ASPERGILLUS ORYZAE FLH2 GENE
PROBLEM TO BE SOLVED: To culture a large amount of a new enzyme FLH2 having NO oxidizing action and a new amino acid sequence (416 amino acid residues) by culturing a transformant to E. coli, and to provide a method for easily and simply transforming eucaryotic organisms and screening a transgenic s...
Gespeichert in:
Hauptverfasser: | , , , , , , , , , , , , , , , , |
---|---|
Format: | Patent |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext bestellen |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | PROBLEM TO BE SOLVED: To culture a large amount of a new enzyme FLH2 having NO oxidizing action and a new amino acid sequence (416 amino acid residues) by culturing a transformant to E. coli, and to provide a method for easily and simply transforming eucaryotic organisms and screening a transgenic strain in introducing the transformant gene to a filamentous fungus by using expression of morphological changes such as coloration of a colony and improvement in spore formation which can be used as a selective marker. SOLUTION: Cloning of the gene coding for the new NO oxidation enzyme FLH2 is carried out. A host (E. coli) is transformed by transducing the new NO oxidation enzyme FLH2 gene into a vector and using an expressed plasmid. The FLH2 protein is confirmed to have maximum absorption at 350-450 nm. Aspergillus oryzae is transformed and compared with the nontrasformed strain to verify performance as the marker for selecting the transgenic strain. COPYRIGHT: (C)2003,JPO |
---|