Literature DB >> 9179840

Energy requirement for pullulanase secretion by the main terminal branch of the general secretory pathway.

O M Possot1, L Letellier, A P Pugsley.   

Abstract

The energy requirement for the second step in pullulanase secretion by the general secretory pathway was studied in Escherichia coli. In order to uncouple the two steps in the secretion pathway (across the cytoplasmic and outer membranes, respectively) and to facilitate kinetic analysis of secretion, a variant form of pullulanase lacking its N-terminal fatty acid membrane anchor was used. The transport of the periplasmic secretion intermediate form of this protein across the outer membrane was not inhibited by concentrations of sodium arsenate in excess of those required to reduce ATP levels to < or = 10% of their normal value. Pullulanase secretion was inhibited by the protonophore carbonyl cyanide m-chlorophenyl hydrazone at concentrations which were similar to those reported by others to be required to prevent solute uptake or the export and processing of preproteins across the cytoplasmic membrane, but which were in excess of those required to fully dissipate the proton-motive force and to reduce lactose uptake to a significant extent.

Entities:  

Mesh:

Substances:

Year:  1997        PMID: 9179840     DOI: 10.1046/j.1365-2958.1997.3451726.x

Source DB:  PubMed          Journal:  Mol Microbiol        ISSN: 0950-382X            Impact factor:   3.501


  23 in total

1.  Structure-function analysis of XcpP, a component involved in general secretory pathway-dependent protein secretion in Pseudomonas aeruginosa.

Authors:  S Bleves; M Gérard-Vincent; A Lazdunski; A Filloux
Journal:  J Bacteriol       Date:  1999-07       Impact factor: 3.490

2.  Membrane association and multimerization of secreton component pulC.

Authors:  O M Possot; M Gérard-Vincent; A P Pugsley
Journal:  J Bacteriol       Date:  1999-07       Impact factor: 3.490

3.  Multiple interactions between pullulanase secreton components involved in stabilization and cytoplasmic membrane association of PulE.

Authors:  O M Possot; G Vignon; N Bomchil; F Ebel; A P Pugsley
Journal:  J Bacteriol       Date:  2000-04       Impact factor: 3.490

4.  Type 4 pilus biogenesis and type II-mediated protein secretion by Vibrio cholerae occur independently of the TonB-facilitated proton motive force.

Authors:  Niranjan Bose; Shelley M Payne; Ronald K Taylor
Journal:  J Bacteriol       Date:  2002-04       Impact factor: 3.490

Review 5.  Type II secretion and pathogenesis.

Authors:  M Sandkvist
Journal:  Infect Immun       Date:  2001-06       Impact factor: 3.441

6.  Type IV-like pili formed by the type II secreton: specificity, composition, bundling, polar localization, and surface presentation of peptides.

Authors:  Guillaume Vignon; Rolf Köhler; Eric Larquet; Stéphanie Giroux; Marie-Christine Prévost; Pascal Roux; Anthony P Pugsley
Journal:  J Bacteriol       Date:  2003-06       Impact factor: 3.490

Review 7.  On the path to uncover the bacterial type II secretion system.

Authors:  Badreddine Douzi; Alain Filloux; Romé Voulhoux
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2012-04-19       Impact factor: 6.237

8.  Bacterial outer membrane secretin PulD assembles and inserts into the inner membrane in the absence of its pilotin.

Authors:  Ingrid Guilvout; Mohamed Chami; Andreas Engel; Anthony P Pugsley; Nicolas Bayan
Journal:  EMBO J       Date:  2006-11-02       Impact factor: 11.598

9.  Structure and Membrane Topography of the Vibrio-Type Secretin Complex from the Type 2 Secretion System of Enteropathogenic Escherichia coli.

Authors:  Iain D Hay; Matthew J Belousoff; Rhys A Dunstan; Rebecca S Bamert; Trevor Lithgow
Journal:  J Bacteriol       Date:  2018-02-07       Impact factor: 3.490

10.  Green fluorescent chimeras indicate nonpolar localization of pullulanase secreton components PulL and PulM.

Authors:  Nienke Buddelmeijer; Olivera Francetic; Anthony P Pugsley
Journal:  J Bacteriol       Date:  2006-04       Impact factor: 3.490

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.