US2012174264A1PendingUtilityA1
Uses of Yerba Santa
Est. expiryJun 20, 2028(~2 yrs left)· nominal 20-yr term from priority
A01H 4/005A61K 2039/5258A61K 2039/542A61K 2039/517A61K 2039/55544A61K 39/145C12N 15/8257A61K 2039/543C12N 2760/16134C12N 15/8205A61K 39/12C12N 15/8258
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Claims
Abstract
Methods of in vitro propagation of plants of the genus Eriodictyon are described, including, in particular embodiments, plants of the species E. californicum, E. trichocalyx and E. sessilifolium . Methods of producing transgenic plants of the genus Eriodictyon are also described, along with methods of producing recombinant proteins in such plants. Compositions and methods for administering recombinant proteins produced in these plants are also described.
Claims
exact text as granted — not AI-modified1 . A transgenic plant of the genus Eriodictyon.
2 . The transgenic plant of claim 1 , wherein the plant is selected from the group consisting of E. californicum, E. trichocalyx and E. sessilifolium.
3 . The transgenic plant of claim 1 , which expresses a recombinant protein.
4 . The transgenic plant of claim 3 wherein the recombinant protein comprises an avian influenza HA1 antigen.
5 . A method for transforming tissue from a plant of the genus Eriodictyon comprising the steps of:
inoculating leaf tissue from an Eriodictyon plant with an Agrobacterium suspension diluted to about OD 600 0.005 to 0.5, the Agrobacterium containing at least one genetic component encoding a desired protein capable of being transferred to the transformable plant tissue and of directing the expression of the desired protein in the plant tissue; co-cultivating the plant tissue with the Agrobacterium; transferring the plant tissue to recovery media containing an antibiotic for eliminating the Agrobacterium ; and selecting transformed plant tissue.
6 . The method of claim 5 wherein the plant species is selected from the group consisting of Eriodictyon californicum, Eriodictyon trichocalyx and Eriodictyon sessilifolium.
7 . The method of claim 5 wherein the Agrobacterium suspension is diluted to about OD 600 0.03.
8 . The method of claim 5 wherein the co-cultivating of the plant tissue with the Agrobacterium suspension is for about 1 to 4 days at about 20 to 25° C.
9 . The method of claim 8 wherein the co-cultivating of the plant tissue with the Agrobacterium suspension is for about 2 days.
10 . A method for producing a recombinant protein in a transgenic plant of the genus Eriodictyon comprising the steps of:
providing a transgenic plant that has been regenerated from a transformed plant cell or tissue of the genus Eriodictyon and that expresses a recombinant protein; and recovering the recombinant protein expressed in the transgenic plant.
11 . The method of claim 10 wherein the recovery step further comprises obtaining an extract of the transgenic plant.
12 . The method of claim 10 wherein the recovery step further comprises harvesting material from at least a portion of the transgenic plant.
13 . The method of claim 12 wherein the at least a portion of the harvested material is edible.
14 . The method of claim 10 wherein the plant cell or tissue is transformed using an Agrobacterium system.
15 . The method of claim 14 wherein the plant cell or tissue is transformed using the method of claim 5 .
16 . The method of claim 10 wherein the recombinant protein is selected from the group consisting of antigens, microbicides, antibodies, hormones, enzymes, blood components, interferons, and anticoagulants.
17 . The method of claim 16 wherein the antigen comprises a viral protein.
18 . The method of claim 17 wherein the protein comprises an avian influenza HA1 antigen.
19 . The method of claim 16 wherein the microbicide comprises an antiretroviral.
20 . The method of claim 19 wherein the antiretroviral comprises griffithsin.Cited by (0)
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