In vitro growth of nine edible ectomycorrhizal fungi under a range of pH conditions

Authors

  • Jaime Olaizola Laboratorio de Entomología y Patología Forestal. Departamento de Producción Vegetal y Recursos Forestales. Universidad de Valladolid. Palencia, Spain. https://orcid.org/0000-0003-0561-9526
  • Oscar Santamaría Laboratorio de Entomología y Patología Forestal. Departamento de Producción Vegetal y Recursos Forestales. Universidad de Valladolid. Palencia, Spain. https://orcid.org/0000-0001-5087-6519
  • Julio J. Diez Laboratorio de Entomología y Patología Forestal. Departamento de Producción Vegetal y Recursos Forestales. Universidad de Valladolid. Palencia, Spain. https://orcid.org/0000-0003-0558-8141

DOI:

https://doi.org/10.51372/bioagro352.8

Keywords:

Forest ecosystems, forest seedlings, fungus biomass, incubation, nurseries

Abstract

Ectomycorrhizal fungi are considered to play an essential role in the development of forest ecosystems and can protect plant against pathogenic infections. Among other factors, soil pH may affect the successful inoculation of forest seedlings in nurseries. The effect of pH on the growth rate of strains of nine species of edible ectomycorrhizal (ECM) fungi was evaluated in vitro. In the experiments, Boletus edulis, B. aereus, B. pinophilus, B. fragrans, Amanita rubescens, Xerocomus ferrugineus, Lactarius deliciosus, Lactarius sanguifluus and Suillus luteus were grown in Petri dishes containing modified Melin Norkrans medium and adjusted at seven different pH levels. Colony area was measured at 7-day intervals for 8 weeks. Final fungal biomass and residual pH of the medium at 8th week were also measured. The optimum pH levels and pH tolerance ranges for the tested ECM fungal species are presented and discussed in the text. The results showed that the greatest growth in vitro was produced by A. rubescens and S. luteus at high pH levels (between 6.5-8.5), and by X. ferrugineus  at low pH (3.5-6.5). Almost all the strains acidified the medium where they were grown after eight incubation weeks.

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References

Barros, L., P. Baptista and I. Ferreira. 2006. Influence of the culture medium and pH on the growth of saprobic and ectomycorrhizal mushroom mycelia. Minerva Biotec. 18: 165-70.

Boeraeve, M., O. Honnay and H. Jacquemyn. 2018. Effects of host species, environmental filtering and forest age on community assembly of ectomycorrhizal fungi in fragmented forests. Fungal Ecology 36: 89-98.

Burke, D.J., S.R. Carrino‐Kyker, C.F. Chervenak, A.J. Hoke and C.R. Hewins. 2021. The function of root mat fungal communities: Changes in response to pH and phosphorus addition. Plants, People, Planet 3(5): 653-666.

Carrino-Kyker, S.R., L.A. Kluber, A.M. Petersen, K.P. Coyle, C.R. Hewins, J.L. DeForest et al. 2016. Mycorrhizal fungal communities respond to experimental elevation of soil pH and P availability in temperate hardwood forests. FEMS Microbiology Ecology 92(3): fiw024.

Daza, A., J.L. Manjón, L. Camacho, L. Romero de la Osa, A. Aguilar and C. Santamaría. 2006. Effect of carbon and nitrogen, pH and temperature on in vitro culture of several isolates of Amanita caesarea (Scop.: Fr.) Pers. Mycorrhiza 16: 133-136.

Díaz-Balteiro, L, A. Álvarez and J.A. Oria de Rueda. 2003. Integración de la producción fúngica en la gestión forestal. Aplicación al monte Urcido (Zamora). Investigación Agraria. Sistemas y recursos forestales 12(1): 5-20.

Domínguez-Núñez, J.A. and A.S. Albanesi. 2019. Ectomycorrhizal fungi as biofertilizers in forestry. Biostimulants in Plant Science. In: S.M. Mirmajlessi and R. Radhakrishnan (eds.). Biostimulants in Plant Science. Chapter 8.

Ge, Z.W., T. Brenneman, G. Bonito and M.E. Smith. 2017. Soil pH and mineral nutrients strongly influence truffles and other ectomycorrhizal fungi associated with commercial pecans (Carya illinoinensis). Plant and soil 418(1): 493-505.

Glassman, S.I., I.J. Wang and T.D. Bruns. 2017. Environmental filtering by pH and soil nutrients drives community assembly in fungi at fine spatial scales. Molecular ecology 26(24): 6960-6973.

Kebert, M., S. Kostić, M. Zlatković, S. Stojnic, E. Čapelja, M. Zorić et al. 2022. Ectomycorrhizal fungi modulate biochemical response against powdery mildew disease in Quercus robur L. Forests 13(9): 1491.

Khan, M.W., M.A. Ali, N.A. Khan, M.A. Khan, A. Rehman and N.J. Javed. 2013. Effect of different levels of lime and pH on mycelial growth and production efficiency of oyster mushroom (Pleurotus spp.). Pak. J. Bot. 45(1): 297-302.

Liu, Y., X. Li and Y. Kou. 2020. Ectomycorrhizal fungi: Participation in nutrient turnover and community assembly pattern in forest ecosystems. Forests 11(4): 453. 16 p.

Matsuoka, S., A.S. Mori, E. Kawaguchi, S. Hobara and T. Osono. 2016. Disentangling the relative importance of host tree community, abiotic environment and spatial factors on ectomycorrhizal fungal assemblages along an elevation gradient. FEMS Microbiology Ecology 92(5): fiw044.

Milton, M., D. Bisarya, V. Kumar, S. Kumar and A.K. Singh. 2021. Mycorrhizae and their importance in agriculture. JETIR 8(9): 201-206.

Mohan, V., R. Nivea and S. Menon. 2015. Evaluation of ectomycorrhizal fungi as potential bio-control agents against selected plant

pathogenic fungi. JAIR 3(9): 408-412.

Rigamonte, T.A., V.S. Pylro and G.F. Duarte. 2010. The role of mycorrhization helper bacteria in the establishment and action of ectomycorrhizae associations. Braz. J. Microbiol. 41(4): 832-40.

Sánchez F, M. Honrubia and P. Torres. 2001. Effect of pH, water stress and temperature on in vitro cultures of ectomycorrhizal fungi from Mediterranean forests. Cryptogamie Mycologie 22(4): 243-258.

Sarker, N.C., M.M. Hossain, N. Sultana, I.H. Mian, A.J. Karim and S.M. Amin. 2007. Effect of different levels of pH on the growth and yield of Pleurotus ostreatus (Jacquin ex. Fr.) Kummer. Bangladesh J. Mush. 1(1): 57-62.

Sebastiana, M., V.T. Pereira, A. Alcântara, M.S. Pais and A.B. Silva. 2013. Ectomycorrhizal inoculation with Pisolithus tinctorius increases the performance of Quercus suber L. (cork oak) nursery and field seedlings. New Forests 44(6): 937-949.

Srinivasan, M., K. Natarajan and G. Nagarajan. 2000. Growth optimization of an ectomycorrhizal fungus with respect to pH and temperature in vitro, using design of experiments. Bioprocess Engineering 22: 267-273.

Sultana, R., M.D. Hossain, M.D. Saifullah, R. Amin and R. Chakraborty. 2018. Influence of substrate pH and watering frequency on the growth of oyster mushroom. Int. J. Plant Biol. Res. 6(4): 1097. 5 p.

Tang, C. and Z. Rengel. 2003. Role of plant cation/anion uptake ratio in soil acidification. In: Z. Rengel (ed.). Handbook of Soil Acidity. CRC Press, Boca Raton, FL. pp. 71-96.

Tedersoo, L., S. Anslan, M. Bahram, R. Drenkhan, K. Pritsch, F. Buegger et al. 2020. Regional-scale in-depth analysis of soil fungal diversity reveals strong pH and plant species effects in Northern Europe. Frontiers in Microbiology 11: 1953.

Turjaman, M., Y. Tamai, H. Segah, S.H. Limin, M. Osaki and K. Tawaraya. 2006. Increase in early growth and nutrient uptake of Shorea seminis seedlings inoculated with two ectomycorrhizal fungi. Journal of Tropical Forest Science 18(4): 243-249.

Vázquez-García, A., G. Santiago-Martinez and A. Estrada-Torres. 2002. Influencia del pH en el crecimiento de quince cepas de hongos ectomicorrizógenos. Anales del Instituto de Biología, Universidad Nacional Autónoma de México, Serie Botánica 73(1): 1-15.

Yamanaka, T. 2003. The effect of pH on the growth of saprotrophic and ectomycorrhizal ammonia fungi in vitro. Mycologia 95(4): 584-589.

Zhu, J.J., F.Q. Li, M.L. Xu, H.Z. Kang and X.Y. Wu. 2008. The role of ectomycorrhizal fungi in alleviating pine decline in semiarid sandy soil of northern China: an experimental approach. Annals of Forest Science 65(304): 12 p.

Published

2023-04-30

How to Cite

Olaizola, J., Santamaría, O., & Diez, J. J. (2023). In vitro growth of nine edible ectomycorrhizal fungi under a range of pH conditions. Bioagro, 35(2), 159-166. https://doi.org/10.51372/bioagro352.8

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Section

Nota Técnica