Cytochemical localization and synthesis mechanism of the glucomannan in pseudobulbs of Bletilla striata Reichb. f.

IF 7.6 Q1 GENETICS & HEREDITY 园艺研究(英文) Pub Date : 2024-04-22 eCollection Date: 2024-05-01 DOI:10.1093/hr/uhae092
Junfeng Huang, Shuang Ma, Ming Zhou, Zhihao Liu, Qiong Liang
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Abstract

The dried pseudobulbs of Bletilla striata, an important traditional Chinese medicine named BaiJi, have an extraordinary polysaccharide content and excellent prospects for medicinal effects. However, the distribution and molecular mechanism underlying biosynthesis are poorly understood. In this study, chemical and immunologic analyses were performed in representative tissues of B. striata, and the results showed that what are conventionally termed Bletilla striata polysaccharides (BSPs) are water-soluble polysaccharides deposited only in pseudobulbs. The structural component of BSPs is glucomannan, with a mannose:glucose mass ratio of ~3:2. BSPs are present in the parenchyma of the pseudobulbs in cells known as glucomannan idioblasts and distributed in the cytoplasm within cellular membranes, but are not contained in the vacuole. Comparative transcriptomics and bioinformatics analyses mapped the pathway from sucrose to BSP and identified BsGPI, BsmanA, and BsCSLAs as the key genes of BSP biosynthesis, suggesting that the functional differentiation of the cellulose synthase-like family A (CSLA) may be critical for the flow of glucomannan to the BSP or cell wall. Subsequently, virus-mediated gene silencing showed that silencing of two CSLAs (Bs03G11846 and Bs03G11849) led to a decrease in BSP content, and yeast two-hybrid and luciferase complementation experiments confirmed that four CSLAs (Bs03G11846, Bs03G11847, Bs03G11848, and Bs03G11849) can form homo- or heterodimers, suggesting that multiple CSLAs may form a large complex that functions in BSP synthesis. Our results provide cytological evidence of BSP and describe the isolation and characterization of candidate genes involved in BSP synthesis, laying a solid foundation for further research on its regulation mechanisms and the genetic engineering breeding of B. striata.

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金针菜假鳞茎中葡甘露聚糖的细胞化学定位和合成机制
白术是一种重要的传统中药,其干燥假鳞茎中含有丰富的多糖,具有极佳的药用前景。然而,人们对其分布和生物合成的分子机制知之甚少。本研究对条纹白芨的代表性组织进行了化学和免疫学分析,结果表明,通常所说的条纹白芨多糖(BSPs)是仅沉积在假鳞茎中的水溶性多糖。BSP 的结构成分是葡甘露聚糖,甘露糖与葡萄糖的质量比约为 3:2。BSP 存在于假球茎的实质细胞中,被称为葡甘露聚糖特异细胞,分布于细胞膜内的细胞质中,但不包含在液泡中。比较转录组学和生物信息学分析绘制了从蔗糖到 BSP 的途径图,并确定 BsGPI、BsmanA 和 BsCSLAs 为 BSP 生物合成的关键基因,这表明纤维素合成酶样家族 A(CSLA)的功能分化可能是葡甘露聚糖流向 BSP 或细胞壁的关键。随后,病毒介导的基因沉默显示,两个 CSLA(Bs03G11846 和 Bs03G11849)的沉默导致 BSP 含量下降,酵母双杂交和荧光素酶互补实验证实了四个 CSLA(Bs03G11846、Bs03G11846、Bs03G11847、Bs03G11848 和 Bs03G11849)可以形成同源或异源二聚体,这表明多个 CSLAs 可能形成一个大型复合物,在 BSP 合成中发挥作用。我们的研究结果提供了 BSP 的细胞学证据,并描述了参与 BSP 合成的候选基因的分离和表征,为进一步研究其调控机制和 B. striata 的基因工程育种奠定了坚实的基础。
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