Literature DB >> 8366055

Chloramphenicol acetyltransferase, a cytoplasmic protein is incompatible for export from Bacillus subtilis.

M W Chen1, V Nagarajan.   

Abstract

Bacillus subtilis cells expressing a hybrid protein (Lvsss-Cat) consisting of the B. amyloliquefaciens levansucrase signal peptide fused to B. pumilus chloramphenicol acetyltransferase (Cat) are unable to export Cat protein into the growth medium. A series of tripartite protein fusions was constructed by inserting various lengths of the Cat sequences between the levansucrase signal peptide and staphylococcal protein A or Escherichia coli alkaline phosphatase. Biochemical characterization of the various Cat protein fusions revealed that multiple regions in the Cat protein were causing the export defect.

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Year:  1993        PMID: 8366055      PMCID: PMC206629          DOI: 10.1128/jb.175.17.5697-5700.1993

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


  19 in total

1.  Isolation and characterization of levansucrase-encoding gene from Bacillus amyloliquefaciens.

Authors:  L B Tang; R Lenstra; T V Borchert; V Nagarajan
Journal:  Gene       Date:  1990-11-30       Impact factor: 3.688

2.  Genetic studies on the inability of beta-galactosidase to be translocated across the Escherichia coli cytoplasmic membrane.

Authors:  C Lee; P Li; H Inouye; E R Brickman; J Beckwith
Journal:  J Bacteriol       Date:  1989-09       Impact factor: 3.490

Review 3.  Uses of lac fusions for the study of biological problems.

Authors:  T J Silhavy; J R Beckwith
Journal:  Microbiol Rev       Date:  1985-12

4.  A conservative amino acid substitution, arginine for lysine, abolishes export of a hybrid protein in Escherichia coli. Implications for the mechanism of protein secretion.

Authors:  R G Summers; C R Harris; J R Knowles
Journal:  J Biol Chem       Date:  1989-11-25       Impact factor: 5.157

5.  Expression of levansucrase-beta-galactosidase hybrids inhibits secretion and is lethal in Bacillus subtilis.

Authors:  M Zagorec; M Steinmetz
Journal:  J Gen Microbiol       Date:  1990-06

6.  A genetic approach to analyzing membrane protein topology.

Authors:  C Manoil; J Beckwith
Journal:  Science       Date:  1986-09-26       Impact factor: 47.728

7.  Structure of chloramphenicol acetyltransferase at 1.75-A resolution.

Authors:  A G Leslie; P C Moody; W V Shaw
Journal:  Proc Natl Acad Sci U S A       Date:  1988-06       Impact factor: 11.205

8.  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

9.  Dihydrofolate reductase (mouse) and beta-galactosidase (Escherichia coli) can be translocated across the plasma membrane of E. coli.

Authors:  R Freudl; H Schwarz; S Kramps; I Hindennach; U Henning
Journal:  J Biol Chem       Date:  1988-11-15       Impact factor: 5.157

10.  Illicit secretion of a cytoplasmic protein into the periplasm of Escherichia coli requires a signal peptide plus a portion of the cognate secreted protein. Demarcation of the critical region of the mature protein.

Authors:  R G Summers; J R Knowles
Journal:  J Biol Chem       Date:  1989-11-25       Impact factor: 5.157

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  3 in total

1.  The secretion of an intrinsically disordered protein with different secretion signals in Bacillus subtilis.

Authors:  Guangqiang Wang; Haiqin Chen; Hao Zhang; Yuanda Song; Wei Chen
Journal:  Curr Microbiol       Date:  2013-01-29       Impact factor: 2.188

2.  A nine-residue synthetic propeptide enhances secretion efficiency of heterologous proteins in Lactococcus lactis.

Authors:  Y Le Loir; A Gruss; S D Ehrlich; P Langella
Journal:  J Bacteriol       Date:  1998-04       Impact factor: 3.490

3.  Escherichia coli signal peptides direct inefficient secretion of an outer membrane protein (OmpA) and periplasmic proteins (maltose-binding protein, ribose-binding protein, and alkaline phosphatase) in Bacillus subtilis.

Authors:  D N Collier
Journal:  J Bacteriol       Date:  1994-05       Impact factor: 3.490

  3 in total

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