Antreich Sebastian J, Permann Charlotte, Xiao Nannan, Tiloca Giuseppe, Holzinger Andreas
Department of Bionanosciences, University of Natural Resource and Life Sciences, Vienna, Austria.
Department of Botany, University of Innsbruck, Innsbruck, Austria.
Front Plant Sci. 2024 Mar 14;15:1358974. doi: 10.3389/fpls.2024.1358974. eCollection 2024.
Sexual reproduction of Zygnematophyceae by conjugation is a less investigated topic due to the difficulties of the induction of this process and zygospore ripening under laboratory conditions. For this study, we collected field sampled zygospores of and three additional strains in Austria and Greece. Serial block-face scanning electron microscopy was performed on high pressure frozen and freeze substituted zygospores and 3D reconstructions were generated, allowing a comprehensive insight into the process of zygospore maturation, involving storage compound and organelle rearrangements. Chloroplasts are drastically changed, while young stages contain both parental chloroplasts, the male chloroplasts are aborted and reorganised as 'secondary vacuoles' which initially contain plastoglobules and remnants of thylakoid membranes. The originally large pyrenoids and the volume of starch granules is significantly reduced during maturation (young: 8 ± 5 µm³, mature: 0.2 ± 0.2 µm³). In contrast, lipid droplets (LDs) increase significantly in number upon zygospore maturation, while simultaneously getting smaller (young: 21 ± 18 µm³, mature: 0.1 ± 0.2 and 0.5 ± 0.9 µm³). Only in the LD volume increases (34 ± 29 µm³), occupying 50% of the zygospore volume. Mature zygospores contain barite crystals as confirmed by Raman spectroscopy with a size of 0.02 - 0.05 µm³. The initially thin zygospore cell wall (0.5 µm endospore, 0.8 µm exospore) increases in thickness and develops a distinct, electron dense mesospore, which has a reticulate appearance (1.4 µm) in sp. from Greece. The exo- and endospore show cellulose microfibrils in a helicoidal pattern. In the denser endospore, pitch angles of the microfibril layers were calculated: ~18 ± 3° in , ~20 ± 3° in sp. from Austria and ~38 ± 8° in sp. from Greece. Overall this study gives new insights into sp. zygospore development, crucial for survival during dry periods and dispersal of this genus.
由于在实验室条件下诱导接合藻纲的有性生殖过程以及合子孢子成熟存在困难,因此对其进行的研究较少。在本研究中,我们在奥地利和希腊采集了野外样本中的合子孢子以及另外三个菌株的合子孢子。对高压冷冻和冷冻替代后的合子孢子进行了连续块面扫描电子显微镜检查,并生成了三维重建图像,从而能够全面了解合子孢子成熟过程,包括储存化合物和细胞器的重排。叶绿体发生了巨大变化,在幼年期含有双亲的叶绿体,雄性叶绿体退化并重新组织成“次生液泡”,这些液泡最初含有质体小球和类囊体膜的残余物。在成熟过程中,原本较大的蛋白核和淀粉粒的体积显著减小(幼年期:8±5立方微米,成熟期:0.2±0.2立方微米)。相比之下,合子孢子成熟时脂滴(LDs)的数量显著增加,同时体积变小(幼年期:21±18立方微米,成熟期:0.1±0.2和0.5±0.9立方微米)。只有在[具体物种]中脂滴体积增加(34±29立方微米),占合子孢子体积的约50%。拉曼光谱证实成熟的合子孢子含有重晶石晶体,尺寸为0.02 - 0.05立方微米。最初较薄的合子孢子细胞壁(约0.5微米的内膜,约0.8微米的外膜)厚度增加,并形成了一层明显的、电子密度高的中膜,在来自希腊的[具体物种]中,该中膜呈现出网状外观(约1.4微米)。外膜和内膜呈现出螺旋状的纤维素微纤丝。在较致密的内膜中,计算了微纤丝层的螺距角:在[具体物种]中约为18±3°,在来自奥地利的[具体物种]中约为20±3°,在来自希腊的[具体物种]中约为38±8°。总体而言,本研究为[具体物种]合子孢子的发育提供了新的见解,这对于该属在干旱时期的生存和传播至关重要。