Literature DB >> 2404939

Alkaline phosphatase fusions: sensors of subcellular location.

C Manoil1, J J Mekalanos, J Beckwith.   

Abstract

Alkaline phosphatase fusions allow genes to be identified solely on the basis of their protein products being exported from the cytoplasm. Thus, the use of such fusions helps render biological processes which involve cell envelope and secreted proteins accessible to a sophisticated genetic analysis. Furthermore, alkaline phosphatase fusions can be used to locate export signals. Specifying such signals is an important component of studies on the structure of individual cell envelope proteins. The basis of the alkaline phosphatase fusion approach is the finding that the activity of the enzyme responds differently to different environments. Thus, the activity of the fusion protein gives evidence as to its location. This general approach of using sensor proteins which vary in their function, depending on their environment, could be extended to the study of other sorts of problems. It may be that certain enzymes will provide an assay for localization to a particular subcellular compartment, if the environment of the compartment differs from that of others. For instance, the lysosome is more acidic than other intracellular organelles. A gene fusion system employing a reporter enzyme that could show activity only at the pH of the lysosome could allow the detection of signals determining lysosomal localization. Analogous types of enzymes may be used as probes for other subcellular compartments.

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Year:  1990        PMID: 2404939      PMCID: PMC208471          DOI: 10.1128/jb.172.2.515-518.1990

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


  47 in total

1.  The use of transposon TnphoA to detect genes for cell envelope proteins subject to a common regulatory stimulus. Analysis of osmotically regulated genes in Escherichia coli.

Authors:  C Gutierrez; J Barondess; C Manoil; J Beckwith
Journal:  J Mol Biol       Date:  1987-05-20       Impact factor: 5.469

2.  Localization and membrane topology of EnvZ, a protein involved in osmoregulation of OmpF and OmpC in Escherichia coli.

Authors:  S Forst; D Comeau; S Norioka; M Inouye
Journal:  J Biol Chem       Date:  1987-12-05       Impact factor: 5.157

3.  Bacterial motility: membrane topology of the Escherichia coli MotB protein.

Authors:  S Y Chun; J S Parkinson
Journal:  Science       Date:  1988-01-15       Impact factor: 47.728

4.  An Escherichia coli mutation preventing degradation of abnormal periplasmic proteins.

Authors:  K L Strauch; J Beckwith
Journal:  Proc Natl Acad Sci U S A       Date:  1988-03       Impact factor: 11.205

5.  Determinants of membrane protein topology.

Authors:  D Boyd; C Manoil; J Beckwith
Journal:  Proc Natl Acad Sci U S A       Date:  1987-12       Impact factor: 11.205

6.  Export of hybrid proteins FhuA'-'LacZ and FhuA'-'PhoA to the cell envelope of Escherichia coli K-12.

Authors:  J W Coulton; G K Reid; A Campana
Journal:  J Bacteriol       Date:  1988-05       Impact factor: 3.490

7.  Alteration of the amino terminus of the mature sequence of a periplasmic protein can severely affect protein export in Escherichia coli.

Authors:  P Li; J Beckwith; H Inouye
Journal:  Proc Natl Acad Sci U S A       Date:  1988-10       Impact factor: 11.205

8.  Use of phoA gene fusions to identify a pilus colonization factor coordinately regulated with cholera toxin.

Authors:  R K Taylor; V L Miller; D B Furlong; J J Mekalanos
Journal:  Proc Natl Acad Sci U S A       Date:  1987-05       Impact factor: 11.205

9.  Nucleotide sequence of the iucD gene of the pColV-K30 aerobactin operon and topology of its product studied with phoA and lacZ gene fusions.

Authors:  M Herrero; V de Lorenzo; J B Neilands
Journal:  J Bacteriol       Date:  1988-01       Impact factor: 3.490

10.  Topology analysis of the SecY protein, an integral membrane protein involved in protein export in Escherichia coli.

Authors:  Y Akiyama; K Ito
Journal:  EMBO J       Date:  1987-11       Impact factor: 11.598

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  92 in total

1.  Mutational analysis and membrane topology of ComP, a quorum-sensing histidine kinase of Bacillus subtilis controlling competence development.

Authors:  F Piazza; P Tortosa; D Dubnau
Journal:  J Bacteriol       Date:  1999-08       Impact factor: 3.490

2.  Membrane topology of the NixA nickel transporter of Helicobacter pylori: two nickel transport-specific motifs within transmembrane helices II and III.

Authors:  J F Fulkerson; H L Mobley
Journal:  J Bacteriol       Date:  2000-03       Impact factor: 3.490

3.  Alkaline phosphatase reporter transposon for identification of genes encoding secreted proteins in gram-positive microorganisms.

Authors:  Carmela M Gibson; Michael G Caparon
Journal:  Appl Environ Microbiol       Date:  2002-02       Impact factor: 4.792

4.  Structural and functional dissection of Sec62p, a membrane-bound component of the yeast endoplasmic reticulum protein import machinery.

Authors:  R J Deshaies; R Schekman
Journal:  Mol Cell Biol       Date:  1990-11       Impact factor: 4.272

5.  TnphoA and TnphoA' elements for making and switching fusions for study of transcription, translation, and cell surface localization.

Authors:  M R Wilmes-Riesenberg; B L Wanner
Journal:  J Bacteriol       Date:  1992-07       Impact factor: 3.490

6.  FtsL, an essential cytoplasmic membrane protein involved in cell division in Escherichia coli.

Authors:  L M Guzman; J J Barondess; J Beckwith
Journal:  J Bacteriol       Date:  1992-12       Impact factor: 3.490

Review 7.  Bacteriophage lysis: mechanism and regulation.

Authors:  R Young
Journal:  Microbiol Rev       Date:  1992-09

8.  Membrane topology analysis of cyclic glucan synthase, a virulence determinant of Brucella abortus.

Authors:  Andrés E Ciocchini; Mara S Roset; Nora Iñón de Iannino; Rodolfo A Ugalde
Journal:  J Bacteriol       Date:  2004-11       Impact factor: 3.490

9.  Use of transposon TnphoA to identify genes for cell envelope proteins of Escherichia coli required for long-chain fatty acid transport: the periplasmic protein Tsp potentiates long-chain fatty acid transport.

Authors:  A Azizan; P N Black
Journal:  J Bacteriol       Date:  1994-11       Impact factor: 3.490

10.  Lyme disease-causing Borrelia species encode multiple lipoproteins homologous to peptide-binding proteins of ABC-type transporters.

Authors:  J A Kornacki; D B Oliver
Journal:  Infect Immun       Date:  1998-09       Impact factor: 3.441

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