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果实木质化的无标记可视化:枇杷木质化细胞的拉曼分子成像

Label-free visualization of fruit lignification: Raman molecular imaging of loquat lignified cells.

作者信息

Zhu Nan, Wu Di, Chen Kunsong

机构信息

College of Agriculture and Biotechnology, Zhejiang Provincial Key Laboratory of Horticultural Plant Integrative Biology/The State Agriculture Ministry Laboratory of Horticultural Plant Growth/Development and Quality Improvement, Zhejiang University, Zijingang Campus, Hangzhou, 310058 People's Republic of China.

出版信息

Plant Methods. 2018 Jul 13;14:58. doi: 10.1186/s13007-018-0328-1. eCollection 2018.

Abstract

BACKGROUND

Flesh lignification, leading to increased fruit firmness, has been reported in several kinds of fruit. Understanding the mechanisms underlying fruit lignification is important to optimize the postharvest storage strategies and reduce the quality deterioration of postharvest fruit. Especially cellular level investigation of lignin deposition in fruits provides novel insight for deciphering the mechanisms underlying fruit lignification. The primary objective of this study was to establish a procedure of using Raman microspectroscopy technique to depict fruit lignification at the cell level.

RESULTS

Lignified cells, a special kind of cells contained high lignin content, were found abundantly scattered in red-fleshed 'Luoyangqing' loquat. Whereas these special lignified cells were barely detected in 'Baisha' loquat flesh. Dominant Raman bands of lignified cells were found primarily attributed to lignin (1664, 1628, 1603, 1467, and 1272 cm), cellulose (1383, 1124 and 1098 cm) and pectin (852 and 1740 cm). The band intensity correlation analysis indicated the peak at 1335 cm assigned to either lignin or cellulose in previous works was related to lignin for the lignified cells. Multi-peaks Gaussian fitting successfully resolved the overlapped fingerprint peaks of lignin in 1550-1700 cm into three independent peaks, which were assigned to different functional groups of lignin. Furthermore, the spatially resolved Raman images of lignified cells were generated, indicating that lignin and cellulose saturated the whole lignified cells, pectin mainly located in the cell corner, and the parenchyma cells contained little lignin. In addition, both phloroglucinol-HCl staining and autofluorescence analysis confirmed the results of lignin distribution of Raman microscopic analysis.

CONCLUSIONS

A procedure for the simultaneous visualization of the main components of the flesh cells without labeling by high-resolution Raman microspectroscopy has been established. With Raman microscopic imaging technique, we can add a microscopic level to cell compositions, essential for a detailed molecular understanding of loquat lignification. Such method can be further used to chemically monitor the textural changes during the ripening process or postharvest storage of other fruits and vegetables.

摘要

背景

在几种水果中都有果肉木质化导致果实硬度增加的报道。了解果实木质化的潜在机制对于优化采后贮藏策略和减少采后果实的品质劣化很重要。特别是在细胞水平上对果实中木质素沉积的研究为解读果实木质化的潜在机制提供了新的见解。本研究的主要目的是建立一种使用拉曼光谱技术在细胞水平描绘果实木质化的方法。

结果

在红肉‘洛阳青’枇杷中发现大量散在分布着一类特殊的、木质素含量高的木质化细胞。而在‘白沙’枇杷果肉中几乎检测不到这些特殊的木质化细胞。木质化细胞的主要拉曼峰主要归因于木质素(1664、1628、1603、1467和1272cm)、纤维素(1383、1124和1098cm)和果胶(852和1740cm)。谱带强度相关分析表明,先前研究中归属于木质素或纤维素的1335cm处的峰对于木质化细胞来说与木质素有关。多峰高斯拟合成功地将1550 - 1700cm范围内木质素重叠的指纹峰解析为三个独立的峰,它们分别归属于木质素的不同官能团。此外,生成了木质化细胞的空间分辨拉曼图像,表明木质素和纤维素充满整个木质化细胞,果胶主要位于细胞角隅,而薄壁细胞几乎不含木质素。另外,间苯三酚 - 盐酸染色和自发荧光分析均证实了拉曼显微镜分析的木质素分布结果。

结论

已建立一种通过高分辨率拉曼光谱技术在不进行标记的情况下同时可视化果肉细胞主要成分的方法。利用拉曼显微镜成像技术,我们能够在细胞组成方面增加微观层面的认识,这对于详细了解枇杷木质化的分子机制至关重要。这种方法可进一步用于化学监测其他水果和蔬菜在成熟过程或采后贮藏期间质地的变化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/164b/6043974/492b958563d6/13007_2018_328_Fig1_HTML.jpg

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