Silica biomineralization in plants alters the structure of lignin.

IF 3.3 3区 化学 Q2 CHEMISTRY, PHYSICAL
Srinath Palakurthy, Michael Elbaum, Rivka Elbaum
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引用次数: 0

Abstract

Biomineralization of silica is a major process in plants, which may contribute 3-10% of tissue dry weight. For reasons that remain unclear, plants containing silica are less sensitive to abiotic and biotic stress. In particular, the mechanisms of silica deposition and stress amelioration are still not fully understood. Silica resides mostly in the extracellular volume (the apoplast) which is made of the lignocellulosic cell wall. In a previous work we showed that synthetic lignin catalyses the formation of silica nanoparticles at RC-OSi(OH)3 positions. Since the phenolic O-4 position is the most reactive during lignin polymerization, the binding sites form at the expense of β-O-4 lignin backbone bonds. Therefore, synthetic lignin becomes more branched when polymerized in the presence of silicic acid, as compared to lignin polymerized without silicic acid. To study lignin-silica relationships in the plant, we extracted lignin from stems of wild type sorghum and compared it to lignin extracted from mutants exhibiting high and low silica contents. The thermal stability of both non-extracted biomass and extracted lignin was measured using thermogravimetric analysis (TGA). High-silica biomass was thermally less stable than low-silica biomass, suggesting lower content of ether (β-O-4) linkages. This interpretation was supported by gas chromatography-mass spectroscopy (GC-MS). Fourier transform infrared (FTIR) and X-ray photoelectron spectra (XPS) indicated lignin with C-O-Si modifications in all genotypes and further showed silicic acid binding to lignin phenolics and carbonyl moieties. Our results show that lignin extracted from genotypes with native-silicon levels have higher affinity to silicic acid, catalysing silica deposition through Si-O-4 (Si-phenoxyl) bonds, and suggest that the presence of silicic acid during in vivo lignin polymerization reduces β-O-4 ether linkages.

植物中二氧化硅生物矿化改变了木质素的结构。
二氧化硅的生物矿化是植物体内的一个重要过程,可能占组织干重的3-10%。由于尚不清楚的原因,含有二氧化硅的植物对非生物和生物胁迫不太敏感。特别是,二氧化硅沉积和应力改善的机制仍未完全了解。二氧化硅主要存在于由木质纤维素细胞壁组成的细胞外体积(外质体)中。在之前的研究中,我们发现合成木质素在RC-OSi(OH)3位置催化二氧化硅纳米颗粒的形成。由于酚醛O-4位置在木质素聚合过程中是最活跃的,结合位点的形成是以牺牲β-O-4木质素主键为代价的。因此,与没有硅酸聚合的木质素相比,在硅酸存在下聚合的合成木质素变得更具支链性。为了研究植物中木质素与二氧化硅的关系,我们从野生型高粱茎中提取木质素,并将其与高、低二氧化硅含量突变体提取的木质素进行比较。采用热重分析法(TGA)测定了未提取的生物质和提取的木质素的热稳定性。高硅生物质的热稳定性低于低硅生物质,表明醚(β-O-4)键的含量较低。气相色谱-质谱(GC-MS)支持了这一解释。傅里叶变换红外(FTIR)和x射线光电子能谱(XPS)表明,所有基因型的木质素都有C-O-Si修饰,并进一步表明硅酸与木质素酚类和羰基部分结合。我们的研究结果表明,从天然硅水平的基因型中提取的木质素对硅酸具有更高的亲和力,通过Si-O-4 (Si-phenoxyl)键催化二氧化硅沉积,并且表明在体内木质素聚合过程中硅酸的存在减少了β-O-4醚键。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Faraday Discussions
Faraday Discussions 化学-物理化学
自引率
0.00%
发文量
259
期刊介绍: Discussion summary and research papers from discussion meetings that focus on rapidly developing areas of physical chemistry and its interfaces
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