Delitschia didyma
Delitschia didyma Auersw., Hedwigia 5: 49 (1866).
Index Fungorum number: IF 177056; Facesoffungi number: FoF 08204, Fig. 1
Description: see Hyde et al. (2013).
Material considered: see Hyde et al. (2013).
Fig. 1 Delitschia didyma (MFLU 12–2217). a, b Appearance of ascomata on host substrate. c Section of ascoma. d Peridium. e Pseudoparaphyses. f, g Asci with ascospores. h, i Ascospores Scale bars: a = 1 mm, b = 500 μm, c = 100 μm, d–g = 50 μm, h, i = 20 μm.
Importance and distribution
There are 79 Delitschia epithets in Index Fungorum (2022), but several species have been transferred to other genera such as Arnium, Cainia, Cercophora, Herpotrichia, Trichodelitschia and Zygospermella. Delitschia comprises 68 species known on several host plants such as Eucalyptus viminalis (Myrtaceae), dung of Alces alces (Cervidae), seawater on Fagus sylvatica (Fagaceae), dung of Capra aegagrus hircus (Bovidae), dung of Equus asinus (Equidae), dung of Ovis aries (Bovidae), Salix sp. (Salicaceae), amongst others. Delitschia is known from Europe (Belgium, United Kingdom, Netherlands), North America (Canada, Mexico), South America (Argentina) and The United States (North Dakota).
Industrial relevance and applications
Delitschia is useful for industry as it produces several compounds such as Benzophenone which is used as a fragrance enhancer and perfume fixative in cosmetics industry (Jayanetti et al. 2017).
Biochemical importance of the genus, chemical diversity or applications
Delitschia produces a wide range of chemicals. Rivera-Chávez et al. (2019) reported Delitpyrones an α-Pyrone Derivatives from a Freshwater Delitschia sp. Jayanetti et al. (2017) reported Benzophenone and Fimetarone derivatives from Delitschia. Delitschia can produce new metabolites such as 6-ethyl-7-hydroxyl-2-methoxyjuglone, sporidesmin A, Delicoferone A, (3S*,4S*,5S*,6R*)-4,5,6-trihydroxy-3-methyl-3,4,6,7-tetrahydro-1H-isochromen-8 (5H)-one, (3R*,4S*)-7-ethyl-3,4,6,8-tetrahydroxy-3,4-dihydronaphthalen-1 (2H)-one, 6-ethyl-2,7-dimethoxyjuglone and 6-(1-hydroxyethyl)-2,7-dimethoxyjuglone (Sun et al. 2011), Delitschiapyrone A (Kurasawa et al. 2018), Azaphilones (Pavesia et al. 2021) amongst others. Singh and Tomassini (2001) isolated Flutimide, a fully substituted 1-hydroxy-3H-pyrazine-2,6-dione, is a fungal metabolite isolated from Delitschia cofertaspora. Cao and Clardy (2012) reported two naphthoquinones, delitzchianones A and B from Delitzchia winteri, an endophytic fungus from Central America (Costa Rica).
References
Romero AI, Samuels GJ. 1991 – Studies on xylophilous fungi from Argentina. VI. Ascomycotina on Eucalyptus viminalis (Myrtaceae). Sydowia 43, 228–248.
Sun R, Gao YX, Shen KZ, Xu YB, Wang CR, Liu HY, Dong JY. 2011 – Antimicrobial metabolites from the aquatic fungus Delitschia corticola. Phytochemistry Letters 4, 101–105.
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