银耳（Tremella fuciformis）原基分化前期双核菌丝细胞和分生孢子的边缘体与质膜体

本文报道银耳（Ｔｒｅｍｅｌｌａｆｕｃｉｆｏｒｍｉｓ）原基分化前期．在双核菌丝的幼细胞、成熟细胞和分生孢子中,与质膜相关联的两类膜结构──边缘体和质膜体的形成与功能。根据相似结构的存在．支持小泡或多泡体排出质膜之外附在细胞壁上成为边缘体和参于细胞壁合成的假定。银耳原基分化前期．双核菌丝迅速分裂的幼细胞．其质膜内陷产生泡状质膜体,内含数个小泡,或产生膜状质膜体;在成熟细胞中．质膜内陷通常形成回旋的膜结构──膜状质膜体．内含１—２个电子致密小泡．当这两类质膜体脱离质膜进入细胞质后,有的膜层和小泡局部被消化．因此,推断质膜体具有内吞和输送养料的作用。另外．在桶孔隔膜闭塞一侧电子致密度高的细胞质中．还观察到一种罕见的只有单个膜层的质膜体．其内充满３个电子致密小泡．估计它的形成与功能同膜状质膜体相似。作者认为．桶孔闭塞和质膜体的出现是与银耳原基细胞分化有关联的两个重要特征。最后,在成熟细胞中,尚可以观察到质膜体的膜层能够散开形成内质网．因此．内质网也可以来源于质膜体。     

The fine structure of psychrophilic and mesophilic Rhodotorula rubra

Transmission electron microscopy of thin sections of two mesophilic and a psychrophilic Rhodotorula rubra revealed structures normally associated with yeast. The capsule of all three strains was thicker in the cells grown in glucose than those grown in glucose-free media. The cell wall of all three strains showed more lamellae in the cells grown in a medium containing glycerol. Budding was of the Rhodoturula type. Endoplasmic reticula running parallel to the nucleus were commonly observed in the psychrophiles but not in the mesophiles. In the psychrophile, in association with the plasmalemma, lomasomes and plasmalemmasomes were observed. Giant mitochondria were commonly seen in the cells grown in a fermentable carbohydrate-free medium. Vacuoles were mostly empty.     

Ultrastructure and Development of Sclerotia of Botrytis cinerea Pers. in vitro

The development of sclerotia of Botrytis cinerea was examined at four stages during their maturation. The surface structure developed a network of profusely branched hyphae through their coalescence to a compact sclerotial body which was maturated by the deposition of melanin pigment. A characteristic feature of the hyphal cells of B. cinerea during the later stages of development was the presence of paramural bodies (plasmalemmasomes and lomasomes). Electrondense bodies with a limiting double-membrane congregated against the transverse septa of hyphal cells as sclerotia matured and may migrate from cell to cell through septal pores. We suggest that these and the lipid bodies found in hyphal cells may have a storage function in the resting sclerotia.     

Fine Structure of Cryptococcus neoformans Grown In Vitro as Observed by Freeze-Etching

Cryptococcus neoformans grown on culture media was observed by the freeze-etching technique. In the capsule, short fibrils were seen when freezeetched. This organism was unique in the appearance of the cell wall, which showed two strata. The outer one was dense with particles of about 20 nm in diameter, whereas the inner one was sparse in particles. The appearance of the cell membrane of this organism differed distinctly depending on the culture media. When grown on glycerol medium, the cell membrane possessed, as do other yeasts, clear but somewhat longer and curved invaginations. The membrane of cells grown on nonglycerol medium exhibited, however, only a few invaginations of irregular shape. Instead, characteristically of this organism, the cell membrane showed round depressions of 40 to 200 nm in diameter which were the surface view of the paramural bodies. In cross-fractured cells, both types of paramural bodies were found. Some of them contained a single vesicle of about 50 nm in diameter. These seem to play a role in secreting the cytoplasmic vesicles. Data suggesting the existence of multivesicular bodies in the cytoplasm and multivesicular lomasomes were also obtained. Some of the baglike paramural bodies showed multilayered membrane. These are thought to be plasmalemmasomes. This organism was similar to other yeasts reported in other respects.     

I Lomasomi: Loro Probabili Rapporti con la Crescita per Distensione della Parete Cellulare

Abstract

« Lomasomes »: their probable role in the expansion growth of the cell wall. — It was previously reported that lomasomes are present in higher plant cells. In a preliminary comunication Authors described the morfological characteristics of the lomasomes and their position in the cell. It was shown that lomasomes vary in organization which appears to be granular or vescicular and in distribution along the cell wall. Both these characters seemed directly related with the level of cellular differentiation.

In this paper it has been reported that the number of lomasomes per cell was sharply decreased when Avena Coleoptiles were illuminated per 3 hours. During this period of time also the growth of the Coleoptiles was inhibited about 8%. These data seem favorable to the hypothesis that lomasomes are tigtly involved in the mechanisms controlling the expansion growth of the cell wall.     

La Flora E La Vegetazione Pel Capo S. Elia (Sardegna Meridionale)

Abstract

Morphological organization of the lomasomes. — From a study on morphological organization of the lomasomes, in Avena coleoptile cells, it has been reported: 1) lomasomes form is quite variable, nevertheless, usually they resemble to a cone having a flattened tip and the base line against the cellular wall. 2) the external border of the lomasoma towards the cytoplasm is represented by the plasma membrane; such external profile results very sinuous and deep invaginations are present. 3) the internal structure is characterized by the presence of an unstructurated matrix containing spherical vescicles, flattened vescicles and tubules all showing an higher density to the electron radiations than the cytoplasmic matrix. Both vescicles and tubules are delimited by a single membrane.     

Histochemical localization of thiamine pyrophosphatase in the lomasomes in asci of Arthroderma vanbreuseghemii

Thiamine pyrophosphatase localization in asci of Arthroderma vanbreuseghemii was investigated histochemically by electron microscopy. The reaction product of this enzyme was demonstrated in some paramural membranous structures that are believed to represent lomasomes. This observation suggests that at least a certain number of lomasomes might be involved in cell wall synthesis and thus behave in a manner similar to the Golgi apparatus in higher eukaryotic cells.     

Lomasomes and plasmalemmasomes in fungi

Summary Electron microscope observations of fungal hyphae and yeast-like cells, using conventional fixation methods and freeze-etching, demonstrate that plasmalemmasomes are not fixation artifacts. The small invaginations of the plasmalemma observed in aldehyde-fixed preparations are also present in frozen-etched samples. The morphology of plasmalemmasomes in the species examined is variable and ranges from vesicles or tubules within the plasmalemma invagination to parallel arrays of membrane lamellae. Plasmalemmasomes thus appear to be primarily excess plasma membrane that has accumulated, perforce, endocellularly. Lomasomes, in contrast, appear to be accumulations of ejected material between the plasmalemma and cell wall that have become sequestered by the deposition of wall material.     

Plasmalemmasomes in cotyledon leaves of germinating Vigna radiata L. (mung beans)

Abstract. Storage parenchyma, vascular parenchyma and phloem companion cells are found adjacent to sieve tubes in the vascular bundles of cotyledon leaves of mung bean ( Vigna radiata L.) seedlings. The paramural bodies of storage parenchyma cells are characterized by flask shaped invaginations of the plasmalemma whereas the plasmalemmasomes of the adjacent vascular parenchyma and companion cells consist of numerous finger-like evaginations which are not enclosed in plasmalemma pockets. Phloem associated transfer cells are not present and it is suggested that the fine tubular plasmalemmasomes may act as the interface between apoplast and symplast in the transport of rapidly mobilized reserves during germination. Tubular structures observed within the protoplasts of storage cells close to vascular tissue were also observed in vascular parenchyma and companion cells between the plasmalemmae and cell walls.     

Una Struttura Comparabile Con I Lomasomi Nelle Cellule Austoriali di Cuscuta Pentagona Engelm

Abstract

A structure comparable with the lomasomes in baustorial cells of « Cuscuta pentagona » Engelm. — Electron microscopic observations of haustorial cells in « Cuscuta pentagona » revealed to the A. the presence of some vesicular structures, outside the plasma membrane, comparable to the lomasomes of Moore and McAlear. The vesicles usually group in a bag of the plasma membrane and show an envelope consisting of unit membrane; their shape and size are variable and some of them are not well distinct while some others show ribosome-like bodies inside .In the examined cells the plasma membrane shows prominences which are in connection with the vesicle membrane, so that the A. thinks it possible the derivation of the vesicles from the peripherical cytoplasm. The function of these structures is not yet explained; they are only found in non photosyntetic cells, such as some Mycophyta, dark grown « Avena » coleoptiles and dodder's haustorial cells. The previously ultrastructural researchs on dodder have not pointed out lomasomes, which seem to be exclusive of the haustoria, so that it is possible to suppose a connection between the lomasome function and that of the haustoria.     

Electron microscope study of Cryptostroma corticale

An ultrastructural study of Cryptostroma corticale has been carried out with scanning and transmission electron microscopes. The usual features in fungi, as well as features characteristic of the family, were shown. It was noted that lomasomes and myelin-type structures were demonstrated by the two fixatives used. Their significance is discussed.     

Plasmalemmasome development in Trichophyton mentagrophytes grown at suboptimal temperature

When the dermatophytic fungus Trichophyton mentagrophytes is cultivated at the suboptimal temperature of 19 degrees C, the plasmalemma of the youngest cells appears to be associated with a variety of membranous bodies, the number of which is much greater than at the optimum temperature of 28 degrees C. These structures can be indicated as plasmalemmasomes both for morphological characteristics and cytochemical reactivity. A possible correlation between the suboptimal condition and plasmalemmasome ontogeny and function is proposed.     

PIP1 Aquaporins Are Concentrated in Plasmalemmasomes of Arabidopsis thaliana Mesophyll

The PIP1 subfamily of water channel proteins (aquaporins) constitute about 1% of the plasma membrane (PM) proteins from Arabidopsis thaliana leaves. Immunogold electron microscopy has confirmed their localization at the PM of mesophyll cells. Very high labeling density at PM invaginations known as plasmalemmasomes was observed. Therefore, we suggest that these subcellular structures are involved in water transport between the apoplast and the vacuole.     

Arabinogalactan-rich glycoproteins are localized on the cell surface and in intravacuolar multivesicular bodies

We investigated the subcellular distribution of antigenic sites immunoreactive to the monoclonal antibody 16.4B4 (PM Norman, VPM Wingate, MS Fitter, CJ Lamb [1986] Planta 167: 452-459) in tobacco (Nicotiana tabacum) leaf cells. This antibody is directed against a glycan epitope in a family of plasma membrane arabinogalactan proteins of 135 to 180 kilodaltons, elaborated from a polypeptide of relative molecular mass 50 kilodaltons (PM Norman, P Kjellbom, DJ Bradley, MG Hahn, CJ Lamb [1990] Planta 181: 365-373). We demonstrated by immunogold electron microscopy that the epitope reactive with monoclonal antibody 16.4B4 is localized on the cell surface in the leaf parenchyma cell periplast. The 16.4B4 antigen is also localized in multivesicular invaginations of the plasma membrane also known as plasmalemmasomes, implying a biochemical and, hence, functional interrelationship between these structures. Monoclonal antibody 16.4B4 also labels intracellular multivesicular bodies that appear to represent internalized plasmalemmasomes. Antibody reactivity was also observed in partially degraded multivesicular bodies sequestered within the central vacuole. We propose that the subcellular distribution of the epitope reactive with monoclonal antibody 16.4B4 defines a plasmalemmasome (or multivesicular body-mediated) pathway for the internalization of the periplasmic matrix for vacuolar mediated disposal. The multivesicular bodies appear to be equivalent to the well-characterized endosomes and multivesicular bodies of animal cells involved in the internalization and lysosome-mediated degradation of extracellular materials.     

Mise en évidence par le cryodécapage de lomasomes dans la basidiospore de Hypholoma fasciculare (Huds. ex Fr.) Kummer

Summary Lomasomes were shown to be present in mature basidiospores of Hypholoma fasciculare using the freeze-etching technique. Grooves in the plasmalemma were also generally observed. It is suggested that lomasomes are related to the elaboration of the chitinous spore wall and, in accordance with the views of Campbell, plasmalemma grooves are connected with the melanisation of its outer parts.     

Electron microscopic studies of saprobic and parasitic forms of Coccidioides immitis

During studies of both saprobic and parasitic cycles of Coccidioides immitis, we found that the hyphae contained septa with simple pores, Woronin bodies, pinocytotic vesicles and/or lomasomes. The alternating thallic arthroconidia were released by fracturing of the adjacent sterile cells. The endospores were formed by progressive cleavage of the spherules. The taxonomic classification of C. immitis still remains obscure.     

ULTRASTRUCTURE OF THE CONCHOCELIS STAGE OF THE MARINE RED ALGA PORPHYRA LEUCOSTICTA1

The ultrastructure of the Conchocelis or filamentous stage of Porphyra leucosticta was investigated. Each cell contains 1 or 2 parietal, stellate chloroplasts with a single pyrenoid in each chloroplast. The centrally located nucleus is irregularly shaped and contains 1–2 nucleoli. The cytoplasm has typical floridean starch grains and nonmernbrane-bound lipid bodies. The cell wall is divided into an outer and an inner wall. Many lomasomes are associated with the cell membrane. Pit connections are found between cells, and their taxonomic significance is discussed.     

Rhizobium sp. Degradation of Legume Root Hair Cell Wall at the Site of Infection Thread Origin

Using a new microinoculation technique, we demonstrated that penetration of Rhizobium sp. into the host root hair cell occurs at 20 to 22 h after inoculation. It did this by dissolving the cell wall maxtrix, leaving a layer of depolymerized wall microfibrils. Colony growth pressure “stretched” the weakened wall, forming a bulge into an interfacial zone between the wall and plasmalemma. At the same time vesicular bodies, similar to plasmalemmasomes, accumulated at the penetration site in a manner which parallels host-pathogen systems.     

Fine Structure of Established Callus Cultures of Taraxacum officinale Weber

The nodular, brown callus cultures of Taraxacum officinale growslowly on a modified White's medium. A section of nodule revealsa meristematic layer bounded both internally and externallyby parenchymatous tissue. No other types of tissue occur withinthe callus. The cells of the inner parenchyma are often compressedand senescing, whereas in the outer tissue localized de-differentiationapparently contributes to the development of new nodules duringcallus growth. Fine-structural observations of both meristematic and parenchymatoustissues show the normal complement of higher plant cell organellesexcept for the apparent absence of cytoplasmic microtubules.The rough endoplasmic reticulum cisternae are often alignedparallel to the cell wall or in whorls and may show pores, thusresembling annulate lamellae. Numerous lipid bodies, up to 7µm wide, occur and these are sometimes invested by arraysof apparently membranous material. The mitochondria are frequentlyhighly branched and often show a scalariform arrangement ofcristae. The plastids show few internal membranes despite cultureof the callus under continuous illumination. Lomasomes are very common in all cells and in the parenchymatissue membranous wall bodies also occur. The latter bodiesare much larger than lomasomes and consist of wall overgrowthsin which vesicular, myelin-like or isolated membranous elementsare enmeshed in fibrillar material. It is suggested that membranouswall bodies may originate from the amalgamation and subsequentproliferation of several adjacent lomasomes. Taraxacum officinale Weber, dandelion callus cultures, fine structure     

Ultrastructural changes accompanying mitosporogenesis inEctocarpus parvus

The plurilocular zoosporangium of Ectocarpus parvus Saunders in initiated as a uniseriate branch from a vegetative cell. Subsequent anticlinal and periclinal divisions of the cells leads to enlargement of the sporangium and the formation of multiple locules. Each locule containes a single biflagellate zoospore. Ultrastructural changes accompanying these events include a reduction in the size of chromatophores, a reduction in the number of dictyosomes and the appearance of plasmalemmasomes in later stages. Enlargement of the mitochondria and a decrease in size of the nucleus occur in the final stages of zoospore formation. Comparison with the vegetative and sporogenous cells of other brown algae are made.