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{"title":"费氏弧菌的基因操作","authors":"David G. Christensen, Jovanka Tepavčević, Karen L. Visick","doi":"10.1002/cpmc.115","DOIUrl":null,"url":null,"abstract":"<p><i>Vibrio fischeri</i> is a nonpathogenic organism related to pathogenic <i>Vibrio</i> species. The bacterium has been used as a model organism to study symbiosis in the context of its association with its host, the Hawaiian bobtail squid <i>Euprymna scolopes</i>. The genetic tractability of this bacterium has facilitated the mapping of pathways that mediate interactions between these organisms. The protocols included here describe methods for genetic manipulation of <i>V. fischeri</i>. Following these protocols, the researcher will be able to introduce linear DNA via transformation to make chromosomal mutations, to introduce plasmid DNA via conjugation and subsequently eliminate unstable plasmids, to eliminate antibiotic resistance cassettes from the chromosome, and to randomly or specifically mutagenize <i>V. fischeri</i> with transposons. © 2020 Wiley Periodicals LLC.</p><p><b>Basic Protocol 1</b>: Transformation of <i>V. fischeri</i> with linear DNA</p><p><b>Basic Protocol 2</b>: Plasmid transfer into <i>V. fischeri</i> via conjugation</p><p><b>Support Protocol 1</b>: Removing FRT-flanked antibiotic resistance cassettes from the <i>V. fischeri</i> genome</p><p><b>Support Protocol 2</b>: Eliminating unstable plasmids from <i>V. fischeri</i></p><p><b>Alternate Protocol 1</b>: Introduction of exogenous DNA using a suicide plasmid</p><p><b>Alternate Protocol 2</b>: Site-specific transposon insertion using a suicide plasmid</p><p><b>Alternate Protocol 3</b>: Random transposon mutagenesis using a suicide plasmid</p>","PeriodicalId":39967,"journal":{"name":"Current Protocols in Microbiology","volume":"59 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2020-09-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/cpmc.115","citationCount":"7","resultStr":"{\"title\":\"Genetic Manipulation of Vibrio fischeri\",\"authors\":\"David G. Christensen, Jovanka Tepavčević, Karen L. Visick\",\"doi\":\"10.1002/cpmc.115\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><i>Vibrio fischeri</i> is a nonpathogenic organism related to pathogenic <i>Vibrio</i> species. The bacterium has been used as a model organism to study symbiosis in the context of its association with its host, the Hawaiian bobtail squid <i>Euprymna scolopes</i>. The genetic tractability of this bacterium has facilitated the mapping of pathways that mediate interactions between these organisms. The protocols included here describe methods for genetic manipulation of <i>V. fischeri</i>. Following these protocols, the researcher will be able to introduce linear DNA via transformation to make chromosomal mutations, to introduce plasmid DNA via conjugation and subsequently eliminate unstable plasmids, to eliminate antibiotic resistance cassettes from the chromosome, and to randomly or specifically mutagenize <i>V. fischeri</i> with transposons. © 2020 Wiley Periodicals LLC.</p><p><b>Basic Protocol 1</b>: Transformation of <i>V. fischeri</i> with linear DNA</p><p><b>Basic Protocol 2</b>: Plasmid transfer into <i>V. fischeri</i> via conjugation</p><p><b>Support Protocol 1</b>: Removing FRT-flanked antibiotic resistance cassettes from the <i>V. fischeri</i> genome</p><p><b>Support Protocol 2</b>: Eliminating unstable plasmids from <i>V. fischeri</i></p><p><b>Alternate Protocol 1</b>: Introduction of exogenous DNA using a suicide plasmid</p><p><b>Alternate Protocol 2</b>: Site-specific transposon insertion using a suicide plasmid</p><p><b>Alternate Protocol 3</b>: Random transposon mutagenesis using a suicide plasmid</p>\",\"PeriodicalId\":39967,\"journal\":{\"name\":\"Current Protocols in Microbiology\",\"volume\":\"59 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2020-09-25\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1002/cpmc.115\",\"citationCount\":\"7\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Current Protocols in Microbiology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/cpmc.115\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Protocols in Microbiology","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cpmc.115","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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Genetic Manipulation of Vibrio fischeri
Vibrio fischeri is a nonpathogenic organism related to pathogenic Vibrio species. The bacterium has been used as a model organism to study symbiosis in the context of its association with its host, the Hawaiian bobtail squid Euprymna scolopes . The genetic tractability of this bacterium has facilitated the mapping of pathways that mediate interactions between these organisms. The protocols included here describe methods for genetic manipulation of V. fischeri . Following these protocols, the researcher will be able to introduce linear DNA via transformation to make chromosomal mutations, to introduce plasmid DNA via conjugation and subsequently eliminate unstable plasmids, to eliminate antibiotic resistance cassettes from the chromosome, and to randomly or specifically mutagenize V. fischeri with transposons. © 2020 Wiley Periodicals LLC.
Basic Protocol 1 : Transformation of V. fischeri with linear DNA
Basic Protocol 2 : Plasmid transfer into V. fischeri via conjugation
Support Protocol 1 : Removing FRT-flanked antibiotic resistance cassettes from the V. fischeri genome
Support Protocol 2 : Eliminating unstable plasmids from V. fischeri
Alternate Protocol 1 : Introduction of exogenous DNA using a suicide plasmid
Alternate Protocol 2 : Site-specific transposon insertion using a suicide plasmid
Alternate Protocol 3 : Random transposon mutagenesis using a suicide plasmid