Didymella exigua
Didymella exigua (Niessl) Sacc., Michelia 2: 57 (1880).
≡ Didymosphaeria exigua Niessl, Oesterr. Bot. Z. 25: 165 (1875).
Index Fungorum number: IF 218525; Facesoffungi number: FoF 11503, Fig.1
Description: see Chen et al. (2015).
Material considered: see Chen et al. (2015).
Fig. 1 Didymella macrostoma (MFLU 15-1319, holotype). a Ascomata on host surface. b Section through ascoma. c Peridium. d, e Asci with ascospores. f, g Ascospores. h Conidiomata in culture. i Section through conidioma. j–l Conidiogenous cells. m Conidia. Scale bars: b, i = 100 μm, c = 20 μm, d, e = 30 μm, f, g, j–m = 10 µm.
Importance and distribution
There are 417 epithets in Index Fungorum (2022), but many species have been transferred to other genera such as Apiosporella, Arthopyrenia, Cercidospora, Constrictolumina, Didymellopsis, Didymolepta, Discostroma, Fenestella, Frigidopyrenia, Gnomoniopsis, Isothea, Keissleriella, Leptorhaphis, Leptosphaeria, Lichenochora, Longipedicellata, Lophiostoma, Monascostroma, Mycoporum, Mycosphaerella, Naetrocymbe, Neoascochyta, Neodidymelliopsis, Oxydothis, Paraboeremia, Phoma, Phomatospora, Prolisea, Pseudomassaria, Pseudosagedia, Seimatosporium, Septoria, Sphaerellothecium, Stagonosporopsis, Xenodidymella and Zwackhiomyces. Members of Didymella are ubiquitous and can be saprobes, pathogens and endophytes on a wide range of plants (Aveskamp et al. 2010; Chen et al. 2015, 2017; Jayasiri et al. 2017). Important diseases caused by Didymella include gummy stem blight of watermelon (Citrullus lanatus) caused by D. bryoniae (Sudisha et al. 2004; Basim et al. 2016), canker of tomato by D. lycopersici (Besri 1982), and tea leaf spot in China by D. bellidis (Wang et al. 2020). Didymella has worldwide distribution.
Industrial relevance and applications
Didymella is beneficial to medical and pharmaceutical industry as it produces nonenolide which has antimalarial activity (Cimmino et al. 2012)
Biochemical importance of the genus, chemical diversity or applications
Didymella produces wide range of chemicals such as Didymellanosine, a decahydrofluorene analogue, and ascolactone C from Didymella sp. IEA-3B.1, an endophyte of Terminalia catappa (Ariantari et al. 2020) and Pinolide, a Nonenolide produced by Didymella pinodes. Luo et al. (2020) reported several chemicals such as didymelol B-D, naphthalenone, didymelol A, naphthols, naphthalenones namely (3S,4R)-3,4,6-trihydroxy-3,4-dihydronaphthalen-1(2H)-one, (4S)-4,6-dihydroxy-3,4-dihydronaphthalen-1(2H)-one, (4S)-4-hydroxy-3,4-dihydronaphthalen-1(2H)-one, from Didymella glomerata.
References
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