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将农业工业废弃物作为原料进行再利用:利用白腐真菌通过固态发酵生产木质素修饰酶提取物。

Agro-industrial wastes revalorization as feedstock: production of lignin-modifying enzymes extracts by solid-state fermentation using white rot fungi.

作者信息

Contreras Elsa, Flores Rodrigo, Gutiérrez Aníbal, Cerro Daniela, Sepúlveda Luisa A

机构信息

Department of Chemical Engineering, Universidad de Santiago de Chile, Santiago, Chile.

出版信息

Prep Biochem Biotechnol. 2023;53(5):488-499. doi: 10.1080/10826068.2022.2109048. Epub 2022 Aug 18.

DOI:10.1080/10826068.2022.2109048
PMID:35980820
Abstract

The purpose of the study was to evaluate the production of lignin-modifying enzyme extracts and delignified biomass from agro-industrial wastes using white rot fungi ( sp. Sp2, Ru-104, sp. BOS55 IJFM 169 and BKM-F-1767). These were screened based on their adaptability and colonization ability on different substrates, as well as by the Laccase, Manganese peroxidase, and Lignin peroxidase enzymatic production. Native strains ( sp. Sp2 and Ru-104) showed the highest growth kinetics under the solid-substrate fermentation conditions and the growth rate parameters of the kinetic logistic model for the different substrates were between 0.39-0.81 (1/d) and 0.42-0.83 (1/d), respectively; the determination coefficients were ≥0.99. sp. Sp2 was subsequently cultured in static flasks to produce crude enzyme extracts, obtaining manganese peroxidase activity levels of 18.5 and 31.3 (U/g) when growing in corn cob husk and spent tea leaves, respectively. Besides, it was to establish that the best conditions for lignin-modifying enzymes production using corn cob husk are 70% of initial moisture and 2.12 mm of particle size; reaching after 30 incubation days a manganese peroxidase activity of 21 ± 6 (U/g) under these conditions; enzyme that showed a suitable thermostability.

摘要

本研究的目的是评估利用白腐真菌(Sp2菌株、Ru-104菌株、BOS55 IJFM 169菌株和BKM-F-1767菌株)从农业工业废弃物中生产木质素改性酶提取物和脱木质素生物质的情况。根据它们在不同底物上的适应性和定殖能力,以及漆酶、锰过氧化物酶和木质素过氧化物酶的酶产量对这些真菌进行了筛选。本地菌株(Sp2菌株和Ru-104菌株)在固体底物发酵条件下表现出最高的生长动力学,不同底物的动力学逻辑模型的生长速率参数分别在0.39 - 0.81(1/d)和0.42 - 0.83(1/d)之间;决定系数≥0.99。随后将Sp2菌株在静态烧瓶中培养以生产粗酶提取物,当在玉米芯壳和废茶叶中生长时,分别获得了18.5和31.3(U/g)的锰过氧化物酶活性水平。此外,还确定了使用玉米芯壳生产木质素改性酶的最佳条件是初始水分含量为70%,粒径为2.12毫米;在这些条件下培养30天后,锰过氧化物酶活性达到21±6(U/g);该酶表现出合适的热稳定性。

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