Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 2 de 2
Filter
Add more filters










Database
Language
Publication year range
1.
Biotechnol J ; 4(2): 230-7, 2009 Feb.
Article in English | MEDLINE | ID: mdl-19156736

ABSTRACT

The expression of proteins in plants both transiently and via permanently transformed lines has been demonstrated by a number of groups. Transient plant expression systems, due to high expression levels and speed of production, show greater promise for the manufacturing of biopharmaceuticals when compared to permanent transformants. Expression vectors based on a tobacco mosaic virus (TMV) are the most commonly utilized and the primary plant used, Nicotiana benthamiana, has demonstrated the ability to express a wide range of proteins at levels amenable to purification. N. benthamiana has two limitations for its use; one is its relatively slow growth, and the other is its low biomass. To address these limitations we screened a number of legumes for transient protein expression. Using the alfalfa mosaic virus (AMV) and the cucumber mosaic virus (CMV) vectors, delivered via Agrobacterium, we were able to identify three Pisum sativum varieties that demonstrated protein expression transiently. Expression levels of 420 +/- 26.24 mg GFP/kgFW in the green pea variety speckled pea were achieved. We were also able to express three therapeutic proteins indicating promise for this system in the production of biopharmaceuticals.


Subject(s)
Alfalfa mosaic virus/genetics , Cucumovirus/genetics , Pisum sativum/physiology , Plants, Genetically Modified/metabolism , Recombinant Proteins/metabolism , Transfection/methods , Genetic Vectors/genetics , Species Specificity
2.
Virology ; 381(1): 136-42, 2008 Nov 10.
Article in English | MEDLINE | ID: mdl-18804833

ABSTRACT

We have developed a Cucumber mosaic virus (CMV)-based expression vector for the production of heterologous proteins in plants. Cell-to-cell movement of CMV is dependent on the presence of coat protein (CP). Previous studies have shown that deletion of 33 amino acids (aa) from the carboxy-terminus of the 3a movement protein facilitates cell-to-cell movement that is independent of CP. The CMV-based expression vector that we have designed utilizes this truncated 3a protein, allowing the expression of target genes from the strong CP subgenomic promoter and without the need for providing CP in trans for cell-to-cell spread. Using this vector we achieved expression levels of ~450 mg/kg leaf tissue of green fluorescent protein (GFP) when the vector was delivered into Nicotiana benthamiana plants by agroinfiltration. Human growth hormone (hGH), on the other hand, accumulated to ~170 mg/kg of leaf tissue when the same approach was used to deliver the vector.


Subject(s)
Cucumovirus/genetics , Cucumovirus/physiology , Genetic Engineering , Genetic Vectors/genetics , Plant Viral Movement Proteins/metabolism , Gene Expression Regulation, Viral , Green Fluorescent Proteins/metabolism , Human Growth Hormone/genetics , Humans , Plant Viral Movement Proteins/genetics , Recombinant Proteins/metabolism , Sequence Deletion , Nicotiana/virology
SELECTION OF CITATIONS
SEARCH DETAIL
...