Kloning Gen CRY dari Bacillus turingiensis var. kurstaki
Bacillus thuringiensis is an entomopathogenic organism. The pathogenic effect is caused by crystalline protein, δ-endotoxin, which is encoded by the cry gene. The aim of this study was to clone the cry gene from B. thuringiensis var. kurstaki with a genomic library approach. HindIII digested B. thur...
Ausführliche Beschreibung
Autor*in: |
Nur Rahmi Ardiani [verfasserIn] Sismindari Sismindari [verfasserIn] Sudjadi Sudjadi [verfasserIn] |
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Format: |
E-Artikel |
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Sprache: |
Englisch ; Indonesisch |
Erschienen: |
1998 |
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Übergeordnetes Werk: |
In: Jurnal Perlindungan Tanaman Indonesia - Universitas Gadjah Mada, 2017, 4(1998), 2, Seite 106-111 |
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Übergeordnetes Werk: |
volume:4 ; year:1998 ; number:2 ; pages:106-111 |
Links: |
Link aufrufen |
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DOI / URN: |
10.22146/jpti.9918 |
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Katalog-ID: |
DOAJ069597863 |
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520 | |a Bacillus thuringiensis is an entomopathogenic organism. The pathogenic effect is caused by crystalline protein, δ-endotoxin, which is encoded by the cry gene. The aim of this study was to clone the cry gene from B. thuringiensis var. kurstaki with a genomic library approach. HindIII digested B. thuringiensis total DNA was ligated to HindIII digested of pUC19, and then used to transform Escherichia coli DH5α. Selection of transformans carrying recombinant was done by α-complementation and a recombinant clone containing the cry gene was further screened by non-radioactive hybridization method using a probe synthesized from the conserved region of the published cry genes. The result suggested that two recombinant clones with the insert size of 3.4 kb and 2.0 kb, respectively, carrying the cry gene. Key words: cloning, cry gene, Bacillus thuringiensis | ||
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10.22146/jpti.9918 doi (DE-627)DOAJ069597863 (DE-599)DOAJ2abee7d75dae45209cbffeba62b8aca8 DE-627 ger DE-627 rakwb eng ind S1-972 SB1-1110 Nur Rahmi Ardiani verfasserin aut Kloning Gen CRY dari Bacillus turingiensis var. kurstaki 1998 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Bacillus thuringiensis is an entomopathogenic organism. The pathogenic effect is caused by crystalline protein, δ-endotoxin, which is encoded by the cry gene. The aim of this study was to clone the cry gene from B. thuringiensis var. kurstaki with a genomic library approach. HindIII digested B. thuringiensis total DNA was ligated to HindIII digested of pUC19, and then used to transform Escherichia coli DH5α. Selection of transformans carrying recombinant was done by α-complementation and a recombinant clone containing the cry gene was further screened by non-radioactive hybridization method using a probe synthesized from the conserved region of the published cry genes. The result suggested that two recombinant clones with the insert size of 3.4 kb and 2.0 kb, respectively, carrying the cry gene. Key words: cloning, cry gene, Bacillus thuringiensis Agriculture (General) Plant culture Sismindari Sismindari verfasserin aut Sudjadi Sudjadi verfasserin aut In Jurnal Perlindungan Tanaman Indonesia Universitas Gadjah Mada, 2017 4(1998), 2, Seite 106-111 (DE-627)1667436341 25484788 nnns volume:4 year:1998 number:2 pages:106-111 https://doi.org/10.22146/jpti.9918 kostenfrei https://doaj.org/article/2abee7d75dae45209cbffeba62b8aca8 kostenfrei https://jurnal.ugm.ac.id/jpti/article/view/9918 kostenfrei https://doaj.org/toc/1410-1637 Journal toc kostenfrei https://doaj.org/toc/2548-4788 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4367 GBV_ILN_4700 AR 4 1998 2 106-111 |
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10.22146/jpti.9918 doi (DE-627)DOAJ069597863 (DE-599)DOAJ2abee7d75dae45209cbffeba62b8aca8 DE-627 ger DE-627 rakwb eng ind S1-972 SB1-1110 Nur Rahmi Ardiani verfasserin aut Kloning Gen CRY dari Bacillus turingiensis var. kurstaki 1998 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Bacillus thuringiensis is an entomopathogenic organism. The pathogenic effect is caused by crystalline protein, δ-endotoxin, which is encoded by the cry gene. The aim of this study was to clone the cry gene from B. thuringiensis var. kurstaki with a genomic library approach. HindIII digested B. thuringiensis total DNA was ligated to HindIII digested of pUC19, and then used to transform Escherichia coli DH5α. Selection of transformans carrying recombinant was done by α-complementation and a recombinant clone containing the cry gene was further screened by non-radioactive hybridization method using a probe synthesized from the conserved region of the published cry genes. The result suggested that two recombinant clones with the insert size of 3.4 kb and 2.0 kb, respectively, carrying the cry gene. Key words: cloning, cry gene, Bacillus thuringiensis Agriculture (General) Plant culture Sismindari Sismindari verfasserin aut Sudjadi Sudjadi verfasserin aut In Jurnal Perlindungan Tanaman Indonesia Universitas Gadjah Mada, 2017 4(1998), 2, Seite 106-111 (DE-627)1667436341 25484788 nnns volume:4 year:1998 number:2 pages:106-111 https://doi.org/10.22146/jpti.9918 kostenfrei https://doaj.org/article/2abee7d75dae45209cbffeba62b8aca8 kostenfrei https://jurnal.ugm.ac.id/jpti/article/view/9918 kostenfrei https://doaj.org/toc/1410-1637 Journal toc kostenfrei https://doaj.org/toc/2548-4788 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4367 GBV_ILN_4700 AR 4 1998 2 106-111 |
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10.22146/jpti.9918 doi (DE-627)DOAJ069597863 (DE-599)DOAJ2abee7d75dae45209cbffeba62b8aca8 DE-627 ger DE-627 rakwb eng ind S1-972 SB1-1110 Nur Rahmi Ardiani verfasserin aut Kloning Gen CRY dari Bacillus turingiensis var. kurstaki 1998 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Bacillus thuringiensis is an entomopathogenic organism. The pathogenic effect is caused by crystalline protein, δ-endotoxin, which is encoded by the cry gene. The aim of this study was to clone the cry gene from B. thuringiensis var. kurstaki with a genomic library approach. HindIII digested B. thuringiensis total DNA was ligated to HindIII digested of pUC19, and then used to transform Escherichia coli DH5α. Selection of transformans carrying recombinant was done by α-complementation and a recombinant clone containing the cry gene was further screened by non-radioactive hybridization method using a probe synthesized from the conserved region of the published cry genes. The result suggested that two recombinant clones with the insert size of 3.4 kb and 2.0 kb, respectively, carrying the cry gene. Key words: cloning, cry gene, Bacillus thuringiensis Agriculture (General) Plant culture Sismindari Sismindari verfasserin aut Sudjadi Sudjadi verfasserin aut In Jurnal Perlindungan Tanaman Indonesia Universitas Gadjah Mada, 2017 4(1998), 2, Seite 106-111 (DE-627)1667436341 25484788 nnns volume:4 year:1998 number:2 pages:106-111 https://doi.org/10.22146/jpti.9918 kostenfrei https://doaj.org/article/2abee7d75dae45209cbffeba62b8aca8 kostenfrei https://jurnal.ugm.ac.id/jpti/article/view/9918 kostenfrei https://doaj.org/toc/1410-1637 Journal toc kostenfrei https://doaj.org/toc/2548-4788 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4367 GBV_ILN_4700 AR 4 1998 2 106-111 |
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10.22146/jpti.9918 doi (DE-627)DOAJ069597863 (DE-599)DOAJ2abee7d75dae45209cbffeba62b8aca8 DE-627 ger DE-627 rakwb eng ind S1-972 SB1-1110 Nur Rahmi Ardiani verfasserin aut Kloning Gen CRY dari Bacillus turingiensis var. kurstaki 1998 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Bacillus thuringiensis is an entomopathogenic organism. The pathogenic effect is caused by crystalline protein, δ-endotoxin, which is encoded by the cry gene. The aim of this study was to clone the cry gene from B. thuringiensis var. kurstaki with a genomic library approach. HindIII digested B. thuringiensis total DNA was ligated to HindIII digested of pUC19, and then used to transform Escherichia coli DH5α. Selection of transformans carrying recombinant was done by α-complementation and a recombinant clone containing the cry gene was further screened by non-radioactive hybridization method using a probe synthesized from the conserved region of the published cry genes. The result suggested that two recombinant clones with the insert size of 3.4 kb and 2.0 kb, respectively, carrying the cry gene. Key words: cloning, cry gene, Bacillus thuringiensis Agriculture (General) Plant culture Sismindari Sismindari verfasserin aut Sudjadi Sudjadi verfasserin aut In Jurnal Perlindungan Tanaman Indonesia Universitas Gadjah Mada, 2017 4(1998), 2, Seite 106-111 (DE-627)1667436341 25484788 nnns volume:4 year:1998 number:2 pages:106-111 https://doi.org/10.22146/jpti.9918 kostenfrei https://doaj.org/article/2abee7d75dae45209cbffeba62b8aca8 kostenfrei https://jurnal.ugm.ac.id/jpti/article/view/9918 kostenfrei https://doaj.org/toc/1410-1637 Journal toc kostenfrei https://doaj.org/toc/2548-4788 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4367 GBV_ILN_4700 AR 4 1998 2 106-111 |
allfieldsSound |
10.22146/jpti.9918 doi (DE-627)DOAJ069597863 (DE-599)DOAJ2abee7d75dae45209cbffeba62b8aca8 DE-627 ger DE-627 rakwb eng ind S1-972 SB1-1110 Nur Rahmi Ardiani verfasserin aut Kloning Gen CRY dari Bacillus turingiensis var. kurstaki 1998 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Bacillus thuringiensis is an entomopathogenic organism. The pathogenic effect is caused by crystalline protein, δ-endotoxin, which is encoded by the cry gene. The aim of this study was to clone the cry gene from B. thuringiensis var. kurstaki with a genomic library approach. HindIII digested B. thuringiensis total DNA was ligated to HindIII digested of pUC19, and then used to transform Escherichia coli DH5α. Selection of transformans carrying recombinant was done by α-complementation and a recombinant clone containing the cry gene was further screened by non-radioactive hybridization method using a probe synthesized from the conserved region of the published cry genes. The result suggested that two recombinant clones with the insert size of 3.4 kb and 2.0 kb, respectively, carrying the cry gene. Key words: cloning, cry gene, Bacillus thuringiensis Agriculture (General) Plant culture Sismindari Sismindari verfasserin aut Sudjadi Sudjadi verfasserin aut In Jurnal Perlindungan Tanaman Indonesia Universitas Gadjah Mada, 2017 4(1998), 2, Seite 106-111 (DE-627)1667436341 25484788 nnns volume:4 year:1998 number:2 pages:106-111 https://doi.org/10.22146/jpti.9918 kostenfrei https://doaj.org/article/2abee7d75dae45209cbffeba62b8aca8 kostenfrei https://jurnal.ugm.ac.id/jpti/article/view/9918 kostenfrei https://doaj.org/toc/1410-1637 Journal toc kostenfrei https://doaj.org/toc/2548-4788 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4367 GBV_ILN_4700 AR 4 1998 2 106-111 |
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Kloning Gen CRY dari Bacillus turingiensis var. kurstaki |
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Bacillus thuringiensis is an entomopathogenic organism. The pathogenic effect is caused by crystalline protein, δ-endotoxin, which is encoded by the cry gene. The aim of this study was to clone the cry gene from B. thuringiensis var. kurstaki with a genomic library approach. HindIII digested B. thuringiensis total DNA was ligated to HindIII digested of pUC19, and then used to transform Escherichia coli DH5α. Selection of transformans carrying recombinant was done by α-complementation and a recombinant clone containing the cry gene was further screened by non-radioactive hybridization method using a probe synthesized from the conserved region of the published cry genes. The result suggested that two recombinant clones with the insert size of 3.4 kb and 2.0 kb, respectively, carrying the cry gene. Key words: cloning, cry gene, Bacillus thuringiensis |
abstractGer |
Bacillus thuringiensis is an entomopathogenic organism. The pathogenic effect is caused by crystalline protein, δ-endotoxin, which is encoded by the cry gene. The aim of this study was to clone the cry gene from B. thuringiensis var. kurstaki with a genomic library approach. HindIII digested B. thuringiensis total DNA was ligated to HindIII digested of pUC19, and then used to transform Escherichia coli DH5α. Selection of transformans carrying recombinant was done by α-complementation and a recombinant clone containing the cry gene was further screened by non-radioactive hybridization method using a probe synthesized from the conserved region of the published cry genes. The result suggested that two recombinant clones with the insert size of 3.4 kb and 2.0 kb, respectively, carrying the cry gene. Key words: cloning, cry gene, Bacillus thuringiensis |
abstract_unstemmed |
Bacillus thuringiensis is an entomopathogenic organism. The pathogenic effect is caused by crystalline protein, δ-endotoxin, which is encoded by the cry gene. The aim of this study was to clone the cry gene from B. thuringiensis var. kurstaki with a genomic library approach. HindIII digested B. thuringiensis total DNA was ligated to HindIII digested of pUC19, and then used to transform Escherichia coli DH5α. Selection of transformans carrying recombinant was done by α-complementation and a recombinant clone containing the cry gene was further screened by non-radioactive hybridization method using a probe synthesized from the conserved region of the published cry genes. The result suggested that two recombinant clones with the insert size of 3.4 kb and 2.0 kb, respectively, carrying the cry gene. Key words: cloning, cry gene, Bacillus thuringiensis |
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Kloning Gen CRY dari Bacillus turingiensis var. kurstaki |
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