Materials and Reagents

Ethyl acetate (Rankem)
Butanol (Qualigens)
Methanol (Qualigens)
Hexane (Qualigens)
Fungus culture
Measuring cylinder
Whatman filter paper
Detergent
Glass jars of 5 L capacity
Malt extract (HiMedia Laboratories)
Yeast extract (HiMedia Laboratories)
Peptone (HiMedia Laboratories)
Glucose (Qualigens)
Needle
Spirit lamp
Commercial disinfectant (70% ethanol)
Vacuum pump
Malt extract
Yeast extract
Wickerham medium (see Recipes)

Equipment

Inoculation flasks
Conical flasks of 1 L capacity
Vacuum rotary evaporator (Heidolph Instruments GmbH)
pH meter (Eutech Instruments pH tutor)
Autoclave (Nat steel)
BOD incubator (Toshiba)
Laminar air flow hood (Toshiba)
Filteration assembly
Hand blender (inalsaappliances.com)
Fume hood
Microbalances (Sartorious, model: RC210P )

Procedure

5 discs of 5 mm diameter of endophytic fungus from petridish were inoculated in Wickerham medium.
Flasks with inoculated media were incubated at 24 °C for 24 days under static culture condition without light.
One flask of medium without any inoculam served as a control.
After 24 days of incubation, 250 ml of ethyl acetate was added to each flask, mixed, and left overnight.
Ethyl acetate immersed fungus culture was blended with a hand blender for 15 min and filtered by whatman filter paper under vacuum (Wicklow et al., 1998).
The filtrate was collected and residual aqueous phase was partitioned thrice times with equal volumes of ethyl acetate in a separator funnel (Figure 1).

Figure 1. Partitioning by separator funnel
Aqueous phase obtained after ethyl acetate extraction was further partitioned three times with equal volumes of saturated butanol.
Aqueous phase obtained after butanol extraction was discarded after immersing in detergent.
The ethyl acetate and butanol extracts were dried with vacuum rotary evaporator.
Dried ethyl acetate extract resuspended in 90% methanol and extracted with n-hexane.
After drying the hexane, butanol, and methanol extracts with vacuum rotary evaporator they were subjected to further experimentation. Schematic diagram for the extraction of the metabolite has been given in Figure 2.

Figure 2. Schematic diagram of extraction procedure for obtaining crude fungal extracts

Recipes

Wickerham medium
Malt extract 3 g/L
Yeast extract 3 g/L
Peptone 5 g/L
Glucose 10 g/L
All the media chemicals were weighed and dissolved in distilled water and pH was measured. After adjusting the pH in range of 7.2-7.4, media was distributed in conical flasks (300 ml in 1 L conical flask). These flasks were subjected to autoclaving at 121 °C temperature and 15 psi pressure for 20 min.

Acknowledgments

This protocol was adopted from Kumar and Kaushik (2013). Authors are grateful to their host institution, The Energy and Resources Institute (TERI), New Delhi, India for funding the research. Susheel Kumar is grateful to University Grant Commission, New Delhi for a research fellowship.

References

Kumar, S. and Kaushik, N. (2013). Endophytic fungi isolated from oil-seed crop Jatropha curcas produces oil and exhibit antifungal activity. PLoS One 8(2): e56202.
Wicklow, D. T., Joshi, B. K., Gamble, W. R., Gloer, J. B. and Dowd, P. F. (1998). Antifungal metabolites (monorden, monocillin IV, and cerebrosides) from Humicola fuscoatra traaen NRRL 22980, a mycoparasite of Aspergillus flavus sclerotia. Appl Environ Microbiol 64(11): 4482-4484.