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Journal ArticleDOI

Transient gene expression in electroporated protoplasts and intact cells of sugar beet

Keith Lindsey, +1 more
- 01 Jan 1987 - 
- Vol. 10, Iss: 1, pp 43-52
TLDR
Factors influencing the transient expression of introduced foreign DNA in electroporated protoplasts and intact cells of sugar beet were determined by assaying for the activity of chloramphenicol acetyltransferase (CAT), using a rectangular pulse generating system.
Abstract
Factors influencing the transient expression of introduced foreign DNA in electroporated protoplasts and intact cells of sugar beet were determined by assaying for the activity of chloramphenicol acetyltransferase (CAT), using a rectangular pulse generating system. Extractable CAT activity depended upon 1) applied plasmid DNA concentration, 2) protoplast density, 3) the interaction between pulse field strength, duration, number, time interval between pulses and the resultant effect on culture viability, and 4) the physiological state of the protoplasts. Mesophyll protoplasts were more susceptible to damage by electroporation, and were more specific in their requirement for electroporations which allowed CAT expression, than were protoplasts derived from suspension culture cells. CAT activity was also demonstrated, at low levels, after electroporation of intact suspension culture cells, and could be increased by pectinase treatment of the cells before electroporation.

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Citations
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Journal ArticleDOI

An Agrobacterium-mediated transient gene expression system for intact leaves

TL;DR: An efficient and reproducible Agrobacterium -mediated transient gene expression system for intact leaf tissue was developed and similar results were obtained with other plant species, such as Phaseolus acutifolius, poplar, and tobacco.
Patent

Methods and compositions for the production of stably transformed fertile monocot plants and cells thereof

TL;DR: In this article, a reproducible system for the production of stable, genetically transformed maize cells, and to methods of selecting cells that have been transformed, is described. But the system is not applicable to the field of agriculture.
PatentDOI

Fertile transgenic corn plants

TL;DR: Fertile transgenic Zea mays (corn) plants which stably express recombinant DNA which is heritable are provided wherein said DNA preferably comprises a recombinant gene which encodes a seed storage protein, so that the amino acid profile of the corn is improved as discussed by the authors.
Patent

Method for preparing fertile transgenic corn plants

TL;DR: In this article, a transgenic Zea mays (corn) plants which stably express heterologous DNA which is heritable are disclosed along with a process for producing said plants.
Journal ArticleDOI

Molecular farming of pharmaceutical proteins.

TL;DR: The promise of using transgenic plants as bioreactors for the molecular farming of recombinant therapeutics, including vaccines, diagnostics, such as recombinant antibodies, plasma proteins, cytokines and growth factors, is demonstrated.
References
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Journal ArticleDOI

A revised medium for rapid growth and bio assays with tobacco tissue cultures

TL;DR: In vivo redox biosensing resolves the spatiotemporal dynamics of compartmental responses to local ROS generation and provide a basis for understanding how compartment-specific redox dynamics may operate in retrograde signaling and stress 67 acclimation in plants.
Journal ArticleDOI

Recombinant genomes which express chloramphenicol acetyltransferase in mammalian cells.

TL;DR: A series of recombinant genomes which directed expression of the enzyme chloramphenicol acetyltransferase (CAT) in mammalian cells provided a uniquely convenient system for monitoring the expression of foreign DNAs in tissue culture cells.
Journal ArticleDOI

Gene transfer into mouse lyoma cells by electroporation in high electric fields.

TL;DR: A simple physical model for the enhanced DNA penetration into cells in high electric fields is proposed, according to which the interaction of the external electric field with the lipid dipoles of a pore configuration induces and stabilizes the permeation sites and thus enhances cross membrane transport.
Journal ArticleDOI

The Use of Fluorescein Diacetate and Phenosafranine for Determining Viability of Cultured Plant Cells

TL;DR: The most suitable dyes tested were fluorescein diacetate for viable cells and phenosafranine for dead cells and these dyes stained specifically whether the cells were from cultures of different ages, of different species or if the cells had been treated in various, often toxic, ways.
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