The isolation and partial characterisation of the chalcone synthase, flavanone 3-hydroxylase and phytoene synthase gene fragments from oncidium taka by using RT-PCR
The RT-PCR technique was used to isolate partial gene fragments for the chalcone synthase (CRS), flavanone 3-hydroxylase (F3H) and phytoene synthase (PSY) genes from 0. taka. The RT-PCR products were amplified by degenerate primers specifically designed for the genes and the templates (total RNA)...
Saved in:
Main Author: | |
---|---|
Format: | Thesis |
Language: | English English |
Published: |
2000
|
Subjects: | |
Online Access: | http://psasir.upm.edu.my/id/eprint/9091/1/FSAS_2000_21%20IR.pdf |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
id |
my-upm-ir.9091 |
---|---|
record_format |
uketd_dc |
spelling |
my-upm-ir.90912024-03-25T00:33:27Z The isolation and partial characterisation of the chalcone synthase, flavanone 3-hydroxylase and phytoene synthase gene fragments from oncidium taka by using RT-PCR 2000-05 Ong, Wai Kean The RT-PCR technique was used to isolate partial gene fragments for the chalcone synthase (CRS), flavanone 3-hydroxylase (F3H) and phytoene synthase (PSY) genes from 0. taka. The RT-PCR products were amplified by degenerate primers specifically designed for the genes and the templates (total RNA) were prepared from the leaves, open flowers and flower buds of 0. taka. A 6S0bp RT -PCR product was successfully amplified from the three different total RNA templates when the degenerate primers for CHS were used. Similarly, a 543bp RT-PCR product was obtained when the degenerate primers for PSY were used on the three different total RNA templates. Only the total RNA preparation from flower buds gave a 503bp RTPCR product when the degenerate primers for F3H were used. The deduced amino acid sequence for the 650bp DNA fragment was found to have a high homology to other CHS sequences in the Genebank, averaging at 66%. Additionally, this sequence also has an exceptionally high homology to previously reported bibenzyl synthase (BibSyl) sequences, with an average percentage of 85%. The 503bp fragment has on average 76% homology to the F3H sequences reported for other plant species. As for the 543bp fragment, it has an avemge of 76% homology to other PSY gene sequences published at Genebank. The results indicate that the CHS and PS Y genes are expressed in all the tissues tested whereas the F3 H gene is only expressed at the flower bud stage in 0. taka. These gene fragments were labelled with DIG and used as probes to screen a genomic DNA library constructed from partially digested genomic DNA of O. taka. Currently, the F3H probe (503bp DNA fragment) has led to the isolation of a genomic clone with an insert size of around 11kb. The genomic clone was restricted into 2 fragments with BamH I and subcloned into the pUC 18 vector separately. The characterisation of the clone is underway. Plant gene isolation - Case studies 2000-05 Thesis http://psasir.upm.edu.my/id/eprint/9091/ http://psasir.upm.edu.my/id/eprint/9091/1/FSAS_2000_21%20IR.pdf text en public masters Universiti Putra Malaysia Plant gene isolation - Case studies Faculty of Science and Environmental Studies Mahmood, Marziah English |
institution |
Universiti Putra Malaysia |
collection |
PSAS Institutional Repository |
language |
English English |
advisor |
Mahmood, Marziah |
topic |
Plant gene isolation - Case studies |
spellingShingle |
Plant gene isolation - Case studies Ong, Wai Kean The isolation and partial characterisation of the chalcone synthase, flavanone 3-hydroxylase and phytoene synthase gene fragments from oncidium taka by using RT-PCR |
description |
The RT-PCR technique was used to isolate partial gene fragments for the chalcone
synthase (CRS), flavanone 3-hydroxylase (F3H) and phytoene synthase (PSY) genes
from 0. taka. The RT-PCR products were amplified by degenerate primers
specifically designed for the genes and the templates (total RNA) were prepared
from the leaves, open flowers and flower buds of 0. taka. A 6S0bp RT -PCR product
was successfully amplified from the three different total RNA templates when the
degenerate primers for CHS were used. Similarly, a 543bp RT-PCR product was
obtained when the degenerate primers for PSY were used on the three different total
RNA templates. Only the total RNA preparation from flower buds gave a 503bp RTPCR
product when the degenerate primers for F3H were used. The deduced amino acid sequence for the 650bp DNA fragment was found to have a
high homology to other CHS sequences in the Genebank, averaging at 66%.
Additionally, this sequence also has an exceptionally high homology to previously
reported bibenzyl synthase (BibSyl) sequences, with an average percentage of 85%.
The 503bp fragment has on average 76% homology to the F3H sequences reported
for other plant species. As for the 543bp fragment, it has an avemge of 76%
homology to other PSY gene sequences published at Genebank. The results indicate
that the CHS and PS Y genes are expressed in all the tissues tested whereas the F3 H
gene is only expressed at the flower bud stage in 0. taka.
These gene fragments were labelled with DIG and used as probes to screen a
genomic DNA library constructed from partially digested genomic DNA of O. taka.
Currently, the F3H probe (503bp DNA fragment) has led to the isolation of a
genomic clone with an insert size of around 11kb. The genomic clone was restricted
into 2 fragments with BamH I and subcloned into the pUC 18 vector separately. The
characterisation of the clone is underway. |
format |
Thesis |
qualification_level |
Master's degree |
author |
Ong, Wai Kean |
author_facet |
Ong, Wai Kean |
author_sort |
Ong, Wai Kean |
title |
The isolation and partial characterisation of the chalcone synthase, flavanone 3-hydroxylase and phytoene synthase gene fragments from oncidium taka by using RT-PCR |
title_short |
The isolation and partial characterisation of the chalcone synthase, flavanone 3-hydroxylase and phytoene synthase gene fragments from oncidium taka by using RT-PCR |
title_full |
The isolation and partial characterisation of the chalcone synthase, flavanone 3-hydroxylase and phytoene synthase gene fragments from oncidium taka by using RT-PCR |
title_fullStr |
The isolation and partial characterisation of the chalcone synthase, flavanone 3-hydroxylase and phytoene synthase gene fragments from oncidium taka by using RT-PCR |
title_full_unstemmed |
The isolation and partial characterisation of the chalcone synthase, flavanone 3-hydroxylase and phytoene synthase gene fragments from oncidium taka by using RT-PCR |
title_sort |
isolation and partial characterisation of the chalcone synthase, flavanone 3-hydroxylase and phytoene synthase gene fragments from oncidium taka by using rt-pcr |
granting_institution |
Universiti Putra Malaysia |
granting_department |
Faculty of Science and Environmental Studies |
publishDate |
2000 |
url |
http://psasir.upm.edu.my/id/eprint/9091/1/FSAS_2000_21%20IR.pdf |
_version_ |
1804888543686819840 |