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Evaluation of different promoters driving the GFP reporter gene in seaweed Kappaphycus alvarezii

Indonesian Journal of Biotechnology · Vol. 19 No. 2 (2014) · hlm. 129–135

DOI
10.22146/ijbiotech.9304
ISSN
2089-2241, 0853-8654
Terbit
2014-12-08
Penerbit
Universitas Gadjah Mada
Bahasa
eng
Lisensi
creativecommons.org/licenses/by-sa/4.0

Abstrak

Promoter regulates expression level of foreign gene in transgenic organism. This study was performed to select asuitable promoter as the fi rst step towards production of valuable trait-enhanced seaweed by transgenic technology. Greenfl uorescent protein (GFP) gene was used as a reporter to determine the activity of promoter in seaweed Kappaphycusalvarezii. GFP gene constructs driven by cytomegalovirus (pCMV-GFP), caulifl ower mosaic virus (pCaMV-GFP),medaka β-actin (pmBA-GFP) and Japanese fl ounder keratin (pJfKer-GFP) promoters were introduced by electroporationmethod. Electroporation was performed using a gene pulser (BIORAD) with voltage of 300 V, pulse length of 0.5 ms,pulse numbers of 4, and pulse interval of 0.1 s. Promoter activity was determined by analyzing GFP gene expressionlevel using a fl uorescent microscope. The results showed that CMV regulated highest number of fi lament callus(34.10%±1.49) expressing GFP at medium to strong fl uorescence levels. CaMV promoter had relatively similar activitywith CMV, but lower number of fi lament callus expressing GFP (10.48%±0.25). mBA promoter drove GFP expressionat medium level and similar number of fi lament callus (8.85%±2.31) expressing GFP with CaMV, while JfKer promoterhad lowest activity by means in number of fi lament callus expressing GFP (4.79%±0.26) and GFP expression level. PCRanalysis for transgenic confi rmation showed a DNA band of PCR product from pCMV-GFP and pCaMV-GFP expressingfi lament callus in the same size (about 0.6 kb) with positive control of plasmid. Thus, CMV and CaMV promoters wasan appropriate promoter and foreign gene could be transferred to fi lament callus by electroporation method. Combiningthis achievement with developing a culture method of fi lament callus to be thallus, stable transgenic breeding in K.alvarezii can be feasible.

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  • Indonesian Center for Agricultural Biotechnology and Genetic Resource Research and Development
  • Universitas Gadjah Mada
  • Politeknik Pertanian Negeri Pangkajene Kepulauan
  • University of Darussalam Gontor
  • Afiliasi tidak diketahui
  • Organisasi berbeda
  • Organisasi sama
  • Afiliasi tidak diketahui
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Tampilkan sebagai tabel
Rekan penulisOrganisasiArtikel bersama
Suharsono SuharsonoAfiliasi tidak diketahui2
Nampiah SukarnoAfiliasi tidak diketahui2
LATIFAH KOSIM DARUSMANAfiliasi tidak diketahui2
ROHANI CINTA BADIA GINTINGAfiliasi tidak diketahui2
SIHEGIKO KANAYAAfiliasi tidak diketahui2
Widya AsmaraUniversitas Gadjah Mada2
Jaka WidadaUniversitas Gadjah Mada2
M. MustofaAfiliasi tidak diketahui2
AlimuddinAfiliasi tidak diketahui2
Komar SumantadinataAfiliasi tidak diketahui2
Ratu Siti AliahAfiliasi tidak diketahui2
Media Fitri Isma NugrahaAfiliasi tidak diketahui1
Hessy NovitaAfiliasi tidak diketahui1
Rossa YunitaIndonesian Center for Agricultural Biotechnology and Genetic Resource Research and Development1
Wening EnggariniIndonesian Center for Agricultural Biotechnology and Genetic Resource Research and Development1
Reflinur ReflinurIndonesian Center for Agricultural Biotechnology and Genetic Resource Research and Development1
Fasya Hadaina MaharaniAfiliasi tidak diketahui1
Berna ElyaAfiliasi tidak diketahui1
Mochamad SyaifudinAfiliasi tidak diketahui1
Agus Oman SudrajatAfiliasi tidak diketahui1
Niken TrisnaningrumUniversity of Darussalam Gontor1
LULUT DWI SULISTYANINGSIHAfiliasi tidak diketahui1
SLAMET SUBYAKTOAfiliasi tidak diketahui1
RUSTIDJAAfiliasi tidak diketahui1
M. SASMITO JATIAfiliasi tidak diketahui1
GEMI TRIASTUTIKAfiliasi tidak diketahui1
Stephanie StephanieAfiliasi tidak diketahui1
Suryo WiyonoAfiliasi tidak diketahui1
Alimuddin AlimuddinAfiliasi tidak diketahui1
Tri HandayaniAfiliasi tidak diketahui1
Andi ParenrengiAfiliasi tidak diketahui1
Emma SuryatiAfiliasi tidak diketahui1
Didy SopandieAfiliasi tidak diketahui1
Radite TistamaAfiliasi tidak diketahui1
AKIHO YOKOTAAfiliasi tidak diketahui1
KINYA AKASHIAfiliasi tidak diketahui1

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Sumber metadata: OAI-PMH (metadata jurnal) https://jurnal.ugm.ac.id/ijbiotech/oai, pertama di-harvest 8 Nov 2026, terakhir terlihat 8 Nov 2026.
Metadata asli (oai_dc)
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	<dc:title xml:lang="en-US">Evaluation of different promoters driving the GFP reporter gene in seaweed Kappaphycus alvarezii</dc:title>
	<dc:creator>Rajamuddin, Muh. Alias L.</dc:creator>
	<dc:creator>Alimuddin, A.</dc:creator>
	<dc:creator>Widyastuti, Utut</dc:creator>
	<dc:creator>Faizal, Irvan</dc:creator>
	<dc:subject xml:lang="en-US">transgenic; promoter; GFP; electroporation; filament callus; Kappaphycus alvarezii</dc:subject>
	<dc:description xml:lang="en-US">Promoter regulates expression level of foreign gene in transgenic organism. This study was performed to select asuitable promoter as the fi rst step towards production of valuable trait-enhanced seaweed by transgenic technology. Greenfl uorescent protein (GFP) gene was used as a reporter to determine the activity of promoter in seaweed Kappaphycusalvarezii. GFP gene constructs driven by cytomegalovirus (pCMV-GFP), caulifl ower mosaic virus (pCaMV-GFP),medaka β-actin (pmBA-GFP) and Japanese fl ounder keratin (pJfKer-GFP) promoters were introduced by electroporationmethod. Electroporation was performed using a gene pulser (BIORAD) with voltage of 300 V, pulse length of 0.5 ms,pulse numbers of 4, and pulse interval of 0.1 s. Promoter activity was determined by analyzing GFP gene expressionlevel using a fl uorescent microscope. The results showed that CMV regulated highest number of fi lament callus(34.10%±1.49) expressing GFP at medium to strong fl uorescence levels. CaMV promoter had relatively similar activitywith CMV, but lower number of fi lament callus expressing GFP (10.48%±0.25). mBA promoter drove GFP expressionat medium level and similar number of fi lament callus (8.85%±2.31) expressing GFP with CaMV, while JfKer promoterhad lowest activity by means in number of fi lament callus expressing GFP (4.79%±0.26) and GFP expression level. PCRanalysis for transgenic confi rmation showed a DNA band of PCR product from pCMV-GFP and pCaMV-GFP expressingfi lament callus in the same size (about 0.6 kb) with positive control of plasmid. Thus, CMV and CaMV promoters wasan appropriate promoter and foreign gene could be transferred to fi lament callus by electroporation method. Combiningthis achievement with developing a culture method of fi lament callus to be thallus, stable transgenic breeding in K.alvarezii can be feasible.</dc:description>
	<dc:publisher xml:lang="en-US">Universitas Gadjah Mada</dc:publisher>
	<dc:contributor xml:lang="en-US"></dc:contributor>
	<dc:date>2014-12-08</dc:date>
	<dc:type>info:eu-repo/semantics/article</dc:type>
	<dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
	<dc:type xml:lang="en-US">Original Research Articles</dc:type>
	<dc:format>application/pdf</dc:format>
	<dc:identifier>https://journal.ugm.ac.id/ijbiotech/article/view/9304</dc:identifier>
	<dc:identifier>10.22146/ijbiotech.9304</dc:identifier>
	<dc:source xml:lang="en-US">Indonesian Journal of Biotechnology; Vol 19, No 2 (2014); 129-135</dc:source>
	<dc:source>2089-2241</dc:source>
	<dc:source>0853-8654</dc:source>
	<dc:language>eng</dc:language>
	<dc:relation>https://journal.ugm.ac.id/ijbiotech/article/view/9304/6898</dc:relation>
	<dc:rights xml:lang="en-US">Copyright (c) 2016 Muh. Alias L. Rajamuddin, Alimuddin A, Utut Widyastuti, Irvan Faizal</dc:rights>
	<dc:rights xml:lang="en-US">http://creativecommons.org/licenses/by-sa/4.0</dc:rights>
</oai_dc:dc>