Versatile and stable vectors for efficient gene expression in Ralstonia eutropha H16

Journal of Biotechnology

Volumn 186, Issue , 2014, Pages 74-82

  Gruber, Steffen ^a   Hagen, Jeremias ^a   Schwab, Helmut ^a   Koefinger, Petra ^a  

^a GRAZ UNIVERSITY OF TECHNOLOGY   (Austria)

Author keywords

Expression system; Origin of replication; Plasmid stability; Promoter; Ralstonia eutropha H16

Indexed keywords

BACTERIA; CARBON DIOXIDE; FERMENTATION; GENE EXPRESSION; PROTEINS; VECTORS;

EXPRESSION SYSTEM; ORIGIN OF REPLICATION; PLASMID STABILITY; PROMOTER; RALSTONIA EUTROPHA;

DNA;

GENTAMICIN; KANAMYCIN; BACTERIAL PROTEIN; GREEN FLUORESCENT PROTEIN; RECOMBINANT PROTEIN;

ARTICLE; BACTERIOPHAGE T5; CONTROLLED STUDY; CUPRIAVIDUS NECATOR; DNA BASE COMPOSITION; DNA REPLICATION ORIGIN; EXPRESSION VECTOR; GENE DOSAGE; GENE EXPRESSION; GENE EXPRESSION SYSTEM; GENE SEQUENCE; METABOLIC ENGINEERING; NONHUMAN; PLASMID; PRIORITY JOURNAL; PROMOTER REGION; RALSTONIA EUTROPHA H16; CHEMISTRY; FERMENTATION; GENE VECTOR; GENETIC ENGINEERING; GENETICS; METABOLISM; PROCEDURES;

BACTERIAL PROTEINS; CUPRIAVIDUS NECATOR; FERMENTATION; GENE DOSAGE; GENETIC ENGINEERING; GENETIC VECTORS; GREEN FLUORESCENT PROTEINS; PLASMIDS; PROMOTER REGIONS, GENETIC; RECOMBINANT PROTEINS;

EID: 84904429534     PISSN: 01681656     EISSN: 18734863     Source Type: Journal    
DOI: 10.1016/j.jbiotec.2014.06.030     Document Type: Article

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