Published 2025

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Publication details

Journal : Microbial Cell Factories , vol. 24 , p. 1–17–0 , 2025

Publisher : BioMed Central (BMC)

International Standard Numbers :
Printed : 1475-2859
Electronic : 1475-2859

Publication type : Academic article

Contributors : Isembart, Clémentine; Zimmermann, Boris; Matić, Josipa; Losada, Cristian Bolaño; Afseth, Nils Kristian; Kohler, Achim; Horn, Svein Jarle; Eijsink, Vincent; Chylenski, Piotr; Shapaval, Volha

Issue : 1

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Kjetil Aune
Chief Librarian
kjetil.aune@nofima.no

Summary

Feathers are a major by-product of the poultry industry, which poses an environmental challenge due to the recalcitrant structure of keratin, making them resistant to degradation. Traditional methods of feather handling, like conversion to feather meal, are energy-intensive and have limited efficiency. Biotechnological approaches, particularly microbial hydrolysis, offer a novel and more sustainable alternative for keratin degradation. This study evaluated feather hydrolysis by two bacterial strains, newly characterized cold-adapted Arthrobacter oryzae (BIM B-1663) and Bacillus licheniformis (CCM 2145T), known as a keratin degrader, under various feather pre-treatment conditions, including washing, autoclaving, drying, and grinding. Results Both bacterial strains were able to degrade pretreated feathers with a degradation efficiency of 75 to 90%, resulting in high ratios of nitrogen to carbon in the hydrolysates. B. licheniformis confirmed its enzymatic capabilities with high levels of general and specific protease activity and furthermore presented enriched amounts of amino acids of industrial interest. A. oryzae showed a much higher keratinase/protease activity ratio, demonstrating high specificity and efficiency of its enzymes. Autoclaving emerged as the most important determinant of microbial degradation efficiency and influenced the composition (peptide pattern, amino acid content, and chemical composition assessed through FTIR) of the resulting hydrolysates. Feather drying, although not improving microbial degradation efficiencies, had a considerable impact on hydrolysate composition. Conclusions The results show that both tested bacterial strains can efficiently degrade autoclaved feathers but use distinct enzymatic strategies to do so. Enriched profiles in amino acids and high nitrogen content in the hydrolysates also advocate for the benefits of microbial feather hydrolysis over an enzymatic one. To the authors’ knowledge this study is the first to report a comprehensive evaluation of the impact of various feather pre-treatment methods on the efficiency of subsequent microbial feather hydrolysis and is the first one to report enrichment in phenylalanine, lysine, and tyrosine secreted by B. licheniformis.

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