Gerardo Mata1, Jean-Michel Savoie. 1. Instituto de Ecología, AC, Carretera antigua a Coatepec 351, El Haya, CP 91070, Xalapa, Veracruz, Mexico. gerardo.mata@inecol.edu.mx
Abstract
BACKGROUND: One of the main problems for the preservation of genetics resources of Agaricus subrufescens is to maintain the viability of the strains because the mycelium is very sensitive to cooling and therefore it ages rapidly. AIMS: Evaluate the viability of A. subrufescens strains stored as cultures on sorghum grain (spawn) at different temperatures. METHODS: Eighteen strains of A. subrufescens and three strains of Agaricus bisporus were studied. Spawn's viability was evaluated under the following conditions: (1) control at 25°C (C), (2) cooling to 4°C (R) and (3) freezing in liquid nitrogen at -196°C (LN). Samples were recovered from week 4 every 2 weeks until week 12 and week 24 in C and R, whereas in LN samples were recovered at 4, 12 and 24 weeks. Viability was evaluated in 50 seeds, by strain and condition, recovering the mycelium in Petri dishes with potato dextrose agar medium (PDA). Mycelium growth was also evaluated on PDA after 14 days of recovery. RESULTS: Most strains showed 100% viability and they were recovered usually in 1 day. In LN the viability ranged between 84 and 100% depending on the strain, but in some cases recovery took more than 10 days. Mycelial growth decreased gradually over time and although the results show significant differences between treatments C and R, the decline is associated with ageing of the mycelium rather than the treatment itself. CONCLUSIONS: Culture on sorghum grain and storage at low temperature is an interesting way to preserve genetic resources of A. subrufescens.
BACKGROUND: One of the main problems for the preservation of genetics resources of Agaricus subrufescens is to maintain the viability of the strains because the mycelium is very sensitive to cooling and therefore it ages rapidly. AIMS: Evaluate the viability of A. subrufescens strains stored as cultures on sorghum grain (spawn) at different temperatures. METHODS: Eighteen strains of A. subrufescens and three strains of Agaricus bisporus were studied. Spawn's viability was evaluated under the following conditions: (1) control at 25°C (C), (2) cooling to 4°C (R) and (3) freezing in liquid nitrogen at -196°C (LN). Samples were recovered from week 4 every 2 weeks until week 12 and week 24 in C and R, whereas in LN samples were recovered at 4, 12 and 24 weeks. Viability was evaluated in 50 seeds, by strain and condition, recovering the mycelium in Petri dishes with potato dextrose agar medium (PDA). Mycelium growth was also evaluated on PDA after 14 days of recovery. RESULTS: Most strains showed 100% viability and they were recovered usually in 1 day. In LN the viability ranged between 84 and 100% depending on the strain, but in some cases recovery took more than 10 days. Mycelial growth decreased gradually over time and although the results show significant differences between treatments C and R, the decline is associated with ageing of the mycelium rather than the treatment itself. CONCLUSIONS: Culture on sorghum grain and storage at low temperature is an interesting way to preserve genetic resources of A. subrufescens.