S3-07
Transformation of African Cassava for Increased Starch Production.
Ihemere
U.E.1, D.I. Arias-Garzon2 and R.T. Sayre1, 2
1.
Departments of Horticulture and Crop Science
2.
Plant Biology, The Ohio State University, Columbus, OH 43210
IHEMERE.1@MAGNUS.ACS.OHIO-STATE.EDU
Cassava
is a good candidate for starch production studies because it has a high
photosynthetic rate, an ability to grow on poor soils and it is
protected from many pests and herbivores due to the presence of
cyanogens. The objective of
this study is to increase the root starch production potential of
cassava by introducing into the plant a modified E.
coli glgC gene, which is driven by the tuber-specific patatin
promoter and is also expressed in cassava roots.
The choice of the E. coli
glgC gene, which encodes ADP-glucose pyrophosphorylase (AGPase),
over the plant’s genes was because the glgC
gene encodes a homodimeric AGPase while the plant’s AGPase is a
heterotetrameric enzyme, that makes cloning difficult.
In addition, the modified E.coli
gene encodes an enzyme with higher activity than the plant enzymes.
Twenty three putative transformed plants were obtained of which
seven have been proven to carry the transgene by PCR and RT-PCR
analysis. Enzyme assays and Southern blotting are being carried out to
confirm the transformation of the plants.
It is proposed that enhanced conversion of sugars to substrates
for starch synthesis in roots will generate plants with higher starch
yields and faster root maturation.
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