Literature DB >> 23794775

Tracing Metabolite Footsteps of Escherichia coli Along the Time Course of Recombinant Protein Expression by Two-Dimensional NMR Spectroscopy.

Young Kee Chae1, Seol Hyun Kim, James J Ellinger, John L Markley.   

Abstract

The recombinant expression of proteins has been the method of choice to meet the demands from proteomics and structural genomics studies. Despite its successful production of many heterologous proteins, Escherichia coli failed to produce many other proteins in their native forms. This may be related to the fact that the stresses resulting from the overproduction interfere with cellular processes. To better understand the physiological change during the overproduction phase, we profiled the metabolites along the time course of the recombinant protein expression. We identified 32 metabolites collected from different time points in the protein production phase. The stress induced by protein production can be characterized by (A) the increased usage of aspartic acid, choline, glycerol, and N-acetyllysine; and (B) the accumulation of adenosine, alanine, oxidized glutathione, glycine, N-acetylputrescine, and uracil. We envision that this work can be used to create a strategy for the production of usable proteins in large quantities.

Entities:  

Keywords:  Metabolite profiling; NMR; Overexpression; Recombinant protein

Year:  2012        PMID: 23794775      PMCID: PMC3686544          DOI: 10.5012/bkcs.2012.33.12.4041

Source DB:  PubMed          Journal:  Bull Korean Chem Soc        ISSN: 0253-2964


  25 in total

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4.  DnaK and DnaJ facilitated the folding process and reduced inclusion body formation of magnesium transporter CorA overexpressed in Escherichia coli.

Authors:  Yong Chen; Jinmei Song; Sen-fang Sui; Da-Neng Wang
Journal:  Protein Expr Purif       Date:  2003-12       Impact factor: 1.650

5.  Fast and precise quantitative analysis of metabolic mixtures by 2D 1H INADEQUATE NMR.

Authors:  Estelle Martineau; Patrick Giraudeau; Illa Tea; Serge Akoka
Journal:  J Pharm Biomed Anal       Date:  2010-08-06       Impact factor: 3.935

6.  A new strategy to produce active human Src from bacteria for biochemical study of its regulation.

Authors:  Yue-Hao Wang; Marina K Ayrapetov; Xiaofeng Lin; Gongqin Sun
Journal:  Biochem Biophys Res Commun       Date:  2006-07-28       Impact factor: 3.575

7.  The role of the thioredoxin and glutaredoxin pathways in reducing protein disulfide bonds in the Escherichia coli cytoplasm.

Authors:  W A Prinz; F Aslund; A Holmgren; J Beckwith
Journal:  J Biol Chem       Date:  1997-06-20       Impact factor: 5.157

8.  Efficient folding of proteins with multiple disulfide bonds in the Escherichia coli cytoplasm.

Authors:  P H Bessette; F Aslund; J Beckwith; G Georgiou
Journal:  Proc Natl Acad Sci U S A       Date:  1999-11-23       Impact factor: 11.205

9.  Heterologous high-level E. coli expression, purification and biophysical characterization of the spine-associated RapGAP (SPAR) PDZ domain.

Authors:  Breann L Brown; Michael Hadley; Rebecca Page
Journal:  Protein Expr Purif       Date:  2008-07-18       Impact factor: 1.650

10.  SUMO fusions and SUMO-specific protease for efficient expression and purification of proteins.

Authors:  Michael P Malakhov; Michael R Mattern; Oxana A Malakhova; Mark Drinker; Stephen D Weeks; Tauseef R Butt
Journal:  J Struct Funct Genomics       Date:  2004
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  2 in total

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Journal:  ISME J       Date:  2015-03-10       Impact factor: 10.302

2.  Relationship between recombinant protein expression and host metabolome as determined by two-dimensional NMR spectroscopy.

Authors:  Young Kee Chae; Seol Hyun Kim; John L Markley
Journal:  PLoS One       Date:  2017-05-09       Impact factor: 3.240

  2 in total

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