Genetic transformation of Labisia Pumila using Agrobacterium Tumefaciens
The present protocol was aimed to establish a routine transformation procedure via Agrobaderium tumefaciens for Labisia puml'la var. pumila. The effect of different factors on T-DNA transfer by measuring transcient expression levels of a disarmed strain lBA 4404 harbouring the binary vector...
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| Format: | Thesis |
| Language: | English |
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2007
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| Online Access: | https://eprints.ums.edu.my/id/eprint/19716/1/Genetic%20transformation%20of%20Labisia%20Pumila.pdf |
| _version_ | 1825713432333123584 |
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| author | Ainul Mardziah Mohamed |
| author_facet | Ainul Mardziah Mohamed |
| author_sort | Ainul Mardziah Mohamed |
| collection | UMS |
| description | The present protocol was aimed to establish a routine transformation procedure
via Agrobaderium tumefaciens for Labisia puml'la var. pumila. The effect of
different factors on T-DNA transfer by measuring transcient expression levels of
a disarmed strain lBA 4404 harbouring the binary vector pBI121 carrying
chimeric glucuronidase (GUS) and neomycin phosphotransferase (NP71l) genes
examined. Parameters optimized were light influence, types of wounding, types
of explant, co-cultivation period, bacterial concentration, shaking influence,
addition of glucose, pH, temperature, addition of acetosyringone and addition of
sucrose. Improved transformation frequencies were btained with an A.
tumefaciens strain carrying kanamycin-type vir genes and when leaves were
infected with Agrobaderium cells in the early log growth phase. Optimized cocultivation
was performed in the presence of 251-1g/1 of kanamycin. Methods
used have expressed up to 77.62% positive transformants. This result were
done using leaf explants co-cultivated for two days using a batch of
Agrobaderium grown until giving the reading of 0.9 absorbance taken at
600nm wavelength. The leaves were poked using sterile needle and co-cultivated
with Agrobacterium at room temperature with the addition of
0.02mg/1 of acetosyringone, 5g/1 of glucose and 15g/1 of sucrose in the pH 7
medium. The mixture was left with 24h lighting and 100rpm aggitation.
Expression and presence of transgene was assayed by histochemical test and
later confirmed with polymerase chain reaction. Seven percent transgenic plants
were micropropagated and successfully acclimatised. The protocol is yet t be
proven t enable it t be reproducible. |
| first_indexed | 2024-03-06T02:56:29Z |
| format | Thesis |
| id | ums.eprints-19716 |
| institution | Universiti Malaysia Sabah |
| language | English |
| last_indexed | 2024-03-06T02:56:29Z |
| publishDate | 2007 |
| record_format | dspace |
| spelling | ums.eprints-197162018-04-04T08:17:13Z https://eprints.ums.edu.my/id/eprint/19716/ Genetic transformation of Labisia Pumila using Agrobacterium Tumefaciens Ainul Mardziah Mohamed RS Pharmacy and materia medica The present protocol was aimed to establish a routine transformation procedure via Agrobaderium tumefaciens for Labisia puml'la var. pumila. The effect of different factors on T-DNA transfer by measuring transcient expression levels of a disarmed strain lBA 4404 harbouring the binary vector pBI121 carrying chimeric glucuronidase (GUS) and neomycin phosphotransferase (NP71l) genes examined. Parameters optimized were light influence, types of wounding, types of explant, co-cultivation period, bacterial concentration, shaking influence, addition of glucose, pH, temperature, addition of acetosyringone and addition of sucrose. Improved transformation frequencies were btained with an A. tumefaciens strain carrying kanamycin-type vir genes and when leaves were infected with Agrobaderium cells in the early log growth phase. Optimized cocultivation was performed in the presence of 251-1g/1 of kanamycin. Methods used have expressed up to 77.62% positive transformants. This result were done using leaf explants co-cultivated for two days using a batch of Agrobaderium grown until giving the reading of 0.9 absorbance taken at 600nm wavelength. The leaves were poked using sterile needle and co-cultivated with Agrobacterium at room temperature with the addition of 0.02mg/1 of acetosyringone, 5g/1 of glucose and 15g/1 of sucrose in the pH 7 medium. The mixture was left with 24h lighting and 100rpm aggitation. Expression and presence of transgene was assayed by histochemical test and later confirmed with polymerase chain reaction. Seven percent transgenic plants were micropropagated and successfully acclimatised. The protocol is yet t be proven t enable it t be reproducible. 2007 Thesis NonPeerReviewed text en https://eprints.ums.edu.my/id/eprint/19716/1/Genetic%20transformation%20of%20Labisia%20Pumila.pdf Ainul Mardziah Mohamed (2007) Genetic transformation of Labisia Pumila using Agrobacterium Tumefaciens. Masters thesis, Universiti Malaysia Sabah. |
| spellingShingle | RS Pharmacy and materia medica Ainul Mardziah Mohamed Genetic transformation of Labisia Pumila using Agrobacterium Tumefaciens |
| title | Genetic transformation of Labisia Pumila using Agrobacterium Tumefaciens |
| title_full | Genetic transformation of Labisia Pumila using Agrobacterium Tumefaciens |
| title_fullStr | Genetic transformation of Labisia Pumila using Agrobacterium Tumefaciens |
| title_full_unstemmed | Genetic transformation of Labisia Pumila using Agrobacterium Tumefaciens |
| title_short | Genetic transformation of Labisia Pumila using Agrobacterium Tumefaciens |
| title_sort | genetic transformation of labisia pumila using agrobacterium tumefaciens |
| topic | RS Pharmacy and materia medica |
| url | https://eprints.ums.edu.my/id/eprint/19716/1/Genetic%20transformation%20of%20Labisia%20Pumila.pdf |
| work_keys_str_mv | AT ainulmardziahmohamed genetictransformationoflabisiapumilausingagrobacteriumtumefaciens |