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pubmed-article:18635055rdf:typepubmed:Citationlld:pubmed
pubmed-article:18635055lifeskim:mentionsumls-concept:C0004651lld:lifeskim
pubmed-article:18635055lifeskim:mentionsumls-concept:C0012854lld:lifeskim
pubmed-article:18635055lifeskim:mentionsumls-concept:C0013878lld:lifeskim
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pubmed-article:18635055pubmed:issue2lld:pubmed
pubmed-article:18635055pubmed:dateCreated2008-7-18lld:pubmed
pubmed-article:18635055pubmed:abstractTextphi29 DNA-containing 12-13- particles (produced by infecting nonsuppressor hosts of Bacillus subtilis with phage containing suppressible mutations in cistrons 12 and 13) can be complemented with lysates containing proteins p12* and p13 to yield infectious phage. Complementation of these particles with lysates containing p12* but not p13 or complementation with purified p12* in the absence of p13 produces a structure (called complex) which has a markedly different organization. Electron microscopy and sedimentation analysis after digestion with DNase I or proteinase K indicate that complex is composed of an intact phage head with a genome-sized linear DNA molecule attached at the collar-tail region. EcoRI digestion establishes that the DNA molecule has a unique orientation. Gel electrophoresis indicates that p12*, the neck appendage protein, is transferred to the particles when complex is formed. Complex can also be produced by incubation of 12-13- particles at 42 degrees , by incubation at pH 6.0, or by incubation in the presence of 20 mM EDTA. Complex is also formed from DNA-containing 12- particles but to a lesser extent.lld:pubmed
pubmed-article:18635055pubmed:languageenglld:pubmed
pubmed-article:18635055pubmed:journalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:18635055pubmed:statusPubMed-not-MEDLINElld:pubmed
pubmed-article:18635055pubmed:monthJunlld:pubmed
pubmed-article:18635055pubmed:issn0042-6822lld:pubmed
pubmed-article:18635055pubmed:authorpubmed-author:SalasMMlld:pubmed
pubmed-article:18635055pubmed:authorpubmed-author:JiménezFFlld:pubmed
pubmed-article:18635055pubmed:authorpubmed-author:GarcíaJ AJAlld:pubmed
pubmed-article:18635055pubmed:authorpubmed-author:VillanuevaNNlld:pubmed
pubmed-article:18635055pubmed:authorpubmed-author:KrawiecSSlld:pubmed
pubmed-article:18635055pubmed:authorpubmed-author:SogoJJlld:pubmed
pubmed-article:18635055pubmed:issnTypePrintlld:pubmed
pubmed-article:18635055pubmed:volume111lld:pubmed
pubmed-article:18635055pubmed:ownerNLMlld:pubmed
pubmed-article:18635055pubmed:authorsCompleteYlld:pubmed
pubmed-article:18635055pubmed:pagination440-54lld:pubmed
pubmed-article:18635055pubmed:year1981lld:pubmed
pubmed-article:18635055pubmed:articleTitleThe orderly, in vitro emergence of DNA from bacteriophage phi29 particles.lld:pubmed
pubmed-article:18635055pubmed:affiliationCentro de Biología Molecular (C.S.I.C.-U.A.M.), Universidad Autónoma de Madrid, Canto Blanco, Madrid-34, Spain.lld:pubmed
pubmed-article:18635055pubmed:publicationTypeJournal Articlelld:pubmed