Literature DB >> 1367632

Structure and morphology of protein inclusion bodies in Escherichia coli.

G A Bowden1, A M Paredes, G Georgiou.   

Abstract

We have studied the structure and characteristics of inclusion bodies formed by the enzyme beta-lactamase in the periplasmic space of Escherichia coli or in the cytoplasm, following expression of the protein without its signal sequence. Electron microscopy of highly purified protein aggregates using a novel sucrose gradient centrifugation procedure revealed striking morphological differences. Periplasmic inclusion bodies were essentially amorphous whereas the protein particles in the cytoplasm were highly regular. Depending on the cellular location, the inclusion bodies exhibited differences in protein composition even though they were formed by the expression of the same polypeptide chain. It was shown that the chaperonins GroEL and SecB are not incorporated into the inclusion bodies. Furthermore, the degree of solubilization of the inclusion bodies in the presence of denaturants and the sensitivity of the aggregated proteins to protease digestion indicated that the differences between cytoplasmic and periplasmic inclusion bodies extend to the conformation of the associated polypeptide chains.

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Year:  1991        PMID: 1367632     DOI: 10.1038/nbt0891-725

Source DB:  PubMed          Journal:  Biotechnology (N Y)        ISSN: 0733-222X


  45 in total

1.  High pressure fosters protein refolding from aggregates at high concentrations.

Authors:  R J St John; J F Carpenter; T W Randolph
Journal:  Proc Natl Acad Sci U S A       Date:  1999-11-09       Impact factor: 11.205

2.  Roles of DegP in prevention of protein misfolding in the periplasm upon overexpression of penicillin acylase in Escherichia coli.

Authors:  Kao-Lu Pan; Hsu-Chou Hsiao; Chiao-Ling Weng; Ming-Sheng Wu; C Perry Chou
Journal:  J Bacteriol       Date:  2003-05       Impact factor: 3.490

3.  Protein compositional analysis of inclusion bodies produced in recombinant Escherichia coli.

Authors:  U Rinas; J E Bailey
Journal:  Appl Microbiol Biotechnol       Date:  1992-08       Impact factor: 4.813

4.  A rapid protein folding assay for the bacterial periplasm.

Authors:  Thomas J Mansell; Stephen W Linderman; Adam C Fisher; Matthew P DeLisa
Journal:  Protein Sci       Date:  2010-05       Impact factor: 6.725

5.  In vivo enzyme immobilization by inclusion body display.

Authors:  Björn Steinmann; Andreas Christmann; Tim Heiseler; Janine Fritz; Harald Kolmar
Journal:  Appl Environ Microbiol       Date:  2010-06-25       Impact factor: 4.792

6.  Two distinct states of Escherichia coli cells that overexpress recombinant heterogeneous β-galactosidase.

Authors:  Yun Zhao; Wei He; Wei-Feng Liu; Chun-Chun Liu; Li-Kui Feng; Lei Sun; Yong-Bin Yan; Hai-Ying Hang
Journal:  J Biol Chem       Date:  2012-02-02       Impact factor: 5.157

7.  Formation of fluorescent proteins by the attachment of phycoerythrobilin to R-phycoerythrin alpha and beta apo-subunits.

Authors:  Dragan Isailovic; Ishrat Sultana; Gregory J Phillips; Edward S Yeung
Journal:  Anal Biochem       Date:  2006-08-23       Impact factor: 3.365

8.  Abnormal fractionation of beta-lactamase in Escherichia coli: evidence for an interaction with the inner membrane in the absence of a leader peptide.

Authors:  G A Bowden; F Baneyx; G Georgiou
Journal:  J Bacteriol       Date:  1992-05       Impact factor: 3.490

9.  Localization of functional polypeptides in bacterial inclusion bodies.

Authors:  Elena García-Fruitós; Anna Arís; Antonio Villaverde
Journal:  Appl Environ Microbiol       Date:  2006-11-03       Impact factor: 4.792

10.  Folding and aggregation of TEM beta-lactamase: analogies with the formation of inclusion bodies in Escherichia coli.

Authors:  G Georgiou; P Valax; M Ostermeier; P M Horowitz
Journal:  Protein Sci       Date:  1994-11       Impact factor: 6.725

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