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TRANSPOSITION AND EXPRESSION OF GEP GENE IN THE GENOME OF Vibrio harveyi TO MONITOR ITS ADHERENCE IN SHRIMP LARVAE

BIOTROPIA · Vol. 13 No. 1 (2011)

DOI
10.11598/btb.2006.13.1.74
ISSN
1907-770X, 0215-6334
Terbit
2011-08-02
Penerbit
SEAMEO BIOTROP
Bahasa
en
Lisensi
creativecommons.org/licenses/by-nc-nd/4.0

Abstrak

Expression of green fluorescent protein encoded by GFP gene in Vibrio harveyi was investigated to understand the ability of the gene as a molecular marker for adherence of this pathogenic Vibrio in shrimp larvae. The GFP gene was inserted into pUC18Not and pUTmini-Tn5 to generate a recombinant plasmid pWGO2 and pWGO3, respectively, which was transferred into the three isolates of V. harveyi employing diparental mating. Recombinant E. coli carrying pWGO2 and pWGO3 resulted in green-fluorescent colonies and cells due to the production of GFP. However, al1 of mini-Tn5, including mini-Tn5-gfp were not successful1y transferred to V. harveyi. Therefore, we used mini-Tn10 (pLOFKm-gfp) for inserting of gfp gene into V. harveyi genome. Although we could obtain relatively high (l0 pangkat -8) transconjugans employing Tn10, only one of Tnl0 derived isolate of V. harveyi G3 (G3-Tn1Ogfp) showed gfp expression and was further employed for adherence assay. Fluorescent 03-TnlOgfp cells could be observed inside the digestive tract of shrimp larvae and could be distinguished from vibrio that naturally exist in shrimp larvae.

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  • IPB University
  • Atma Jaya Catholic University of Indonesia
  • Universitas Sumatera Utara
  • University of Indonesia
  • Universitas Pattimura
  • Montana State University
  • State University of Makassar
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Rekan penulisOrganisasiArtikel bersama
Esti PuspitasariIPB University4
İman RusmanaIPB University4
Nisa Rachmania MubarikIPB University4
Dwi SuryantoUniversitas Sumatera Utara3
Anja MeryandiniIPB University3
Aris Tri WahyudiIPB University3
Andreas Adhi SatyaAfiliasi tidak diketahui3
Widanarni WidanarniIPB University2
Amarila MalikUniversity of Indonesia2
Bibiana W. LayIPB University2
Yulin LestariIPB University2
Dedy Duryadi SolihinIPB University2
Cecilia Anna SeumahuUniversitas Pattimura2
Maria Indah PurnamasariMontana State University2
Rika Indri AstutiIPB University2
Yepy H. RustamAfiliasi tidak diketahui2
Nurul AiniIPB University1
Walter R. ErdelenIPB University1
Muhammad ZairinIPB University1
Ridwan AffandiIPB University1
Yusminah HalaState University of Makassar1
Sukenda SukendaIPB University1
Budi TjahjonoIPB University1
R. HarlingScottish Agricultural College1
SumardiAfiliasi tidak diketahui1
Maggy T HenawidjajaIPB University1
T Resnawati P UrwadariaAfiliasi tidak diketahui1
Andi KhaeruniUniversitas Halu Oleo1
Budi TjahjonoIPB University1
Meity Suradji SinagaIPB University1
Ari SusilowatiSebelas Maret University1
Suryo WiyonoIPB University1
Rasti SaraswatiAfiliasi tidak diketahui1
Ratih Dewi HastutiIPB University1
. EFRIWATIAfiliasi tidak diketahui1
Lilis NuraidaIPB University1
Gayuh RahayuIPB University1
Tati BarusAtma Jaya Catholic University of Indonesia1
IVAN HANJAYAAtma Jaya Catholic University of Indonesia1

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Sumber metadata: OAI-PMH (metadata jurnal) http://journal.biotrop.org/index.php/biotropia/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">TRANSPOSITION AND EXPRESSION OF GEP GENE IN THE GENOME OF Vibrio harveyi TO MONITOR ITS ADHERENCE IN SHRIMP LARVAE</dc:title>
	<dc:creator xml:lang="en">Suwanto, Antonius</dc:creator>
	<dc:description xml:lang="en">Expression of green fluorescent protein encoded by GFP gene in Vibrio harveyi was investigated to understand the ability of the gene as a molecular marker for adherence of this pathogenic Vibrio in shrimp larvae. The GFP gene was inserted into pUC18Not and pUTmini-Tn5 to generate a recombinant plasmid pWGO2 and pWGO3, respectively, which was transferred into the three isolates of V. harveyi employing diparental mating. Recombinant E. coli carrying pWGO2 and pWGO3 resulted in green-fluorescent colonies and cells due to the production of GFP. However, al1 of mini-Tn5, including mini-Tn5-gfp were not successful1y transferred to V. harveyi. Therefore, we used mini-Tn10 (pLOFKm-gfp) for inserting of gfp gene into V. harveyi genome. Although we could obtain relatively high (l0 pangkat -8) transconjugans employing Tn10, only one of Tnl0 derived isolate of V. harveyi G3 (G3-Tn1Ogfp) showed gfp expression and was further employed for adherence assay. Fluorescent 03-TnlOgfp cells could be observed inside the digestive tract of shrimp larvae and could be distinguished from vibrio that naturally exist in shrimp larvae.</dc:description>
	<dc:publisher xml:lang="en">SEAMEO BIOTROP</dc:publisher>
	<dc:date>2011-08-02</dc:date>
	<dc:type>info:eu-repo/semantics/article</dc:type>
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	<dc:identifier>https://journal.biotrop.org/index.php/biotropia/article/view/74</dc:identifier>
	<dc:identifier>10.11598/btb.2006.13.1.74</dc:identifier>
	<dc:source xml:lang="en">BIOTROPIA; Vol. 13 No. 1 (2006): BIOTROPIA Vol. 13 No. 1 June 2006</dc:source>
	<dc:source>1907-770X</dc:source>
	<dc:source>0215-6334</dc:source>
	<dc:source>10.11598/btb.2006.13.1.</dc:source>
	<dc:language>en</dc:language>
	<dc:relation>https://journal.biotrop.org/index.php/biotropia/article/view/74/447</dc:relation>
	<dc:rights xml:lang="en">Copyright (c) 2017 BIOTROPIA - The Southeast Asian Journal of Tropical Biology</dc:rights>
	<dc:rights xml:lang="en">http://creativecommons.org/licenses/by-nc-nd/4.0</dc:rights>
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