Dihydroxyhexanoic acid biosynthesis controls turgor in pathogenic fungi
Naoyoshi Kumakura1, Takayuki Motoyama1, Keisuke Miyazawa2,3
1RIKEN Center for Sustainable Resource Science, Yokohama, Kanagawa, Japan.
Abstract:
Many plant pathogenic fungi penetrate host surfaces mechanically, using turgor pressure generated by specialized infection cells called appressoria. These appressoria develop semipermeable cell walls and accumulate osmolytes internally to create turgor by osmosis. Although melanin is known to be important for turgor generation, the mechanism underlying wall semipermeability remains unclear. By using reverse genetics, we identified that the enzymes PKS2 and PBG13 are required for forming the semipermeable barrier in fungi causing anthracnose and rice blast diseases. These enzymes synthesize 3,5-dihydroxyhexanoic acid polymers that are essential for pathogenicity. These polymers reduce cell wall permeability and generate turgor, independently of melanization. Our findings uncover a mechanism of fungal turgor generation, linking enzyme function to pathogen penetration and disease potential, presenting new targets for disease control.
Insights
Plant pathogenic fungi use specialized cells to penetrate hosts. New research identifies enzymes PKS2 and PBG13 essential for forming a semipermeable barrier, crucial for fungal pathogenicity and disease control.
Area of Science:
- Plant Pathology
- Mycology
- Biochemistry
Background:
- Plant pathogenic fungi utilize appressoria to mechanically penetrate host surfaces.
- Appressoria generate turgor pressure via internal osmolyte accumulation and semipermeable cell walls.
- The precise mechanism of appressorial wall semipermeability, independent of melanin, is not fully understood.
Purpose of the Study:
- To elucidate the molecular mechanism behind the semipermeable barrier formation in fungal appressoria.
- To identify key enzymes and pathways involved in generating turgor pressure for host penetration.
- To explore novel targets for controlling plant diseases caused by fungal pathogens.
Main Methods:
- Employed reverse genetics to investigate gene functions in fungal pathogens.
- Focused on the enzymes PKS2 and PBG13, known to be involved in fungal development.
- Analyzed the role of synthesized polymers in cell wall permeability and turgor generation.
Main Results:
- Identified PKS2 and PBG13 as essential enzymes for forming the semipermeable barrier in appressoria.
- These enzymes synthesize 3,5-dihydroxyhexanoic acid polymers, critical for pathogenicity.
- The synthesized polymers reduce cell wall permeability and generate turgor pressure independently of melanization.
Conclusions:
- Uncovered a novel mechanism of fungal turgor generation mediated by specific enzymes and polymer synthesis.
- Demonstrated the essential role of 3,5-dihydroxyhexanoic acid polymers in fungal pathogenicity.
- These findings provide new targets for developing strategies to control anthracnose and rice blast diseases.
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