US2009104701A1PendingUtilityA1
Method for the production of biomass from plant differentiated tissue
Est. expiryDec 20, 2026(~0.4 yrs left)· nominal 20-yr term from priority
C12N 5/0025
41
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Claims
Abstract
The present invention provides a method and a culture medium for the production of food biomass by directly culturing seed kernel tissue, or seed cotyledonary differentiated tissue. The culture medium of the present invention contains at least DKW culture medium, Vitamin MS culture medium with an enriched concentration of thiamine, sacarose, kinetine, adenine, 2,4 d iclorofenoxiacético (2,4D), L-Glutamine, cysteine, ascorbic acid, and Gelrite®.
Claims
exact text as granted — not AI-modified1 . A method for the production of biomass from Sterculiacea plant differentiated tissue comprising:
A. Obtaining a fruit that is between three and five months old; B. Cleaning and sterilizing said fruit; C. Extracting seeds from said fruit; D. Discarding the embryo and obtaining a sample of cotyledonary differentiated tissue; E. Putting the sample of cotyledonary differentiated tissue in contact with culture medium; F. Incubating under light with a determined wave length, and at a temperature between 15 and 35° C., until biomass is produced; and, G. Collecting grown biomass by retiring said grown biomass from the culture medium.
2 . The method of claim 1 , wherein the culture medium contains at least DKW culture medium, Vitamin MS culture medium with an enriched concentration of thiamine, sacarose in a concentration between 15 and 40 g/L, kinetine in a concentration between 0.5 and 4 mg/L, adenine in a concentration between 0.2 and 5 mg/L, 2,4diclorofenoxiacético (2,4D) in a concentration between 1 and 5 mg/L, L-Glutamine in a concentration between 20 and 100 mg/L, cysteine in a concentration between 10 and 100 mg/L, ascorbic acid in a concentration between 20 and 110 mg/L, and Gelrite® in a concentration between 0.7 and 2.0 g/L; and wherein the pH of the culture medium is adjusted to a range between 5.5 and 6.0.
3 . The method of claim 1 , wherein the Sterculiacea plant is from the Theobroma genus.
4 . The method of claim 1 , wherein the Sterculiacea plant is from the T. cacao species.
5 . The method of claim 1 , wherein the sample of cotyledonary differentiated tissue in contact with the culture medium is incubated under total darkness.
6 . A method for the production of biomass from Proteaceae plant differentiated tissue comprising:
a. Obtaining a sample of kernel differentiated tissue; b. Putting the sample of kernel differentiated tissue in contact with culture medium; c. Incubating under light with a determined wave length, and at a temperature between 15 and 35° C., until biomass is produced; and, d. Collecting grown biomass by retiring said grown biomass from the culture medium.
7 . The method of claim 6 , wherein the culture medium contains at least DKW culture medium, Vitamin MS culture medium with an enriched concentration of thiamine, sacarose in a concentration between 15 and 40 g/L, kinetine in a concentration between 0.5 and 4 mg/L, adenine in a concentration between 0.2 and 5 mg/L, 2,4diclorofenoxiacético (2,4D) in a concentration between 1 and 5 mg/L, L-Glutamine in a concentration between 20 and 100 mg/L, cysteine in a concentration between 10 and 100 mg/L, ascorbic acid in a concentration between 20 and 110 mg/L, and Gelrite® in a concentration between 0.7 and 2.0 g/L; and wherein the pH of the culture medium is adjusted to a range between 5.5 and 6.0.
8 . The method of claim 6 , wherein the Proteaceae plant is from the Macadamia genus.
9 . The method of claim 6 , wherein the Proteaceae plant is from the Macadamia species.
10 . The method of claim 6 , wherein the sample of kernel differentiated tissue in contact with the culture medium is incubated under total darkness.Join the waitlist — get patent alerts
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