Pseudomonas syringae pv syringae hrpZ gene

Chemistry: natural resins or derivatives; peptides or proteins; – Proteins – i.e. – more than 100 amino acid residues

Patent

Rate now

  [ 0.00 ] – not rated yet Voters 0   Comments 0

Details

536 237, 435874, C07K 1421, C12N 1531

Patent

active

057081395

ABSTRACT:
The nucleic acid and amino acid sequences for proteinaceous elicitors of the plant defense reaction known as the hypersensitive response against Pseudomonas syringae are described along with method for preparation.

REFERENCES:
patent: 4569841 (1986-02-01), Liu
patent: 4597972 (1986-07-01), Taylor
patent: 4601842 (1986-07-01), Caple et al.
patent: 4740593 (1988-04-01), Gonzalez et al.
patent: 4851223 (1989-07-01), Sampson
patent: 5061490 (1991-10-01), Paau et al.
patent: 5135910 (1992-08-01), Blackburn et al.
patent: 5173403 (1992-12-01), Tang
patent: 5217950 (1993-06-01), Blackburn et al.
patent: 5243038 (1993-09-01), Ferrari et al.
patent: 5244658 (1993-09-01), Parke
patent: 5260271 (1993-11-01), Blackburn et al.
Stryer, "Enzymes are Highly Specific," Biochemoistry, San Francisco: W.H. Freeman and Company, p. 116 (1975).
Keen et al., "Inhibition of the Hypersensitive Reaction of Soybean Leaves to Incompatible Pseudomonas spp. by Blasticidin S, or Elevated Temperature," Physiological Plant Pathology, 18:325-337 (1981).
Lerner "Tapping the Immunological Repertoire to Produce Antibodies of Predetermined Specificity," Nature, 299:592-596 (1982).
Staskawicz et al., "Cloned Avirulence Gene of Pseudomonas syringae pv. glycinea Determines Race-specific Incompatibility on Glycine max (L.) Merr., " Proc. Natl. Acad. Sci., 81:6024-6028 (1984).
Atkinson et al., "The Hypersensitive Reaction of Tobacco to Pseudomonas syringae pv. pisi .sup.1," Plant Physiol., 79:843-847 (1985).
Huynh et al., "Bacterial Blight of Soybean: Regulation of a Pathogen Gene Determining Host Cultivar Specificity," Science, 245:1374-1377 (1986).
Lindgren et al., "Gene Cluster of Pseudomonas syringae pv. Phaseolicola J. Bacteriology, Controls Pathogenicity of Bean Plants and Hypersensitivity on Nonhost Plant," 168(2):512-522 (1986).
Bauer et al., "Cloning of a Gene from Erwinia amylovora Involved in Induction of Hypersensitivity and Pathogenicity," Plant Pathogenic Bacteria, 425-429 (1987).
Collinge et al., "Plant Gene Expression in Response to Pathogens," Plant Molecular Biology, 9:389-410 (1987).
Shatzman et al., "Expression, Identification, and Characterization of Recombinant Gene Products in Escherichia coli," Methods in Enzymology, 152:661-673 (1987).
Shields, "towards Insect-Resistant Plants," Nature, 328:12-13 (1987).
Huang et al., "Molecular Cloning of a Pseudomonas syringae pv. syringae Gene Cluster That Enables Pseudomonas fluorescens To Elicit the Hypersensitive Response in Tobacco Plants," Journal of Bacteriology, 170(10):4748-4756 (1988).
Schottens-Toma et al., "Purification and Primary Structure of a Necrosis-inducing Peptide from the Apoplastic Fluids of Tomato Infected with Cladosporium fulvum (syn. Fulvia fulva)," Physiological and Molecular Plant pathology, 33:59-67 (1988).
Steinberger et al., "Creation and Complementation of Pathogenicity Mutants of Erwinia amylovora," Molecular Plant-Microbe Interactions, 1(3):135-144 (1988).
Beer et al., "The Hypersensitive Response is Elicited by Escherichia coli containing a cluster of Pathogenicity Genes from Erwinia amylovora," Phytophathology, 79(10):1156 (Abstract 169) (1989).
Hiatt et al., "Production of Antibodies in Transgenic Plants," Nature, 342:76-78 (1989).
Hippe et al., "In Situ Localization of a Foreign Protein in Transgenic Plants by Immunoelectron Microscopy Following High Pressure Freeze Substitution and Low Temperature Embedding," European Journal of Cell Biology, 50:230-234 (1989).
Huang et al., "Isolation and Purification of a Factor from Pseudomonas solanacearum That Induces a Hypersensitive-like Response in Potato Cells," Molecular Plant-Microbe Interactions, 2(3):132-138 (1989).
James et al., "Genetic Transformation of Apple (Malus pumila Mill.) Using a Disarmed Ti-binary Vector," Plant Cell Reports, 7:658-661 (1989).
Laby et al., "Cloning and Preliminary Characterization of an HRP Gene Cluster of Erwinia amylovora," Phytopathology, 79(10):1211 (Abstract 607) (1989).
Dow et al., "Extracellular Proteases from Xanthomonas campestris pv. Campestris, the Black Rot Pathogen," Applied and Environmental Microbiology, 56(10):2994-2998 (1990).
Walters et al., "Gene for Pathogenicity and Ability to Cause the Hypersensitive Reaction Cloned from Erwinia amylovora," Physiological and Molecular Plant Pathology, 36:509-521 (1990).
Wu et al., "Cloning, Genetic Organization, and Characteriation of a Structural Gene Encoding Bacillopeptidase F from Bacillus subtilis," The Journal of Biological Chemistry, 265(12):6845-6850 (1990).
Bauer et al., "Further Characterization of an hrp Gene Cluster of Erwinia amylovora," Molecular Plant Microbe Interactions,4(5):493-499 (1991).
Beer et al., "The HRP Gene Cluster of Erwinia amylovora," Advances in Molecular Genetics of Plant-Microbe Interactions, 1:53-60 (1991).
Benvenuto et al., "`Phytoantibodies`: A General Vector for the Expression of Immunoglobulin Domains in Transgenic Plants," Plant Molecular Biology, 17:865-874 (1991).
Milat et al., "Physiological and Structural Changes in Tobacco Leaves Treated with Cryptogein, a Proteinaceous Elicitor from Phytophthora cryptogea," Phytopathology, 81(11):1364-1368 (1991).
Ruberti et al., "A Novel Class of Plant Proteins Containing a Homeodomain with a Closely Linked Leucine Zipper Motif," The EMBO Journal, 10(7):1787-1791 (1991).
Quigley et al., "Nucleotide Sequence and Expression of a Novel Glycine-Rich Protein Gene from Arabidopsis thaliana," Plant Molecular Biology, 17:949-952 (1991).
van Kan et al., "Cloning and Characterization of cDNA of Avirulence Gene avr9 of the Fungal Pathogen Cladosporium fulvum, Causal Agent of Tomato Leaf Mold," Molecular Plant-Microbe Interactions, 4(1):52-59 (1991).
Waldmann, "Monoclonal Antibodies in Diagnosis and Therapy," Science, 252:1657-1662 (1991).
Willis et al., "hrp Genes of Phytopathogenic Bacteria," Molecular Plant-Microbe Interactions, 4:(2) 132-138 (1991).
Beer et al., "Are Harpins Universal Elicitors of the Hypersensitive Response of Phytopathogenic Bacteria?," Advances in Molecular Genetics of Plant-Microbe Interactions, 2:281-286 (1992).
Laby et al., Molecular Plant-Microbe Interactions, 5(5):412 (1992).
Sandhu, Crit. Rev. in Biotech., (92-review) 12:437-462.
Wei et al. "Harpin, Elicitor of the Hypersensitive Response Produced by the Plant Pathogen Erwinia amylovora," Science, 257:85-88 (1992).
He et al., "Pseudomonas syringae pv. syringae Harpin.sub.P86 : A Protein that is Secreted Via the Hrp Pathway and Elicits the Hypersensitive Response in Plants," Cell, 73:1255-1266 (1993).
H. Huang et al. "Molecular Cloning of a Pseudomonas syringae pv. syringae Gene Cluster That Enables Pseudomonas fluorescens to Elicit the Hypersensitive Response in Tobacco Plants", J. Bacteriology 170(10) 4748-4756 (Oct. 1988).
Z. Wei et al., "Harpin, Elicitor of the Hypersensitive Response Produced by the Plant Pathogen Erwinia amylovora", Science 257: 85-88 (Jul. 1992).
S. Beer et al., "Are Harpins Universal Elicitors of the Hypersensitive Response of Phytopathogenic Bacteria" in Advances in Molecular Genetics of Plant-Microbe Interactions, Nester et al. (eds.) Kluwer Academic Publishers, Dordrecht, Netherlands pp. 281-286 (1993).

LandOfFree

Say what you really think

Search LandOfFree.com for the USA inventors and patents. Rate them and share your experience with other people.

Rating

Pseudomonas syringae pv syringae hrpZ gene does not yet have a rating. At this time, there are no reviews or comments for this patent.

If you have personal experience with Pseudomonas syringae pv syringae hrpZ gene, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Pseudomonas syringae pv syringae hrpZ gene will most certainly appreciate the feedback.

Rate now

     

Profile ID: LFUS-PAI-O-327603

  Search
All data on this website is collected from public sources. Our data reflects the most accurate information available at the time of publication.