Cloning and expression of the Bacillus thuringiensis crystal protein gene in Escherichia coli.

Sau 3A1 partial digestion fragments from Bacillus thuringiensis var. kurstaki HD-1 plasmid DNA were ligated into the BamHI site of the cloning vector pBR322 and transformed into Escherichia coli strain HB101. Colonies presumed to contain recombinant plasmids were screened for production of an antige...

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Veröffentlicht in:	Proc Natl Acad Sci U S A
Hauptverfasser:	Schnepf, H E, Whiteley, H R
Format:	Artigo
Sprache:	Inglês
Veröffentlicht:	National Academy of Sciences 1981
Schlagworte:	Research Article
Online-Zugang:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC319465/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/7019914/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.78.5.2893
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