Literature DB >> 6284711

Role of proton motive force in genetic transformation of Bacillus subtilis.

M H van Nieuwenhoven, K J Hellingwerf, G Venema, W N Konings.   

Abstract

This study explored the role of the proton motive force in the processes of DNA binding and DNA transport of genetic transformation of Bacillus subtilis 168 strain 8G-5 (trpC2). Transformation was severely inhibited by the ionophores valinomycin, nigericin, and 3,5-di-tert-4-hydroxybenzylidenemalononitrite (SF-6847) and by tetraphenylphosphonium. The ionophores valinomycin and nigericin also severely inhibited binding of transforming DNA to the cell envelope, whereas SF-6847 and carbonylcyanide-p-trifluoromethoxyphenylhydrazone hardly affected binding. The proton motive force, therefore, does not contribute to the process of DNA binding, and valinomycin and nigericin interact directly with the DNA binding sites at the cell envelope. The effects of ionophores, weak acids, and tetraphenylphosphonium on the components of the proton motive force and on the entry of transforming DNA after binding to the cell envelope was investigated. DNA entry, as measured by the amount of DNase I-resistant cell-associated [3H]DNA and by the formation of DNA breakdown products, was severely inhibited under conditions of a small proton motive force and also under conditions of a small delta pH and a high electrical potential. These results suggest that the proton motive force and especially the delta pH component functions as a driving force for DNA uptake in transformation.

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Year:  1982        PMID: 6284711      PMCID: PMC220324          DOI: 10.1128/jb.151.2.771-776.1982

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


  22 in total

1.  Competence in Bacillus subtilis transformation system.

Authors:  F E Young
Journal:  Nature       Date:  1967-02-25       Impact factor: 49.962

2.  Changes of total water and sucrose space accompanying induced ion uptake or phosphate swelling of rat liver mitochondria.

Authors:  E J Harris; K van Dam
Journal:  Biochem J       Date:  1968-02       Impact factor: 3.857

3.  Kinetic analysis of the products of donor deoxyribonucleate in transformed cells of Bacillus subtilis.

Authors:  R Davidoff-Abelson; D Dubnau
Journal:  J Bacteriol       Date:  1973-10       Impact factor: 3.490

4.  Conditions affecting the isolation from transformed cells of Bacillus subtilis of high-molecular-weight single-stranded deoxyribonucleic acid of donor origin.

Authors:  R Davidoff-Abelson; D Dubnau
Journal:  J Bacteriol       Date:  1973-10       Impact factor: 3.490

5.  Fate of transforming DNA following uptake by competent Bacillus subtilis. IV. The endwise attachment and uptake of transforming DNA.

Authors:  D Dubnau; C Cirigliano
Journal:  J Mol Biol       Date:  1972-02-28       Impact factor: 5.469

6.  Fate of transforming deoxyribonucleic acid after uptake by competent Bacillus subtilis: size and distribution of the integrated donor segments.

Authors:  D Dubnau; C Cirigliano
Journal:  J Bacteriol       Date:  1972-08       Impact factor: 3.490

7.  Fate of transforming DNA following uptake by competent Bacillus subtilis. Formation and properties of products isolated from transformed cells which are derived entirely from donor DNA.

Authors:  D Dubnau; C Cirigliano
Journal:  J Mol Biol       Date:  1972-02-28       Impact factor: 5.469

8.  Fate of transforming deoxyribonucleate in Bacillus subtilis.

Authors:  M Piechowska; M S Fox
Journal:  J Bacteriol       Date:  1971-11       Impact factor: 3.490

9.  Different nuclease activities in competent and noncompetent Bacillus subtilis.

Authors:  H Joenje; G Venema
Journal:  J Bacteriol       Date:  1975-04       Impact factor: 3.490

10.  The integration of donor and recipient deoxyribonucleic acid during transformation of Bacillus subtilis.

Authors:  S R Ayad; G R Barker
Journal:  Biochem J       Date:  1969-06       Impact factor: 3.857

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  9 in total

1.  DNA transport into Bacillus subtilis requires proton motive force to generate large molecular forces.

Authors:  Berenike Maier; Ines Chen; David Dubnau; Michael P Sheetz
Journal:  Nat Struct Mol Biol       Date:  2004-06-06       Impact factor: 15.369

Review 2.  Membrane-associated DNA transport machines.

Authors:  Briana Burton; David Dubnau
Journal:  Cold Spring Harb Perspect Biol       Date:  2010-06-23       Impact factor: 10.005

3.  Characterization of DNA uptake by the cyanobacterium Anacystis nidulans.

Authors:  H Daniell; B A McFadden
Journal:  Mol Gen Genet       Date:  1986-08

4.  Uptake and expression of bacterial and cyanobacterial genes by isolated cucumber etioplasts.

Authors:  H Daniell; B A McFadden
Journal:  Proc Natl Acad Sci U S A       Date:  1987-09       Impact factor: 11.205

5.  Regulation of the competence pathway as a novel role associated with a streptococcal bacteriocin.

Authors:  Delphine Dufour; Martha Cordova; Dennis G Cvitkovitch; Céline M Lévesque
Journal:  J Bacteriol       Date:  2011-10-07       Impact factor: 3.490

6.  K+ modulates genetic competence and the stress regulon of Streptococcus mutans.

Authors:  Gursonika Binepal; Iwona B Wenderska; Paula Crowley; Richard N Besingi; Dilani B Senadheera; L Jeannine Brady; Dennis G Cvitkovitch
Journal:  Microbiology       Date:  2017-06-22       Impact factor: 2.777

7.  Role of the electrochemical proton gradient in genetic transformation of Haemophilus influenzae.

Authors:  W Bremer; J Kooistra; K J Hellingwerf; W N Konings
Journal:  J Bacteriol       Date:  1984-03       Impact factor: 3.490

8.  Optimal conditions for genetic transformation of the cyanobacterium Anacystis nidulans R2.

Authors:  S S Golden; L A Sherman
Journal:  J Bacteriol       Date:  1984-04       Impact factor: 3.490

Review 9.  Genetic competence in Bacillus subtilis.

Authors:  D Dubnau
Journal:  Microbiol Rev       Date:  1991-09
  9 in total

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