Browsing by Author "Odeniyi, Olubusola Ayoola"
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Item Amylase production by Streptomyces species and its application in orange juice clarification(Trakya University Journal of Natural Sciences, 2026-01-13) Odjoji, Elizabeth Aghogho; Fasiku, Samuel Adedayo; Alao, Olaoluwa Kehinde; Salawu, Kehinde Olamide; Dada, Micheal Tunde; Odeniyi, Olubusola Ayoola; Wakil, Sherifah MonilolaAmylases are enzymes that break down starch and help clarify fruit juices. This study focused on screening amylolytic Streptomyces spp. isolated from soil samples for their potential for amylase production and fruit juice clarification. Select organisms produced amylase, which was assayed by measuring the reducing sugar content of the fermentation medium. The effects of pH, carbon and nitrogen source, as well as agitation and incubation periods, were evaluated to optimize amylase synthesis. A total of 22 species were isolated, with five—FE4, ELI1, FL2, MS2, and MS5—demonstrating high amylase production ability, which occurred at a pH ranging from slightly acidic to slightly alkaline. Cassava peels supported optimal amylase production in Streptomyces spp. A4 (0.834), ELI1 (0.910), and FE4 (0.814 U/mL). The maximum yield of 0.930 U/mL was observed with ELI1 when urea was used as the nitrogen source, at an agitation speed of 100–150 rpm, and peaking on the fourth day of fermentation. It was identified as S. griseoflavus ELI_1 using 16S rRNA gene sequencing and submitted to the GenBank with accession number OQ930232. The amylase produced by it was partially purified, markedly increasing its specific activity from 1.50 to 4.56 U/mL. Its ability to clarify orange juice was tested; the turbidity reduced significantly by 16.8% after amylase treatment (p <0.05). Amylolytic Streptomyces spp. were isolated from soil samples, and their amylase yield was optimized. The Amylase of S. griseoflavus ELI_1 could optimally clarify orange juice.Item Production of xylanase by Aspergillus niger GIO and Bacillus megaterium through solid-state fermentation(Microbiology Society, 2023-06-14) Fasiku, Samuel Adedayo; Bello, Mobolaji Akeem; Odeniyi, Olubusola AyoolaXylanase breaks xylan down to xylose, which is used in industries such as pulp and paper, food and feed, among others. The utilization of wastes for xylanase production is economical, hence this work aimed at producing xylanase through solidstate fermentation and characterizing the enzyme. Xylanase-producing strains of Bacillus megaterium and Aspergillus niger GIO were inoculated separately in a 5 and 10 day solid fermentation study on maize straw, rice straw, sawdust, corn cob, sugarcane bagasse, conifer litters, alkaline-pretreated maize straw (APM) and combined alkaline and biological-pretreated maize straw, respectively. The best substrate was selected for xylanase production. The crude enzyme was extracted from the fermentation medium and xylanase activity was characterized using parameters such as temperature, cations, pH and surfactants. Among different substrates, the highest xylanase activity of 3.18 U ml−1 was recorded when A. niger GIO was grown on APM. The xylanase produced by A. niger GIO and B. megaterium had the highest activities (3.67 U ml−1 and 3.36 U ml−1) at 40 °C after 30 and 45 min of incubation, respectively. Optimal xylanase activities (4.58 and 3.58 U ml−1) of A. niger GIO and B. megaterium, respectively, were observed at pH 5.0 and 6.2. All cations used enhanced xylanase activities except magnesium ion. Sodium dodecyl sulfate supported the highest xylanase activity of 6.13 and 6.90 U ml−1 for A. niger GIO and B. megaterium, respectively. High yields of xylanase were obtained from A. niger GIO and B. megaterium cultivated on APM. The xylanase activities were affected by pH, temperature, surfactants and cations.