Production of peptone from chicken feathers

By: Subosa, Bemboy Nino F [author]
Contributor(s): Mirando, Jevie S [author] | Velasquez, Allan Paolo V [author] | Alamar, Vera Loise Q [author] | Capinpin, Geordan Gerald L [author] | Sablan, Khrizelle Angelique D [author] | De Leon, Rizalinda L [author]
Copyright date: 2016Subject(s): Culture media (Biology) In: Philippine Engineering Journal vol. 37, no. 1: (June 2016), pages 63-78Abstract: Peptones are the product of a protein hydrolysis, which serve as the main nutrient source for bacteria in a culture media. This study aimed to provide a locally feasible process for peptone production. Optimization results for Phase 1 showed that a temperature of 90°C, a digestion time of 4 hours, and a ratio of 0.06 g feathers/mL produced a yield of 50.6%. Statistical analysis showed that E. coli growth on the laboratory-produced peptone is significantly greater than the growth realized on commercial peptone and plate count agar. B. cereus growth on laboratory-produced peptone, however, was significantly lower than the growth on commercial peptone and plate count agar. Purification, drying, and characterization techniques were integrated into the existing process for Phase 2 to obtain peptones with better commercial quality. The maximum yield obtained was 30 g peptone per 100 g feathers. Freeze-dried powders from the purified hydrolysates had reduced odor and moisture as compared to the vacuum dried peptone. The vacuum-filtered batch also approximated the physical characteristics of the standard peptone hydrolysate. Performance testing for Phase 2 showed increased support for bacterial growth.
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Peptones are the product of a protein hydrolysis, which serve as the main nutrient source for bacteria in a culture media. This study aimed to provide a locally feasible process for peptone production. Optimization results for Phase 1 showed that a temperature of 90°C, a digestion time of 4 hours, and a ratio of 0.06 g feathers/mL produced a yield of 50.6%. Statistical analysis showed that E. coli growth on the laboratory-produced peptone is significantly greater than the growth realized on commercial peptone and plate count agar. B. cereus growth on laboratory-produced peptone, however, was significantly lower than the growth on commercial peptone and plate count agar. Purification, drying, and characterization techniques were integrated into the existing process for Phase 2 to obtain peptones with better commercial quality. The maximum yield obtained was 30 g peptone per 100 g feathers. Freeze-dried powders from the purified hydrolysates had reduced odor and moisture as compared to the vacuum dried peptone. The vacuum-filtered batch also approximated the physical characteristics of the standard peptone hydrolysate. Performance testing for Phase 2 showed increased support for bacterial growth.

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