Abstract: A soybean cultivar designated 04220959 is disclosed. The invention relates to the seeds of soybean cultivar 04220959, to the plants of soybean cultivar 04220959, to the plant parts of soybean cultivar 04220959, and to methods for producing progeny of soybean cultivar 04220959. The invention also relates to methods for producing a soybean plant containing in its genetic material one or more transgenes and to the transgenic soybean plants and plant parts produced by those methods. The invention also relates to soybean cultivars or breeding cultivars, and plant parts derived from soybean cultivar 04220959. The invention also relates to methods for producing other soybean cultivars, lines, or plant parts derived from soybean cultivar 04220959, and to the soybean plants, varieties, and their parts derived from use of those methods. The invention further relates to hybrid soybean seeds, plants, and plant parts produced by crossing cultivar 04220959 with another soybean cultivar.

Abstract: A novel soybean variety, designated 5PAHV91 is provided. Also provided are the seeds of soybean variety 5PAHV91, cells from soybean variety 5PAHV91, plants of soybean 5PAHV91, and plant parts of soybean variety 5PAHV91. Methods provided include producing a soybean plant by crossing soybean variety 5PAHV91 with another soybean plant, methods for introgressing a transgenic trait, a mutant trait, and/or a native trait into soybean variety 5PAHV91, methods for producing other soybean varieties or plant parts derived from soybean variety 5PAHV91, and methods of characterizing soybean variety 5PAHV91. Soybean seed, cells, plants, germplasm, breeding lines, varieties, and plant parts produced by these methods and/or derived from soybean variety 5PAHV91 are further provided.

Abstract: The present disclosure discloses an AtPPR1 gene (negative regulatory factor) for Phytophthora resistance and homologous genes thereof, involving an AtPPR1 gene and a protein encoded by the AtPPR1 gene. The AtPPR1 gene has a nucleotide sequence of SEQ ID NO:6, and the protein encoded by the AtPPR1 gene has an amino acid sequence of SEQ ID NO:7. A function of the AtPPR1 gene of the present disclosure to improve Phytophthora resistance of plants can be used for the selective breeding of Phytophthora-resistant varieties. As a new type of negative immunoregulatory factor in plants, AtPPR1 negatively regulates the resistance of plants to Phytophthora by interfering with downstream signal transduction of endogenous jasmonic acid (JA) and salicylic acid (SA) and ROS signals in plants.

Abstract: The present disclosure provides compositions and methods for providing broad-based resistance to fungal pathogens, such as a Fusarium fungi, and plants derived therefrom.

Abstract: The present invention relates to a method of improving soybean transformation efficiency, which comprises: transforming a plant cell using a recombinant vector containing a gene of interest and a gene encoding a sulfonylurea herbicide hydrolase; screening and culturing the transformed plant cell by external application of an ALS inhibitor, using the gene encoding the sulfonylurea herbicide hydrolase as a selective marker; selecting a plant cell that has not been killed and/or not been inhibited.

Abstract: New lettuce variety designated ‘Pensacola’ is described. ‘Pensacola’ is a lettuce variety exhibiting stability and uniformity.

Abstract: A novel soybean variety, designated 5PMHT38 is provided. Also provided are the seeds of soybean variety 5PMHT38, cells from soybean variety 5PMHT38, plants of soybean 5PMHT38, and plant parts of soybean variety 5PMHT38. Methods provided include producing a soybean plant by crossing soybean variety 5PMHT38 with another soybean plant, methods for introgressing a transgenic trait, a mutant trait, and/or a native trait into soybean variety 5PMHT38, methods for producing other soybean varieties or plant parts derived from soybean variety 5PMHT38, and methods of characterizing soybean variety 5PMHT38. Soybean seed, cells, plants, germplasm, breeding lines, varieties, and plant parts produced by these methods and/or derived from soybean variety 5PMHT38 are further provided.

Abstract: A lettuce cultivar, designated Apollo Creed, is disclosed. The invention relates to the seeds, plants, and plant parts of lettuce cultivar Apollo Creed and to methods for producing a lettuce plant by crossing cultivar Apollo Creed with itself or another lettuce cultivar. The invention further relates to methods for producing a lettuce plant containing in its genetic material one or more transgenes and to the transgenic lettuce plants and plant parts produced by those methods. This invention also relates to lettuce cultivars or breeding cultivars and plant parts derived from lettuce cultivar Apollo Creed, to methods for producing other lettuce cultivars, lines or plant parts derived from lettuce cultivar Apollo Creed and to the lettuce plants, varieties, and their parts derived from the use of those methods. The invention further relates to hybrid lettuce seeds, plants, and plant parts produced by crossing cultivar Apollo Creed with another lettuce cultivar.

Abstract: Provided is a canola variety designated 18GG0453L and seed, plants and plant parts thereof produced from a cross of inbred varieties. Methods for producing a canola variety comprise crossing canola variety 18GG0453L with another canola plant. Methods for producing a canola plant containing in its genetic material one or more traits introgressed into 18GG0453L through backcross conversion and/or transformation, and to the canola seed, plant and plant part produced thereby are described. Canola variety, the seed, the plant produced from the seed, plant parts and variants, mutants, and minor modifications of canola variety are disclosed.

Abstract: Disclosed herein are compositions and methods for effecting alterations at a defined location in the genome of a plant cell or plant protoplast. Further disclosed are methods using an RNA-guided nuclease to alter a target nucleotide sequence in a cell or protoplast of a plant; embodiments of such methods include treatments with chemical or physical reagents or treatment of the cell or protoplast with a specific thermal regime, such as a heat treatment.

Abstract: Compositions and methods for controlling pests are provided. The methods involve transforming organisms with a nucleic acid sequence encoding an insecticidal protein. In particular, the nucleic acid sequences are useful for preparing plants and microorganisms that possess insecticidal activity. Thus, transformed bacteria, plants, plant cells, plant tissues and seeds are provided. Compositions are insecticidal nucleic acids and proteins of bacterial species. The sequences find use in the construction of expression vectors for subsequent transformation into organisms of interest including plants, as probes for the isolation of other homologous (or partially homologous) genes. The pesticidal proteins find use in controlling, inhibiting growth or killing Lepidopteran, Coleopteran, Dipteran, fungal, Hemipteran and nematode pest populations and for producing compositions with insecticidal activity.

Abstract: A genetically engineered land plant that expresses a plant CCP1-like mitochondrial transporter protein is provided. The genetically engineered land plant comprises a modified gene for the plant CCP1-like mitochondrial transporter protein. The plant CCP1-like mitochondrial transporter protein is an ortholog of CCP1 of Chlamydomonas reinhardtii of SEQ ID NO: 1 derived from a source land plant. The plant CCP1-like mitochondrial transporter protein is localized to mitochondria of the genetically engineered land plant based on a mitochondrial targeting signal intrinsic to the plant CCP1-like mitochondrial transporter protein. The modified gene comprises (i) a promoter and (ii) a nucleic acid sequence encoding the plant CCP1-like mitochondrial transporter protein. The promoter is non-cognate with respect to the nucleic acid sequence.

Abstract: The present invention relates to an allele designated alpha-WOLF 26 which confers resistance to at least one Peronospora farinosa f. sp. spinacea race, wherein the protein encoded by said allele is a CC-NBS-LRR protein that may comprise in its amino acid sequence: a) the motif “MAEIGYSVC” SEQ ID NO: 1 at its N-terminus; and b) the motif “KWMCLR” SEQ ID NO: 2; and wherein the LRR domain of the protein has in order of increased preference at least 91%, 91.5%, 92%, 92.5%, 93%, 93.5%, 94%, 94.5%, 95%, 95.5%, 96%, 96.5%, 97%, 97.5%, 98%, 98.5%, 99%, 99.5%, 100% sequence identity to SEQ ID NO: 10. The allele when present in a spinach plant confers complete resistance to at least Peronospora farinosa f. sp. spinacea race Pfs:7, Pfs:10, Pfs:11, Pfs:12, Pfs:13, Pfs:14, Pfs:15, Pfs:16, Pfs:17, and does not confer resistance to downy mildew race Pfs:8 and Pfs:9.

Abstract: The present invention provides transgenic Brassica events LBFLFK and LBFDAU and progeny thereof, and cells, seeds, plants comprising DNA diagnostic for these events. The invention also provides artificial oligonucleotide primers and probes that are diagnostic for the LBFLFK and LBFDAU events and their progeny in a sample, and methods for detecting the presence of the LBFLFK and LBFDAU events and their progeny in a sample. The invention further provides oil and commodity products derived from the LBFLFK and LBFDAU events.

Abstract: The present invention provides a method and means to change fatty acid and ultimately triacylglycerol production in plants and algae. Methods of the invention comprise the step of altering the activity levels of the committed step for de novo fatty acid biosynthesis, acetyl-CoA carboxylases (ACCase). More specifically, methods of the invention directly enhance the activity of ACCase by overexpression of ?-CT or a catalytic portion thereof.

Abstract: The invention relates to the wheat cultivar designated 01092991. Provided by the invention are the seeds, plants and derivatives of the wheat cultivar 01092991. Also provided by the invention are tissue cultures of the wheat cultivar 01092991 and the plants regenerated therefrom. Still further provided by the invention are methods for producing wheat plants by crossing the wheat cultivar 01092991 with itself or another wheat cultivar and plants produced by such methods.

Abstract: A wheat variety designated 6PLSK70B, the plants and seeds of wheat variety 6PLSK70B, methods for producing a wheat plant produced by crossing the variety 6PLSK70B with another wheat plant, and hybrid wheat seeds and plants produced by crossing the variety 6PLSK70B with another wheat line or plant, and the creation of variants by backcrossing, mutagenesis or transformation of variety 6PLSK70B are disclosed. Methods for producing other wheat varieties or breeding lines derived from wheat variety 6PLSK70B and to wheat varieties or breeding lines produced by those methods are also provided.

Abstract: Plant cell cultures as well as related methods, systems, and compositions for increasing the frequency and efficiency of plant genome editing are provided. Various plant cell growth conditions and/or treatments where such increases in gene editing frequencies are obtained are disclosed.

Abstract: The present invention provides a method for improving a one-time seedling rate of microspore embryoids of Brassica campestris ssp. Chinensis Makino, including the steps of: spraying 6-BA onto a flower bud of a plant; sterilizing the flower bud with alcohol and HgCl2; releasing microspores, filtering and centrifuging to obtain purified microspores; diluting the microspores with a NLN medium, subpackaging into culture dishes, and adding phytic acid; finally, subjecting to heat shock treatment and transferring to culture in the dark until embryoids appear, and then conducting shaking culture; transferring the cultured embryos in a cotyledon stage onto a MS medium for differentiation culture, wherein the culture conditions are: 4° C., 14 h of illumination by blue-red compound light/day, and 14 days of culture; and then continuing to culture under the condition of 25° C. and 14 h of illumination by blue-red compound light/day until seedlings.

Abstract: A lettuce cultivar, designated Patton, is disclosed. The invention relates to the seeds, plants, and plant parts of lettuce cultivar Patton and to methods for producing a lettuce plant by crossing the cultivar Patton with itself or another lettuce cultivar. The invention further relates to methods for producing a lettuce plant containing in its genetic material one or more transgenes and to the transgenic lettuce plants and plant parts produced by those methods. This invention also relates to lettuce cultivars or breeding cultivars and plant parts derived from lettuce cultivar Patton, to methods for producing other lettuce cultivars, lines or plant parts derived from lettuce cultivar Patton and to the lettuce plants, varieties, and their parts derived from the use of those methods. The invention further relates to hybrid lettuce seeds, plants, and plant parts produced by crossing cultivar Patton with another lettuce cultivar.