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BIOLOGICAL CONTROL OF PLANT
DISEASES
Biocontrol agent
Any practice which reduce the survival or
activity of pathogen through other living organism
which results reducing disease incidence
(Garrett -1970)
• Living organism – Antagonist
Two types
Fungal biocontrol agent
• Eg. Trichoderma viride
• Trichoderma harzianum
Bacterial biocontrol agent
• Eg.Pseudomonas fluorescence
• Bacillus subtilis
Advantage
• Low cost
• Safe to environment and person who apply them.
• Gives protection throughout the life
• Encourage soil microflora and increase yield
• Easy to manufacture
• Combined with bio- fertilizer.
Disadvantage
• Only used against specific disease
• Slow effect than the fungicides
• Preventive not curative method
• Required skilled persons
LiquidPowder
Culture
Liquid
Powder
Culture
Mechanism of bio-control
• Parasitism
• Competition
• Antibiosis
• Lysis
• Induced Systemic Resistance
Parasitism
• The antagonistic micro organism parasitize the
pathogen by coiling around the hyphae
• Ex:Trichoderma - Pythium
Pythium
Trichoderma
Competition
• The antagonistic microorganism compete
with the pathogen for food and space making
them unavailable for the pathogen.
Antibiosis
The antibiotic compound(toxic metabolites)
secreted by the biocontrol agent suppresses the
growth of the pathogen.
Eg:
• P. fluorescens - Phenazine -1- carboxlic - suppress the wheat
diseases.
• Trichoderma spp - Trichodermin,gliotoxin and viridin.
Antibiosis
Lysis
Different fungi and bacteria secrete hydrolytic
enzymes degrade the cell wall of the pathogen.
Eg :
• Trichoderma sp.- β-1,3, glucanase and chitinases
which degrade the chitins and glucans in cell wall and
causes its lyses in R. solani
ISR/ SAR
• Enhanced defensive capacity of the
entire plant against pathogen
• Mediated by jasmonic acid/ ethylene
• Mediated by salicylic acid
Mass multiplication of Trichoderma viride
• Sterilized molasses yeast medium
• (Molasses 30g + yeast 5g + 1000ml of distilled water)
• Trichoderma viride culture is inoculated into the medium
• Incubated for 10 days - Mother culture
• Medium is prepared in a fermentor and sterilized
• Mother culture is added to the fermentor @ 1.5 liter/50
liters of medium
• Incubate for 10 days
• Carrier substances sterilized at 20 p.s.i for 30 minutes for
two successive days.
• Carrier substances pH adjusted to 7 by adding CaCo3
@150g/kg.
• Medium is mixed with carrier substrates viz., flyash,
peatsoil, talc powder at 1:2 ratio
• Mixture is air dried & mixed with Carboxyl Methyl
Cellulose (CMC) @ 50g/kg of the product for sticking.
• Packed in white polythene bags
Mass multiplication of Pseudomonas fluorescence
• Sterilized King’s ‘B’ broth medium
• Pseudomonas fluorescence inoculate in to the medium
• Incubate for 72 hrs - Mother culture
• Medium is prepared in a fermentor and sterilized
• Mother culture is added to the fermentor @ 1 liter/100
liters of medium
• Incubate for 72 hrs
• Carrier substances sterilized at 20 p.s.i for 30 minutes for
two successive days.
• Carrier substances pH adjusted to 7 by adding CaCo3
@150g/kg.
• Medium is mixed with carrier substrates viz., flyash,
peatsoil, talc powder at 1:2 ratio
• Mixture is air dried & mixed with Carboxyl Methyl
Cellulose (CMC) @ 50g/kg of the product for sticking.
• Packed in white polythene bags
Mass multiplication of Bacillus subtilis
• Sterilized King’s ‘B’ broth medium
• A loopful of bacillus subtilis culture is inoculated to the
medium, incubated for 24hrs. - Mother culture
• Medium is prepared in a fermentor and sterilized
• Mother culture is added to the fermentor @ 1 liter/100
liters of medium
• Incubate for 72 hrs
• Carrier substances sterilized at 20 p.s.i for 30 minutes for
two successive days.
• Carrier substances pH adjusted to 7 by adding CaCo3
@150g/kg.
• Medium is mixed with carrier substrates viz., flyash,
peatsoil, talc powder at 1:2 ratio
• Mixture is air dried & mixed with Carboxyl Methyl
Cellulose (CMC) @ 50g/kg of the product for sticking.
• Packed in white polythene bags
QUALITY CONTROL OF BIOCONTROL AGENTS:
• Fresh product should contain 10-6 cfu/g (Trichoderma viride),
10-8 cfu/g (Pseudomonas fluorescence & Bacillus subtilis)
• Maximum storage period is 120 days (Trichoderma viride)
and 90days(Pseudomonas fluorescence & Bacillus subtilis)
• After storage period at room temperature the population
should be 10-6 cfu/g (Trichoderma viride), 10-7cfu/g
(Pseudomonas fluorescence & Bacillus subtilis)
• Size of the carrier substrate should be 50µ
• Moisture content of the final product should not be more
than 20%
Characteristics of good Bio-control
agents
• It should not be pathogenic to plants
• It should have fast growth and sporulation
• It should be amenable for mass multiplication
• It should be compatible with bio fertilizer
• It should not be toxic to human beings & animals
• It should have more shelf life
• It should not be toxic to beneficial organisms.

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Biological control

  • 1. BIOLOGICAL CONTROL OF PLANT DISEASES
  • 2. Biocontrol agent Any practice which reduce the survival or activity of pathogen through other living organism which results reducing disease incidence (Garrett -1970) • Living organism – Antagonist
  • 3. Two types Fungal biocontrol agent • Eg. Trichoderma viride • Trichoderma harzianum Bacterial biocontrol agent • Eg.Pseudomonas fluorescence • Bacillus subtilis
  • 4. Advantage • Low cost • Safe to environment and person who apply them. • Gives protection throughout the life • Encourage soil microflora and increase yield • Easy to manufacture • Combined with bio- fertilizer.
  • 5. Disadvantage • Only used against specific disease • Slow effect than the fungicides • Preventive not curative method • Required skilled persons
  • 8. Mechanism of bio-control • Parasitism • Competition • Antibiosis • Lysis • Induced Systemic Resistance
  • 9. Parasitism • The antagonistic micro organism parasitize the pathogen by coiling around the hyphae • Ex:Trichoderma - Pythium
  • 11. Competition • The antagonistic microorganism compete with the pathogen for food and space making them unavailable for the pathogen.
  • 12.
  • 13.
  • 14. Antibiosis The antibiotic compound(toxic metabolites) secreted by the biocontrol agent suppresses the growth of the pathogen. Eg: • P. fluorescens - Phenazine -1- carboxlic - suppress the wheat diseases. • Trichoderma spp - Trichodermin,gliotoxin and viridin.
  • 16. Lysis Different fungi and bacteria secrete hydrolytic enzymes degrade the cell wall of the pathogen. Eg : • Trichoderma sp.- β-1,3, glucanase and chitinases which degrade the chitins and glucans in cell wall and causes its lyses in R. solani
  • 17. ISR/ SAR • Enhanced defensive capacity of the entire plant against pathogen • Mediated by jasmonic acid/ ethylene • Mediated by salicylic acid
  • 18. Mass multiplication of Trichoderma viride • Sterilized molasses yeast medium • (Molasses 30g + yeast 5g + 1000ml of distilled water) • Trichoderma viride culture is inoculated into the medium • Incubated for 10 days - Mother culture • Medium is prepared in a fermentor and sterilized • Mother culture is added to the fermentor @ 1.5 liter/50 liters of medium • Incubate for 10 days
  • 19. • Carrier substances sterilized at 20 p.s.i for 30 minutes for two successive days. • Carrier substances pH adjusted to 7 by adding CaCo3 @150g/kg. • Medium is mixed with carrier substrates viz., flyash, peatsoil, talc powder at 1:2 ratio • Mixture is air dried & mixed with Carboxyl Methyl Cellulose (CMC) @ 50g/kg of the product for sticking. • Packed in white polythene bags
  • 20.
  • 21. Mass multiplication of Pseudomonas fluorescence • Sterilized King’s ‘B’ broth medium • Pseudomonas fluorescence inoculate in to the medium • Incubate for 72 hrs - Mother culture • Medium is prepared in a fermentor and sterilized • Mother culture is added to the fermentor @ 1 liter/100 liters of medium • Incubate for 72 hrs
  • 22. • Carrier substances sterilized at 20 p.s.i for 30 minutes for two successive days. • Carrier substances pH adjusted to 7 by adding CaCo3 @150g/kg. • Medium is mixed with carrier substrates viz., flyash, peatsoil, talc powder at 1:2 ratio • Mixture is air dried & mixed with Carboxyl Methyl Cellulose (CMC) @ 50g/kg of the product for sticking. • Packed in white polythene bags
  • 23.
  • 24. Mass multiplication of Bacillus subtilis • Sterilized King’s ‘B’ broth medium • A loopful of bacillus subtilis culture is inoculated to the medium, incubated for 24hrs. - Mother culture • Medium is prepared in a fermentor and sterilized • Mother culture is added to the fermentor @ 1 liter/100 liters of medium • Incubate for 72 hrs
  • 25. • Carrier substances sterilized at 20 p.s.i for 30 minutes for two successive days. • Carrier substances pH adjusted to 7 by adding CaCo3 @150g/kg. • Medium is mixed with carrier substrates viz., flyash, peatsoil, talc powder at 1:2 ratio • Mixture is air dried & mixed with Carboxyl Methyl Cellulose (CMC) @ 50g/kg of the product for sticking. • Packed in white polythene bags
  • 26. QUALITY CONTROL OF BIOCONTROL AGENTS: • Fresh product should contain 10-6 cfu/g (Trichoderma viride), 10-8 cfu/g (Pseudomonas fluorescence & Bacillus subtilis) • Maximum storage period is 120 days (Trichoderma viride) and 90days(Pseudomonas fluorescence & Bacillus subtilis) • After storage period at room temperature the population should be 10-6 cfu/g (Trichoderma viride), 10-7cfu/g (Pseudomonas fluorescence & Bacillus subtilis) • Size of the carrier substrate should be 50µ • Moisture content of the final product should not be more than 20%
  • 27. Characteristics of good Bio-control agents • It should not be pathogenic to plants • It should have fast growth and sporulation • It should be amenable for mass multiplication • It should be compatible with bio fertilizer • It should not be toxic to human beings & animals • It should have more shelf life • It should not be toxic to beneficial organisms.