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Plants as Factories for Protein Production (Hardcover, 2002 ed.)
Loot Price: R4,306
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Plants as Factories for Protein Production (Hardcover, 2002 ed.)
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For over 10 years, TMV -based vectors have been used as plant
expression tools to examine gene regulation and function, protein
processing, pathogen elicitors, to manipulate biosynthetic
pathways, and to produce high levels of enzymes, proteins, or
peptides of interest in different locations in a plant cell. TMV
vectors often exhibit genetic stability of foreign RNA sequences
through multiple passages in plant hosts. Foreign coding sequences
can be expressed in plants where the stability, intracellular fate
and enzymatic or biological activities of the recombinant proteins
can be rapidly evaluated and optimized. These properties make viral
vectors attracti ve expression vehicles for testing and production
of a wide variety of recombinant peptides and proteins, for
structural analyses of post-translational modifications and for
assessing gene function and metabolic control. Finally, the utility
of both CP fusion and dual subgenomic vectors has extended beyond
the laboratory and greenhouse to field-scale production and
purification of recombinant products for commercial use (Grill,
1992; Grill, 1993; Turpen et at. , 1997). REFERENCES Copeman RJ,
Hartman IR and Watterson IC. 1969. Tobacco mosaic virus in
inoculated and systemically infected tobacco leaves. Phytopathology
59: 1012-1013. Dawson WO, Beck DL, Knorr DA and Grantham GL. 1986.
cDNA cloning of the complete genome of tobacco mosaic virus and
production of infectious transcripts. Proc. Natl. Acad. Sci. (USA)
83: 1832-1836. Dawson WO and Lehto KM. 1990. Regulation of
tobamovirus gene expression. Ad. Virus Res. 38:307-342. Dawson WOo
1992. Tobamovirus-Plant Interactions. Virology 186:359-367.
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