Construction of the expression vector based on the growth phase- and growth rate-dependent rmf promoter: Use of cell growth rate to control the expression of cloned genes in Escherichia coli

Biotechnology Letters

Volumn 23, Issue 1, 2001, Pages 5-11

  Chao, Yun Peng ^a   Wen, Chih Sheng ^a   Chiang, Chung Jen ^b   Wang, Jenn Jye ^b  

^a FENG CHIA UNIVERSITY   (Taiwan)

^b Widetex Chemical Co   (Taiwan)

Author keywords

Bioremediation; Expression vector; Growth phase; Ribosome modulation factor

Indexed keywords

BCR ABL PROTEIN; BETA GALACTOSIDASE; FUSION PROTEINS, BCR ABL; HYBRID PROTEIN; TRANSACTIVATOR PROTEIN;

ARTICLE; BACTERIAL GENE; BACTERIAL GROWTH; BIOPROCESS; BIOTRANSFORMATION; CHRONIC MYELOID LEUKEMIA; DNA VECTOR; ESCHERICHIA COLI; EXPRESSION VECTOR; FERMENTATION; GENE EXPRESSION; GENE EXPRESSION REGULATION; GENETICS; METABOLISM; MOLECULAR CLONING; NONHUMAN; POLYACRYLAMIDE GEL ELECTROPHORESIS; PROMOTER REGION; PROTEIN SYNTHESIS;

ELECTROPHORESIS, POLYACRYLAMIDE GEL; ESCHERICHIA COLI; FUSION PROTEINS, BCR-ABL; GENE EXPRESSION; GENE PRODUCTS, TAT; GENETIC VECTORS; LEUKEMIA, MYELOGENOUS, CHRONIC, BCR-ABL POSITIVE; RECOMBINANT FUSION PROTEINS;

BACTERIA (MICROORGANISMS); ESCHERICHIA COLI;

EID: 0035136224     PISSN: 01415492     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1026775906596     Document Type: Article

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