Identification of new isolates of Bacillus thuringiensis using rep-PCR products and delta-endotoxin electron microscopy
Autor(a) principal: | |
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Data de Publicação: | 2002 |
Outros Autores: | , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Genetics and Molecular Biology |
Texto Completo: | http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572002000200017 |
Resumo: | PCR has been used to analyze the distribution of REP (Repetitive Extragenic Palindromic) and ERIC (Enterobacterial Repetitive Intergenic Consensus) sequences (rep-PCR) found within the genome of the bacterium Bacillus thuringiensis, with the purpose to analyze the genetic similarities among 56 subspecies samples and 95 field isolates. The PCR products were analyzed by EB-AGE (ethidium bromide-agarose electrophoresis) and then submitted to banding comparisons, based on the Phyllip software algorithm. When the banding similarities were considered for comparison purposes among all the strains, the phylogenic tree patterns varied according to the rep-PCR primers considered, but, from a broader point of view, the ERIC sequences produced better results, which, together with electron microscopy analysis of the released parasporal bodies and colony morphology characteristics, allowed to detect two possible new subspecies of B. thuringiensis. |
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Genetics and Molecular Biology |
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Identification of new isolates of Bacillus thuringiensis using rep-PCR products and delta-endotoxin electron microscopyREPERICcrystal proteinparasporal bodiesPCR has been used to analyze the distribution of REP (Repetitive Extragenic Palindromic) and ERIC (Enterobacterial Repetitive Intergenic Consensus) sequences (rep-PCR) found within the genome of the bacterium Bacillus thuringiensis, with the purpose to analyze the genetic similarities among 56 subspecies samples and 95 field isolates. The PCR products were analyzed by EB-AGE (ethidium bromide-agarose electrophoresis) and then submitted to banding comparisons, based on the Phyllip software algorithm. When the banding similarities were considered for comparison purposes among all the strains, the phylogenic tree patterns varied according to the rep-PCR primers considered, but, from a broader point of view, the ERIC sequences produced better results, which, together with electron microscopy analysis of the released parasporal bodies and colony morphology characteristics, allowed to detect two possible new subspecies of B. thuringiensis.Sociedade Brasileira de Genética2002-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572002000200017Genetics and Molecular Biology v.25 n.2 2002reponame:Genetics and Molecular Biologyinstname:Sociedade Brasileira de Genética (SBG)instacron:SBG10.1590/S1415-47572002000200017info:eu-repo/semantics/openAccessLima,A.S.G.Guidelli,A.M.Abreu,I.L.Lemos,M.V.F.eng2002-09-11T00:00:00Zoai:scielo:S1415-47572002000200017Revistahttp://www.gmb.org.br/ONGhttps://old.scielo.br/oai/scielo-oai.php||editor@gmb.org.br1678-46851415-4757opendoar:2002-09-11T00:00Genetics and Molecular Biology - Sociedade Brasileira de Genética (SBG)false |
dc.title.none.fl_str_mv |
Identification of new isolates of Bacillus thuringiensis using rep-PCR products and delta-endotoxin electron microscopy |
title |
Identification of new isolates of Bacillus thuringiensis using rep-PCR products and delta-endotoxin electron microscopy |
spellingShingle |
Identification of new isolates of Bacillus thuringiensis using rep-PCR products and delta-endotoxin electron microscopy Lima,A.S.G. REP ERIC crystal protein parasporal bodies |
title_short |
Identification of new isolates of Bacillus thuringiensis using rep-PCR products and delta-endotoxin electron microscopy |
title_full |
Identification of new isolates of Bacillus thuringiensis using rep-PCR products and delta-endotoxin electron microscopy |
title_fullStr |
Identification of new isolates of Bacillus thuringiensis using rep-PCR products and delta-endotoxin electron microscopy |
title_full_unstemmed |
Identification of new isolates of Bacillus thuringiensis using rep-PCR products and delta-endotoxin electron microscopy |
title_sort |
Identification of new isolates of Bacillus thuringiensis using rep-PCR products and delta-endotoxin electron microscopy |
author |
Lima,A.S.G. |
author_facet |
Lima,A.S.G. Guidelli,A.M. Abreu,I.L. Lemos,M.V.F. |
author_role |
author |
author2 |
Guidelli,A.M. Abreu,I.L. Lemos,M.V.F. |
author2_role |
author author author |
dc.contributor.author.fl_str_mv |
Lima,A.S.G. Guidelli,A.M. Abreu,I.L. Lemos,M.V.F. |
dc.subject.por.fl_str_mv |
REP ERIC crystal protein parasporal bodies |
topic |
REP ERIC crystal protein parasporal bodies |
description |
PCR has been used to analyze the distribution of REP (Repetitive Extragenic Palindromic) and ERIC (Enterobacterial Repetitive Intergenic Consensus) sequences (rep-PCR) found within the genome of the bacterium Bacillus thuringiensis, with the purpose to analyze the genetic similarities among 56 subspecies samples and 95 field isolates. The PCR products were analyzed by EB-AGE (ethidium bromide-agarose electrophoresis) and then submitted to banding comparisons, based on the Phyllip software algorithm. When the banding similarities were considered for comparison purposes among all the strains, the phylogenic tree patterns varied according to the rep-PCR primers considered, but, from a broader point of view, the ERIC sequences produced better results, which, together with electron microscopy analysis of the released parasporal bodies and colony morphology characteristics, allowed to detect two possible new subspecies of B. thuringiensis. |
publishDate |
2002 |
dc.date.none.fl_str_mv |
2002-01-01 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572002000200017 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572002000200017 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/S1415-47572002000200017 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
text/html |
dc.publisher.none.fl_str_mv |
Sociedade Brasileira de Genética |
publisher.none.fl_str_mv |
Sociedade Brasileira de Genética |
dc.source.none.fl_str_mv |
Genetics and Molecular Biology v.25 n.2 2002 reponame:Genetics and Molecular Biology instname:Sociedade Brasileira de Genética (SBG) instacron:SBG |
instname_str |
Sociedade Brasileira de Genética (SBG) |
instacron_str |
SBG |
institution |
SBG |
reponame_str |
Genetics and Molecular Biology |
collection |
Genetics and Molecular Biology |
repository.name.fl_str_mv |
Genetics and Molecular Biology - Sociedade Brasileira de Genética (SBG) |
repository.mail.fl_str_mv |
||editor@gmb.org.br |
_version_ |
1752122378243014656 |