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020 _a9781617379673
024 7 _a10.1007/978-1-61737-967-3
_2doi
040 _aES-MaUEC
_bspa
_cES-MaUEC
_dES-MaUEC
050 4 _aQH450
_b2011 EB
245 0 0 _aHeterologous Gene Expression in E.coli :
_bMethods and Protocols
_cedited by Thomas C. Evans, Jr., Ming-Qun Xu
250 _a1st edition 2011
264 1 _aTotowa, NJ
_bHumana Press
_c2011
300 _a1 recurso en línea (XI, 310 páginas)
336 _atexto
_btxt
_2rdacontent
337 _aelectrónico
_bc
_2rdamedia
338 _arecurso electrónico
_bcr
_2rdacarrier
347 _aarchivo de texto
_bPDF
490 0 _aMethods in Molecular Biology
_x1940-6029
_v705
505 0 _aAdjustment of Codon Usage Frequencies by Codon Harmonization Improves Protein Expression and Folding -- SUMO Fusion Technology for Enhanced Protein Expression and Purification in Prokaryotes and Eukaryotes -- Molecular and Chemical Chaperones for Improving the Yields of Soluble Recombinant Proteins -- Genetic Selection of Solubility-Enhanced Proteins Using the Twin-Arginine Translocation System -- Protein Folding Liquid Chromatography -- Site-Specific Protein Labeling by Intein-Mediated Protein Ligation -- Efficient Expression of Human Aromatase (CYP19) in E. coli -- Expression of Recombinant Cytochromes c in E. coli -- Semi-Synthesis of Glycoproteins from E. coli through Native Chemical Ligation -- Expression of Recombinant Proteins with Uniform N-Termini -- Recent Developments in Difficult Protein Expression: A Guide to E. coli Strains, Promoters, and Relevant Host Mutations -- Periplasmic Chaperones Used to Enhance Functional Secretion of Proteins in E. coli -- Engineering Unusual Amino Acids into Peptides Using Lantibiotic Synthetase -- The Targeted Expression of Nucleotide Sugar Transporters to the E. coli Inner Membrane -- Detection of Protein-Protein Interactions in Bacteria by GFP-Fragment Reconstitution -- Enhancing the Solubility of Recombinant Proteins in Escherichia coli by Using Hexahistidine-Tagged Maltose-Binding Protein as a Fusion Partner -- Introducing Predetermined Mutations throughout a Target Gene Using TDEM (Transposon Directed Base-Exchange Mutagenesis) -- Fluorescent Site-Specific Labeling of Escherichia coli Expressed Proteins with Sfp Phosphopantetheinyl Transferase.
520 _aProtein expression in a heterologous host is a cornerstone of biomedical research and of the biotechnology industry. Despite the advanced state of protein expression technology improvements are still needed. For example, membrane proteins constitute a significant percentage of the total cellular proteins but as a class are very difficult to overexpress, especially in a heterologous host. The ideal host would have the ability to express any protein, with relevant post-translational modifications, and be as easy to work with as E. coli. In Heterologous Gene Expression in E. coli: Methods and Protocols, expert scientists intimately familiar with the relevant techniques offer chapters that greatly expand the utility of this expression host. The contributions in this detailed volume describe methods, for example, to successfully express proteins in E. coli that would otherwise form aggregates in this host, to add post-translational modifications, to incorporate non-standard amino acid residues or moieties into E. coli expressed proteins, to identify binding partners, and to express membrane proteins. Written in the highly successful Methods in Molecular Biology™ format, chapters include introductions to their respective subjects, lists of the necessary materials and reagents, step-by-step, readily reproducible laboratory protocols, and tips on troubleshooting and avoiding known pitfalls. Practical and cutting-edge, Heterologous Gene Expression in E. coli: Methods and Protocols seeks to familiarize the researcher with the myriad of E. coli expression strains available and move E. coli closer to that ideal of the perfect host.
988 _aSpringer_Protocols_2011
650 7 _2embne
_9162770
_aExpresión génica
_vManuales de laboratorio
776 0 8 _iPrinted edition:
_z9781617379666
776 0 8 _iPrinted edition:
_z9781617379680
776 0 8 _iPrinted edition:
_z9781493957255
856 4 0 _uhttps://go.openathens.net/redirector/universidadeuropea.es?url=https://doi.org/10.1007/978-1-61737-967-3
_zAcceso a este recurso digital (usuarios Universidad Europea de Madrid)
942 _2lcc
_cLE
998 _b12/2023
_dz
_eu
_zSI