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.

A method for obtaining regenerated seedlings of Brassica campestris L. ssp. chinensis from embryonic tip tissues, including the following steps. A seed is inoculated to a germination medium for dark culture for 60 h. The testa, root tip, two cotyledons and middle growing point of the resultant germinated seed are removed, and an embryonic tip with a length of 3-5 mm is retained as an explant. The explant is sequentially subjected to low-temperature pre-culture in a pre-culture medium for 36 h, room-temperature shaking culture in a liquid bud induction culture medium for 10 min, and bud induction culture in a bud induction culture medium for 20 d. A regenerated plant with 5-6 leaves is transferred to a rooting medium for rooting culture for about 2 weeks, and a well-rooted plant is collected, and subjected to hardening and transplantation into a filed.

The present invention relates to a method for the production of haploid, polyhaploid and/or doubled haploid embryos, calli, seeds and/or plants of the species Beta vulgaris from isolated microspore cultures, more specifically to a method comprising contacting the isolated microspores with a histone deacetylase inhibitor (HDACi) and a complex protein composition. The present invention also provides a kit for producing a haploid, polyhaploid and/or doubled haploid embryo, callus, seed and/or plant of the species Beta vulgaris from at least one isolated microspore as well as the use of a histone deacetylase inhibitor (HDACi) and a complex protein composition for producing a haploid, polyhaploid and/or doubled haploid embryo, callus, seed and/or plant of the species Beta vulgaris. Finally, the present invention also relates to a population of haploid, polyhaploid and/or doubled haploid Beta vulgaris plants directly derived from a single flower, single inflorescence or single bud.

The present invention relates to the use of PDE inhibitors, preferably mammalian PDE inhibitors, to enhance the induction of in vitro plant cell reprogramming towards plant embryogenesis or microcallus formation for further plant regeneration. The present invention also relates to a method to promote this process comprising culturing an isolated plant material with at least one PDE inhibitor, preferably mammalian PDE inhibitor.

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 invention provides: a callus induction method that efficiently induces callus from a tissue fragment from an isoprenoid-producing plant; a callus culture method that efficiently grows callus; a somatic embryo induction method that efficiently forms a somatic embryo; a plant regeneration method that can stably regenerate callus into plants; a plant propagation method that can stably propagate a plant without being affected by e.g. weather and seasons; and a method of inducing rooting in a mature embryo. The present invention relates, inter alia, to a method of plant regeneration that can stably regenerate callus into plants and a method of plant propagation that can stably propagate a plant.

Described herein are apparatus and methods for wounding plant tissue. A method of the present invention includes blending a plant tissue (e.g., a plant and/or plant part) in a blender (e.g., an electric blender) to provide wounded plant tissue.

The present invention provides a method of producing a photosynthetic product, the method comprising maintaining a photosynthetic plant or algal cell suspension culture, in the presence of water, light and a carbonic acid-enriched growth medium. The carbonic acid may, for example be provided by feeding the photosynthetic plant cell suspension culture with a carbonic acid solution, a solid or liquid precursor thereof, or a gaseous mixture of carbon dioxide and one or more other gases. The invention also provides a method for producing a photosynthetic product, the method comprising maintaining a photosynthetic plant or algal cell suspension culture, in the presence of water, light and a carbon source selected from carbon dioxide and carbonic acid, wherein the culture is maintained at a pH of less than 7.0, preferably 4.5 to 5.5.

There are provided a radiofrequency device for increasing amount of a bioactive substance in a plant cell and a plant cell culture method for increasing amount of useful intracellular secondary metabolites by using the radiofrequency device. The cell culture method of the present invention makes it possible to increase specific secondary metabolites such as daidzein, equol, and the like in a cell and thus can be used for development into various medicines, agricultural pesticides, spices, pigments, food additives, and cosmetics containing bioactive substances. Further, the cell culture method of the present invention improves conventional cell culture methods limitedly used for specific cells or specific metabolites for increasing amount of intracellular bioactive substances and thus can be widely applied to production of cells and secondary metabolites.

A method, apparatus, and system are provided for the printing and maturation of living tissue in an Earth-referenced reduced gravity environment such as that found on a spacecraft or on other celestial bodies. The printing may be three-dimensional structures. The printed structures may be manufactured from low viscosity biomaterials.