Evidence map›Paper›PMID 42667443›Full record

ArticleBiodegradation2026

Biodegradation of hair waste for keratinase production using Bacillus altitudinis VK-1120 and its application in enzymatic dehairing.

Vijan Lal Vikash, Pradeep Srinivasan, Parthasarathy Baskaran Sujiritha, Anandasadagopan Suresh Kumar, Ponesakki Ganesan, Balaraman Madhan, Numbi Ramudu Kamini

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Article in Biodegradation, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

7 authors.

Vijan Lal VikashBiochemistry and Biotechnology Laboratory, CSIR - Central Leather Research Institute (CLRI), Chennai, 600020, India. vikashnegi11@gmail.com.
Pradeep SrinivasanBiochemistry and Biotechnology Laboratory, CSIR - Central Leather Research Institute (CLRI), Chennai, 600020, India.
Parthasarathy Baskaran SujirithaBiochemistry and Biotechnology Laboratory, CSIR - Central Leather Research Institute (CLRI), Chennai, 600020, India.
Anandasadagopan Suresh KumarBiochemistry and Biotechnology Laboratory, CSIR - Central Leather Research Institute (CLRI), Chennai, 600020, India.
Ponesakki GanesanBiochemistry and Biotechnology Laboratory, CSIR - Central Leather Research Institute (CLRI), Chennai, 600020, India.
Balaraman MadhanBiochemistry and Biotechnology Laboratory, CSIR - Central Leather Research Institute (CLRI), Chennai, 600020, India.
Numbi Ramudu KaminiBiochemistry and Biotechnology Laboratory, CSIR - Central Leather Research Institute (CLRI), Chennai, 600020, India. nrkamini@yahoo.com.

Funding

Council of Scientific and Industrial Research, India sanction letter no. 31/006(0468)/2019-EMR-I
6 · The paper itself

Abstract

The leather industry impacts the environment through the use of hazardous chemicals for dehairing and the improper disposal of waste from these processes. In this study, a newly isolated Bacillus altitudinis VK-1120 was utilized for hair waste valorization and keratinase production. The keratinase production was optimized, and the maximum activity of 220.82 U/mL was achieved at 40 °C, pH 8.0, and 100 rpm after 48 h. The activity of purified enzyme was inhibited by PMSF and EDTA, suggesting that the enzyme functions as a serine-metalloprotease. SDS-PAGE results revealed a molecular weight of ~25 kDa for the purified keratinase. The optimum temperature and pH for the purified keratinase were 50 °C and 9.0, respectively. The keratinase solution was applied to the dehairing of goatskins using the industrial drum-based method, and complete dehairing was observed within 5 h. The enzymatic treatment significantly improved the waste liquor quality, reducing Biochemical Oxygen Demand (BOD) by 38.67%, Chemical Oxygen Demand (COD) by 50.16%, Total Dissolved Solids (TDS) by 65.25%, and Total Solids (TS) by 52.22%. The physical and organoleptic properties of enzymatically dehaired leather were comparable to those processed by the conventional lime and sulfide method. Additionally, the recyclability of the dehairing enzyme for up to 3 cycles enhanced the application of the keratinase for industrial-scale depilation. Therefore, this study could pave the way for more environmentally responsible solid waste management and depilation practices in the leather industry.

Indexed as

BacillusBacterial ProteinsHairHair RemovalPeptide HydrolasesAnimalsBiodegradation, EnvironmentalGoatsHydrogen-Ion ConcentrationTemperatureBacterial ProteinskeratinasePeptide HydrolasesCircular economyEnzymatic depilationKeratinaseKeratin wasteValorization

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.