Mori Tetsuya, Tsuboi Yuuri, Ishida Nobuhiro, Nishikubo Nobuyuki, Demura Taku, Kikuchi Jun
1] Graduate School of Bioagricultural Sciences, Nagoya University, 1 Furo-cho, Chikusa-ku, Nagoya 464-0810, Japan [2] Biotechnology Laboratory, Toyota Central R&D Labs, Inc., 41-1, Nagakute 480-1192, Japan.
RIKEN Center for Sustainable Resource Science, 1-7-22 Suehiro-cho, Tsurumi-ku, Yokohama 230-0045, Japan.
Sci Rep. 2015 Jul 6;5:11848. doi: 10.1038/srep11848.
Lignocellulose, which includes mainly cellulose, hemicellulose, and lignin, is a potential resource for the production of chemicals and for other applications. For effective production of materials derived from biomass, it is important to characterize the metabolites and polymeric components of the biomass. Nuclear magnetic resonance (NMR) spectroscopy has been used to identify biomass components; however, the NMR spectra of metabolites and lignocellulose components are ambiguously assigned in many cases due to overlapping chemical shift peaks. Using our (13)C-labeling technique in higher plants such as poplar samples, we demonstrated that overlapping peaks could be resolved by three-dimensional NMR experiments to more accurately assign chemical shifts compared with two-dimensional NMR measurements. Metabolites of the (13)C-poplar were measured by high-resolution magic angle spinning NMR spectroscopy, which allows sample analysis without solvent extraction, while lignocellulose components of the (13)C-poplar dissolved in dimethylsulfoxide/pyridine solvent were analyzed by solution-state NMR techniques. Using these methods, we were able to unambiguously assign chemical shifts of small and macromolecular components in (13)C-poplar samples. Furthermore, using samples of less than 5 mg, we could differentiate between two kinds of genes that were overexpressed in poplar samples, which produced clearly modified plant cell wall components.
木质纤维素主要包括纤维素、半纤维素和木质素,是生产化学品及用于其他用途的一种潜在资源。为了有效地生产源自生物质的材料,表征生物质的代谢物和聚合物成分非常重要。核磁共振(NMR)光谱已被用于鉴定生物质成分;然而,由于化学位移峰重叠,代谢物和木质纤维素成分的NMR光谱在很多情况下难以明确归属。利用我们在杨树等高等植物样本中采用的¹³C标记技术,我们证明与二维NMR测量相比,三维NMR实验可以分辨重叠峰,从而更准确地归属化学位移。¹³C杨树的代谢物通过高分辨率魔角旋转NMR光谱进行测量,该技术无需溶剂萃取即可进行样品分析,而溶解于二甲基亚砜/吡啶溶剂中的¹³C杨树的木质纤维素成分则通过溶液态NMR技术进行分析。使用这些方法,我们能够明确归属¹³C杨树样本中小分子和大分子成分的化学位移。此外,使用少于5毫克的样本,我们能够区分杨树样本中两种过表达的基因,这些基因产生了明显改变的植物细胞壁成分。