The present invention provides medium compositions and methods for the regeneration of the whole plant from explants obtained from plants belonging to the Malvaceae family, particularly the Abelmoschus genus, more preferably Abelmoschus esculentus L, through somatic embryogenesis. The present invention also provides an efficient methodology for genetic transformation of plants belonging to the Malvaceae family through somatic embryogenesis in semisolid culture with the use of the Agrobacterium. The present invention is also related to a method for the development of virus-resistant transgenic plants belonging to the Malvaceae family.

A plant propagation system, process and method are provided for promoting the growth of plant tissue into propagules using a photoautotrophic gel system. The plant propagation system includes a sterile growth vessel that has a vented lid to permit passive diffusion of gases. The process is initiated with one or more sterile rooted explants, which are then cultured in a large container with a vented lid photoautotrophically, which simulates ex-vitro growth conditions. These nodal explants can then be rooted onto photoautotrophic rooting agar gel in vented lid containers and subsequently transferred onto a substrate of choice for mature growth ex-vitro.

A tree eggplant and a cultivation method, a rapid propagation method and an application thereof are provided by the present disclosure. In the present disclosure, the Solanum wrightii is specifically selected as the female parent, and the Solanum torvum is used as the male parent, and the tree eggplant variety obtained by hybridization has fast growth, developed trunk, strong growth potential, and is perennial, and is strong in photosynthesis, strong in nutrient and water absorption capacity, high in affinity with the scion, fast in healing at the scion interface of the rootstock and good in healing; and has good resistance to soil-borne diseases such as fusarium wilt, verticillium wilt, bacterial wilt and root knot nematode; and the rapid propagation method of the tree eggplant has strong operability and high efficiency, and is easy to popularize in practical application.

A method of producing cannabinoids for use in medical treatments by growing cultured Cannabis sativa plant cells through tissue culture, the method comprising the steps of: selecting Cannabis sativa leaf tissue for culture; and growing a tissue culture from the selected leaf tissue in a liquid based medium whilst controlling the light exposure of the tissue culture to control the cannabinoid content of the tissue culture. Control of the light exposure can enable the phytocannabinoid content of the grown tissue culture to be tailored to the use intended for the tissue culture. For example, the THC content of the tissue culture can be controlled to be maximised or minimised depending on the intended use. Use of tissue culture is beneficial as compared to prior art methods as it allows for genetic consistency and reduces the resources necessary to produce plant cells containing phytocannabinoids.

This invention relates to an agent for inducing a callus comprising a compound represented by Formula (I) or a hydrolysis product of an amide bond thereof: ##STR00001##
wherein Ar.sup.1 represents phenyl substituted with substituent or substituents selected from alkoxy and methylenedioxy; Ar.sup.2 represents phenyl substituted with halogen; R.sup.1 and R.sup.2 each represent hydrogen, alkyl, cyano, or carboxyl; R.sup.1 and R.sup.2 may together form oxo; R.sup.3 to R.sup.10 each represent hydrogen or methyl; and R.sup.3 and R.sup.4, R.sup.5 and R.sup.6, R.sup.7 and R.sup.8, and/or R.sup.9 and R.sup.10 may together form oxo; a method for inducing a callus and a method for plant transformation using such agent for inducing a callus.

The present invention relates to a method for the production of a (poly)hydroxylated pentacyclic triterpene composition including a 3-O-p-coumaroyl ester of tormentic acid from a plant suspension cell culture, to a pharmaceutical composition comprising at least 3-O-p-coumaroyl ester of tormentic acid for a use in the prevention and/or the treatment of trypanosomiasis, optionally in admixture with other (poly)hydroxylated pentacyclic triterpenes, and to 3-O-p-coumaroyl ester of tormentic acid for its use as an antiparasitic agent for the prevention and/or the treatment of trypanosomiasis, optionally in admixture with other (poly)hydroxylated pentacyclic triterpenes.

The methods disclosed herein provide for clonal plant production using a morphogenic gene to produce non-transgenic and transgenic plants wherein the morphogenic gene does not integrate into the genome of the plant.

A method to expedite the growth of the agave plant by growing the plant tissue from a cell culture in a laboratory utilize incubator cells that are taken from the leaf of an agave plant and grown in a medium containing all the nutrients required for the production of new cells and the maturation of those new cells. The cells are then exposed to photosynthetic active radiation and fed with extra carbon dioxide, causing the cells to undergo photosynthesis and form the sugars that are found in a naturally growing agave plant. These cultivated cells are given an optimum amount of light and carbon dioxide to promote an unexpected and substantially higher growth rate than heretofore achieved.

A recombinant protein for use in a liquid culture medium for photo-autotrophic micropropagation of Cannabis sativa L. is disclosed. The recombinant protein comprises a fusion of a growth induction part and a uptake enhancement part. The growth induction part comprises an Arabinogalactan protein and/or a plant transcription factor associated with plant growth and development. The uptake enhancement part comprises a cell penetrating peptide sequence and a nuclear localization signal encoded by the peptide sequence SEQ ID NO 1.

Provided is an in vitro rescue method for immature embryo of avocado, and the method includes: collecting immature avocado hybrid fruits, stripping immature zygotic embryos from the sterilized fruits; inducing maturation of zygotic embryos in different mediums selected according to the maturities of zygotic embryos; and avocado seed embryos growing to normal plants under light conditions after germination. Provided is a technology for the in vitro culture rescue of immature embryo of avocado, wherein the zygotic embryos at different developmental stages are induced to maturation under in vitro conditions, and after maturation, the seed embryos are induced to germinate and form healthy plants. The technology of the present invention can effectively improve the survival rate of hybrid avocado zygotic embryo, increase the success rate of hybrid avocado, rescue the hybrid offspring, reduce the loss of hybrid offspring, ensure the genetic integrity of hybrid group, and provide the key technology for hybrid breeding and genetic research of avocado, etc.