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Keratinous hydrolysate profiling: comparison of the differences obtained from different extraction methods

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Abstract

The extraction of keratin from chicken feathers is of research interest due to the beneficiation of biomass. This study investigates the impact of the keratin hydrolysate obtained using four different methods. There are two different chemical extraction methods, CH1 and CH2, and two enzymatic hydrolyses, EH1 and EH2. The investigation includes the characterization and analysis using different types of equipment for different applications. The keratin hydrolysates formed were all characterized using FTIR, TGA, SDS PAGE, and CHNS analysis, Bradford assay, and ash content. All the keratin hydrolysate from different methods showed all the amide bonds present in the keratinous structure from the FTIR, while TGA followed the three-phase trend loss of the keratinous structure. Protein concentrations obtained from CH1, CH2, EH1, and EH2 were 1.40, 1.02, 1.08, and 0.45 mg/ml respectively and their protein content was 86.56, 67.63, 78.06, and 90.00%. Their molecular weights were all in different ranges while the ash content for CH1 was 20.7, CH2 was 5.27, and EH1 was 9.19. All the results obtained were compared to the pure keratin azure and EH2 showed high protein content but low protein concentration. CH1 showed the second-highest protein content but with high impurities from the extraction method shown from the ash content.

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Acknowledgements

The authors thank the Biorefinery Industrial Development Facility-Council of Scientific and Industrial Research (BIDF-CSIR) for the laboratory facility, Technology Innovation Agency (TIA) for the funding, University of KwaZulu Natal (UKZN), and University of Fort Hare.

Funding

Lizzy Kekana reports financial support was provided by University of KwaZulu-Natal. Bruce Sithole reports a relationship with The Council Of Scientific And Industrial Research that includes: equity or stocks, funding grants, and non-financial support.

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Contributions

I am responsible for the study, conception and design. Material were supplied by M. Khumalo, O. Fagbemi, O. Mnguni and T. Dlume. All data collection and analysis were performed by L. Kekana. The first draft and the final version of the manuscript were written by L. Kekana and all authors read and approved the final manuscript.

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Correspondence to L. M. Kekana.

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The authors declare the following financial interests/personal relationships which may be considered as potential competing interests.

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

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Novelty Statement

The main objective of this article is to compare the different keratin hydrolysates produced from different extraction methods. Most authors focus on the extraction methods and optimization but not the detailed characteristics of the keratin hydrolysate obtained for a specific application.

The quality and quantity of the keratin hydrolysate are dependent on the method used. Comparing the different hydrolysates helps with determining which method to use to obtain a specific hydrolysate with the quality and quantity required for the application in the study.

This research has not been done before where the same characterizations techniques are used on different keratin hydrolysate from different methods, then comparing their qualities and quantities. The applications of the keratin hydrolysates are all dependent on the quality of the hydrolysate obtained which is dependent on the method used, this is the reason why this research is important.

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Kekana, L.M., Sithole, B.B., Govinden, R. et al. Keratinous hydrolysate profiling: comparison of the differences obtained from different extraction methods. Biomass Conv. Bioref. 14, 6749–6757 (2024). https://doi.org/10.1007/s13399-022-02965-5

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