21st Century Guidebook to Fungi, SECOND EDITION, by David Moore, Geoffrey D. Robson and Anthony P. J. Trinci

Table of Contents

1. Chapter 11: Exploiting fungi for food
2. Chapter 12: Development and morphogenesis
   1. Development and morphogenesis
   2. The formal terminology of developmental biology
   3. The observational and experimental basis of fungal developmental biology
   4. Ten ways to make a mushroom
   5. Competence and regional patterning
   6. The Coprinopsis fruit body: making hymenia
   7. Coprinopsis and Volvariella making gills (not forgetting how polypores make tubes)
   8. The Coprinopsis fruit body: making stems
   9. Co-ordination of cell inflation throughout the maturing fruit body
   10. Mushroom mechanics
   11. Metabolic regulation in relation to morphogenesis
   12. Developmental commitment
   13. Comparisons with other tissues and other organisms
   14. Genetic approaches to study development: through the classic to genomic systems analysis
   15. Degeneration, senescence and death
   16. Basic principles of fungal developmental biology
   17. Relevance to commercially cultivated fungi
   18. Chapter 12 References and further reading
   19. Buy a PDF of Chapter 12
3. Chapter 13: Ecosystem mycology: saprotrophs, and mutualisms between plants and fungi

Chapter 12.18 References and further reading

Adamatzky, A., Gandia, A., Ayres, P., Wösten, H. & Tegelaar, M. (2021a). Adaptive Fungal Architectures. In: LINKs-series; Vol. 5-6. pp. 66-77. URL: https://www.researchgate.net/publication/348937077_Adaptive_Fungal_Architectures.

Adamatzky, A., Gandia, A. & Chiolerio, A. (2021b). Towards fungal sensing skin. Fungal Biology and Biotechnology, 8: article number 6. DOI: https://doi.org/10.1186/s40694-021-00113-8.

Agudelo-Valencia, D., Uribe-Echeverry, P.T. & Betancur-Pérez, J.F. (2020). De novo assembly and annotation of the Ganoderma australe genome. Genomics, 112: 930-933. DOI: https://doi.org/10.1016/j.ygeno.2019.06.008.

Ahmed, Y.L., Gerke, J., Park, H.-S., Bayram, Ö., Neumann, P., and six others. (2014). The Velvet family of fungal regulators contains a DNA-binding domain structurally similar to NF-κB. PLoS Biology, 11: article number e1001750. DOI: https://doi.org/10.1371/journal.pbio.1001750.

Ahuactzin-Pérez, M., Tlecuitl-Beristain, S., García-Dávila, J., Santacruz-Juárez, E., González-Pérez, M., Gutiérrez-Ruíz, M.C. & Sánchez, C. (2018). A novel biodegradation pathway of the endocrine-disruptor di(2-ethylhexyl) phthalate by Pleurotus ostreatus based on quantum chemical investigation. Ecotoxicology Enviromental Safety, 147: 494-499. DOI: https://doi.org/10.1016/j.ecoenv.2017.09.004.

Al-Gharawi, A. & Moore, D. (1977). Factors affecting the amount and the activity of the glutamate dehydrogenases of Coprinus cinereus. Biochimica et Biophysica Acta, 496: 95-102. DOI: http://dx.doi.org/10.1016/0304-4165(77)90118-0. CLICK HERE to download the full text.

Allen, J.J., Moore, D. & Elliott, T.J. (1992). Persistent meiotic arrest in basidia of Agaricus bisporus. Mycological Research, 96: 125-127. DOI: https://doi.org/10.1016/S0953-7562(09)80926-X. CLICK HERE to download the full text.

An, H., Lee, H.Y., Shim, D., Choi, S.H., Cho, H., Hyun, T.K., Jo, I.H. & Chung, J.W. (2021). Development of CAPS markers for evaluation of genetic diversity and population structure in the germplasm of Button Mushroom (Agaricus bisporus). Journal of Fungi, 7(5): article number 375. DOI: https://doi.org/10.3390/jof7050375.

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Baars, J.J.P., Scholtmeijer, K., Sonnenberg, A.S.M. & van Peer, A. (2020). Critical factors involved in primordia building in Agaricus bisporus: a review. Molecules, 25: article 2984. DOI: https://doi.org/10.3390/molecules25132984.

Bailey, A.M., Collopy, P.D., Thomas, D.J., Sergeant, M.R., Costa, A.M.S.B., Barker, G.L.A. Mills, P.R., Challen, M.P., Foster, G.D. (2013). Transcriptomic analysis of the interactions between Agaricus bisporus and Lecanicillium fungicola. Fungal Genetics and Biology, 55: 67-76. DOI: https://doi.org/10.1016/j.fgb.2013.04.010.

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Bayram, Ö., Krappmann, S., Ni, M., Bok, J.W., Helmstaedt, K., and six others. (2008). VelB/VeA/LaeA complex coordinates light signal with fungal development and secondary metabolism. Science, 320: 1504-1506. DOI: https://doi.org/10.1126/science.1155888.

Berne, S., Pohleven, J., Vidic, I., Rebolj, K., Pohleven, F., Turk, T., Macek, P., Sonnenberg, A. & Sepčić, K. (2007). Ostreolysin enhances fruiting initiation in the oyster mushroom (Pleurotus ostreatus). Mycological Research, 111: 1431-1436. DOI: https://doi.org/10.1016/j.mycres.2007.09.005.

Bleuler-Martínez, S., Butschi, A., Garbani, M., Wälti, M.A., Wohlschlager, T., and seven others (2011). A lectin-mediated resistance of higher fungi against predators and parasites. Molecular Ecology, 20: 3056-3070. DOI: https://doi.org/10.1111/j.1365-294X.2011.05093.x.

Bobola, N. & Merabet, S. (2017). Homeodomain proteins in action: similar DNA binding preferences, highly variable connectivity. Current Opinion in Genetics & Development, 43: 1-8. DOI: https://doi.org/10.1016/j.gde.2016.09.008.

Borgognone, A., Castanera, R., Morselli, M., Lopez-Varas, L., Rubbi, L., Pisabarro, A.G., Pellegrini, M. & Ramirez, L. (2018). Transposon associated epigenetic silencing during Pleurotus ostreatus life cycle. DNA Research, 25: 451-464. DOI: https://doi.org/10.1093/dnares/dsy016.

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Updated August, 2021