Your browser doesn't support javascript.
loading
Metabolic engineering of medicinal plants: transgenic Atropa belladonna with an improved alkaloid composition.
Yun, D J; Hashimoto, T; Yamada, Y.
Afiliação
  • Yun DJ; Department of Agricultural Chemistry, Faculty of Agriculture, Kyoto University, Japan.
Proc Natl Acad Sci U S A ; 89(24): 11799-803, 1992 Dec 15.
Article em En | MEDLINE | ID: mdl-1465402
ABSTRACT
The tropane alkaloid scopolamine is a medicinally important anticholinergic drug present in several solanaceous plants. Hyoscyamine 6 beta-hydroxylase (EC 1.14.11.11) catalyzes the oxidative reactions in the biosynthetic pathway leading from hyoscyamine to scopolamine. We introduced the hydroxylase gene from Hyoscyamus niger under the control of the cauliflower mosaic virus 35S promoter into hyoscyamine-rich Atropa belladonna by the use of an Agrobacterium-mediated transformation system. A transgenic plant that constitutively and strongly expressed the transgene was selected, first by screening for kanamycin resistance and then by immunoscreening leaf samples with an antibody specific for the hydroxylase. In the primary transformant and its selfed progeny that inherited the transgene, the alkaloid contents of the leaf and stem were almost exclusively scopolamine. Such metabolically engineered plants should prove useful as breeding materials for obtaining improved medicinal components.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Métodos Terapêuticos e Terapias MTCI: Terapias_biologicas Assunto principal: Plantas Medicinais / Plantas Tóxicas / Atropina / Escopolamina / Atropa belladonna / Plantas Geneticamente Modificadas / Oxigenases de Função Mista Idioma: En Revista: Proc Natl Acad Sci U S A Ano de publicação: 1992 Tipo de documento: Article País de afiliação: Japão

Texto completo: 1 Base de dados: MEDLINE Métodos Terapêuticos e Terapias MTCI: Terapias_biologicas Assunto principal: Plantas Medicinais / Plantas Tóxicas / Atropina / Escopolamina / Atropa belladonna / Plantas Geneticamente Modificadas / Oxigenases de Função Mista Idioma: En Revista: Proc Natl Acad Sci U S A Ano de publicação: 1992 Tipo de documento: Article País de afiliação: Japão