Literature DB >> 18760314

Size characterization of inclusion bodies by sedimentation field-flow fractionation.

Gerd Margreiter1, Paul Messner, Karin D Caldwell, Karl Bayer.   

Abstract

Sedimentation field-flow fractionation (sedFFF) was evaluated to characterize the size of Delta(4-23)TEM-beta-lactamase inclusion bodies (IBs) overexpressed in fed-batch cultivations of Escherichia coli. Heterologous Delta(4-23)TEM-beta-lactamase protein formed different sizes of IBs, depending upon the induction conditions. In the early phases of recombinant protein expression, induced with low concentrations of IPTG (isopropyl-beta-d-thiogalactoside), IB masses were larger than expected and showed heterogeneous size distributions. During cultivation, IB sizes showed a Gaussian distribution and reached a broad range by the end of the fed-batch cultivations. The obtained result proved the aptitude of sedFFF to rapidly assess the size distribution of IBs in a culture.

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Year:  2008        PMID: 18760314      PMCID: PMC4388406          DOI: 10.1016/j.jbiotec.2008.07.1995

Source DB:  PubMed          Journal:  J Biotechnol        ISSN: 0168-1656            Impact factor:   3.307


  19 in total

1.  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

2.  Particle characterization in centrifugal fields. Comparison between ultracentrifugation and sedimentation field-flow fractionation.

Authors:  J M Li; K D Caldwell; W Mächtle
Journal:  J Chromatogr       Date:  1990-09-26

3.  Localization of chaperones DnaK and GroEL in bacterial inclusion bodies.

Authors:  M Mar Carrió; Antonio Villaverde
Journal:  J Bacteriol       Date:  2005-05       Impact factor: 3.490

4.  Field-flow fractionation of macromolecules.

Authors:  J C Giddings
Journal:  J Chromatogr       Date:  1989-05-26

5.  T7-directed protein synthesis.

Authors:  F W Studier; J V Maizel
Journal:  Virology       Date:  1969-11       Impact factor: 3.616

6.  Size characterization of green fluorescent protein inclusion bodies in E. coli using asymmetrical flow field-flow fractionation-multi-angle light scattering.

Authors:  Jian Luo; Mats Leeman; Andras Ballagi; Anders Elfwing; Zhiguo Su; Jan-Christer Janson; Karl-Gustav Wahlund
Journal:  J Chromatogr A       Date:  2006-01-18       Impact factor: 4.759

7.  Localization of inclusion bodies in Escherichia coli overproducing beta-lactamase or alkaline phosphatase.

Authors:  G Georgiou; J N Telford; M L Shuler; D B Wilson
Journal:  Appl Environ Microbiol       Date:  1986-11       Impact factor: 4.792

Review 8.  Bioprocessing of therapeutic proteins from the inclusion bodies of Escherichia coli.

Authors:  Amulya K Panda
Journal:  Adv Biochem Eng Biotechnol       Date:  2003       Impact factor: 2.635

9.  Molecular characterization of beta-lactamase inclusion bodies produced in Escherichia coli. 1. Composition.

Authors:  P Valax; G Georgiou
Journal:  Biotechnol Prog       Date:  1993 Sep-Oct

10.  Nativelike secondary structure in interleukin-1 beta inclusion bodies by attenuated total reflectance FTIR.

Authors:  K Oberg; B A Chrunyk; R Wetzel; A L Fink
Journal:  Biochemistry       Date:  1994-03-08       Impact factor: 3.162

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  9 in total

1.  Diffusion within the cytoplasm: a mesoscale model of interacting macromolecules.

Authors:  Fabio Trovato; Valentina Tozzini
Journal:  Biophys J       Date:  2014-12-02       Impact factor: 4.033

2.  Recombinant production of ESAT-6 antigen in thermoinducible Escherichia coli: the role of culture scale and temperature on metabolic response, expression of chaperones, and architecture of inclusion bodies.

Authors:  Sara Restrepo-Pineda; Carlos G Bando-Campos; Norma A Valdez-Cruz; Mauricio A Trujillo-Roldán
Journal:  Cell Stress Chaperones       Date:  2019-06-04       Impact factor: 3.667

3.  Comparison of two codon optimization strategies to enhance recombinant protein production in Escherichia coli.

Authors:  Hugo G Menzella
Journal:  Microb Cell Fact       Date:  2011-03-03       Impact factor: 5.328

4.  Kinetics of inclusion body formation and its correlation with the characteristics of protein aggregates in Escherichia coli.

Authors:  Arun K Upadhyay; Aruna Murmu; Anupam Singh; Amulya K Panda
Journal:  PLoS One       Date:  2012-03-29       Impact factor: 3.240

5.  The pre-induction temperature affects recombinant HuGM-CSF aggregation in thermoinducible Escherichia coli.

Authors:  Sara Restrepo-Pineda; Nuria Sánchez-Puig; Néstor O Pérez; Enrique García-Hernández; Norma A Valdez-Cruz; Mauricio A Trujillo-Roldán
Journal:  Appl Microbiol Biotechnol       Date:  2022-04-12       Impact factor: 5.560

6.  Bacterial inclusion bodies as potential synthetic devices for pathogen recognition and a therapeutic substance release.

Authors:  Klaudia Talafová; Eva Hrabárová; Dušan Chorvát; Jozef Nahálka
Journal:  Microb Cell Fact       Date:  2013-02-07       Impact factor: 5.328

7.  Influence of pH control in the formation of inclusion bodies during production of recombinant sphingomyelinase-D in Escherichia coli.

Authors:  Andrea Castellanos-Mendoza; Ricardo M Castro-Acosta; Alejandro Olvera; Guadalupe Zavala; Miguel Mendoza-Vera; Enrique García-Hernández; Alejandro Alagón; Mauricio A Trujillo-Roldán; Norma A Valdez-Cruz
Journal:  Microb Cell Fact       Date:  2014-09-12       Impact factor: 5.328

8.  Coiled-coil inspired functional inclusion bodies.

Authors:  Marcos Gil-Garcia; Susanna Navarro; Salvador Ventura
Journal:  Microb Cell Fact       Date:  2020-06-01       Impact factor: 5.328

Review 9.  Catalytically-active inclusion bodies for biotechnology-general concepts, optimization, and application.

Authors:  Vera D Jäger; Robin Lamm; Kira Küsters; Gizem Ölçücü; Marco Oldiges; Karl-Erich Jaeger; Jochen Büchs; Ulrich Krauss
Journal:  Appl Microbiol Biotechnol       Date:  2020-07-10       Impact factor: 4.813

  9 in total

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