutants by amino acid limitation, suggesting that the relaxation of catabolite repression observed is not due to a defect in the mechanism of catabolite repression. Although others have shown a perturbation in cytochrome regulation in spoA and spoB mutants, the primary dehydrogenases, succinate dehydrogenase and reduced nicotinamide adenine dinucleotide dehydrogenase, leading to these cytochromes are unimpaired in all mutant classes. A comparison of the structural components of cell walls and membranes of spoA and the wild type is made. The pleiotropic phenotypes of these mutants are discussed.

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Year:  1973        PMID: 4199504      PMCID: PMC246354          DOI: 10.1128/jb.115.3.1063-1070.1973

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  22 in total

1.  THE SEPARATION OF SIMPLE SUGARS BY CELLULOSE THIN-LAYER CHROMATOGRAPHY.

Authors:  D W VOMHOF; T C TUCKER
Journal:  J Chromatogr       Date:  1965-02

2.  Reconstitution of succinate-coenzyme Q reductase (complex II) and succinate oxidase activities by a highly purified, reactivated succinate dehydrogenase.

Authors:  M L Baginsky; Y Hatefi
Journal:  J Biol Chem       Date:  1969-10-10       Impact factor: 5.157

Review 3.  Unique biochemical events in bacterial sporulation.

Authors:  R S Hanson; J A Peterson; A A Yousten
Journal:  Annu Rev Microbiol       Date:  1970       Impact factor: 15.500

Review 4.  Sporulation and the production of antibiotics, exoenzymes, and exotonins.

Authors:  P Schaeffer
Journal:  Bacteriol Rev       Date:  1969-03

5.  Induction and repression of the histidine-degrading enzymes of Bacillus subtilis.

Authors:  L A Chasin; B Magasanik
Journal:  J Biol Chem       Date:  1968-10-10       Impact factor: 5.157

6.  The teichoic acid from the walls of Lactobacillus buchneri N.C.I.B. 8007.

Authors:  N Shaw; J Baddiley
Journal:  Biochem J       Date:  1964-11       Impact factor: 3.857

7.  Genetic analysis of pleiotropic negative sporulation mutants in Bacillus subtilis.

Authors:  J A Hoch
Journal:  J Bacteriol       Date:  1971-03       Impact factor: 3.490

8.  Characterization of proteinases excreted by Bacillus subtilis Marburg strain during sporulation.

Authors:  J Millet
Journal:  J Appl Bacteriol       Date:  1970-03

9.  Physiological studies on early-blocked sporulation mutants of Bacillus subtilis.

Authors:  J F Michel; J Millet
Journal:  J Appl Bacteriol       Date:  1970-03

10.  Isolation and properties of a temperature-sensitive sporulation mutant of Bacillus subtilis.

Authors:  J Szulmajster; C Bonamy; J Laporte
Journal:  J Bacteriol       Date:  1970-03       Impact factor: 3.490

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  39 in total

1.  Identification of a second region of the Spo0A response regulator of Bacillus subtilis required for transcription activation.

Authors:  D A Rowe-Magnus; M J Richer; G B Spiegelman
Journal:  J Bacteriol       Date:  2000-08       Impact factor: 3.490

Review 2.  Genetic aspects of bacterial endospore formation.

Authors:  P J Piggot; J G Coote
Journal:  Bacteriol Rev       Date:  1976-12

3.  YneA, an SOS-induced inhibitor of cell division in Bacillus subtilis, is regulated posttranslationally and requires the transmembrane region for activity.

Authors:  Allison H Mo; William F Burkholder
Journal:  J Bacteriol       Date:  2010-04-16       Impact factor: 3.490

4.  The SpoOA protein of Bacillus subtilis is a repressor of the abrB gene.

Authors:  M Strauch; V Webb; G Spiegelman; J A Hoch
Journal:  Proc Natl Acad Sci U S A       Date:  1990-03       Impact factor: 11.205

5.  Structural alterations in the Bacillus subtilis Spo0A regulatory protein which suppress mutations at several spo0 loci.

Authors:  G Spiegelman; B Van Hoy; M Perego; J Day; K Trach; J A Hoch
Journal:  J Bacteriol       Date:  1990-09       Impact factor: 3.490

Review 6.  [Molecular biology and regulatory mechanisms of antibiotic production in Bacillus].

Authors:  M A Marahiel
Journal:  Naturwissenschaften       Date:  1992-05

7.  Use of green fluorescent protein for visualization of cell-specific gene expression and subcellular protein localization during sporulation in Bacillus subtilis.

Authors:  C D Webb; A Decatur; A Teleman; R Losick
Journal:  J Bacteriol       Date:  1995-10       Impact factor: 3.490

8.  Repression of sporulation in Bacillus subtilis by L-malate.

Authors:  M Ohné; B Rutberg
Journal:  J Bacteriol       Date:  1976-02       Impact factor: 3.490

9.  Deoxyribonucleic acid-binding proteins in vegetative Bacillus subtilis: alterations caused by stage O sporulation mutations.

Authors:  S P Brehm; F Le Hegarat; J A Hoch
Journal:  J Bacteriol       Date:  1975-11       Impact factor: 3.490

10.  Viral mutation affecting bacteriophage phi 1 development in Bacillus subtilis 168.

Authors:  C W Rettenmier; H E Hemphill
Journal:  J Virol       Date:  1975-04       Impact factor: 5.103

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