Abstract

Plant pathogenic fungi produce a wide variety of secondary metabolites with unique and complex structures. However, most fungal secondary metabolism genes are poorly expressed under laboratory conditions. Moreover, the relationship between pathogenicity and secondary metabolites remains unclear. To activate silent gene clusters in fungi, successful approaches such as epigenetic control, promoter exchange, and heterologous expression have been reported. Pyricularia oryzae, a well-characterized plant pathogenic fungus, is the causal pathogen of rice blast disease. P. oryzae is also rich in secondary metabolism genes. However, biosynthetic genes for only four groups of secondary metabolites have been well characterized in this fungus. Biosynthetic genes for two of the four groups of secondary metabolites have been identified by activating secondary metabolism. This review focuses on the biosynthesis and roles of the four groups of secondary metabolites produced by P. oryzae. These secondary metabolites include melanin, a polyketide compound required for rice infection; pyriculols, phytotoxic polyketide compounds; nectriapyrones, antibacterial polyketide compounds produced mainly by symbiotic fungi including endophytes and plant pathogens; and tenuazonic acid, a well-known mycotoxin produced by various plant pathogenic fungi and biosynthesized by a unique NRPS-PKS enzyme.

Highlights

  • Filamentous fungi, including plant pathogenic fungi, produce a wide variety of secondary metabolites with unique and complex structures

  • Whole-genome sequencing analyses have revealed that filamentous fungi possess many more secondary metabolism genes than expected, suggesting that most secondary metabolite biosynthetic genes are silent under laboratory conditions

  • P. oryzae is rich in secondary metabolism genes, and some of the secondary metabolites are expected to be involved in rice infection

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Summary

Introduction

Filamentous fungi, including plant pathogenic fungi, produce a wide variety of secondary metabolites with unique and complex structures. P. oryzae produces the black pigment melanin (Figure 1), which is essential for rice infection [8]. The rice secondary plants is achieved by an that is formed at mechanism the base of Melanin is not a invasion toxin, butofthis metabolite is infection essential peg for infection by the an appressorium, which adheres tightly to the host surface. P. oryzae forms an infection-specific organ, appressorium, and infects rice plants through infection peg, mechanical force exerted by appressoria is necessary. Turgor forces semipermeable membrane that passes water but not glycerol and as a structural support for this very are focused toward the epidermal surfaces of the rice plant, and the pressure inside the appressoria has high beenpressure. 1,8-DHN by using three enzymes: reductase (4HNR), Colletotrichum lagenarium, it has been shown that melanin is a hexaketide compound and the backbone scytalone dehydratase (SDH1/RSY1), 1,3,8-trihydroxynaphthalene (1,3,8-THN).

Pyriculols
Nectriapyrones
Tenuazonic Acid
Other Secondary Metabolites
Conclusions
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