Optimizing Periplasmic Expression in Escherichia coli for the Production of Recombinant Proteins Tagged with the Small Metal-Binding Protein SmbP.
Bacterial Proteins
/ genetics
Carrier Proteins
/ genetics
Cation Transport Proteins
/ genetics
Cloning, Molecular
/ methods
Copper Transport Proteins
Escherichia coli
/ genetics
Escherichia coli Proteins
/ genetics
Gene Expression
Genes, Reporter
Genetic Vectors
/ chemistry
Iron-Binding Proteins
/ genetics
Luminescent Proteins
/ genetics
Nitrosomonas europaea
/ genetics
Oxidoreductases, N-Demethylating
/ genetics
Periplasm
/ chemistry
Polysaccharide-Lyases
/ genetics
Protein Sorting Signals
Protein Transport
Recombinant Fusion Proteins
/ genetics
Red Fluorescent Protein
CusF
GFP
IMAC
PelB
Periplasm
Protein expression and purification
RFP
Sec pathway
Signal sequence
SmbP
Tat pathway
TorA
Journal
Molecular biotechnology
ISSN: 1559-0305
Titre abrégé: Mol Biotechnol
Pays: Switzerland
ID NLM: 9423533
Informations de publication
Date de publication:
Jun 2019
Jun 2019
Historique:
pubmed:
19
4
2019
medline:
24
8
2019
entrez:
19
4
2019
Statut:
ppublish
Résumé
We have previously shown that the small metal-binding protein (SmbP) extracted from the gram-negative bacterium Nitrosomonas europaea can be employed as a fusion protein for the expression and purification of recombinant proteins in Escherichia coli. With the goal of increasing the amounts of SmbP-tagged proteins produced in the E. coli periplasm, we replaced the native SmbP signal peptide with three different signal sequences: two were from the proteins CusF and PelB, for transport via the Sec pathway, and one was the signal peptide from TorA, for transport via the Tat pathway. Expression of SmbP-tagged Red Fluorescent Protein (RFP) using these three alternative signal peptides individually showed a considerable increase in protein levels in the periplasm of E. coli as compared to its level using the SmbP signal sequence. Therefore, for routine periplasmic expression and purification of recombinant proteins in E. coli, we highly recommend the use of the fusion proteins PelB-SmbP or CusF-SmbP, since these signal sequences increase periplasmic production considerably as compared to the wild-type. Our work, finally, demonstrates that periplasmic expression for SmbP-tagged proteins is not limited to the Sec pathway, in that the TorA-SmbP construct can export reasonable quantities of folded proteins to the periplasm. Although the Sec route has been the most widely used, sometimes, depending on the nature of the protein of interest, for example, if it contains cofactors, it is more appropriate to consider using the Tat route over the Sec. SmbP therefore can be recommended in terms of its particular versatility when combined with signal peptides for the two different routes.
Identifiants
pubmed: 30997666
doi: 10.1007/s12033-019-00176-4
pii: 10.1007/s12033-019-00176-4
doi:
Substances chimiques
Bacterial Proteins
0
Carrier Proteins
0
Cation Transport Proteins
0
Copper Transport Proteins
0
CusF protein, E coli
0
Escherichia coli Proteins
0
Iron-Binding Proteins
0
Luminescent Proteins
0
Protein Sorting Signals
0
Recombinant Fusion Proteins
0
copper-binding protein
0
zinc-binding protein
0
Oxidoreductases, N-Demethylating
EC 1.5.-
trimethylamine dehydrogenase
EC 1.5.8.2
Polysaccharide-Lyases
EC 4.2.2.-
pectate lyase
EC 4.2.2.2
Types de publication
Journal Article
Langues
eng
Pagination
451-460Subventions
Organisme : UANL-PAICYT-2015
ID : CN567-15
Organisme : CONACYT
ID : CB 2012-179774-B
Références
EMBO J. 1999 Jun 1;18(11):2982-90
pubmed: 10357811
J Biol Chem. 2001 Mar 16;276(11):8159-64
pubmed: 11099493
Mol Microbiol. 2001 Jan;39(1):47-53
pubmed: 11123687
Trends Microbiol. 2001 Oct;9(10):494-500
pubmed: 11597451
Eur J Biochem. 2002 Nov;269(22):5564-71
pubmed: 12423355
J Bacteriol. 2003 Oct;185(19):5706-13
pubmed: 13129941
Biochemistry. 2004 Sep 7;43(35):11206-13
pubmed: 15366930
J Biol Inorg Chem. 2005 May;10(3):221-30
pubmed: 15770503
Biochemistry. 2005 Aug 9;44(31):10533-40
pubmed: 16060662
Appl Microbiol Biotechnol. 2006 Sep;72(2):211-22
pubmed: 16791589
Appl Environ Microbiol. 2007 Feb;73(3):906-12
pubmed: 17142370
Biochim Biophys Acta. 2008 Sep;1778(9):1735-56
pubmed: 17935691
Methods Enzymol. 2009;463:29-34
pubmed: 19892164
Proteome Sci. 2010 Jun 15;8:32
pubmed: 20546627
Mol Syst Biol. 2011 Oct 11;7:539
pubmed: 21988835
Protein Expr Purif. 2012 Feb;81(2):145-50
pubmed: 22019762
Nat Methods. 2012 Jul;9(7):671-5
pubmed: 22930834
Protein Expr Purif. 2013 Feb;87(2):129-35
pubmed: 23168094
Appl Microbiol Biotechnol. 2013 May;97(9):3811-26
pubmed: 23529680
Protein J. 2013 Aug;32(6):419-25
pubmed: 23897421
Biochim Biophys Acta. 2014 Aug;1843(8):1620-8
pubmed: 24583120
Comput Struct Biotechnol J. 2012 Nov 22;3:e201210013
pubmed: 24688673
J Ind Microbiol Biotechnol. 2014 Sep;41(9):1435-42
pubmed: 25038884
Protein Expr Purif. 2015 Apr;108:9-12
pubmed: 25573388
Protein Expr Purif. 2015 Jul;111:18-22
pubmed: 25795130
Appl Biochem Biotechnol. 2015 Sep;177(2):458-71
pubmed: 26198023
Microb Cell Fact. 2015 Sep 02;14:125
pubmed: 26330219
Protein Expr Purif. 2016 Feb;118:49-54
pubmed: 26494603
Protein Expr Purif. 2016 May;121:61-5
pubmed: 26805756
Data Brief. 2016 Mar 04;7:502-8
pubmed: 27014739
J Chromatogr B Analyt Technol Biomed Life Sci. 2017 Feb 1;1043:122-127
pubmed: 27372913
Adv Pharm Bull. 2016 Jun;6(2):187-94
pubmed: 27478780
J Biotechnol. 2017 Sep 20;258:101-109
pubmed: 28238807
Microbiology. 1995 Mar;141 ( Pt 3):649-54
pubmed: 7711904
Curr Biol. 1996 Feb 1;6(2):178-82
pubmed: 8673464