Purification of an isoform of patatin with antimicrobial activity against Phytophthora infestans

• Published in: Plant physiology and biochemistry 2004-07, Vol.42 (7), p.647-655
• Main Authors: Sharma, Neelam, Gruszewski, Hope A., Park, Sang-Wook, Holm, David G., Vivanco, Jorge M.
• Format: Article
• Language: English
• Subjects: Anti-Infective Agents - isolation & purification; Anti-Infective Agents - pharmacology; Antifungal protein; Biological and medical sciences; Carboxylic Ester Hydrolases - isolation & purification; Carboxylic Ester Hydrolases - pharmacology; Enzymes; Fundamental and applied biological sciences. Psychology; Late blight; Metabolism; Microbial Sensitivity Tests; Patatin; Phytophthora - drug effects; Phytophthora infestans; Plant Diseases; Plant physiology and development; Plant Proteins - isolation & purification; Plant Proteins - pharmacology; Potato; Solanum tuberosum
• ISSN: 0981-9428; 1873-2690
• DOI: 10.1016/j.plaphy.2004.05.010

Phytophthora infestans (Mont.) de Bary is infamous as the causal agent of the late blight epidemic contributing to the Irish potato famine of the mid 19th century and remains agriculture’s most destructive disease as new mutations and migrations confound control measures. In efforts to develop resistant varieties, a somatic hybrid (the Wisconsin J series) between potato ( Solanum tuberosum) and a wild relative ( Solanum bulbocastanum) has been found to convey durable resistance against the pathogen. We screened the total protein (100 μg ml –1) of somatic hybrid varieties J138, J138A12, J101K12, J103K12, and J101K9 for in vitro spore germination inhibition of P. infestans. Since J138 exhibited maximum inhibition at 150 μg ml –1 in comparison to other varieties, we purified a 40 kD protein from J138 tubers by assaying its ability to inhibit spore germination in P. infestans spores. The highly purified protein was able to inhibit P. infestans spore germination by 70% at the 2.5 μg ml –1 concentration. The N-terminal sequence of this protein was found to have exact amino acid homology to patatin, the major storage protein of potato tubers. The inhibitory protein has the same molecular weight as patatin and cross-reacts with patatin antibodies. The infection of J138 plants with spores of P. infestans under greenhouse conditions showed that patatin is expressed in stem tissue 72 h after the plant is inoculated with field isolates of P. infestans (US8). In this communication, we report the purification, characterization and antifungal activity against spores of P. infestans of patatin-J from potato tubers.