Production of surfactant-stable keratinase from Bacillus cereus YQ15 and its application as detergent additive

BMC Biotechnol. 2022 Sep 8;22(1):26. doi: 10.1186/s12896-022-00757-3.

Abstract

Background: With the growing concern for the environment, there are trends that bio-utilization of keratinous waste by keratinases could ease the heavy burden of keratinous waste from the poultry processing and leather industry. Especially surfactant-stable keratinases are beneficial for the detergent industry. Therefore, the production of keratinase by Bacillus cereus YQ15 was improved; the characterization and use of keratinase in detergent were also studied.

Results: A novel alkaline keratinase-producing bacterium YQ15 was isolated from feather keratin-rich soil and was identified as Bacillus cereus. Based on the improvement of medium components and culture conditions, the maximum keratinase activity (925 U/mL) was obtained after 36 h of cultivation under conditions of 35 °C and 160 rpm. Moreover, it was observed that the optimal reacting temperature and pH of the keratinase are 60 °C and 10.0, respectively; the activity was severely inhibited by PMSF and EDTA. On the contrary, the keratinase showed remarkable stability in the existence of the various surfactants, including SDS, Tween 20, Tween 60, Tween 80, and Triton X-100. Especially, 5% of Tween 20 and Tween 60 increased the activity by 100% and 60%, respectively. Furtherly, the keratinase revealed high efficiency in removing blood stains.

Conclusion: The excellent compatibility with commercial detergents and the high washing efficiency of removing blood stains suggested its suitability for potential application as a bio-detergent additive.

Keywords: Bacillus cereus; Detergent compatibility; Keratinase; Production.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bacillus cereus* / metabolism
  • Detergents* / chemistry
  • Enzyme Stability
  • Feathers / metabolism
  • Hydrogen-Ion Concentration
  • Keratins / metabolism
  • Peptide Hydrolases / metabolism
  • Polysorbates
  • Surface-Active Agents
  • Temperature

Substances

  • Detergents
  • Polysorbates
  • Surface-Active Agents
  • Keratins
  • Peptide Hydrolases
  • keratinase