Adebami Gboyega E, Adebayo-Tayo Bukola C, Kuila Arindam, Babalola Benjamin A, Abiala Moses A
Department of Biological Sciences, Mountain Top University, Ibafo, Nigeria.
Department of Microbiology, University of Ibadan, Ibadan, Nigeria.
Sci Rep. 2025 Jul 1;15(1):20967. doi: 10.1038/s41598-025-06505-9.
The quest for economically viable sources of microbial lipases has been a primary focus for microbial enzymologists. This research aimed to screen, identify, and produce lipase from fungi using inexpensive agro-wastes as substrates. Samples of palm oil mill effluent were screened for lipolytic fungi using solid agar and submerged fermentation. Morphological and molecular methods were employed for isolate identification. Lipase activity was measured via spectrophotometric assays with p-nitrophenyl palmitate (p-NPP) as the substrate. The effect of medium composition on lipase production, the mineral and proximate compositions of the agro waste used as carbon sources via solid state fermentation were evaluated, followed by lipase purification and kinetic studies. Out of the 25 fungi screened, isolate GP11 identified as Aspergillus oryzae (Accession number: MN416218) exhibited the highest lipase activity and was selected for further studies. Medium composition significantly affected (p ≤ 0.05) lipase and biomass production across six fermentation media yielding 148.75 ± 2.94 to 274.05 ± 13.70 (U/mL) and 28.5 ± 1.41 to 35.4 ± 1.77 (g/L) respectively. Production media having glucose and peptone as carbon and organic nitrogen sources supported the highest lipase production. Agro waste composition influenced lipase production which ranged from 103.97 ± 2.88 to 259.78 ± 8.45 (U/mL). Wheat bran (WTB) (230.78 ± 7.79 U/mL) and rice bran (RCB) (211.62 ± 3.20 U/mL) with the highest carbohydrate contents supported the highest lipase production compared to orange peel, unripe plantain peel, ripe banana peel, ripe plantain peel, and sugar cane bagasse respectively. The purified lipase had 12.74- and 50.81%-fold purification and yield via Sephadex G-100 chromatography with a molecular weight of 53 kDa.
寻找经济可行的微生物脂肪酶来源一直是微生物酶学家的主要研究重点。本研究旨在以廉价的农业废弃物为底物,从真菌中筛选、鉴定并生产脂肪酶。采用固体琼脂和深层发酵法,对棕榈油厂废水样品进行脂肪分解真菌的筛选。采用形态学和分子方法对分离菌株进行鉴定。以对硝基苯基棕榈酸酯(p-NPP)为底物,通过分光光度法测定脂肪酶活性。评估了培养基组成对脂肪酶生产的影响,以及通过固态发酵用作碳源的农业废弃物的矿物质和近似成分,随后进行脂肪酶纯化和动力学研究。在筛选的25株真菌中,鉴定为米曲霉(登录号:MN416218)的分离株GP11表现出最高的脂肪酶活性,并被选作进一步研究。培养基组成对六种发酵培养基中的脂肪酶和生物量产量有显著影响(p≤0.05),脂肪酶产量分别为148.75±2.94至274.05±13.70(U/mL),生物量产量分别为28.5±1.41至35.4±1.77(g/L)。以葡萄糖和蛋白胨作为碳源和有机氮源的生产培养基支持最高的脂肪酶产量。农业废弃物组成影响脂肪酶产量,产量范围为103.97±2.88至259.78±8.45(U/mL)。与橙皮、未成熟芭蕉皮、成熟香蕉皮、成熟芭蕉皮和甘蔗渣相比,碳水化合物含量最高的麦麸(WTB)(230.78±7.79 U/mL)和米糠(RCB)(211.62±3.20 U/mL)支持最高的脂肪酶产量。经Sephadex G-100色谱纯化的脂肪酶纯化倍数为12.74倍,产率为50.81%,分子量为53 kDa。