Plant vector
AssigneePhytogen
InventorDavid M. Anderson
Life of this patent
Estimating the term…
Abstract
There are provided herewith vector precursors and vectors based on Pst I cleaved left and right border fragments of the T region of the Ti plasmid Agrobacterium tumefaciens strain of C58 interligated and ligated into the Pst I site of plasmid pBR322. Antibiotic resistance gene sequence is used to establish vector expression and presence in host cells.
Claims7
A vector precursor comprising the Pst I cleaved left and right border fragments of the T region of the Ti plasmid Agrobacterium tumefaciens strain of C58 interligated and ligated into the Pst I site of plasmid pBR322.
A vector comprising the Pst I-cleaved left and right border fragments of the T region of the Ti plasmid Agrobacterium tumefaciens strain of C58 ligated to the Pst I sites of the plasmid pBR322 and in which there is contained within the border segments a eukaryotic transcription sequence next to an antibiotic resistance gene sequence.
A vector comprising the Pst I cleaved left and right border fragments of the T region of the Ti plasmid Agrobacterium tumefaciens strain of C58 ligated to the Pst I sites of the plasmid pBR322 in proper orientation and in which there is contained within the right border segment at the BamHI site the thymidine kinase promoter and neomycin resistance genes.
A vector comprising a first segment comprising the Pst I cleaved left and right border sequences of the T region of the Ti plasmid Agrobacterium tumefaciens strain C58 ligated to the Pst I sites of the plasmid pBR322 in proper orientation and in which there is contained within the right border segment at the BamHI site thymidine kinase promoter and neomycin resistance genes ligated into the Hpa I site of the cauliflower mosaic virus at blunted Kpn I sites of the right border sequence.
A process for vector formation which comprises:
- (a) isolating from the Ti plasmid Agrobacterium tumefaciens strain of C58 right- and left-hand border sequences generated by XbaI cleavage;
- (b) cleaving the right-hand and left-hand border sequences with Pst I;
- (c) combining the Pst I cleaved left- and right-hand border sequences in the same orientation as in the Ti plasmid into the Pst I site of the plasmid pBR322 at a temperature of about 30.degree. C. or less;
- and
- (d) introducing to the border sequences an antibiotic gene sequence and an adjacent eukaryotic transcription promoter sequence.
Dependencies are inferred from the claim text.