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Screening, Identification and
Isolation of Cellulolytic fungi
By sreeremya.s
Asst professor,sree narayana guru
college,cbe
• Fungi constitute a group of microorganisms
• that are widely distributed in environment
• especially in soil (Boer et al., 2005). Since
• they produce wide variety of hydrolytic
• enzymes and hence exist in nature in
• saprophytic mode (Ng TB, 2004).
• Cellulases bring about the hydrolysis of
• cellulose, a homopolymer of -1,4 linked
• glucose units that comprises amorphous and
• crystalline regions, by synergistic action of
• its constituent enzymes (Bhat M and Bhat
• S,1997). Cellulases are group of
• extracellular enzymes commonly employed
• in many industries for the hydrolysis
• of cellulolytic material.(Mahmood RT et al.,
• 2013).
• Characterization and Identification of
• fungal Isolates
• Fungal colonies were isolated form soil
• samples enriched for cellulase producing
• microorganisms by serial dilution method
• wherein, PDA (potato dextrose agar) media
• was prepared, autoclaved and poured in
• sterile petriplates. 50μl of soil samples
• diluted upto 10-5 dilutions were spread on
• respective solidified PDA plates. The
• inoculated petriplates were incubated at
• 28°C for 48 hours.
• Cellulase assay for Enzyme production
• The activity of -glucosidase ( G), total
• cellulase (FPase) and endoglucanase
• (CMCase) was studied as cellulolytic
• activity. Filter paper activity (FPase) for
• total cellulase activity in the culture filtrate
• was determined according to the standard
• method (Eveleigh DE et al.2009). CMCase
• (carboxy methyl cellulase) activity was
• assayed using Dinitrosalicylic acid (DNS)
• method (Mandels and Weber, 1969).
• Therefore,
• there is a growing interest in assessing soil
• biodiversity and its biological functioning
• (Barrios E, 2007). At the ecosystem scale,
• extracellular enzyme activity is influenced
• by organic matter abundance and
• composition (Sinsabaugh RL et al., 2008).
Screening, identification and isolation of cellulolytic fungi
Screening, identification and isolation of cellulolytic fungi
Screening, identification and isolation of cellulolytic fungi
Screening, identification and isolation of cellulolytic fungi
Screening, identification and isolation of cellulolytic fungi
Screening, identification and isolation of cellulolytic fungi
Screening, identification and isolation of cellulolytic fungi
Screening, identification and isolation of cellulolytic fungi
Screening, identification and isolation of cellulolytic fungi
Screening, identification and isolation of cellulolytic fungi
Screening, identification and isolation of cellulolytic fungi
Screening, identification and isolation of cellulolytic fungi
Screening, identification and isolation of cellulolytic fungi
Screening, identification and isolation of cellulolytic fungi

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Screening, identification and isolation of cellulolytic fungi

  • 1. Screening, Identification and Isolation of Cellulolytic fungi By sreeremya.s Asst professor,sree narayana guru college,cbe
  • 2. • Fungi constitute a group of microorganisms • that are widely distributed in environment • especially in soil (Boer et al., 2005). Since • they produce wide variety of hydrolytic • enzymes and hence exist in nature in • saprophytic mode (Ng TB, 2004).
  • 3. • Cellulases bring about the hydrolysis of • cellulose, a homopolymer of -1,4 linked • glucose units that comprises amorphous and • crystalline regions, by synergistic action of • its constituent enzymes (Bhat M and Bhat • S,1997). Cellulases are group of • extracellular enzymes commonly employed • in many industries for the hydrolysis • of cellulolytic material.(Mahmood RT et al., • 2013).
  • 4. • Characterization and Identification of • fungal Isolates • Fungal colonies were isolated form soil • samples enriched for cellulase producing • microorganisms by serial dilution method • wherein, PDA (potato dextrose agar) media • was prepared, autoclaved and poured in • sterile petriplates. 50μl of soil samples • diluted upto 10-5 dilutions were spread on • respective solidified PDA plates. The • inoculated petriplates were incubated at • 28°C for 48 hours.
  • 5. • Cellulase assay for Enzyme production • The activity of -glucosidase ( G), total • cellulase (FPase) and endoglucanase • (CMCase) was studied as cellulolytic • activity. Filter paper activity (FPase) for • total cellulase activity in the culture filtrate • was determined according to the standard • method (Eveleigh DE et al.2009). CMCase • (carboxy methyl cellulase) activity was • assayed using Dinitrosalicylic acid (DNS) • method (Mandels and Weber, 1969).
  • 6. • Therefore, • there is a growing interest in assessing soil • biodiversity and its biological functioning • (Barrios E, 2007). At the ecosystem scale, • extracellular enzyme activity is influenced • by organic matter abundance and • composition (Sinsabaugh RL et al., 2008).