Using promoter libraries to reduce metabolic burden due to plasmid-encoded proteins in recombinant Escherichia coli

New Biotechnology

Volumn 33, Issue 1, 2016, Pages 78-90

  Pasini, Martina ^a   Fernández Castané, Alfred ^b   Jaramillo, Alfonso ^c,d   de Mas, Carles ^a   Caminal, Gloria ^e   Ferrer, Pau ^a  

^a UNIVERSITAT AUTÒNOMA DE BARCELONA   (Spain)

^b UNIVERSITY OF BIRMINGHAM   (United Kingdom)

^c UNIVERSITY OF WARWICK   (United Kingdom)

^d UNIVERSITÉ D EVRY VAL D ESSONNE   (France)

^e INSTITUTE OF ADVANCED CHEMISTRY OF CATALONIA IQAC CSIC   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACIDS; ANTIBIOTICS; DNA; ESCHERICHIA COLI; GENES; METABOLISM; PHYSIOLOGICAL MODELS; SYNTHETIC BIOLOGY;

ACETIC ACID PRODUCTIONS; ANTIBIOTIC RESISTANCE GENES; AUXOTROPHIC MARKERS; HETEROLOGOUS PROTEINS; PHYSIOLOGICAL RESPONSE; RECOMBINANT ESCHERICHIA COLI; SECOND GENERATION SYSTEMS; SECONDARY METABOLISM;

RECOMBINANT PROTEINS;

ACETIC ACID; FRUCTOSE BISPHOSPHATE ALDOLASE; FUCULOSE PHOSPHATE ALDOLASE; GLYCINE; GLYCINE AUXOTROPHIC MARKER; LAC REPRESSOR; PLASMID DNA; RECOMBINANT PROTEIN; REPRESSOR PROTEIN; UNCLASSIFIED DRUG; ANTIINFECTIVE AGENT; ESCHERICHIA COLI PROTEIN; GLUCOSE; METHYLTRANSFERASE;

ANTIBIOTIC RESISTANCE; ARTICLE; BACTERIAL STRAIN; COMPARATIVE STUDY; CONTROLLED STUDY; DNA SEQUENCE; ESCHERICHIA COLI; GENE CONSTRUCT; GENE EXPRESSION SYSTEM; GENE LIBRARY; HETEROLOGOUS EXPRESSION; MARKER GENE; METABOLIC ENGINEERING; MOLECULAR BIOLOGY; NONHUMAN; PLASMID; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; PROMOTER REGION; PROTEIN EXPRESSION; SYNTHETIC BIOLOGY; BIOMASS; CELL CULTURE TECHNIQUE; DRUG EFFECTS; GENE EXPRESSION REGULATION; GENE VECTOR; GENETIC RECOMBINATION; GENETICS; GROWTH, DEVELOPMENT AND AGING; METABOLISM;

ACETIC ACID; ANTI-BACTERIAL AGENTS; BIOMASS; CELL CULTURE TECHNIQUES; ESCHERICHIA COLI; ESCHERICHIA COLI PROTEINS; GENE EXPRESSION REGULATION, BACTERIAL; GENETIC VECTORS; GLUCOSE; METHYLTRANSFERASES; PLASMIDS; PROMOTER REGIONS, GENETIC; RECOMBINATION, GENETIC;

EID: 84942133361     PISSN: 18716784     EISSN: 18764347     Source Type: Journal    
DOI: 10.1016/j.nbt.2015.08.003     Document Type: Article

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