New robust subtilisins from halotolerant and halophilic Bacillaceae
Applied Microbiology and Biotechnology, vol. 107, pp. 3939–3954
Abstract
Abstract The aim of the present study was the characterisation of three true subtilisins and one phylogenetically intermediate subtilisin from halotolerant and halophilic microorganisms. Considering the currently growing enzyme market for efficient and novel biocatalysts, data mining is a promising source for novel, as yet uncharacterised enzymes, especially from halophilic or halotolerant Bacillaceae, which offer great potential to meet industrial needs. Both halophilic bacteria Pontibacillus marinus DSM 16465T and Alkalibacillus haloalkaliphilus DSM 5271T and both halotolerant bacteria Metabacillus indicus DSM 16189 and Litchfieldia alkalitelluris DSM 16976T served as a source for the four new subtilisins SPPM, SPAH, SPMI and SPLA. The protease genes were cloned and expressed in Bacillus subtilis DB104. Purification to apparent homogeneity was achieved by ethanol precipitation, desalting and ion-exchange chromatography. Enzyme activity could be observed between pH 5.0–12.0 with an optimum for SPPM, SPMI and SPLA around pH 9.0 and for SPAH at pH 10.0. The optimal temperature for SPMI and SPLA was 70 °C and for SPPM and SPAH 55 °C and 50 °C, respectively. All proteases showed high stability towards 5% (w/v) SDS and were active even at NaCl concentrations of 5 M. The four proteases demonstrate potential for future biotechnological applications. Key points • Halophilic and halotolerant Bacillaceae are a valuable source of new subtilisins. • Four new subtilisins were biochemically characterised in detail. • The four proteases show potential for future biotechnological applications.
Authors 5
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Affiliation as printed
Institute of Nano- and Biotechnologies, Aachen University of Applied Sciences, 52428, Jülich, Germany
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Affiliation as printed
Institute of Nano- and Biotechnologies, Aachen University of Applied Sciences, 52428, Jülich, Germany
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Affiliation as printed
Institute of Bio- and Geosciences, IBG-1: Biotechnology, Forschungszentrum Jülich, 52425, Jülich, Germany
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Affiliation as printed
Institute of Nano- and Biotechnologies, Aachen University of Applied Sciences, 52428, Jülich, Germany
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Affiliation as printed
Institute of Nano- and Biotechnologies, Aachen University of Applied Sciences, 52428, Jülich, Germany. siegert@fh-aachen.de
Institute of Nano- and Biotechnologies, Aachen University of Applied Sciences, 52428, Jülich, Germany
Cited by 11 stored of 13
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Cited by patents worldwide 1 (Lens.org)
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PROTEASE-CONTAINING DETERGENT COMPOSITION HAVING INCREASED STORAGE STABILITYWO2025108803A1 2025-05-30 Pending
References 97
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W2140538197details pending0citations
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W190784933details pending0citations
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W1601264718details pending0citations
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W1605815951details pending0citations