PCR isolation of catechol 2,3-dioxygenase gene fragments from environmental samples and their assembly into functional genes

Gene

Volumn 212, Issue 2, 1998, Pages 221-228

  Okuta, Akiko ^a   Ohnishi, Kouhei ^a   Harayama, Shigeaki ^a  

^a MARINE BIOTECHNOLOGY INSTITUTE   (Japan)

Author keywords

Catechol 2,3 dioxygenase; DNA diversity; DNA library; Hybrid enzyme; PCR

Indexed keywords

BACTERIAL DNA; CATECHOL 2,3 DIOXYGENASE; DNA FRAGMENT; OXYGENASE; UNCLASSIFIED DRUG;

AMINO ACID SEQUENCE; ARTICLE; BACTERIAL GENE; CLONING VECTOR; DNA LIBRARY; ENVIRONMENT; ENZYME SPECIFICITY; ESCHERICHIA COLI; GENE AMPLIFICATION; GENE ISOLATION; GENETIC TRANSFORMATION; HYBRID GENE; MOLECULAR CLONING; NONHUMAN; NUCLEOTIDE SEQUENCE; PHYLOGENY; PLASMID; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; STRUCTURAL GENE; THERMOSTABILITY;

AMINO ACID SEQUENCE; BACTERIAL PROTEINS; CATECHOL 2,3-DIOXYGENASE; DIOXYGENASES; ENVIRONMENTAL MICROBIOLOGY; ENZYME STABILITY; GENES, BACTERIAL; MOLECULAR SEQUENCE DATA; OXYGENASES; PEPTIDE FRAGMENTS; PETROLEUM; POLYMERASE CHAIN REACTION; RECOMBINANT PROTEINS; SEAWATER; SEQUENCE ALIGNMENT; SEQUENCE HOMOLOGY, AMINO ACID; SOIL MICROBIOLOGY; SUBSTRATE SPECIFICITY;

BACTERIA (MICROORGANISMS); ESCHERICHIA COLI;

EID: 0032496652     PISSN: 03781119     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0378-1119(98)00153-X     Document Type: Article

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