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Registro Completo |
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Biblioteca(s): |
Embrapa Meio-Norte; Embrapa Recursos Genéticos e Biotecnologia. |
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Data corrente: |
22/12/2011 |
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Data da última atualização: |
03/06/2022 |
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Tipo da produção científica: |
Artigo em Periódico Indexado |
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Autoria: |
GOODWIN, S. B.; M’BAREK, S. B.; DHILLON, B.; WITTENBERG, A. H. J.; CRANE, C. F.; HANE, J. K.; FOSTER, A. J.; LEE, T. A. J. van der; GRIMWOOD, J.; AERTS, A.; ANTONIW, J.; BAILEY, A.; BLUHM, B.; BOWLER, J.; BRISTOW, J.; BURGT, A. van der; CANTO CANCHE, B.; CHURCHILL, A. C. L.; CONDE FERRÀEZ, L.; COOLS, H. J.; COUTINHO, P. M.; CSUKAI, M.; DEHAL, P.; WIT, P. de; DONZELLI, B.; GEEST, H. C. van de; HAM, R. C. H. H. van; HAMMOND KOSACK, K. E.; HENRISSAT, B.; KILIAN, A.; KOBAYASHI, A. K.; KOOPMANN, E.; KOURMPETIS, Y.; KUZNIAR, A.; LINDQUIST, E.; LOMBARD, V.; MALIEPAARD, C.; MARTINS, N. F.; MEHRABI, R.; NAP, J. P. H.; PONOMARENKO, A.; RUDD, J. J.; SALAMOV, A.; SCHMUTZ, J.; SCHOUTEN, H. J.; SHAPIRO, H.; STERGIOPOULOS, I.; TORRIANI, S. F. F.; TU, H.; VRIES, R. P. de; WAALWIJK, C.; WARE, S. B.; WIEBENGA, A.; ZWIERS, L.; OLIVER, R. P.; GRIGORIEV, I. V.; KEMA, G. H. J. |
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Afiliação: |
STEPHEN B. GOODWIN, USDA–AGRICULTURAL RESEARCH SERVICE; SARRAH BEN M’BAREK, PLANT RESEARCH INTERNATIONAL B.V., WAGENINGEN, THE NETHERLANDS; BRAHAM DHILLON, PURDUE UNIVERSITY, USA; ALEXANDER H. J. WITTENBERG, PLANT RESEARCH INTERNATIONAL B.V., WAGENINGEN, THE NETHERLANDS; CHARLES F. CRANE, USDA–AGRICULTURAL RESEARCH SERVICE; JAMES K. HANE, MURDOCH UNIVERSITY, PERTH, AUSTRALIA; ANDREW J. FOSTER, IBWF e.V., GERMANY; THEO A. J. VAN DER LEE, PLANT RESEARCH INTERNATIONAL B.V., WAGENINGEN, THE NETHERLANDS; JANE GRIMWOOD, HUDSONALPHA INSTITUTE OF BIOTECHNOLOGY, USA; ANDREA AERTS, DOE JOINT GENOME INSTITUTE, USA; JOHN ANTONIW, ROTHAMSTED RESEARCH, UNITED KINGDOM; ANDY BAILEY, UNIVERSITY OF BRISTOL, UNITED KINGDOM; BURT BLUHM, UNIVERSITY OF ARKANSAS, USA; JUDITH BOWLER, SYNGENTA, UNITED KINGDOM; JIM BRISTOW, HUDSONALPHA INSTITUTE OF BIOTECHNOLOGY, USA; ATE VAN DER BURGT, PLANT RESEARCH INTERNATIONAL B.V., WAGENINGEN, THE NETHERLANDS; BLONDY CANTO CANCHE, CENTRO DE INVESTIGACIÓN CIENTÍFICA DE YUCATÁN, MÉXICO; ALICE C. L. CHURCHILL, CORNELL UNIVERSITY, USA; LAURA CONDE FERRÀEZ, CENTRO DE INVESTIGACIÓN CIENTÍFICA DE YUCATÁN, MÉXICO; HANS J. COOLS, ROTHAMSTED RESEARCH, UNITED KINGDOM; PEDRO M. COUTINHO, ARCHITECTURE ET FONCTION DES MACROMOLECULES BIOLOGIQUES, CNRS, FRANCE; MICHAEL CSUKAI, SYNGENTA, UNITED KINGDOM; PARAMVIR DEHAL, DOE JOINT GENOME INSTITUTE, USA; PIERRE DE WIT, WAGENINGEN UNIVERSITY AND RESEARCH CENTRE, THE NETHERLANDS; BRUNO DONZELLI, USDA–AGRICULTURAL RESEARCH SERVICE; HENRI C. VAN DE GEEST, PLANT RESEARCH INTERNATIONAL B.V., WAGENINGEN, THE NETHERLANDS; ROELAND C. H. J. VAN HAM, PLANT RESEARCH INTERNATIONAL B.V., WAGENINGEN, THE NETHERLANDS; KIM E. HAMMOND KOSACK, ROTHAMSTED RESEARCH, UNITED KINGDOM; BERNARD HENRISSAT, ARCHITECTURE ET FONCTION DES MACROMOLECULES BIOLOGIQUES, CNRS, FRANCE; ANDRZEJ KILIAN, DIVERSITY ARRAYS TECHNOLOGY PTY LTD, AUSTRALIA; ADILSON KENJI KOBAYASHI, CPAMN; EDDA KOOPMANN, BAYER CROPSCIENCE AG, GERMANY; YIANNIS KOURMPETIS, WAGENINGEN UNIVERSITY AND RESEARCH CENTRE, THE NETHERLANDS; ARNOLD KUZNIAR, WAGENINGEN UNIVERSITY AND RESEARCH CENTRE, THE NETHERLANDS; ERIKA LINDQUIST, DOE JOINT GENOME INSTITUTE, USA; VINCENT LOMBARD, ARCHITECTURE ET FONCTION DES MACROMOLECULES BIOLOGIQUES, CNRS, FRANCE; CHRIS MALIEPAARD, WAGENINGEN UNIVERSITY AND RESEARCH CENTRE, THE NETHERLANDS; NATALIA FLORENCIO MARTINS, CENARGEN; RAHIM MEHRABI, SEED AND PLANT IMPROVEMENT INSTITUTE, IRAN; JAN P. H. NAP, PLANT RESEARCH INTERNATIONAL B.V., WAGENINGEN, THE NETHERLANDS; ALISA PONOMARENKO, PURDUE UNIVERSITY, USA; JASON J. RUDD, ROTHAMSTED RESEARCH, UNITED KINGDOM; ASAF SALAMOV, DOE JOINT GENOME INSTITUTE, USA; JEREMY SCHMUTZ, HUDSONALPHA INSTITUTE OF BIOTECHNOLOGY, USA; HENK J. SCHOUTEN, PLANT RESEARCH INTERNATIONAL B.V., WAGENINGEN, THE NETHERLANDS; HARRIS SHAPIRO, DOE JOINT GENOME INSTITUTE, USA; IOANNIS STERGIOPOULOS, WAGENINGEN UNIVERSITY AND RESEARCH CENTRE, THE NETHERLANDS; STEFANO F. F. TORRIANI, SWISS FEDERAL INSTITUTE OF TECHNOLOGY (ETH), SWITZERLAND; HANK TU, DOE JOINT GENOME INSTITUTE, USA; RONALD P. DE VRIES, CBS–KNAW FUNGAL BIODIVERSITY CENTRE, THE NETHERLANDS; CEES WAALWIJK, PLANT RESEARCH INTERNATIONAL B.V., WAGENINGEN, THE NETHERLANDS; SARAH B. WARE, PLANT RESEARCH INTERNATIONAL B.V., WAGENINGEN, THE NETHERLANDS; AD WIEBENGA, CBS–KNAW FUNGAL BIODIVERSITY CENTRE, THE NETHERLANDS; LUTE-HARM ZWIERS, CBS–KNAW FUNGAL BIODIVERSITY CENTRE, THE NETHERLANDS; RICHARD P. OLIVER, CURTIN UNIVERSITY, AUSTRALIA; IGOR V. GRIGORIEV, DOE JOINT GENOME INSTITUTE, USA; GERT H. J. KEMA, PLANT RESEARCH INTERNATIONAL B.V., WAGENINGEN, THE NETHERLANDS. |
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Título: |
Finished genome of the fungal wheat pathogen Mycosphaerella graminicola Reveals dispensome structure, chromosome plasticity, and stealth pathogenesis. |
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Ano de publicação: |
2011 |
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Fonte/Imprenta: |
Plos Genetics, v. 7, n. 6, e1002070, 2011. |
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Idioma: |
Inglês |
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Palavras-Chave: |
Fungus. |
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Thesagro: |
Fungo. |
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Thesaurus Nal: |
Mycosphaerella graminicola. |
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Categoria do assunto: |
-- |
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URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/53161/1/AdilsonKobayashi.pdf
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Marc: |
LEADER 02207naa a2200817 a 4500
001 1913905
005 2022-06-03
008 2011 bl uuuu u00u1 u #d
100 1 $aGOODWIN, S. B.
245 $aFinished genome of the fungal wheat pathogen Mycosphaerella graminicola Reveals dispensome structure, chromosome plasticity, and stealth pathogenesis.$h[electronic resource]
260 $c2011
650 $aMycosphaerella graminicola
650 $aFungo
653 $aFungus
700 1 $aM’BAREK, S. B.
700 1 $aDHILLON, B.
700 1 $aWITTENBERG, A. H. J.
700 1 $aCRANE, C. F.
700 1 $aHANE, J. K.
700 1 $aFOSTER, A. J.
700 1 $aLEE, T. A. J. van der
700 1 $aGRIMWOOD, J.
700 1 $aAERTS, A.
700 1 $aANTONIW, J.
700 1 $aBAILEY, A.
700 1 $aBLUHM, B.
700 1 $aBOWLER, J.
700 1 $aBRISTOW, J.
700 1 $aBURGT, A. van der
700 1 $aCANTO CANCHE, B.
700 1 $aCHURCHILL, A. C. L.
700 1 $aCONDE FERRÀEZ, L.
700 1 $aCOOLS, H. J.
700 1 $aCOUTINHO, P. M.
700 1 $aCSUKAI, M.
700 1 $aDEHAL, P.
700 1 $aWIT, P. de
700 1 $aDONZELLI, B.
700 1 $aGEEST, H. C. van de
700 1 $aHAM, R. C. H. H. van
700 1 $aHAMMOND KOSACK, K. E.
700 1 $aHENRISSAT, B.
700 1 $aKILIAN, A.
700 1 $aKOBAYASHI, A. K.
700 1 $aKOOPMANN, E.
700 1 $aKOURMPETIS, Y.
700 1 $aKUZNIAR, A.
700 1 $aLINDQUIST, E.
700 1 $aLOMBARD, V.
700 1 $aMALIEPAARD, C.
700 1 $aMARTINS, N. F.
700 1 $aMEHRABI, R.
700 1 $aNAP, J. P. H.
700 1 $aPONOMARENKO, A.
700 1 $aRUDD, J. J.
700 1 $aSALAMOV, A.
700 1 $aSCHMUTZ, J.
700 1 $aSCHOUTEN, H. J.
700 1 $aSHAPIRO, H.
700 1 $aSTERGIOPOULOS, I.
700 1 $aTORRIANI, S. F. F.
700 1 $aTU, H.
700 1 $aVRIES, R. P. de
700 1 $aWAALWIJK, C.
700 1 $aWARE, S. B.
700 1 $aWIEBENGA, A.
700 1 $aZWIERS, L.
700 1 $aOLIVER, R. P.
700 1 $aGRIGORIEV, I. V.
700 1 $aKEMA, G. H. J.
773 $tPlos Genetics$gv. 7, n. 6, e1002070, 2011.
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Registro original: |
Embrapa Meio-Norte (CPAMN) |
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 | Acesso ao texto completo restrito à biblioteca da Embrapa Soja. Para informações adicionais entre em contato com valeria.cardoso@embrapa.br. |
Registro Completo
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Biblioteca(s): |
Embrapa Soja. |
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Data corrente: |
15/05/2007 |
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Data da última atualização: |
16/05/2007 |
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Autoria: |
OLIVEIRA, J. V. de C.; WOLFF, J. L. C.; GARCIA-MARUNIAK, A.; RIBEIRO, B. M.; CASTRO, M. E. B. de; SOUZA, M. L. de; MOSCARDI, F.; MARUNIAK, J. E.; ZANOTTO, P. M. de A. |
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Título: |
Genome of the most widely used viral biopesticide: Anticarsia gemmatalis multiple nucleopolyhedrovirus. |
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Ano de publicação: |
2006 |
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Fonte/Imprenta: |
Journal of General Virology, v. 87, p. 3233-3250, 2006. |
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Idioma: |
Inglês |
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Conteúdo: |
The genome of Anticarsia gemmatalis multiple nucleopolyhedrovirus isolate 2D (AgMNPV-2D), which is the most extensively used virus pesticide in the world, was completely sequenced and shown to have 132 239 bp (G+C content 44.5 mol%) and to be capable of encoding 152 non-overlapping open reading frames (ORFs). Three ORFs were unique to AgMNPV-2D, one of which (ag31) had similarity to eukaryotic poly(ADP-ribose) polymerases. The lack of chiA and v-cath may explain some of the success and growth of the AgMNPV biological control programme, as it may explain the high recovery of polyhedra sequestered inside dead larvae in the field, which are collected and used for further application as biological pesticides in soybean fields. The genome organization was similar to that of the Choristoneura fumiferana defective MNPV (CfDefNPV). Most of the variation between the two genomes took place near highly repetitive regions, which were also closely associated with bro-coding regions. The separation of the NPVs into groups I and II was supported by: (i) a phenogram of the complete genomes of 28 baculovirus and Heliothis zea virus 1, (ii) the most parsimonious reconstruction of gene content along the phenograms and (iii) comparisons of genomic features. Moreover, these data also reinforced the notion that group I of the NPVs can be split further into the AgMNPV lineage (AgMNPV, CfDefNPV, Epiphyas postvittana NPV, Orgyia pseudotsugata MNPV and C. fumiferana MNPV), sharing eight defining genes, and the Autographa californica MNPV (AcMNPV) lineage (AcMNPV, Rachiplusia ou NPV and Bombyx mori NPV), sharing nine defining genes. MenosThe genome of Anticarsia gemmatalis multiple nucleopolyhedrovirus isolate 2D (AgMNPV-2D), which is the most extensively used virus pesticide in the world, was completely sequenced and shown to have 132 239 bp (G+C content 44.5 mol%) and to be capable of encoding 152 non-overlapping open reading frames (ORFs). Three ORFs were unique to AgMNPV-2D, one of which (ag31) had similarity to eukaryotic poly(ADP-ribose) polymerases. The lack of chiA and v-cath may explain some of the success and growth of the AgMNPV biological control programme, as it may explain the high recovery of polyhedra sequestered inside dead larvae in the field, which are collected and used for further application as biological pesticides in soybean fields. The genome organization was similar to that of the Choristoneura fumiferana defective MNPV (CfDefNPV). Most of the variation between the two genomes took place near highly repetitive regions, which were also closely associated with bro-coding regions. The separation of the NPVs into groups I and II was supported by: (i) a phenogram of the complete genomes of 28 baculovirus and Heliothis zea virus 1, (ii) the most parsimonious reconstruction of gene content along the phenograms and (iii) comparisons of genomic features. Moreover, these data also reinforced the notion that group I of the NPVs can be split further into the AgMNPV lineage (AgMNPV, CfDefNPV, Epiphyas postvittana NPV, Orgyia pseudotsugata MNPV and C. fumiferana MNPV), sharing eight defining gene... Mostrar Tudo |
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Palavras-Chave: |
Biopesticida: Anticarsia gemmatalis multiple nucleopolyhedrovirus. |
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Thesagro: |
Controle Biológico; Genoma. |
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Categoria do assunto: |
-- |
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Marc: |
LEADER 02429naa a2200253 a 4500
001 1469999
005 2007-05-16
008 2006 bl --- 0-- u #d
100 1 $aOLIVEIRA, J. V. de C.
245 $aGenome of the most widely used viral biopesticide$bAnticarsia gemmatalis multiple nucleopolyhedrovirus.
260 $c2006
520 $aThe genome of Anticarsia gemmatalis multiple nucleopolyhedrovirus isolate 2D (AgMNPV-2D), which is the most extensively used virus pesticide in the world, was completely sequenced and shown to have 132 239 bp (G+C content 44.5 mol%) and to be capable of encoding 152 non-overlapping open reading frames (ORFs). Three ORFs were unique to AgMNPV-2D, one of which (ag31) had similarity to eukaryotic poly(ADP-ribose) polymerases. The lack of chiA and v-cath may explain some of the success and growth of the AgMNPV biological control programme, as it may explain the high recovery of polyhedra sequestered inside dead larvae in the field, which are collected and used for further application as biological pesticides in soybean fields. The genome organization was similar to that of the Choristoneura fumiferana defective MNPV (CfDefNPV). Most of the variation between the two genomes took place near highly repetitive regions, which were also closely associated with bro-coding regions. The separation of the NPVs into groups I and II was supported by: (i) a phenogram of the complete genomes of 28 baculovirus and Heliothis zea virus 1, (ii) the most parsimonious reconstruction of gene content along the phenograms and (iii) comparisons of genomic features. Moreover, these data also reinforced the notion that group I of the NPVs can be split further into the AgMNPV lineage (AgMNPV, CfDefNPV, Epiphyas postvittana NPV, Orgyia pseudotsugata MNPV and C. fumiferana MNPV), sharing eight defining genes, and the Autographa californica MNPV (AcMNPV) lineage (AcMNPV, Rachiplusia ou NPV and Bombyx mori NPV), sharing nine defining genes.
650 $aControle Biológico
650 $aGenoma
653 $aBiopesticida: Anticarsia gemmatalis multiple nucleopolyhedrovirus
700 1 $aWOLFF, J. L. C.
700 1 $aGARCIA-MARUNIAK, A.
700 1 $aRIBEIRO, B. M.
700 1 $aCASTRO, M. E. B. de
700 1 $aSOUZA, M. L. de
700 1 $aMOSCARDI, F.
700 1 $aMARUNIAK, J. E.
700 1 $aZANOTTO, P. M. de A.
773 $tJournal of General Virology$gv. 87, p. 3233-3250, 2006.
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