“…Enzymatic lignin degradation has several advantages such as mild conditions and potentially fewer inhibitors for microbes. However, the degradation of lignin in LCBM still gave a very low yield of fragmented and soluble lignin, which may due to the limitations on efficient electron transfer [28] in the process.…”
Section: Cellulolytic Enzyme Ligninmentioning
confidence: 99%
“…Furthermore, a significant reduction in the weight-average molecular weight (M w ) of extracted lignin was also achieved. Synergistic effects were found in the combination of pretreatments to enhance the isolation or conversion of lignins [28,46]. In the sequential fractionation of Tamarix spp., MWL, organosolv lignin, and alkaline lignin were conducted with dioxane, alkaline organosolv, and alkaline solutions, respectively.…”
Lignin is highly branched phenolic polymer and accounts 15-30% by weight of lignocellulosic biomass (LCBM). The acceptable molecular structure of lignin is composed with three main constituents linked by different linkages. However, the structure of lignin varies significantly according to the type of LCBM, and the composition of lignin strongly depends on the degradation process. Thus, the elucidation of structural features of lignin is important for the utilization of lignin in high efficient ways. Up to date, degradation of lignin with destructive methods is the main path for the analysis of molecular structure of lignin. Spectroscopic techniques can provide qualitative and quantitative information on functional groups and linkages of constituents in lignin as well as the degradation products. In this review, recent progresses on lignin degradation were presented and compared. Various spectroscopic methods, such as ultraviolet spectroscopy, Fourier-transformed infrared spectroscopy, Raman spectroscopy, and nuclear magnetic resonance (NMR) spectroscopy, for the characterization of structural and compositional features of lignin were summarized. Various NMR techniques, such as 1 H, 13 C, 19 F, and 31 P, as well as 2D NMR, were highlighted for the comprehensive investigation of lignin structure. Quantitative 13 C NMR and various 2D NMR techniques provide both qualitative and quantitative results on the detailed lignin structure and composition produced from various processes which proved to be ideal methods in practice.
“…Enzymatic lignin degradation has several advantages such as mild conditions and potentially fewer inhibitors for microbes. However, the degradation of lignin in LCBM still gave a very low yield of fragmented and soluble lignin, which may due to the limitations on efficient electron transfer [28] in the process.…”
Section: Cellulolytic Enzyme Ligninmentioning
confidence: 99%
“…Furthermore, a significant reduction in the weight-average molecular weight (M w ) of extracted lignin was also achieved. Synergistic effects were found in the combination of pretreatments to enhance the isolation or conversion of lignins [28,46]. In the sequential fractionation of Tamarix spp., MWL, organosolv lignin, and alkaline lignin were conducted with dioxane, alkaline organosolv, and alkaline solutions, respectively.…”
Lignin is highly branched phenolic polymer and accounts 15-30% by weight of lignocellulosic biomass (LCBM). The acceptable molecular structure of lignin is composed with three main constituents linked by different linkages. However, the structure of lignin varies significantly according to the type of LCBM, and the composition of lignin strongly depends on the degradation process. Thus, the elucidation of structural features of lignin is important for the utilization of lignin in high efficient ways. Up to date, degradation of lignin with destructive methods is the main path for the analysis of molecular structure of lignin. Spectroscopic techniques can provide qualitative and quantitative information on functional groups and linkages of constituents in lignin as well as the degradation products. In this review, recent progresses on lignin degradation were presented and compared. Various spectroscopic methods, such as ultraviolet spectroscopy, Fourier-transformed infrared spectroscopy, Raman spectroscopy, and nuclear magnetic resonance (NMR) spectroscopy, for the characterization of structural and compositional features of lignin were summarized. Various NMR techniques, such as 1 H, 13 C, 19 F, and 31 P, as well as 2D NMR, were highlighted for the comprehensive investigation of lignin structure. Quantitative 13 C NMR and various 2D NMR techniques provide both qualitative and quantitative results on the detailed lignin structure and composition produced from various processes which proved to be ideal methods in practice.
“…68,99 Other than single enzymes, fungal secretome (i.e., enzyme mixture) was also directly added into the lignin fermentation broth, which led to a reduction of lignin molecular weight by more than 60%. Fungal ligninolytic enzymes with strong oxidative ability can be supplemented into lignin fermentation system to facilitate the destruction of complex lignin molecules.…”
Section: Advanced Process Design For Lignin Bioconversionmentioning
As one of the most abundant polymers in biosphere, lignin has attracted extensive attention as a kind of promising feedstock for biofuel and bio-based products. However, the utilization of lignin presents various challenges in that its complex composition and structure and high resistance to degradation. Lignin conversion through biological platform harnesses the catalytic power of microorganisms to decompose complex lignin molecules and obtain value-added products through biosynthesis.Given the heterogeneity of lignin, various microbial metabolic pathways are involved in lignin bioconversion processes, which has been characterized in extensive research work. With different types of lignin substrates (e.g., model compounds, technical lignin, and lignocellulosic biomass), several bacterial and fungal species have been proved to own lignin-degrading abilities and accumulate microbial products (e.g., lipid
“…To obtain smaller molecular weight Kraft lignin, oxygen-pretreatment (O 2 -pretreatment) was carried out on Kraft lignin under alkaline conditions which lowered the molecular weight of the lignin and when treated with R. opacus resulted in increased oleaginicity (14%) and an increase in lipid titers (0.07 mg/ml) [57] (Table 1, #4). Alternatively, Zhao supplemented R. opacus fermentation with Kraft lignin with laccases which resulted in an increase in lipid titers (0.15 mg/ ml) [78] (Table 1, #5). Laccases aid in lignin depolymerization allowing for selective degradation of different lignin functional groups probably improving the usage of the lower molecular weight lignin molecules [78].…”
“…Alternatively, Zhao supplemented R. opacus fermentation with Kraft lignin with laccases which resulted in an increase in lipid titers (0.15 mg/ ml) [78] (Table 1, #5). Laccases aid in lignin depolymerization allowing for selective degradation of different lignin functional groups probably improving the usage of the lower molecular weight lignin molecules [78].…”
Rhodococcus opacus produces intracellular lipids from the biodegradation of lignocellulosic biomass. These lipids can be used to produce biofuels that could potentially replace petroleum-derived chemicals. Current studies are focusing on deconstructing lignin through efficient and cost-effective pretreatment methods and improving microbial lipid titers. R. opacus can reach high levels of oleaginicity (>80%) when grown on glucose and other aromatic model compounds but intracellular lipid production is much lower on complex recalcitrant lignin substrates. This review will discuss recent advances in studying R. opacus lignin degradation by exploring different pretreatment methods, increasing lignin solubility, enriching for low molecular weight lignin compounds and laccase supplementation.
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