Terpenoid backbone biosynthesis pathway identified in Hericium erinaceus and differentially expressed proteins in the fruiting body vs. mycelium.

Terpenoid backbone biosynthesis pathway identified in Hericium erinaceus and differentially expressed proteins in the fruiting body vs. mycelium.

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Background: Hericium erinaceus, a famous edible mushroom, is also a well-known traditional medicinal fungus. To date, a large number of bioactive metabolites with antitumor, antibacterial, and immune-boosting effects were isolated from the free-living mycelium and fruiting body of H. erinaceus. Objective: Here we used the proteomic approach to e...

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... on H. erinaceus genome, we found there were 12 genes involved in terpenoid backbone biosynthesis in KEGG pathway. Similarly, 8 proteins were responsible for terpenoid backbone synthesis, including 4 DEPs between mycelium and fruiting body proteome. As shown in in Fig. 5 and Table 1, acetyl-CoA acetyltransferase B (Her1A4929) and diphosphomevalonate decarboxylase (Her1A3732) from the mevalonate (MEP) pathway were significantly up-regulated in fruiting body compared with mycelium. In contrast, farnesyl pyrophosphate synthase (HerlA4642) and dehydrodolichyl diphosphate synthase (Her1A2677) from the lower ...

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... Lowering the temperature and providing exposure to light have proven to be effective factors in inducing fruiting bodies in the species H. americanum, H. erinaceus, and H. coralloides (Gonkhom et al., 2022;Grace & Mudge, 2015;Sokół et al., 2015). Comparative data in biochemical analyses of mycelia and fruiting bodies is lacking, and this is particularly crucial given the different expression of genes associated with proteins involved in the synthesis of secondary metabolites between mycelium and fruiting bodies (Zeng et al., 2018). ...
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This book spotlights macrofungi with health-promising properties, which mainly belong to Basidiomycota (Agaricomycotina) and Ascomycota (Pezizomycotina). Macrofungi or higher fungi are ascomycetous and basidiomycetous mushrooms forming conspicuous, epigeous, or hypogeous sporocarps and are large enough to be seen by the naked eye. The consumption of wild macrofungi by man goes back 13,000 years. Macrofungi vary in structure and reproduction and occur in a wide range of habitats in different ecogeographic zones of the world. Ethnomycological surveys across the globe reveal the food value and therapeutic significance of wild species in diet and folk medicine. Scientific research proves the nutritional and pharmacological properties of these macrofungi. The latter are consecrated with a wealth of nutrients such as carbohydrates, proteins, fats, fatty acids, amino acids, minerals, and vitamins contributing to their food value. The sporocarps/cultured mycelia or cultured broths of these fungi are rich in numerous high and low molecular weight bioactive constituents. These bioactive components include polysaccharides, proteins, fatty acids, proteoglycans, terpenoids, and phenolics, accounting for a broad spectrum of pharmacological activities such as antioxidant, antitumor, antidiabetic, antibacterial, antifungal, immunomodulatory, antimalarial, and antiviral. Several health-promoting products of macrofungal origin are available in market in the form of tablets, capsules, syrups, pastes, and powders. In spite of huge benefits of macrofungi, these are often overlooked as far as conservation efforts are concerned. Many macrofungal species are red listed by IUCN and need immediate attention to conserve and ensure sustainable use of this inexpensive natural treasure with huge health benefits. In this book, we endeavored to highlight the future prospects of macrofungi and tried to shed light on the taxonomy, ecology, ethnomycology, nutraceutical composition, bioactive active and pharmacological activities, commercialization, and conservation. Some information on cultivation and toxigenic macrofungi is also provided.
... Advances in omics technologies such as transcriptomics and proteomics have clearly facilitated the comprehensive analysis of gene and protein expression levels under multiple experimental conditions. For example, gene and protein expression profiling have provided a viewpoint into the genes and proteins involved in nutrition transport in Morchella importuna [16], bioactive metabolites in Hericium erinaceus [17], temperature stress in Lentinula edodes [18], Cd 2+ stress in Pleurotus eryngii [19], special odor formation in Schizophyllum commune [20] and fruiting body development in Flammulina velutipes and Dictyophora indusiata [21][22]. ...
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... Chen et al. (2017) sequenced the genome in the monokaryotic mycelium, dikaryotic mycelium and fruiting body of H. erinaceus to investigate the biosynthesis of bioactive secondary metabolites from H. erinaceus. Zeng et al. (2018) identified numerous proteins involved in terpenoid, polyketide and sterol biosynthesis by proteome analysis of H. erinaceus. These two studies successfully provided a theoretical basis for elucidating the synthesis of active components. ...
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Background: Hericium erinaceus, also known as lion's mane mushroom, is a widely distributed edible and medicinal fungus in Asian countries. H. erinaceus harbors diverse bioactive metabolites with anticancer, immunomodulating, anti-inflammatory, antimicrobial, antihypertensive, antidiabetic and neuroprotective properties. Although the chemical synthesis processes of these bioactive metabolites are known, the biosynthetic processes remain unknown. Results: In this study, we obtained the transcriptomes of six H. erinaceus strains using next-generation RNA sequencing and investigated the characteristics of the transcriptomes and biosynthesis of bioactive compounds, especially polysaccharides. The transcriptomes ranged in size from 46.58 to 58.14 Mb, with the number of unigenes ranging from 20,902 to 37,259 across the six H. erinaceus strains. Approximately 60% of the unigenes were successfully annotated by comparing sequences against different databases, including the nonredundant (NR), Gene Ontology (GO), Kyoto Encyclopedia of Genes and Genomes (KEGG), clusters of orthologous groups for eukaryotic complete genomes (KOG) and Swiss-Prot databases. Most of the transcripts were putatively involved in signal transduction, carbohydrate metabolism, translation, transport and catabolism, and amino acid metabolism. Genes involved in polysaccharide biosynthesis were identified, and these genes encoded phosphoglucomutase (PGM), glucose phosphate isomerase (PGI), UDP-glucose pyrophosphorylase (UGP), glycoside hydrolase family proteins, glycosyltransferase family proteins and other proteins. Moreover, the putative pathway for the intracellular polysaccharide biosynthesis of H. erinaceus was analyzed. Additionally, the open reading frames (ORFs) and simple sequence repeats (SSRs) were predicted from the transcriptome data of the six strains. Conclusions: Overall, the present study may facilitate the discovery of polysaccharide biosynthesis processes in H. erinaceus and provide useful information for exploring the secondary metabolites in other members of the Basidiomycetes genus.