Cai Lixi, Zheng Ying, Chu Yunmeng, Lin Yuanqing, Liu Lixing, Zhang Guangya
College of Basic Medicine, Putian University, Putian, China.
Department of Bioengineering and Biotechnology, Huaqiao University, Xiamen, China.
Front Nutr. 2022 Oct 19;9:970540. doi: 10.3389/fnut.2022.970540. eCollection 2022.
Enzyme-assisted valorization of lichenan represents a green and sustainable alternative to the conventional chemical industry. The recently discovered lytic polysaccharide monooxygenases (LPMOs) are essential components of state-of-the-art enzyme cocktails for lichenin bioconversion. The LPMOs named SpyTag fused LPMOs (AST) from was functionally expressed in and exhibited 1.25-fold synergism with lichenase, whereas AST alone produced no detectable reducing sugars. HPLC results further confirm that AST does not alter the endogenous hydrolysis mode of lichenase but rather enhances its hydrolysis efficiency by disrupting the long chain of lichenan and releasing more reducing ends. To the best of our knowledge, this was the first report on the synergistic effect of LPMOs and lichenase, which may have great synergistic potential in the conversion of lichen biomass. Furthermore, a novel strategy for the covalently immobilizing AST and lichenase on silica nanoparticles (SNPs) from the cell lysate in a single step was proposed, which exhibited high activity recovery (82.9%) and high immobilization yield (94.8%). After 12 independent runs, about 67.4 % of the initial activity of the immobilized enzymes was retained. The resulted biocatalyst systems exhibited the green and sustainable strategy in the bioconversion of lichen biomass as well as other diverse polysaccharides.
地衣多糖的酶促增值是传统化学工业的一种绿色可持续替代方案。最近发现的裂解多糖单加氧酶(LPMOs)是用于地衣多糖生物转化的先进酶混合物的重要组成部分。来自的名为SpyTag融合LPMO(AST)的LPMOs在中功能表达,并与地衣酶表现出1.25倍的协同作用,而单独的AST没有产生可检测到的还原糖。高效液相色谱结果进一步证实,AST不会改变地衣酶的内源性水解模式,而是通过破坏地衣多糖的长链并释放更多还原端来提高其水解效率。据我们所知,这是关于LPMOs与地衣酶协同效应的首次报道,其在地衣生物质转化中可能具有巨大的协同潜力。此外,还提出了一种将AST和地衣酶从细胞裂解物中一步共价固定在二氧化硅纳米颗粒(SNPs)上的新策略,该策略表现出高活性回收率(82.9%)和高固定化产率(94.8%)。经过12次独立运行后,固定化酶保留了约67.4%的初始活性。所得的生物催化剂系统在地衣生物质以及其他多种多糖的生物转化中展现出绿色可持续策略。