Lamia Medouni-HarouneSonia Medouni-AdrarAicha Asma HoufaniCilia BouicheZahra AzzouzSevastianos RoussosVéronique DesseauxKhodir MadaniMouloud Kecha2026-07-232026-07-232023-07-171559-0291https://dspace.crtaa.dz/handle/123456789/91Xylanase production by Streptomyces sp. S1M3I was optimized by response surface meth- odology (RSM), followed by a partial characterization of these enzymes. Olive pomace was used as a substrate for growing Streptomyces sp. S1M3I in submerged fermentation. Effects of incubation time, pH, temperature, carbon source, nitrogen source, and inoculum size on xylanase production were studied, through the one-factor-at-a-time method. Then, a 33-factorial experimental design with RSM and the Box–Behnken design was investi- gated for the major influence factors. Maximum xylanase production (11.28 U/mL) was obtained when the strain was grown in mineral medium supplemented with 3% (w/v) of olive pomace powder and 0.3% (w/v) of ammonium sulfate, at a pH 7.4 and an incuba- tion temperature of 40 °C. The xylanases in the supernatant degraded all tested substrates, with higher activity for the low-viscosity wheat arabinoxylan substrate. Two xylanases with close molecular masses were detected by zymogram analysis: Xyl-1 and Xyl-2 with molecular masses of 24.14 kDa and 27 kDa, respectively. The optimization of enzyme pro- duction parameters of Streptomyces sp. S1M3I and the characterization of these enzymes are prerequisites to enhancing xylanase production yield, which is crucial for further bio- technological processes.enActinobacteriaXylanaseOlive pomaceOptimizationCharacterizationArticle