SNA (Synthetic Nutrient Deficient) Agar for Identification fungi

Gabriela Gabriela Paredes

Published: 2024-08-15 DOI: 10.17504/protocols.io.261ge5jkjg47/v1

Disclaimer

This protocol is provided for educational and research purposes only. The procedures described herein should be conducted by trained personnel in a properly equipped laboratory, adhering to all relevant safety and ethical guidelines. The authors and publishers of this protocol are not responsible for any injuries, damages, or legal consequences that may result from the improper use of this protocol. The use of chemicals, reagents, and equipment should be done with caution, and users must ensure they are compliant with all local, national, and institutional regulations.

Users are responsible for ensuring that their work complies with applicable biosafety and bioethics standards, particularly when handling genetically modified organisms (GMOs), pathogens, or other hazardous materials. This protocol does not constitute medical, legal, or professional advice, and should not be used as a substitute for consultation with qualified professionals in those fields.

Abstract

SNA (Spezieller Nährstoffarmer Agar) , or Synthetic Nutrient Deficient Agar, is a specialized culture medium designed for the identification and study of fungi such as Fusarium and Cylindrocarpon . This medium is nutrient-deficient, promoting specific morphological characteristics in these fungi that are critical for accurate identification. SNA is frequently used in mycological research and diagnostics, particularly in laboratories focused on plant pathology and fungal taxonomy. If the goal is to observe and document specific growth patterns, sporulation, or other morphological traits of these fungi under nutrient-limited conditions, SNA agar provides an optimal environment.

When Not to Use SNA Agar:

Isolation of Nutrient-Demanding Fungi :

  • For fungi that require richer nutrient environments for growth, such as certain saprophytic or pathogenic fungi not belonging to Fusarium or Cylindrocarpon , SNA agar would not provide the necessary nutrients for their development.

Rapid Growth and Mass Production :

  • If the objective is to rapidly grow and mass-produce fungal cultures for spore collection or other applications, a nutrient-rich medium such as Potato Dextrose Agar (PDA) or Sabouraud Dextrose Agar (SDA) would be more appropriate

Before start

Before starting the preparation of SNA medium, ensure that all necessary materials and equipment are available and properly sterilized. Measure out all the required chemical components accurately.

Steps

Dissolve SNA Components:

1.

In a 1-liter Erlenmeyer flask, dissolve the following components in 1 liter of distilled water (dH2O):

  • 1g of KH2PO4 (Potassium dihydrogen phosphate)
  • 1g of KNO3 (Potassium nitrate)
  • 0.5gof MgSO4·7H2O (Magnesium sulfate heptahydrate)
  • 0.5gof KCl (Potassium chloride)
  • 0.2gof Glucose
  • 0.2µLof Sucrose
  • 20g of Agar

Sterilize:

2.

Autoclave the solution at 121°C for 20 minutes to sterilize the medium.* After autoclaving, allow the medium to cool to around 50°C before pouring it into Petri dishes.

Pour into Petri Dishes:

3.

Work aseptically to pour the medium into sterile Petri dishes.* Allow the agar to solidify at room temperature before use.

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