A comparative study of periplast structure inCryptomonas cryophila andC. ovata (Cryptophyceae)

Summary Freeze-fracture followed by deep-etch was used with transmission electron microscopy to characterize and compare the periplasts of two cryptomonads,Cryptomonas ovata andC. cryophila. The periplast ofC. ovata consists of a dense surface mat of granular/fibrillar material overlying a series of polygonal plates attached to the undersurface of the plasma membrane (PM) at their upturned edges. Fracture faces of the PM reveal a highly stable substructure with distinct patterns of intra-membrane particles (IMPs) associated with the underlying plates; a role for the PM in plate development is indicated. The surface periplast component ofC. cryophila exhibits a cover of morphologically complex, overlapping heptagonal scales (termed rosette scales) in addition to elongate fibrils. The arrangement of IMPs within the PM is predominantly random and the inner periplast component consists of a sheet with regular pores where ejectisomes are located. The sheet does not appear closely associated with the PM. The combination of features exhibited by the periplast ofC. cryophila warrants its inclusion as a new type within theCryptophyceae.     

Periplast structure of the cryptomonad flagellateHemiselmis brunnescens

Summary The periplast ofHemiselmis brunnescens Butcher is a complex cell covering comprised of the plasma membrane (PM) sandwiched between a surface periplast component (SPC) and an inner periplast component (IPC). The SPC is revealed by deep-etching, and consists of hexagonal plates composed of tripartite subunits that appear to self-assemble into a crystalline layer with a hexagonal symmetry. Small scales (termed fibrillar scales) accumulate on the crystalline plates during cell growth, eventually forming a carpet that itself may appear crystalline when fully formed. Heptagonal rosette scales are occasionally observed on the surface as well. The position of the crystalline plates is precisely mirrored by both the E and P fracture faces of the PM. The plate proper is underlain by membrane with a high concentration of intramembrane particles (IMPs) while the bands of membrane underlying the plate borders lack IMPs. Access of subunits and fibrillar scales to the cell surface following initial plate formation appears to be at the plate boundaries. This study suggests that cryptomonad flagellates may provide model systems for studying the self-assembly of cell surface components, and for relating membrane structure to function, as evidence suggests a major role for the PM in mediating periplast assembly and development.     

Observations on the ultrastructure of the flagella and periplast in the Cryptophyceae

The flagella in Cryptomonas ovata Ehrenberg and two other un-named strains of Cryptomonas both bear stiff hairs with fine distal filaments of the same type as those found in the Xanthophyceae, the Chrysophyceae sensu stricto, the Phaeophyceae, the Bacillariophyceae, the Eustigmatophyceae and the Oomycetes. On the longer of the two flagella the hairs are 2·5 µm long and in two opposite rows whereas on the shorter flagellum they measure only 1 µm, are arranged in a single row and are more closely spaced. The long flagellum also bears a characteristic lateral swelling with a tuft of hairs of the same type as on the remainder of the flagellum, at approximately the level at which it emerges from the gullet. The hairs on the flagella of Hemiselmis rufescens Parke are distributed in a similar manner to those in Cryptomonas but they are more flexible and the swelling and tuft of hairs appear to be absent from the long flagellum. Hairs are apparently absent from the short flagellum of Chroomonas sp. The periplast in Cryptomonas ovata shows a hexagonal pattern in surface view and in sections of all three Cryptomonas strains appears as a typical plasmalemma underlain by a discontinuous layer of electron-dense material with variable substructure. The distribution of flagellar hairs and the structure of the periplast appear to be characters unique to the Cryptophyceae and these features emphasise the isolated position of this class of algae.     

Periplast development in cryptophyceae I. Changes in periplast arrangement throughout the cell cycle

Summary The cell covering (or periplast) of many cryptomonads consists of discrete plate areas precisely arranged over most of the cell periphery. Developmental changes in periplast arrangement that occur throughout the cell cycle are examined here forKomma caudata andProteomonas sulcata [haplomorph]. In both cryptomonads, pole reversal occurs during cytokinesis, necessitating major realignment of the plate areas. Growth of the periplast occurs by addition of new plate areas to specialized regions (termed anamorphic zones) located around the vestibular margins and along the mid-ventral line of cells. Development of the periplast from these regions enables elongation and lateral expansion of cryptomonads throughout cell growth. Observed differences in cell division and periplast development between these genera are closely associated with variations in the arrangement of anamorphic zones.     

Regular arrays of intramembranous particles in the plasmalemma of guard cell and mesophyll cell protoplasts of Vicia faba

Freeze fractures of the plasmalemma membranes of guard-cell and mesophyll protoplasts of Vicia faba demonstrate that the inner monolayer of the plasmalemma is compartmentalized into areas with distinct, highly organized structures. Between areas of intramembranous particles dispersed randomly on a relatively smooth fracture face, membrane domains showing an extremely regular planar, hexagonal array of particles are interspersed. The dimensions of these hexagonal lattices are about 0.5 m in diameter, the center-to-center spacing is about 22 nm, and the particle size is about 9 nm. The particle in the hexagonal arrays are accompanied by complementary pits in the opposite monolayer fracture of the plasmalemma membrane.The freeze-fracture preparation was performed by using an improved Leybold Bioetch device which provides a sufficiently high cooling rate and allows the omission of cryoprotectants, like glycerol.Presented by H. Schnabl on the Workshop on Plant Membrane Transport, Toronto, Canada, July 1979     

Observations on Rhinomonas reticulata comb. nov. and R. reticulata var. eleniana var. nov. (Cryptophyceae), with comments on the genera Pyrenomonas and Rhodomonas

Seven marine red strains of Cryptophyceae were examined using scanning and transmission electron microscopy. Six of these, possessing a nucleomorph housed within the pyrenoid and a periplast with distinctly hexagonal periplast areas, are assigned to Rhinomonas reticulata comb. nov. Rhinomonas reticulata var. eleniana var. nov. is described on the basis of the smaller size of the periplast areas. In a strain of the genus Pyrenomonas , which Rhinomonas otherwise resembles, the periplast areas appear more or less rectangular. Since it is impossible to know with certainty which red marine forms fall within the original concept of the genus Rhodomonas , the name Pyrenomonas should be preferred to a recent emendation of Rhodomonas.     

Morphology and ultrastructure ofOlisthodiscus luteus (Raphidophyceae) with special reference to the taxonomy

A flattened discoid flagellate collected from the Seto Inland Sea, Japan, has been examined by light and electron microscopy. This alga agrees well withClisthodiscus luteus Carter. It has two heterodynamic flagella emerging from a furrow on the upward side of the cell that contains six to 13 yellow-green parietal chloroplasts. It does not rotate but smoothly glide while swimming. The cell has a thin periplast lying between the plasmalemma and chloroplasts. Neither lipid bodies nor mucocysts are seen in the periplast. The pyrenoid matrix being free from thylakoids is penetrated by several cytoplasmic canals from various directions. There are no vesicles of periplastidal network in the narrow space between chloroplast envelope and chloroplast ER. The ultrastructural features ofO. luteus are unique, sharing certain characters with the raphidophycean algae but others withPseudopedinella pyriformis, a unique member of the Chrysophyceae.     

MICROMORPHOLOGY OF THE PERIPLAST OF CHROOMONAS SP. (CRYPTOPHYCEAE)1,2

An ultrastructural examination of the periplast of Chroomonas sp. revealed a surface pattern composed of rows of plate areas. The plate areas are delineated by a series of ridges, which emanate from a common line at the posterior cell end, and lateral grooves which intersect the anterior-posterior ridges. Small ejectosomes (trichocysts) are generally located at the intersection of the lateral grooves and the ridges. Size of the plate areas varies, being smallest at the posterior and anterior ends and largest in the midregion of the cell. The average plate area is 1 μ in length and 0.7 μ in width. In section the periplast is seen to consist of 3 intimately attached layers of which the middle (plasma membrane) layer is continuous with the gullet region, flagella, and ejectosome chambers. Trypsin digestion resulted in the disappearance of the inner and outer layers, and in the loss of periplast stiffness.     

Zum Feinbau des Periplasten und der Geißel von Trypanosoma brucei und Trypanosoma gambiense

Zusammenfassung Elektronenmikroskopische Untersuchungen an Geißelfibrillen und Mikrotubuli des Periplasten von Trypanosomen ergaben, daß beide Strukturen aus Protofilamenten aufgebaut sind. Die Protofilamente bestehen aus kettenförmig angeordneten globulären Untereinheiten von 45–50 Å Durchmesser. Die Mikrotubuli des Periplasten sind in ungefähr 150 Å-Abständen durch Querbrücken miteinander vernetzt. Es wird angenommen, daß diese Querbrücken durch abzweigende Protofilamente gebildet werden. Im Zusammenhang mit diesen Ergebnissen wird der Bau des Periplasten diskutiert.

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Ultrastructure of the periplast and the flagellum of Trypanosoma brucei and Trypanosoma gambiense

Summary Flagellar fibres and microtubules of the periplast of Trypanosomes are studied by electron microscopy. They both are shown to consist of protofilaments which are composed of globular subunits in beadlike array measuring 45–50 Å in diameter. The periplastic microtubules are connected by bridges which appear to be formed by protofilaments, branching off at intervals of approximately 150 Å from the microtubules. The structure of the periplast is discussed in detail.

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Durchgeführt mit Unterstützung durch die Deutsche Forschungsgemeinschaft.     

Mikromorphologie der Samenoberflächen der GattungEuphorbia

Seed coat surfaces of 127 species, representing 23 sections of the genusEuphorbia L. (Euphorbiaceae) have been examined with the scanning electron microscope (SEM). Various surface patterns and cell wall structures are described. In some groups the seed coat is rather uniform (e.g. in sect.Euphorbium), in other sections even closely related species can be separated by seed coat morphology (e.g.Tithymalus). The taxonomic application of testa micromorphology and the possible systematic position of certain taxa are briefly discussed. The seed coat cells of all species in sect.Tithymalus show remarkable intercellulares filled with small particles, which are described in detail for the first time.

     

Rhodomonas lacustris (Pascher & Ruttner) Javornicky (Cryptomonadida): Ultrastructure of the Vegetative Cell

The ultrastructure of Rhodomonas lacustris was examined using scanning and transmission electron microscopy, and the pigments were scanned in vivo by the opal plate technique. The periplast is composed of hexagonal plates, with trichocysts at the corners. This cryptomonad lacks a gullet but has a deep ventral furrow, in which more than 20 large ejectosomes are located. The chloroplast has mainly three thylakoids per lamella, and it is structurally reminiscent of that of certain haptophycean flagellates. The pigments appear to be as usual within the photosynthetic cryptomonads, with phycoerythrin type PE I (phycocyanin was not detected). Other cellular inclusions (e.g., lysosome-like vesicles and the contractile vacuolar complex) are also discussed.     

Feinstrukturelle und mikroanalytische Untersuchungen an den Kristallen und Lithosomen des CiliatenEuplotes vannus

Summary In the cytoplasm of the marine ciliateEuplotes vannus, there exist two conspicuous types of membrane bound inclusions: 1. irregularly shaped crystals which are highly anisotropic; 2. globular lithosomes characterized by concentrically arranged layers of deposits which exhibit only faint birefringence. Normally, both structures form distinct accumulations. Energy dispersive X-ray microanalysis of these accumulations reveals a high content of calcium and phosphorus, besides magnesium, sulphur and chlorine. Analysis of cell areas devoid of the inclusions show significantly lower calcium- and phosphorus-peaks.

     

Intracelluläre Organisation phagenschwanz-ähnlicher Bacteriocine der Gruppe A in Serratia marcescens

Zusammenfassung Die Genese eines phagenschwanzähnlichen Bacteriocins in Zellen des Gruppe A-bacteriocinogenen (bA⁺) Serratia marcescens-Stammer Nr. 16 wurde nach Mitomycin C (MC) Induktion elektronenoptisch untersucht. Dieses Bacteriocin (Gesamtlänge 117 nm) besteht aus einem hohlen Stift mit kontraktiler Scheide. Nach 60 min Induktion wurden in Dünnschnitten stäbchenförmige Bacteriocine identifiziert. Sie erscheinen in drei Aggregationsformen: 1. als hexagonale Einschlüsse, 2. als Bänder dicht nebeneinanderliegender Bacteriocine und 3. als Stapel von übereinanderliegenden Bacteriocinschichten, wenn nach 120 min Induktion ein Maximum von ca. 450 Bacteriocinen pro Zelle erreicht wird.Bacteriocine konnten nach der gleichen Induktionszeit von 60 min auch mit der in situ lysis technique nachgewiesen werden. Neben Bacteriocinen traten relativ selten und unregelmäßig auch Phagenköpfe auf.Die Stäbchenform teilungsfähiger Zellen blieb bis zum Auftreten von intracellulären Bacteriocinen erhalten. Ihre Umwandlung in geblähte, sphäroplastenähnliche Zellformen, die nach 120 min Induktion lysierten, war zeitlich korreliert mit Feinstrukturveränderungen der Zellwand.

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Intracellular organisation of bacteriophage tail-like Bacteriocins of group A in Serratia marcescens

The biosynthesis of a phage tail-like Bacteriocin by cells of the group A-bacteriocinogenic (bA⁺ Serratia marcescens strain no. 16 after induction with mitomycin C (MC) was examined electronmicroscopically. This bacteriocin (total length 117 nm) consists of a hollow core and a contractile sheath. At 60 min following induction, rod-like bacteriocin-partieles were identifiable in ultrathin sections. The particles were found to comprise three morphologically different forms of aggregation: 1. hexagonal inclusions, 2. contiguous, bank-like particles, and 3. staples of superimposed layers of bacteriocin particles. At 120 min after induction bA⁺ cells revealed maximally 450 bacteriocin particles.Similarly, the phage tail particles could be demonstrated with the in situ lysis technique at 60 min following induction. Occasionally, phage heads were demonstrable, but in no instance were complete phage particles discernible.Dividing cells of the bA⁺ strain of S. marcescens maintained their rod-form following induction with MC until intracellular phage tail bacteriocin particles were seen. However, at 120 min after induction, the swollen, sphaeroplast-like cells lysed, an event that could be correlated with fine structural alterations of the cell wall.

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Abkürzungen B Bacteriocine in Bandform - C core - CM Cytoplasmamembran - F Schwanzfasern - H hexagonale Aggregationsform - M Mesosom - MC Mitomycin C - OM outer membrane - ZW Zellwand     

Ultrastruktur und Entwicklungsgeschichte des Pollenkitts vonEuphorbia cyparissias,E. palustris undMercurialis perennis (Euphorbiaceae)

Development, fine structure and distribution of pollenkitt is investigated inEuphorbia cyparissias, E. palustris, andMercurialis perennis. The predominantly anemophilousM. perennis produces a great amount of strictly homogeneous pollenkitt, which is deposited in the exine caves. In contrast to this and to all other angiosperms so far investigated, bothEuphorbia species produce large quantities of an extremely inhomogeneous and particular pollenkitt. Its ultrastructure is quite different, both during its development and after its deposition on the exine surface: Lipid particles with different electron density and size are wrapped in a strictly homogeneous electron transparent matrix. This can be considered as new and additional proof for the secondary entomophily ofEuphorbia.

     

Structure and development of the cryptomonad periplast: A review

Summary The structure and development of the complex periplast, or cell covering, of cryptomonads is reviewed. The periplast consists of the plasma membrane (PM) plus an associated surface periplast component (SPC) and cytoplasmic or inner periplast component (IPC). The structure of the SPC and IPC, and their association with the PM, varies considerably between genera. This review, which concentrates on cryptomonads with an IPC of discrete plates, discusses relationships between periplast components and examines the development of this unique cell covering. Formation and growth of inner plates occurs throughout the cell cycle from specialized regions termed anamorphic zones. Crystalline surface plates, which comprise the SPC in many cryptomonad species, appear to form by self-assembly of disorganized subunits. InKomma caudata the subunits are composed of a high molecular weight glycoprotein that is produced within the endomembrane system and deposited onto the cell surface within anamorphic zones. The self-assembly of subunits into highly ordered surface plates appears closely associated with developmental changes in the underlying IPC and PM.     

Die Perikarpentwicklung geflügelter Klausen aus demParacaryum-Verwandtschaftskreis (Cynoglosseae,Boraginaceae)

The anatomy and development of mericarps in four representatives ofBoraginaceae-Cynoglosseae has been investigated. In each case, the nutlets grow from a six-layered carpel. While the mesocarp becomes multilayered and thick in correlation with epizoochory inCynoglossum, it remains six-layered inMattiastrum, Paracaryum, andRindera. The wings are formed by both exo- and mesocarp and later on the inflated rim becomes hollow. Development of wings and reduction of glochids are discussed as adaptations to anemochory.

     

Stephanosporaceae — eine neue Familie derBasidiomycetes mit aphyllophoralen und gastroiden Fruchtkörpern

The new familyStephanosporaceae (Basidiomycetes, Fungi) is proposed. As far as known, the range of the family covers aphyllophoroid (Lindtneria) and gastroid genera (Stephanospora) which are characterized by strongly sculptured and coloured spores. From the micro- and ultrastructural point of viewLindtneria andStephanospora are practically undistinguishable. Therefore, the two genera are considered to be closely related, despite their striking differences concerning the macromorphology of their carpophores.

     

REM-Untersuchungen anMilesia vogesiaca undMilesia whitei (Uredinales)

Central European specimens of twoMilesia species, both growing onPolystichum, were investigated by SEM. The uredospores ofM. vogesiaca are not smooth, as stated in literature, but finely verrucose; size and density of the verrucae are rather variable. In contrast, the uredospores ofM. whitei are finely echinulate.

     

STRUCTURE OF THE PERIPLAST OF CRYPTOMONAS OVATA VAR. PALUSTRIS1,2

The periplast of Cryptomonas ovata var. palustris is composed of polygonal plates which are delineated by shallow ridges. A small ejectosome is located at each corner of the plate area. The plate areas vary in size; they are smallest at the anterior and posterior ends and are largest in the middle of the cell with an average length of 0.5 μ and of width 0.4 μ. In cross section a plate area is composed of 2 distinct layers, an outer plasma membrane layer with a fine particulate, appearance, and an inner layer consisting of two sheets. The sheets of the inner layer have a striated lattice pattern with a periodicity of about 20 nm. In negatively stained preparations one lattice appears to underlie another at certain angles. Protease digestion removed polygonal shaped inner layer.     

A new species of <Emphasis Type="Italic">Acalypha</Emphasis> (Euphorbiaceae: Acalyphoideae: Acalypheae) from Belize and adjacent Mexico and Guatemala

Acalypha gentlei is described, illustrated and mapped. The species is endemic to Belize and adjacent areas of Mexico and Guatemala and restricted to semi-deciduous moist forests on limestone. The species is referred to Acalypha subgenus Linostachys.

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Resumen  Se describe, ilustra y grafica la distribución de Acalypha gentlei. Esta especie nueva es endémica a Belice y áreas adyacentes de México y Guatemala, y está restringida a bosques húmedos semi-deciduos sobre caliza. La especie es referida a Acalypha subgénero Linostachys.