摘要:
A method for in vitro culturing Sphagnum is provided. The method comprises providing a vegetative fragment of Sphagnum and surface cleaning the fragment with alcohol. The method further comprises dissecting the fragment to provide a piece (106) of Sphagnum. The method further comprises initiating the piece (106) of Sphagnum in a culture medium (104).
摘要:
The invention provides method for producing a plant cell or plant with increased phlorizin or phloretin glycosyltransferase activity, the method comprising transformation of a plant cell or plant with a polynucleotide encoding a polypeptide with phloretin glycosyltransferase activity. The invention also provides host cells, plant cells and plants, genetically modified to contain and or express the polynucleotides.
摘要:
The present invention pertains to compositions and methods for more efficiently and effectively growing microalgae suitable for biofuel production. In one aspect, the invention pertains to a composition comprising microalgae and a suitable growth medium. The suitable growth medium comprises a nutritionally acceptable nitrate salt, and a carbonate salt. The concentration of nutritionally acceptable nitrate salt is from about 75 to about 200 μM while the concentration of carbonate salt is from about 1 to about 6 mM.
摘要:
The invention relates to the technical field of plant biotechnology and, more specifically, to the OCP3 gene of Arabidopsis and the ocp3 mutation of same, as well as to the use thereof in the regulation of resistance to diseases caused by necrotrophic pathogens and to the applications of same in the generation of transgenic plants that are resistant to said type of pathogens.
摘要:
The present invention provides nucleic acid sequences having an altered viral movement protein and 126/183 kDa replicase proteins further characterized in its ability tostabilize a transgene contained in a virus that expresses the altered movement protein. The present invention also provides viral vectors expressing the altered movement protein, cells transformed with the vectors, and host plants infected by the viral vectors.
摘要:
A method for producing an interspecific hybrid Euphorbia plant. The method comprises: (a) providing a first plant which is a Euphorbia pulcherrima plant and a second plant which is a species of Euphorbia selected from the group consisting of Euphorbia cornastra, Euphorbia radians, Euphorbia colorata and Euphorbia fulgens; (b) pollinating a flower of the second plant with pollen from the first plant or a flower of the first plant with pollen from the second plant in a manner which permits formation of an embryo in at least one ovule of the pollinated plant; (c) cutting the embryo; and (d) culturing the cut embryo by placing the cut embryo in contact with culture medium to permit growth of the embryo to thereby produce a primary plant.
摘要:
The present invention relates to a genotype-independent method for transforming and selecting plant explants. The transformation method includes pre-culturing the explants in the presence of an Agrobacterium inducer and exposing the transformed explants to a shoot regeneration media that accelerates shoot development. Plants generated from this transformation method are provided. In particular, methods for obtaining transgenic Eucalyptus and pine cells and regenerating stably transformed Eucalyptus and pine trees are provided. The invention also provides media, methods, and plasmids for selecting and regenerating plants, particularly forest trees.
摘要:
The present invention relates to a rapid transformation and regeneration system for plants. In particular, the invention relates to a plant tissue preparation system. The transformation method is efficient and reliable for production of fertile plants with improved agronomic qualities.
摘要:
The present invention provides for the identification and cloning of functional plant centromeres in Arabidopsis. This will permit construction of stably inherited minichromosomes which can serve as vectors for the construction of transgenic plant and animal cells. In addition, information on the structure and function of these regions will prove valuable in isolating additional centromeric and centromere related genetic elements and polypeptides from other species.