Source:http://linkedlifedata.com/resource/pubmed/id/11040123
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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
2
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| pubmed:dateCreated |
2000-11-9
|
| pubmed:abstractText |
Two putative structural genes, orf tmp (tape measure protein) and orf bpp (baseplate protein), of the temperate lactococcal phage TP901-1 were examined by introduction of specific mutations in the prophage strain Lactococcus lactic ssp. cremoris 901-1. The adsorption efficiencies of the mutated phages to the indicator strain L. lactic ssp. cremoris 3107 were determined and electron micrographs were obtained. Specific mutations in orf tmp resulted in the production of mostly phage head structures without tails and a few wild-type looking phages. Furthermore, construction of an inframe deletion or duplication of 29% in orf tmp was shown to shorten or lengthen the phage tail by approximately 30%, respectively. The orf tmp is proposed to function as a tape measure protein, TMP, important for assembly of the TP901-1 phage tail and involved in tail length determination. Specific mutations in orf bpp produced phages which were unable to adsorb to the indicator strain and electron microscopy revealed particles lacking the baseplate structure. The orf bpp is proposed to encode a highly immunogenic structural baseplate protein, BPP, important for assembly of the baseplate. Finally, an assembly pathway of the TP901-1 tail and baseplate structure is presented.
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| pubmed:language |
eng
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| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:chemical | |
| pubmed:status |
MEDLINE
|
| pubmed:month |
Oct
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| pubmed:issn |
0042-6822
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| pubmed:author | |
| pubmed:copyrightInfo |
Copyright 2000 Academic Press.
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| pubmed:issnType |
Print
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| pubmed:day |
25
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| pubmed:volume |
276
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| pubmed:owner |
NLM
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| pubmed:authorsComplete |
Y
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| pubmed:pagination |
315-28
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| pubmed:dateRevised |
2006-11-15
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| pubmed:meshHeading |
pubmed-meshheading:11040123-Adsorption,
pubmed-meshheading:11040123-Blotting, Western,
pubmed-meshheading:11040123-DNA, Viral,
pubmed-meshheading:11040123-Electrophoresis, Polyacrylamide Gel,
pubmed-meshheading:11040123-Enzyme-Linked Immunosorbent Assay,
pubmed-meshheading:11040123-Escherichia coli,
pubmed-meshheading:11040123-Genes, Viral,
pubmed-meshheading:11040123-Lactococcus lactis,
pubmed-meshheading:11040123-Mutagenesis,
pubmed-meshheading:11040123-Open Reading Frames,
pubmed-meshheading:11040123-Restriction Mapping,
pubmed-meshheading:11040123-Sequence Analysis, DNA,
pubmed-meshheading:11040123-Siphoviridae,
pubmed-meshheading:11040123-Viral Proteins,
pubmed-meshheading:11040123-Viral Structural Proteins,
pubmed-meshheading:11040123-Viral Tail Proteins,
pubmed-meshheading:11040123-Virus Activation,
pubmed-meshheading:11040123-Virus Assembly
|
| pubmed:year |
2000
|
| pubmed:articleTitle |
Mutational analysis of two structural genes of the temperate lactococcal bacteriophage TP901-1 involved in tail length determination and baseplate assembly.
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| pubmed:affiliation |
Department of Dairy and Food Science, The Royal Veterinary and Agricultural University, Rolighedsvej 30, Frederiksberg C, DK-1958, Denmark.
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| pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|