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STRAIN IMPROVEMENT OF A FUNGUS PRODUCING CHITINASE BY A CHEMICAL MUTAGEN

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Microbial chitinases are commercially exploited for their biocontrol properties and generation of useful products from chitinous waste. Availability of highly active chitinolytic enzymes is a major problem. The present study was carried out to improve chitinase production by Aspergillus terreus using a chemical mutagen, ethidium bromide. The organism was cultivated on lactose- yeast extract medium. The production medium consisting of chitin- yeast extract medium was seeded at 10% level. The wild strains were exposed to ethidium bromide in the concentration range 1.5- 6.0 µg/mL. Generally, all the mutated strains showed an improved chitinase yield compared to the control. Highest yield was observed with the strain exposed to 6 µg/mL of ethidium bromide. The yield was 25.03 % higher compared to the wild strain. The mutated strain was slimy in nature. Protein content of the mutated strain decreased by 11%. Ethidium bromide at a concentration of 1.5 µg/mL was considered optional, at which the strain was stable with increase of 21.80 % in enzyme activity and 4.41% increase in protein content. Increased enzyme yield with decreased non-specific protein could be useful in producing cost effective enzyme.
Title: STRAIN IMPROVEMENT OF A FUNGUS PRODUCING CHITINASE BY A CHEMICAL MUTAGEN
Description:
Microbial chitinases are commercially exploited for their biocontrol properties and generation of useful products from chitinous waste.
Availability of highly active chitinolytic enzymes is a major problem.
The present study was carried out to improve chitinase production by Aspergillus terreus using a chemical mutagen, ethidium bromide.
The organism was cultivated on lactose- yeast extract medium.
The production medium consisting of chitin- yeast extract medium was seeded at 10% level.
The wild strains were exposed to ethidium bromide in the concentration range 1.
5- 6.
0 µg/mL.
Generally, all the mutated strains showed an improved chitinase yield compared to the control.
Highest yield was observed with the strain exposed to 6 µg/mL of ethidium bromide.
The yield was 25.
03 % higher compared to the wild strain.
The mutated strain was slimy in nature.
Protein content of the mutated strain decreased by 11%.
Ethidium bromide at a concentration of 1.
5 µg/mL was considered optional, at which the strain was stable with increase of 21.
80 % in enzyme activity and 4.
41% increase in protein content.
Increased enzyme yield with decreased non-specific protein could be useful in producing cost effective enzyme.

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