UMR SPO INRA/SupAgro/UM I.
Ann Bot. 2013 Oct;112(6):1003-14. doi: 10.1093/aob/mct168. Epub 2013 Sep 11.
Condensed tannins (also called proanthocyanidins) are widespread polymers of catechins and are essential for the defence mechanisms of vascular plants (Tracheophyta). A large body of evidence argues for the synthesis of monomeric epicatechin on the cytosolic face of the endoplasmic reticulum and its transport to the vacuole, although the site of its polymerization into tannins remains to be elucidated. The aim of the study was to re-examine the cellular frame of tannin polymerization in various representatives of the Tracheophyta.
Light microscopy epifluorescence, confocal microscopy, transmission electron microscopy (TEM), chemical analysis of tannins following cell fractionation, and immunocytochemistry were used as independent methods on tannin-rich samples from various organs from Cycadophyta, Ginkgophyta, Equisetophyta, Pteridophyta, Coniferophyta and Magnoliophyta. Tissues were fixed in a caffeine-glutaraldehyde mixture and examined by TEM. Other fresh samples were incubated with primary antibodies against proteins from both chloroplastic envelopes and a thylakoidal chlorophyll-carrying protein; they were also incubated with gelatin-Oregon Green, a fluorescent marker of condensed tannins. Coupled spectral analyses of chlorophyll and tannins were carried out by confocal microscopy on fresh tissues and tannin-rich accretions obtained through cell fractionation; chemical analyses of tannins and chlorophylls were also performed on the accretions.
The presence of the three different chloroplast membranes inside vacuolar accretions that constitute the typical form of tannin storage in vascular plants was established in fresh tissues as well as in purified organelles, using several independent methods. Tannins are polymerized in a new chloroplast-derived organelle, the tannosome. These are formed by pearling of the thylakoids into 30 nm spheres, which are then encapsulated in a tannosome shuttle formed by budding from the chloroplast and bound by a membrane resulting from the fusion of both chloroplast envelopes. The shuttle conveys numerous tannosomes through the cytoplasm towards the vacuole in which it is then incorporated by invagination of the tonoplast. Finally, shuttles bound by a portion of tonoplast aggregate into tannin accretions which are stored in the vacuole. Polymerization of tannins occurs inside the tannosome regardless of the compartment being crossed. A complete sequence of events apparently valid in all studied Tracheophyta is described.
缩合单宁(也称为原花青素)是儿茶素广泛存在的聚合物,是维管植物(管植物)防御机制的关键。大量证据表明,单体表儿茶素在内质网细胞质面合成,并被运输到液泡,但单宁聚合的部位仍有待阐明。本研究的目的是重新检查管植物各代表种中单宁聚合的细胞框架。
在富含单宁的样品上,使用光镜荧光、共聚焦显微镜、透射电子显微镜(TEM)、单宁的化学分析(继细胞分离后)和免疫细胞化学,作为来自苏铁纲、银杏纲、木贼纲、蕨类植物、裸子植物和被子植物的各种器官的独立方法。组织用咖啡因-戊二醛混合物固定,并用 TEM 检查。其他新鲜样品用针对质体包膜和类囊体叶绿素携带蛋白的蛋白质的初级抗体孵育;它们还与明胶-Oregon Green(一种缩合单宁的荧光标记物)孵育。用共聚焦显微镜对新鲜组织和通过细胞分离获得的富含单宁的沉积物进行叶绿素和单宁的耦合光谱分析;对沉积物进行单宁和叶绿素的化学分析。
使用几种独立的方法,在新鲜组织和纯化的细胞器中均证实了构成维管植物典型单宁储存形式的液泡沉积物内存在三种不同的质体膜。单宁在一个新的叶绿体衍生的细胞器中聚合,即单宁体。这些是由类囊体珠化形成 30nm 球体,然后由叶绿体出芽形成的单宁体穿梭体包裹,并由两个质体包膜融合形成的膜结合。穿梭体通过细胞质将许多单宁体输送到液泡中,然后通过液泡被膜的内陷而被包裹。最后,由一部分液泡被膜结合的穿梭体聚集形成单宁沉积物,储存在液泡中。单宁的聚合发生在单宁体内部,无论穿过的隔室如何。描述了一个显然在所有研究的管植物中都有效的完整事件序列。