Disclosed herein are media, kits, systems and methods for achieving micropropagation of a HDT date palm on a commercially relevant scale. Compositions and methods for each stage of micropropagation, including initiation, elongation, and rooting are disclosed in the present application. Also disclosed are conditions for harvesting and sterilizing explant tissue for micropropagation.

Disclosed herein are media, kits, systems and methods for achieving micropropagation of a date palm on a commercially relevant scale. Compositions and methods for each stage of micropropagation, including initiation, elongation, and rooting are disclosed in the present application. Also disclosed are conditions for harvesting and sterilizing explant tissue for micropropagation.

Disclosed herein are media, kits, systems and methods for achieving micropropagation of an Abada date palm on a commercially relevant scale. Compositions and methods for each stage of micropropagation, including initiation, elongation, and rooting are disclosed in the present application. Also disclosed are conditions for harvesting and sterilizing explant tissue for micropropagation.

Disclosed herein are media, kits, systems and methods for achieving micropropagation of a Black Barhee date palm on a commercially relevant scale. Compositions and methods for each stage of micropropagation, including initiation, elongation, and rooting are disclosed in the present application. Also disclosed are conditions for harvesting and sterilizing explant tissue for micropropagation.

Cosmos bipinnatus cotyledons are isolated as explants, and the isolated explants are cultured onto a regeneration medium to obtain regenerated Cosmos bipinnatus shoots. The regeneration medium optionally includes a basal medium, a cytokinin, an ethylene action inhibitor, and a nitrogen source.

Methods of producing sugar cane transplant units that includes planting a sugar cane propagation material in a planting container that has a volume of 10 to 200 cubic centimeters; growing the sugar plant to an age of at least 4 months; harvesting the stalks of the sugar cane plant when the stalks have a length of 10 to 50 centimeters; cutting the harvested stalks into stalk segments, wherein the stalk segments are cut to a length of 1 to 5 centimeters; and planting one or more of the stalk segments into a planting container that has a volume from 10 to 200 cubic centimeters.

The disclosure relates to a method for increasing the resistance of a plant to a plant RNA virus, comprising expressing in said plant a mutant protein-only RNase P enzyme lacking a nuclear localization signal domain or an organelle targeting sequence domain, and related compositions.

The present application relates generally to the field of plant propagation. In particular, the present invention relates to a method for the propagation of vegetatively reproducing plants and plants and plant parts produced by such methods. The invention also provides encapsulated propagules. The invention also provides various end uses for the encapsulated propagules and for plants grown from the same. The invention also provides a method for the modification of the architecture of rhizomes and rhizomes having modified architecture and a method for the modification of the architecture of stem cuttings and stem cuttings having modified architecture. The invention also provides a coating for a propagule and a propagule coated therewith.

There are provided compositions and methods for transforming plants, preferably monocot, and even more preferably, sugarcane. The transformation methods involve infection of plant tissue with Agrobacterium, and co-cultivation using culture medium comprising high concentrations of gelling agent, with the result of inhibiting the exacerbated growth of the bacteria and increasing the transformation frequencies. The invention includes regenerating transformed plants, and the transformed plants themselves.

Provided are a method for improving rice yield by jointly knocking out ABA receptor PYL family genes and a use thereof.