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PMID: 7531275 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Selection for transport competence of C-terminal polypeptides derived from Escherichia coli hemolysin: the shortest peptide capable of autonomous HlyB/HlyD-dependent secretion comprises the C-terminal 62 amino acids of HlyA.

Molecular & general genetics : MGG ·Vol. 245 ·No. 1 ·1994-10-17 ·Pages 53-60

Jarchau T, Chakraborty T, Garcia F, Goebel W

Abstract

Escherichia coli hemolysin (HlyA) is secreted by a specific export machinery which recognizes a topogenic secretion signal located at the C-terminal end of HlyA. This signal sequence has been variously defined as comprising from 27 to about 300 amino acids at the C-terminus of HlyA. We have used here a combined genetic and immunological approach to select for C-terminal HlyA peptides that are still secretion-component. A deletion library of HlyA mutant proteins was generated in vitro by successive degradation of hylA from the 5' end with exonuclease III. Secretion competence was tested by immunoblotting of the supernatant of each clone with an antiserum raised against a C-terminal portion of hemolysin. It was found that the hemolysin secretion system has no apparent size limitation for HlyA proteins over a range from 1024 to 62 amino acids. The smallest autonomously secretable peptide isolated in this selection procedure consists of the C-terminal 62 amino acids of HlyA. This sequence is shared by all secretion-competent, truncated HlyA proteins, which suggests that secretion of the E. coli hemolysin is strictly post-translational. The capacity of the hemolysin secretion machinery was found to be unsaturated by the steady-state level of its natural HlyA substrate and large amounts of truncated HlyA derivatives could still be secreted in addition to full-length HlyA.

MeSH Terms
Antibodies, Bacterial/immunology Bacterial Proteins/metabolism Biological Transport Carrier Proteins Epitopes/immunology Escherichia coli/metabolism Escherichia coli Proteins Hemolysin Proteins/metabolism Membrane Proteins Membrane Transport Proteins Peptide Fragments/metabolism
Chemicals
Antibodies, Bacterial Bacterial Proteins Carrier Proteins Epitopes Escherichia coli Proteins Hemolysin Proteins HlyD protein, E coli Hlya protein, E coli Membrane Proteins Membrane Transport Proteins Peptide Fragments
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Jarchau T
Theodor-Boveri-Institut für Biowissenschaften, Würzburg, Germany.
Chakraborty T
Garcia F
Goebel W
References (29)
29 references, click to expand
  1. Alterations of amino acid repeats in the Escherichia coli hemolysin affect cytolytic activity and secretion.
    Proc Natl Acad Sci U S A. 1988 Jul;85(14):5269-73 PMID: 2839840
  2. TolC, an Escherichia coli outer membrane protein required for hemolysin secretion.
    Proc Natl Acad Sci U S A. 1990 Jun;87(12):4776-80 PMID: 2112747
  3. Protein secretion in gram-negative bacteria. The extracellular metalloprotease B from Erwinia chrysanthemi contains a C-terminal secretion signal analogous to that of Escherichia coli alpha-hemolysin.
    J Biol Chem. 1990 Oct 5;265(28):17118-25 PMID: 2211614
  4. Cleavage of structural proteins during the assembly of the head of bacteriophage T4.
    Nature. 1970 Aug 15;227(5259):680-5 PMID: 5432063
  5. Functional complementation between bacterial MDR-like export systems: colicin V, alpha-hemolysin, and Erwinia protease.
    J Bacteriol. 1991 Dec;173(23):7549-56 PMID: 1938950
  6. The C-terminal, 23 kDa peptide of E. coli haemolysin 2001 contains all the information necessary for its secretion by the haemolysin (Hly) export machinery.
    FEBS Lett. 1986 Aug 18;204(2):331-5 PMID: 3525227
  7. Sequence information required for protein translocation from the cytoplasm.
    J Bacteriol. 1987 Dec;169(12):5339-42 PMID: 3316179
  8. Escherichia coli hemolysin is released extracellularly without cleavage of a signal peptide.
    J Bacteriol. 1985 Jul;163(1):88-93 PMID: 3891742
  9. Isolation and analysis of the C-terminal signal directing export of Escherichia coli hemolysin protein across both bacterial membranes.
    EMBO J. 1989 Feb;8(2):595-605 PMID: 2656259
  10. Processing by OmpT of fusion proteins carrying the HlyA transport signal during secretion by the Escherichia coli hemolysin transport system.
    Mol Gen Genet. 1992 May;233(1-2):42-8 PMID: 1603076
  11. Structural and functional relationships among the RTX toxin determinants of gram-negative bacteria.
    FEMS Microbiol Rev. 1992 Feb;8(2):137-61 PMID: 1558765
  12. Electroblotting of multiple gels: a simple apparatus without buffer tank for rapid transfer of proteins from polyacrylamide to nitrocellulose.
    J Biochem Biophys Methods. 1984 Dec;10(3-4):203-9 PMID: 6530509
  13. Characterization of monoclonal antibodies against the Escherichia coli hemolysin.
    Infect Immun. 1990 Mar;58(3):822-7 PMID: 1689701
  14. Change in the cellular localization of alkaline phosphatase by alteration of its carboxy-terminal sequence.
    Mol Gen Genet. 1990 Jul;222(2-3):211-6 PMID: 2274026
  15. A dot-immunobinding assay for monoclonal and other antibodies.
    Anal Biochem. 1982 Jan 1;119(1):142-7 PMID: 7072935
  16. Release of a chimeric protein into the medium from Escherichia coli using the C-terminal secretion signal of haemolysin.
    EMBO J. 1987 Sep;6(9):2835-41 PMID: 3119330
  17. Secretion of CyaA-PrtB and HlyA-PrtB fusion proteins in Escherichia coli: involvement of the glycine-rich repeat domain of Erwinia chrysanthemi protease B.
    J Bacteriol. 1992 Aug;174(15):4920-7 PMID: 1629152
  18. Analysis of cytoskeletal structures using blot-purified monospecific antibodies.
    Methods Enzymol. 1986;134:467-72 PMID: 3547038
  19. Transport of hemolysin across the outer membrane of Escherichia coli requires two functions.
    J Bacteriol. 1983 Apr;154(1):200-10 PMID: 6300033
  20. The secretion genes of Pseudomonas aeruginosa alkaline protease are functionally related to those of Erwinia chrysanthemi proteases and Escherichia coli alpha-haemolysin.
    Mol Microbiol. 1991 Feb;5(2):447-53 PMID: 1904127
  21. Genetical and functional organisation of the Escherichia coli haemolysin determinant 2001.
    Mol Gen Genet. 1985;201(2):282-8 PMID: 3003531
  22. The Rhizobium nodulation gene nodO encodes a Ca2(+)-binding protein that is exported without N-terminal cleavage and is homologous to haemolysin and related proteins.
    EMBO J. 1990 Feb;9(2):349-54 PMID: 2303029
  23. Peptide mapping in one dimension by limited proteolysis of sodium dodecyl sulfate-solubilized proteins.
    Methods Enzymol. 1983;96:222-9 PMID: 6361454
  24. Transport of hemolysin by Escherichia coli.
    J Cell Biochem. 1983;22(2):87-97 PMID: 6368575
  25. Nucleotide sequence of an Escherichia coli chromosomal hemolysin.
    J Bacteriol. 1985 Jul;163(1):94-105 PMID: 3891743
  26. Cloning and expression in Escherichia coli of the Serratia marcescens metalloprotease gene: secretion of the protease from E. coli in the presence of the Erwinia chrysanthemi protease secretion functions.
    J Bacteriol. 1991 Apr;173(7):2160-6 PMID: 2007544
  27. Analysis of the haemolysin secretion system by PhoA-HlyA fusion proteins.
    Mol Gen Genet. 1990 Nov;224(2):201-8 PMID: 2277639
  28. Unidirectional digestion with exonuclease III in DNA sequence analysis.
    Methods Enzymol. 1987;155:156-65 PMID: 3323819
  29. Analysis of the haemolysin transport process through the secretion from Escherichia coli of PCM, CAT or beta-galactosidase fused to the Hly C-terminal signal domain.
    Mol Microbiol. 1991 Oct;5(10):2557-68 PMID: 1791766
Article Info
Journal
Molecular & general genetics : MGG
Abbr.
Mol Gen Genet
ISSN
0026-8925
Published
1994-10-17
Pages
53-60
Language
English
Region
Germany
NLM ID
0125036
Subset
IM
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