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Valorization of lignocellulosic wastes for sustainable xylanase production from locally isolated Bacillus subtilis exploited for xylooligosaccharides' production with potential antimicrobial activity.
El-Gendi, Hamada; Badawy, Ahmed S; Bakhiet, Elsayed K; Rawway, Mohammed; Ali, Salah G.
Affiliation
  • El-Gendi H; Bioprocess Development Department, Genetic Engineering and Biotechnology Research Institute, City of Scientific Research and Technological Applications (SRTA-City), New Borg El-Arab City, Alexandria, 21934, Egypt. Elgendi1981@yahoo.com.
  • Badawy AS; Botany and Microbiology Department, Faculty of Science, AL-Azhar University, Assiut, Egypt.
  • Bakhiet EK; Botany and Microbiology Department, Faculty of Science, AL-Azhar University, Assiut, Egypt.
  • Rawway M; Botany and Microbiology Department, Faculty of Science, AL-Azhar University, Assiut, Egypt.
  • Ali SG; Botany and Microbiology Department, Faculty of Science, AL-Azhar University, Assiut, Egypt.
Arch Microbiol ; 205(9): 315, 2023 Aug 21.
Article de En | MEDLINE | ID: mdl-37605001
ABSTRACT
The worldwide availability of lignocellulosic wastes represents a serious environmental challenge with potential opportunities. Xylanases are crucial in lignocellulosic bio-hydrolysis, but the low enzyme productivity and stability are still challenges. In the current study, Bacillus subtilis (coded ARSE2) revealed potent xylanase activity among other local isolates. The enzyme production optimization revealed that maximum enzyme production (490.58 U/mL) was achieved with 1% xylan, 1.4% peptone, and 5% NaCl at 30 °C and pH 9. Furthermore, several lignocellulosic wastes were exploited for sustainable xylanase production, where sugarcane bagasse (16%) under solid-state fermentation and woody sawdust (2%) under submerged fermentation supported the maximum enzyme titer of about 472.03 and 485.7 U/mL, respectively. The partially purified enzyme revealed two protein bands at 42 and 30 kDa. The partially purified enzyme revealed remarkable enzyme activity and stability at 50-60 °C and pH 8-9. The enzyme also revealed significant stability toward tween-80, urea, DTT, and EDTA with Vmax and Km values of 1481.5 U/mL and 0.187 mM, respectively. Additionally, the purified xylanase was applied for xylooligosaccharides production, which revealed significant antimicrobial activity toward Staphylococcus aureus with lower activity against Escherichia coli. Hence, the locally isolated Bacillus subtilis ARSE2 could fulfill the xylanase production requirements in terms of economic production at a high titer with promising enzyme characteristics. Additionally, the resultant xylooligosaccharides revealed a promising antimicrobial potential, which paves the way for other medical applications.
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Bacillus subtilis / Saccharum Langue: En Journal: Arch Microbiol Année: 2023 Type de document: Article Pays d'affiliation: Égypte

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Bacillus subtilis / Saccharum Langue: En Journal: Arch Microbiol Année: 2023 Type de document: Article Pays d'affiliation: Égypte