In
metabolic engineering approach, isolation and characterization of promoters
leads to an understanding of which cis-acting elements are responsible for the
regulation of gene expression. DBR2 is a key enzyme in Artemisinin biosynthetic
pathway. In order to allow chromosome walking beyond the 5'-flanking region of
DBR2, two specific primers were used in combination with 6 arbitrary primers in
TAIL-PCR method. A 696bp upstream of DBR2 start codon was isolated and cloned.
The subsequent sequence analysis using bioinformatics softwares revealed that
there were several cis-acting elements such as TATA-box, CAAT-box, and
MeJA-responsive element, and several W-box and light-responsive elements inside
the DBR2 promoter. These results can be helpful in understanding of artemisinin
biosynthesis regulation and will facilitate metabolic engineering of the compound.
Website: http://www.arjonline.org/agricultural-sciences/american-research-journal-of-agriculture/
Website: http://www.arjonline.org/agricultural-sciences/american-research-journal-of-agriculture/
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