Chlorosis-inducing products from Pseudomonas syringae pathovars: new N-coronafacoyl compounds
Author:
Publisher
Elsevier BV
Subject
Horticulture,Plant Science,Molecular Biology,General Medicine,Biochemistry
Reference13 articles.
1. The structure of coronatine
2. Production of different pathogenic symptoms and different toxins by strains of Pseudomonas syringae pv. tomato not distinguishable by gel -immunodiffusion assay
3. Norcoronatine and N-coronafacoyl-L-valine, phytotoxic analogues of coronatine produced by a strain of Pseudomonas syringae pv. glycinea
4. N-Coronafacoyl-L-isoleucine and N-coronafacoyl-L-alloisoleucine, potential biosynthetic intermediates of the phytotoxin coronatine
5. The structure-activity relationships in coronatine analogs and amino compounds derived from (+)-coronafacic acid.
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1. Discovery, characterization and engineering of ligases for amide synthesis;Nature;2021-05-19
2. Scalable total synthesis and comprehensive structure–activity relationship studies of the phytotoxin coronatine;Nature Communications;2018-03-16
3. Characterization of the Coronatine-Like Phytotoxins Produced by the Common Scab Pathogen Streptomyces scabies;Molecular Plant-Microbe Interactions®;2015-04
4. ChemInform Abstract: Chlorosis-Inducing Products from Pseudomonas Syringae Pathovars: New N-Coronafacoyl Compounds.;ChemInform;2010-06-16
5. Simple and Rapid Capillary Zone Electrophoresis Method for the Detection of Coronamic Acid, a Precursor to the Pseudomonas syringae Phytotoxin Coronatine;Journal of Agricultural and Food Chemistry;2009-11-03
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