Solid-state fermentation for protease production using agro-industrial residues by a novel thermotolerant Streptomyces sp. isolated from algerian arid soil

The process of solid-state fermentation (SSF) offers a sustainable platform for enzyme production, particularly proteases with industrial relevance. In this study, protease synthesis was investigated using a thermotolerant Streptomyces sp. strain C8, isolated from arid soil of Tamanrasset, Algeria. The strain, Gram-positive with biverticillate spore chains, grew optimally at 45°C, pH 7, tolerated 5% NaCl, and exhibited 93.21% 16S rRNA similarity to Streptomyces griseorubens NBRC 12780 (GenBank accession PV834194), suggesting novelty. Under SSF, various agro-industrial wastes were tested, with spent brewing grains (SBGs) emerging as the most promising substrate. Initial optimization via the One-Factor-at-a-Time approach identified incubation time, temperature, pH, and moisture as critical parameters, yielding maximum activity (82 U/mL) under 30°C, pH 7, 4 days, and 75% humidity. Further optimization using response surface methodology of Box-Behnken design confirmed significant model performance (F = 8.47, P = 0.0003, R² = 0.9081), highlighting moisture, incubation time, and pH as key factors. The refined conditions (31°C, 55% moisture, 3 days, and pH 7) resulted in 128.70 U/mL activity. Overall, these findings demonstrate that low-cost agro-industrial byproducts, particularly SBGs, can serve as efficient, eco-friendly substrates for protease production using thermotolerant Streptomyces strains, offering promising applications in biotechnology.

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Publication Details

Journal
FEMS Microbiology Letters
Published
2025-01-01
DOI
https://doi.org/10.1093/femsle/fnaf095
Citations
1
Primary Topic
Enzyme Production and Characterization
Type
article
Field-Weighted Citation Impact
1.23
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article

Solid-state fermentation for protease production using agro-industrial residues by a novel thermotolerant Streptomyces sp. isolated from algerian arid soil

Faiza Boughachiche, Habiba Zerizer, Zahra Azzouz, Messaoudi Mohammed et al.
1 citations
FEMS Microbiology Letters
Enzyme Production and Characterization
1.23
article

Solid-state fermentation for protease production using agro-industrial residues by a novel thermotolerant Streptomyces sp. isolated from algerian arid soil

Faiza Boughachiche, Habiba Zerizer, Zahra Azzouz, Messaoudi Mohammed, Houria Benhamiche
article en
1 citations

Abstract

The process of solid-state fermentation (SSF) offers a sustainable platform for enzyme production, particularly proteases with industrial relevance. In this study, protease synthesis was investigated using a thermotolerant Streptomyces sp. strain C8, isolated from arid soil of Tamanrasset, Algeria. The strain, Gram-positive with biverticillate spore chains, grew optimally at 45°C, pH 7, tolerated 5% NaCl, and exhibited 93.21% 16S rRNA similarity to Streptomyces griseorubens NBRC 12780 (GenBank accession PV834194), suggesting novelty. Under SSF, various agro-industrial wastes were tested, with spent brewing grains (SBGs) emerging as the most promising substrate. Initial optimization via the One-Factor-at-a-Time approach identified incubation time, temperature, pH, and moisture as critical parameters, yielding maximum activity (82 U/mL) under 30°C, pH 7, 4 days, and 75% humidity. Further optimization using response surface methodology of Box-Behnken design confirmed significant model performance (F = 8.47, P = 0.0003, R² = 0.9081), highlighting moisture, incubation time, and pH as key factors. The refined conditions (31°C, 55% moisture, 3 days, and pH 7) resulted in 128.70 U/mL activity. Overall, these findings demonstrate that low-cost agro-industrial byproducts, particularly SBGs, can serve as efficient, eco-friendly substrates for protease production using thermotolerant Streptomyces strains, offering promising applications in biotechnology.

FEMS Microbiology LettersVol. 372
University Frères Mentouri Constantine 1 (DZ), University of Béjaïa (DZ), Ahmed Draia University (DZ)
Openalex Percentile: Top 18%
Enzyme Production and Characterization
1.23
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