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Literature summary for 1.13.12.19 extracted from

  • Araki, S.; Matsuoka, M.; Tanaka, M.; Ogawa, T.
    Ethylene formation and phenotypic analysis of transgenic tobacco plants expressing a bacterial ethylene-forming enzyme (2000), Plant Cell Physiol., 41, 327-334.
    View publication on PubMed

Application

Application Comment Organism
agriculture introduction of a gene encoding a chimeric protein consisting of EFE and beta-glucuronidase GUS into the tobacco genome using a binary vector which directs expression of the EFE-beta-glucuronidase fusion protein under the control of constitutive promoter of cauliflower mosaic virus 35S RNA. Transgenic plants produce ethylene at consistently higher rates than the untransformed plant, and their beta-glucuronidase activities are expressed in different tissues. A significant dwarf morphology observed in the transgenic tobacco displaying the highest ethylene production resembles the phenotype of a wild-type plant exposed to excess ethylene Pseudomonas syringae

Cloned(Commentary)

Cloned (Comment) Organism
expression in Nicotiana tabacum Pseudomonas syringae

Protein Variants

Protein Variants Comment Organism
additional information introduction of a gene encoding a chimeric protein consisting of EFE and beta-glucuronidase GUS into the tobacco genome using a binary vector which directs expression of the EFE-GUS fusion protein under the control of constitutive promoter of cauliflower mosaic virus 35S RNA Pseudomonas syringae

Organism

Organism UniProt Comment Textmining
Pseudomonas syringae P32021 pv. phaseolicola PK2
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