Department of Biological Systems Engineering, University of Nebraska-Lincoln, Lincoln, NE 68583, USA.
Department of Biotechnology, University of São Paulo, Lorena, SP, Brazil.
Bioresour Technol. 2021 Apr;325:124700. doi: 10.1016/j.biortech.2021.124700. Epub 2021 Jan 12.
Enzymatic lignin depolymerization is considered a favorable approach to utilize lignin due to the higher selectivity and less energy requirement when compared to thermochemical lignin valorization. Lignin peroxidase (LiP) is one of the key enzymes involved in lignin degradation and possesses high redox potential to oxidize non-phenolic structures and phenolic compounds in lignin. However, the production of LiP is mainly from white-rot fungi at small scales. It is critical to discover new LiP from other microorganisms and produce LiP at large scales. This study aims to produce a novel LiP originally from Thermothelomyces thermophiles using a recombinant Aspergillus nidulans strain. The LiP production medium was optimized, and different fed-batch strategies for LiP production were investigated to improve LiP activity, yield, and productivity. Results demonstrated that LiP production was enhanced by using multi-pulse fed-batch fermentation. A maximum LiP activity of 1,645 mU/L with a protein concentration of 0.26 g/L was achieved.
酶法木质素解聚被认为是一种利用木质素的有利方法,因为与热化学木质素增值相比,它具有更高的选择性和更少的能量需求。木质素过氧化物酶(LiP)是参与木质素降解的关键酶之一,具有较高的氧化还原电位,可氧化木质素中的非酚类结构和酚类化合物。然而,LiP 的生产主要来自于小规模的白腐真菌。从其他微生物中发现新的 LiP 并进行大规模生产至关重要。本研究旨在使用重组 Aspergillus nidulans 菌株生产一种新型的来源于 Thermothelomyces thermophiles 的 LiP。优化了 LiP 生产培养基,并研究了不同的补料分批策略以提高 LiP 活性、产量和生产效率。结果表明,采用多脉冲补料分批发酵可提高 LiP 生产。最大 LiP 活性为 1645 mU/L,蛋白浓度为 0.26 g/L。