Seed structure and histochemistry in the palm Euterpe edulis

The Euterpe edulis embryo consists of a prominent single cotyledon, a very short radicle-hypocotyl axis and an epicotyl. The epicotyl is obliquely angled with respect to the cotyledon; consequently it corresponds to one of the two categories recognized for palm seeds by DeMason (1988 ). Parenchyma, protoderm and procambium can be distinguished on the basis of position and shape of their cells, which are highly vacuolated with one central vacuole and the cytoplasm restricted to a thin parietal layer. Initial cells from both apical meristems are also vacuolated but they have small vacuoles distributed around the nuclei. Silica occurs in cell walls of some protodermal cells. Raphides, silica bodies and tannins all occur occasionally in vacuoles, especially in the basal cotyledon region. Most embryo cells lack storage reserves and exhibit an active state, with numerous mitochondria, RER cisternae and Golgi apparatus, indicating a strategy of continuous development without the interposition, at maturity, of a dry state. The endosperm consists of living cells with very large nuclei and thickened cell walls. Similar to the endosperm of other studied palm species, their cells exhibit a quiescent appearance with lipid, protein, minerals (in the cytoplasm) and mannans (in the cell walls) as the insoluble storage reserves.  © 2004 The Linnean Society of London, Botanical Journal of the Linnean Society , 2004, 145 , 445–453.     

Recalcitrant seeds of horse chestnut lack protein bodies

In recalcitrant seeds of horse chestnut (Aesculus hippocastanum L.), the bulk of protein in axial organs and cotyledons is accounted for by water-soluble proteins (albumins). In the cells of embryo, proteins are predominantly located in the cytosol, whereas the fraction of cell structures precipitate in the range from 1000 to 20000 g, accounting for only an insignificant part of total protein. Among the proteins of this fraction, there were no major components that could play a role of storage proteins. The aim of this work was to study deposition of protein in the vacuoles of cells of recalcitrant seeds of horse chestnut. Light microscopy and specific staining of protein and phytin did not detect protein bodies in the vacuoles of axial organs and cotyledons. Electron microscopy revealed traces of phytin in the vacuoles, but there were no formed globoids or considerable amount of protein therein. It is possible that precisely the absence of typical storage proteins and genetically determined desiccation in the course of maturation of recalcitrant seeds of horse chestnut stipulated preservation of the vacuoles that in mature recalcitrant seeds were not transformed into protein bodies.     

Biogenesis of Protein Bodies in Embryonic Axes of Soybean Seeds (Glycine max. cv. Enrei)

Protein bodies in embryonic axes of soybean seeds have inclusion structures containing phytin globoids. Biogenesis of the protein bodies during seed development was examined by transmission electron microscopy. Protein bodies in embryonic axes originated from central vacuoles. The central vacuole in embryonic axes subdivided into smaller vacuoles with internal membranous structure. Then the subdivided vacuoles were directly associated with rough endoplasmic reticulum (rER), and were filled with proteinaceous matrix from the peripheral region. The increase of matrix was simultaneous with accumulation of β-conglycinin estimated by SDS-polyacrylamide gel electrophoresis. Glycinin-rich granules that had been found in developing cotyledons were not observed in embryonic axes. After proteinaceous matrix filled the protein bodies, electron-transparent regions presumably surrounded by a single membrane appeared in the matrix. Phytin globoids were constructed in this internal structures of protein bodies as the final step of protein body formation.     

Hormonal Complex and Ultrastructure of Maturing Aesculus hippocastanum Seeds

The content and temporal changes in the endogenous IAA, cytokinins, gibberellin-like compounds (GLC), and ABA were determined during horse chestnut (Aesculus hippocastanum L.) seed development (the stages of embryo axis development, its active growth, and storage compound deposition). The active growth of the embryo was characterized by the highest amounts of free phytohormones. Later, by the end of seed maturation, we observed the accumulation of the bound forms of IAA and ABA and a trend to a decrease in the content of free IAA, zeatin, and GLC (butanol fraction). The electron-microscopic examination of the embryo from the mature seed demonstrated that some structural components of the cytoplasm were similar in the cells of embryo axes and cotyledons. During the entire period of maturation, the embryo cells preserved native vacuoles and protein bodies were not formed. Thus, the structure of cotyledonary and axial cells and the distribution of free and bound phytohormones in the horse-chestnut seeds are similar to those in maturing seeds characterized by exogenous dormancy.     

Stomatal myrosin cells in Caricaceae. Taxonomic implications for a glucosinolate-containing family

Jørgensen, L. B. 1995. Stomatal myrosin cells in Caricaceae. Taxonomic implications for a glucosinolate-containing family. — Nord. J. Bot. 15: 523–540. Copenhagen. ISSN 0107–055X.
Stomatal myrosin cells are shown to be present in Carica goudotiana, C. papaya, C. guercifolia and Jarilla caudata of the Caricaceae. They are found in the epidermis of all green parts, viz. leaves, stems, and immature fruits, and also of cotyledons from germinating seeds. They are structurally the same as the stomatal myrosin cells in other glucosinolate- and myrosinase-containing families, Resedaceae, Tovariaceae and Bata-ceae, and comparable to the idioblastic myrosin cells from e.g. Brassicaceae and Capparaceae. The stomatal myrosin cells have vacuoles filled with proteinaceous material and cytoplasm rich in rough endoplasmic reticulum. During embryogenesis single adaxial epidermal cells of the cotyledons can be distinguished as myrosin cells, since their protein bodies are homogeneous and without globoids and become filled with protein earlier than the protein bodies with globoids present in the other epidermal cells or the mesophyll cells of the cotyledons. This is analogous to myrosin cells in embryos from Brassicaceae. In germinating seeds the single epidermal myrosin cells divide to form precursors of guard cells, thus turning into stomatal myrosin cells in the green cotyledons. The presence of myrosin cells supports a taxonomic treatment of Caricaceae together with the majority of the other glucosinolate-containing families in the major glucosinolate clade.     

Subcellular Organization of Developing Embryos of Bidens cernua

Anatomical and submicroscopical changes in the cotyledons and radicles of Bidens cernua L. have been studied at five developmental stages. In the subcellular structure, these two plant organs are relatively similar but each developmental stage is characterized by a distinct fine structure. Protein bodies, which occupy the bulk of the cell in dormant embryos, develop as filling products of vacuoles. Ribosomes are seen abundantly at this stage, both in the nucleus and the plasma strands. Small vesicles which are the initials of globoids can be detected in the vacuoles even of rather young cells. They later associate at the periphery of protein masses secreted in the vacuoles. Many light globoids are seen in the protein bodies of mature cells. Some amyloplasts are present in the early developmental stages but not in the dormant cells. The endoplasmic reticulum becomes filled with osmiophilic storage fat, and later many spherosomes are seen between the protein bodies. Some osmiophilic material is also found in the intercellular spaces.     

The Cytological and Histochemical Studies of Developing Soybean,Cotyledons

In the late globular proembryos, three regions could be identified, i. e. the cotyledon primordium, the epiphysis and the hypocotyl-hypophysis. In the cotyledon primordia, the mitotic frequency of the cells was comparitively high, the directions of the mitotic planes were mostly perpendicular to the long axis of the embryo, the size of the nucleolus was comparitively large, and the cytoplasm density was high. In the epiphysis region, however, the mitotic frequency of the cells was low, the size of the nucleolus was small, and as the first pair of leaf primordia appeared the mitotic frequency of the cells in that region began to increase. In the hypocotyls hypophysis region the mitotic frequency of the cells as well as the size of the nucleolus lied in between the corresponding values of those of the above two regions, the cytoplasm density was low and the size of the vacuoles was large. As the proembryo continued to develop the direction of the mitotic plane changed gradually, from mostly perpendicular to the long axis of the embryo to mainly inclined, or even parallel to that axis. As a result, the proembryo developed from a heart-shaped embryo into a torpedo-shaped embryo. After the first pair of leaf primordia appeared from the young embryo, the vacuoles in the cells of the cotyledons grew in size rapidly. About twenty to twenty five days after flowering, the starch grains, the protein bodies and the lipid granules began to accumulate in the cells of the cotyledons and gradually increased both in size as well as in quantity. About fifty days after flowering the diameter of the starch grains reached its maximum value of 6.2–7.0 μm, and decreased in value thereafter till the time of harvesting when most of the starch grains disappeared except those in the palisades. On the other hand, fifty to sixty days after flowering, the diameters of the lipid granules and of the protein bodies reached their maximum values of 5.4–7.0 μm and 6.2–7.0 μm, respectively. The observation revealed that the formation of the protein bodies was related to the vacules.     

Energy dispersive X-ray analysis of protein bodies in Protea compacta cotyledons

Summary The elemental composition of globoids in the protein bodies of Protea compacta cotyledons was studied by means of energy dispersive X-ray analysis. The globoid crystal was rich in phosphorus and calcium with lesser amounts of magnesium and potassium suggesting the presence of phytin in these structures.Abbreviation EDX energy dispersive X-ray analysis     

Protein bodies from the cotyledons of Cytisus scoparius L. (Link). Ultrastructure,isolation, and subunit composition of albumin,legumin and vicilin

The structure of protein bodies differs in the upper and lower parts of the cotyledons of mature seeds of Cytisus scoparius L. The palisade-mesophyll cells contain essentially homogeneous protein bodies, without globoids, but the protein bodies of the spongy-mesophyll cells are heterogeneous, with numerous globoids. Albumins, legumins and vicilins were selectively extracted from isolated protein bodies and their subunits separated by SDS-PAGE, under non-reducing and reducing conditions.Abbreviations SDS-PAGE sodium dodecyl sulfate-polyacrylamide gel electrophoresis     

Seed Structure and Localization of Reserves inChenopodium quinoa

The three areas of food reserves in quinoa seeds are: a largecentral perisperm, a peripheral embryo and a one to two-celllayered endosperm surrounding the hypocotyl-radicle axis ofthe embryo. Cytochemical and ultrastructural analysis revealedthat starch grains occupy the cells of the perisperm, whilelipid bodies, protein bodies with globoid crystals of phytin,and proplastids with deposits of phytoferritin are the storagecomponents of the cells of the endosperm and embryo tissues.EDX analysis of the endosperm and embryo protein bodies revealedthat globoid crystals contain phosphorus, potassium and magnesium.These results are compared with studies on other perispermousseeds published to date.Copyright 1998 Annals of Botany Company Chenopodium quinoa,EDX analysis, phytoferritin, phytin, protein bodies, quinoa, seed structure, seed reserves, starch grains.     

冠果草种子萌发过程的组织化学动态

冠果草的种子中没有胚乳,营养物质贮藏在胚中,其成分主要是淀粉和蛋白质。胚各部分的物质积累情况差异较大,子叶和下胚轴细胞中的淀粉粒、蛋白体数目多、体积大,胚芽和胚根分生细胞中则只贮藏少量的淀粉粒、蛋白体。在种子萌发过程中,胚各部分的淀粉粒逐渐解体,至二叶幼苗期全部消失。蛋白体的降解有严格顺序,远离胚芽的细胞中蛋白体降解较早,胚芽附近细胞中的降解较晚,而且胚芽细胞中还有新的蛋白体形成。单个蛋白体的降解     

Development of protein bodies in cotyledons of Fagus sylvatica

Electron microscopic analysis of cotyledons of beech ( Fagus sylvatica ) at different stages of seed maturation indicates that protein bodies originate by gradual subdivision of the vacuoles in which reserve proteins are deposited. The majority of protein bodies show a proteinaceous matrix and a number of globoid inclusions of different sizes. In a small number of cells, druse-like inclusions were observed. Analysis by SDS-PAGE of proteins extracted from isolated protein bodies shows that the majority correspond to beech seed storage globulins.     

Ultrastructure of Protein Bodies and Plastids in Cotyledon of Nelumbo nucifera Gaertn.at Seed Germination

The present article deals mainly with the formation and dissolution of protein bodies and development of plastids in cotyledon cells of Nelumbo nucifera during seed germination. Electron microscopic studies reveal that protein bodies are formed after imbibition of the cotyledons before germination. They are produced through accumulation of protein material in small vacuoles delivered from the exudates of endoplasmic reticulum or by fragmentation of endoplasmic reticulum itself. In the period of germination, most of the material in the protein bodies dissolute and they coalesce with each other forming large vacuoles. The protein residue of the vacuoles condenses into small blocks with high electron density adhering to the tonoplast or freely floating in the vacuole. Thus, it suggests that the protein bodies of the germinating N. nucifera cotyledons are originated from vacuoles formed by endoplasmic reticulum. Part of the plastids found in cotyledonous cells of mature N. nucifera seeds exists as proplastids. They develop continuously after imbibition of the cotyledons. During the period of seed germination, many concentric lamellae are developed along the plastid membrane on which they later coalesce with the neighboring concentric lameUae forming loosely organized prolamellar bodies which condense into paracrystalline lattices. No ribosomes are present in the inter spaces of paracrystatline lattice. One to several prolamellar bodies can be developed in one plastid.     

Ultrastructure of post-fertilization development in the red alga Nienburgia andersoniana (Delesseriaceae, Ceramiales, Rhodophyta)

The ultrastructure of post-fertilization development in Nienburgia andersoniana (J. Ag.) Kyl. is described. Above the auxiliary cell there is a group of four sterile cells. The presence of abundant storage products (starch granules, lipid bodies and protein crystals) in these cells indicates that the sterile cells function as nutrient suppliers to the young auxiliary and gonimoblast cells of the carposporophyte during its early steps of development. Following fertilization and transfer of the diploid nucleus to the auxiliary cell, the trichogyne disappears and large multinucleate gonimoblast initials are produced. These subsequently produce generative gonimoblast cells which cleave successively to form young carpospores. Those of the gonimoblast cells which will not differentiate into carpospores are transformed into cells producing mucilage. Both kinds of gonimoblast cells contain plastids, starch granules, cytoplasmic concentric membrane bodies and small vesicles. Dark-staining spherical masses occurring in the cytoplasm of the auxiliary and gonimoblast cells may represent degenerating haploid nuclei. Septal plugs interconnecting the auxiliary cell and gonimoblast cells increase considerably in size during carposporophyte development. The fusion cell at the late stage of carposporophyte development appears degenerative. Young carpospores have plastids and mitochondria, and concentric membrane bodies that will form mucilage sacs. Medium-aged carpospores have fully developed plastids, starch granules and fibrous vacuoles. Mature carpospores possess, in addition, cored vesicles. The inner pericarp cells contribute large amounts of mucilage to the cytostocarpic cavity and eventually are consumed. © 2003 The Linnean Society of London, Botanical Journal of the Linnean Society , 2003, 142 , 289–299.     

Histochemical and ultrastructural studies on <Emphasis Type="Italic">Salix alba</Emphasis> and <Emphasis Type="Italic">S. matsudana</Emphasis> seeds

Mature seeds of Salix alba L. and Salix matsudana Koidz. are exendospermous and consist of an embryo and a seed coat. Ultrastructural studies show the presence of protein bodies, lipid bodies, chloroplasts, and a nucleus in the cells of most of the embryo tissues. Protein bodies always contain two or more globoid crystals. Energy-dispersive X-ray analysis of globoid crystals revealed the presence of P, K, Mg and Ca as the main constituents in all tissues. The chloroplasts present well-developed grana and, frequently, starch grains in the stroma. In cells of apical meristems, plastid endomembranes are non-organised in grana and deposits of phytoferritin are present in the stroma. Some cells of the subdermal layers of the cotyledons and hypocotyl-radicle axis present a large central vacuole and a narrow peripheral band of cytoplasm within which the protein bodies are scarce. Seeds of the two species studied here have recently been characterised as orthodox with short viability. The present study was carried out in an attempt to advance in the characterisation of these seeds as part of a comprehensive study of Salicaceae seeds.     

Distribution of minerals in quinoa (Chenopodium quinoa Willd.) seeds

The distribution of minerals in quinoa (Chenopodium quinoa Willd.) seed was examined using energy dispersive X-ray microanalysis (EDX) in combination with scanning electron microscopy (SEM). Phosphorus, K, and Mg coincided in localization in embryonic tissue. Since phytin globoids have been known to localize in protein bodies in embryonic cells of quinoa seed, it is thought that P is attributed to phytic acid and that K and Mg form to phytate. Calcium and K were present in the pericarp, where the cell wall is thickly developed, suggesting that these minerals are associated with pectin. Sulfur occurred in embryonic tissues, which would be derived from sulfur amino acid residues of storage proteins concentrated in the tissues. Abrasion of quinoa seeds resulted particularly in decrease in Ca content.     

An unusual case of epigeal cryptocotylar germination in Rollinia salicifolia (Annonaceae)

An unusual case of epigeal cryptocotylar germination found in Rollinia salicifolia Schltdl. (Annonaceae) is described and is discussed in relation to the terminology used for germination studies. The terms cryptocotylar and phanerocotylar are used to describe the permanence of cotyledons within the seed coat or endocarp; the terms epigeal and hypogeal are used to refer the position of cotyledons in relation to ground level. The terms to describe position about ground level and permanence of cotyledons within the seed coat or endocarp are not used simultaneously in many papers, and some authors consider the terms cryptocotylar and hypogeal to be synonyms. Cases of epigeal cryptocotylar germination seem to be scarce in the literature. The morphological characters shown by R. salicifolia seeds and seedlings − a non-chlorophyllous embryo, abundant endosperm, thick woody seed coat, thickened hypocotyl and non-photosynthetic haustorial cotyledons − are closely related to its epigeal cryptocotylar germination. This is the first record of this type of germination in Argentina.  © 2004 The Linnean Society of London, Botanical Journal of the Linnean Society , 2004, 146 , 53–56.     

Ultrastructural and biochemical investigations of protein mobilization of Mucuna pruriens (L.) DC. cotyledons and embryo axis

The mobilization of storage reserves, with particular emphasis on storage proteins of Mucuna pruriens (L.) DC., cotyledons, and embryo was investigated from the ultrastructural and biochemical points of view. Proteins and starch were the two main storage substances in cotyledons, and proteins and lipids were the main ones in the embryo. Embryo protein bodies were smaller and fewer in number than those of cotyledons. Structural and ultrastructural data determined between 24 and 48 h after imbibition and between 48 and 72 h after imbibition, the end of significant embryo and cotyledon protein mobilization, respectively, indicating more precocious storage protein mobilization in the axis than cotyledons. Moreover, storage protein mobilization in embryo and cotyledons occurred before the end of germination. Water soluble proteins were separated by sodium dodecyl sulfate polyacrylamide gel electrophoresis, producing 29 bands with molecular weights from 14 to 90 KDa. Embryo extract contained more proteins than cotyledon extract, contained seven characteristic bands, and showed a higher variability of the optical density trend than cotyledon.     

莲种子萌发和幼苗生长时期营养物质的代谢变化

莲子叶细胞中储存了丰富的营养物质,主要为蛋白质、淀粉和淀粉质体DNA.这些贮藏物质为种子萌发和幼苗的生长提供必需的能量和养料.通过组织化学和显微镜观察,研究莲从种子萌发到植株生长至具有4个节时,子叶中贮藏物质消耗的全过程.在此过程中,子叶中的贮藏物质不断降解,营养物质发生转运.蛋白体首先发生降解,其大量降解主要发生在幼苗三叶期.淀粉质体降解时会聚集成团,之后体积逐渐减小,最后完全降解.种子萌发后65天是子叶贮藏物质消耗末期,淀粉质体DNA的含量比萌发后20天的三叶期明显减少.细胞壁的形态结构发生多种形式的变化,细胞壁发生的这些变化与子叶细胞间物质的运输有关.含多糖的球形颗粒通过维管束在子叶中运输.