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Lambda phage

About: Lambda phage is a research topic. Over the lifetime, 1609 publications have been published within this topic receiving 84675 citations. The topic is also known as: Enterobacteria phage lambda.


Papers
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Journal ArticleDOI
01 Oct 1984-Gene
TL;DR: The phi 29 DNA restriction fragment HindIII-D, shown to contain gene 10 coding for the connector protein, has been cloned in plasmid pPLc28 under the control of the pL promoter of phage lambda.

23 citations

Journal ArticleDOI
01 Nov 1991-Genomics
TL;DR: A full-length cDNA is cloned from the Mov-34 gene, the transcription unit disrupted by the proviral integration, predicted to encode a novel 321-amino acid, 36-kDa protein of unknown function.

23 citations

Journal ArticleDOI
01 Dec 1982-Gene
TL;DR: Plasmid ppBest 322, a derivative of pBR322 carrying this portable packager and both amp and tet genes, was constructed, and this plasmid is useful for cloning of large DNA fragments.

23 citations

Journal ArticleDOI
11 Aug 1997-Gene
TL;DR: Sequence comparison of the early genes has confirmed that the C-immunity region of ES18 is identical with that of P22, whereas the same region of phage L shows poor (repressor gene) or no similarity.

23 citations

Journal ArticleDOI
TL;DR: The Hind III G fragment from the Bacillus subtilis phage phi 29 DNA, inserted downstream from the bacteriophage lambda promoter PL carried by a pBR322 derivative plasmid (pPLc28), directed the synthesis in E. coli of two proteins of apparent molecular weight 27500 and 12500.
Abstract: The Hind III G fragment from the Bacillus subtilis phage phi 29 DNA, inserted downstream from the bacteriophage lambda promoter PL carried by a pBR322 derivative plasmid (pPLc28), directed the synthesis in E. coli of two proteins of apparent molecular weight 27500 and 12500. With the use of the recombinants obtained with the DNA from mutants sus3(91) and sus4(56), the two proteins were identified as a modified p3 (p3'), the protein covalently linked to the 5' ends of phi 29 DNA, and p4, responsible for the phi 29 late transcription, respectively. Under the best conditions used, proteins p4 and p3' were produced in E. coli from the cloned DNA fragments in an amount corresponding to approximately 30% and 6% of total de novo protein synthesis, respectively.

23 citations


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Performance
Metrics
No. of papers in the topic in previous years
YearPapers
20226
20219
20209
20195
20188
20177