An Analysis of Ultrastructural Changes during Oosphere-initial Development in Oogonia from Ca2+-sufficient and Ca2+-deficient cultures of Saprolegnia terrestris Cookson ex Seymour

The central vacuole system of oogonia of Saprolegnia terrestrisfrom Ca²⁺-sufficient cultures was fully enlarged prior to theformation of oosphere initials, which did not involve cleavagevesicles. In oogonia with fully-enlarged central vacuole systems,subsidiary vacuoles at the periphery of the system sometimescontained dense bodies, and dense-body profiles were sometimespresent within sections of the central vacuole system itself.As the central vacuole system enlarged, volume densities ofdense-body vesicles, peripheral vacuoles, lipid bodies and thecytoplasmic matrix decreased relative to total oogonial volume(peripheral protoplasm volume plus central vacuole volume),while the volume density of nuclei increased and that of mitochondriaremained constant. Relative to the peripheral protoplasm only,volume densities of dense-body vesicles, lipid bodies and mitochondriaincreased and volume densities of peripheral vacuoles and ofthe cytoplasmic matrix decreased, while the volume density ofnuclei increased during central vacuole enlargement but subsequentlydecreased during formation of oosphere initials. Under conditionsof Ca²⁺ deficiency, the volume densities of mitochondria andof the cytoplasmic matrix were significantly increased, whilethat of lipid bodies was significantly decreased, at early stagesof oogonial development; the volume densities of other organelleswere not significantly altered at any stage. Saprolegnia terrestris, oogonia, development, calcium, ultrastructure, stereology     

Vacuolation and Storage Protein Breakdown in the Castor Bean Endosperm following Imbibition

Cytochemical staining of sections prepared for light microscopy,electron microscope sections, and sodium dodecyl sulphate-polyacrylamidegel electrophoresis reveal that, following imbibition, storageproteins are mobilized from the protein bodies of the endospermof castor bean (Ricinus communis L. cv. Hale). This is accompaniedby fusion of protein bodies to form a central vacuole, beforeall the protein is hydrolyzed. Mobilization of the US crystalloidprotein complex and of the 2S albumin fraction commences 2 dafter imbibition and is completed within 2 d. This loss of proteinis accompanied by an increase in activity of three proteolyticenzymes, one carboxypeptidase and two -SH-dependent aminopeptidases.In contrast to the 11S and 2S protein fractions the lectins,located within the protein body, are mobilized only slowly andare present after the other proteins have been completely brokendown. Hence lectins may have a role other than as storage proteins. Key words: Castor bean, Protein breakdown, Storage protein, Lectin, Vacuolation, Seed germination     

Ultrastructural and Cytochemical Evidence for the Presence of Peroxisomes in the Generative Cell of Magnolia x soulangeana Pollen Grain

The generative cell (GC) development during three sequentialstages of Magnolia x soulangeana pollen grain maturation wasinvestigated by light and electron microscopy. Plastids werenot identified in this cell but mitochondria, Golgi bodies andvesicles as well as rough endoplasmic reticulum profiles werealways present. Microtubules were also present, their numberincreasing and their disposition varying during GC maturation.The most conspicuous components of the GC cytoplasm were themicrobodies. The latter were few in number in the newly formedGC, and the appearance of their matrix was different from laterdevelopmental stages. A clear microbodial proliferation occurredin the GC during an intermediate stage of pollen maturation.Then, the microbody matrix was either fibrillar to granularas in the vegetative cell microbodies or very dense and compact.The polymorphism and size range and the frequent aggregationof these organelles in one or more clusters were also noteworthy.Tilting of semithin sections as well as the analysis of serialsections suggested that a number or enlarged and irregularlyshaped microbodies co-exist with smaller and more sphericalones, the latter probably originating by budding. In the GCof the mature pollen the microbody-like organelles were in generalmore uniform both in shape and size. The cytochemical test ofDAB was positive in the microbodies of both the pollen cells,thus demonstrating their peroxisomic nature. The function ofthe microbodies in the GC is not clear. In this cell, a fewlipid droplets only exist during the first developmental stageand the microbodies were apparently unrelated to any other organelle.Possibly, these are unspecialized microbodies which are paternallytransmitted, but it is not excluded that, temporarily, theymay play some special role during GC maturation.Copyright 1994,1999 Academic Press Peroxisomes, generative cell, pollen maturation, Magnolia x soulangeana Soul.-Bod     

Effects of Light and Dark on the Ultrastructure of Lichen Algae

Quantitative ultrastructural observations have been made onthe algal cells (Trebouxia) in two lichens, Parmelia sulcataand P. laevigata, stored for 48 h in the dark or under a light/darkregime. The response of the alga was found to differ in theselichens. In P. sulcata the dark treatment caused a decreasein starch grains, lipid-rich pyrenoglobuli and peripheral cytoplasmicstorage bodies and an increase in pyrenoid and chloroplast proteinbodies. The algae in P. laevigata contained little starch andno chloroplast protein bodies. However, after dark treatment,starch, cytoplasmic storage bodies and pyrenoid dimensions sometimesdeclined, while pyrenoglobuli numbers increased. Some of theseapparent changes depended upon the units used for calculatingthe cross-sectional areas of structures, e.g. absolute units,percentage of cell wall, protoplast or chloroplast cross-sectionalarea. Chloroplast area increased in the dark (as a % of cellwall area) in both species while mitochondria were larger inthe dark in P. sulcata but not in P. laevigata. Ultrastructuralchanges were not clearly correlated with changes in photosyntheticand respiratory rates. These results directly support the suggestionthat some intra-cellular structures are energy-generating reservesthe dimensions of which can rapidly change. Parmelia sulcata, Parmelia laevigata, lichen algae, light and dark storage, starvation, reserve substances, organdie dimensions     

Inclusion bodies in several species of Ceratium Schrank (Dinophyceae) from the Caribbean Sea examined with DNA-specific staining

Several dinoflagellate species in the genus Ceraiium Schrankwere examined, with the help of a DNA-specific dye, for thepresence of a nucleus, chloroplasts and inclusion bodies. Theabundance of Ceratium in the Caribbean Sea in April 1990 wasbetween 1.3 and 4.9 x 10⁵ cells m^–3 Most Ceratium teresKofoid contained 5–10 small chloroplasts and among 529C.teres cells. 8% possessed an inclusion body. The shape andsize of inclusion bodies varied, and 7% of the inclusions hada DNA-containing particle inside. Similar inclusion bodies werealso observed in Ceratium declinatum f. normale Jörgensen,Ceratium furca (Ehrenberg) Claparede and Lachmann, and Ceratiumfusus (Ehrenberg) Dujardin. Our observations indicated thatinclusion bodies are common in oceanic Ceratium. ¹Present address: Institute of Marine Biology, National TaiwanOcean University, Keelung 20224, Taiwan, ROC     

The Ultrastructure of the Alkaloidal Vesicles of Papaver somniferum latex

Papaver somniferum latex contains abundant small vesicles. Theirultrastructure was studied in tissue sections from adult plantsand in sections of sequential fractions of centrifuged latex.The vesicles were found to exist in two forms, the first witha smooth but progressively granulated outer membrane and thesecond, probably derived from the first, with adherent ‘cap-like’structures which in the heavier centrifuged fractions possesseda zonally-ordered interior. These vesicle fractions were active in synthesizing morphineand the name ‘alkaloidal vesicle’ is proposed forthem. Papaver somniferum latex also contains an organelle whichwas found to resemble a complex organelle present in the latexof Hevea brasiliensis. Its function is not yet known.     

Pigment Bodies in Fruits of Crimson and High Pigment Lines of Tomatoes

Pigment bodies in fruits of crimson (og^c), high pigment (hp),and crimson-high pigment (og^c hp) lines of tomatoes were observedby electron and light microscopy and compared with those ofnormal red lines and a yellow cultivar. During chloroplast-chromoplasttransformation, two main structurally distinct bodies are produced,their total and relative amounts apparently accounting for theentire range of colours (from very deep red to yellow) characterizingthe mature fruits of these different colour lines. The longnarrow crystalloids, believed to be lycopene, form in associationwith an extended thylakoid system; in senescing (over-ripe)fruit many of these are reduced to shorter irregular forms.The rounded globules are believed to be beta-carotene dissolvedin lipid material derived from membrane lysis. Analytical resultscorroborate microscopic observations that the effect of theog^c gene, as compared with the r⁺ gene for normal red colour,is to increase the lycopene content and lower the beta-carotenecontent. The effect of the hp gene is to increase the levelsof both pigments. The results support the view that the genescontrol the development of fruit pigments which affect chromoplastultrastructure. Lycopersicon esculentum Mill, tomato, fruit, pigment bodies, beta-carotene, lycopene     

Adaptive Growth Responses to Osmotic Stress of Hypocotyl Sections of Vigna unguiculata: Roles of the Xylem Proton Pump and IAA

The growth responses to osmotic stress of hypocotyl sectionsof Vigna unguiculata were studied by the xylem perfusion method.Hypocotyl sections shrank upon exposure to osmotic stress. Sectionsshowed no adaptive responses to osmotic stress when they werein an IAA-depleted condition as a result of perfusion with solutionsthat lacked IAA for 3–4 h. The correlation between thegrowth rate and the membrane potential of the xylem/symplastboundary (V^px) was very limited in the absence of IAA. By contrast,hypocotyl sections showed distinct adaptive responses to osmoticstress after perfusion with solutions that contained 10 µMIAA. In the presence of IAA, V^px increased in the negative directionand growth resumed in spite of the osmotic stress. The growthrate was closely correlated with the xylem membrane potential.Hyper-polarization of the membranes of the xylem/symplast boundaryalways preceded the recovery of growth under osmotic stress.It appears that IAA is essential for the adaptive recovery ofgrowth under osmotic stress and, moreover, that the xylem protonpump plays an indispensable role in modulating the growth ofhypocotyl sections. This result confirms prediction of an earliersimulation study using the apoplast canal model [Katou and Furumoto(1986) Protoplasma 133: 174, Katou and Enomoto (1991) PlantCell Physiol. 32: 343]. (Received June 27, 1996; Accepted October 28, 1996)     

Structure and Development of Plastids in Epidermal Cells of African Violet (Saintpaulia ionantha Wendl.) in Culture

The structure of plastids in epidermal cells of African violet(Saintpaulia ionantha Wendl.) ‘Marge Winters’ wasexamined using transmission electron microscopy before and afterplacement of leaf tissue in culture. The plastids from matureepidermal cells contained membrane-bound inclusion bodies andprolamellar bodies in various stages of development. Starchgrains and poorly developed granal stacks were observed in asmall number of plastids. After placement of the leaves on suitableculture medium, inclusion bodies decreased in size and the lamellarsystem became more organized. The plastids in the epidermaltissue are believed to be in an arrested state of developmentand are released from this state by placement on a medium inductiveto organogenesis. Saintpaulia ionantha Wendl., African violet, membrane-bound inclusion, tissue culture, plastid development     

Ultrastructural Studies on Development in Mature Seeds; Embryos of Euonymus europaea L. Dormant or Cultured at +25 ?C

Ultrastructural observations on naturally dispersed and dehydratedseeds of Euonymus europaea L. were performed. It was shown thatduring the culture of isolated embryos at 25 ?C for 7 d thematuration of protein bodies continued; the initial juvenileform (single protein body per cell with dispersed contents)was developing into a more advanced form (single body splitto form several sub-units with condensed contents). Parallelbiochemical determinations pointed to an increase in insolubleprotein levels. There were no changes in other storage organelles,lipid bodies, either in the fine structure or in the level oftriacylglycerols. Deterioration of cellular membranes (in mitochondria,proplastids and protein bodies) similar to that described forageing was observed in cells at the periphery of the embryonicaxis. It is concluded that during the culture of E. europaeaembryos the maturation programme of development in protein bodiesis being continued. Key words: Embryonic axis, storage protein and lipid body, maturation     

Fine Structure of Botrytis fabae Sardina Conidia

The fine structure of Botrytis fabae conidia was studied usinga variety of electron-microscope techniques. The spore walllacks conspicuous ornamentation and consists of microfibrilsembedded in a granular matrix. The two distinct wall layersseen in chemically fixed sections cannot be detected in cross-fracturedreplicas; the two layers are probably structurally similar.The outer surface of the plasmalemma is covered with branchedinvaginations and two kinds of particles. Three distinct typesof particles are present on the inner surface of the plasmalemma.In freeze-etched replicas nuclei, vacuoles, and other organellesalways appear smoothly rounded. Small vesicles pass throughthe plasmalemma into the cell wall. Particles approximately10 nm in diameter occur in compact rows on the cristae of cross-fracturedmitochondria: dense spherical particles, probably of calciumphosphate, are present in chemically fixed mitochondria. Prevacuolesand vesicles with membranous inclusions can be seen in bothcross-fractured replicas and chemically fixed sections. In cross-fracturedreplicas vacuoles and lipid bodies are frequently joined bystrands of endoplasmic reticulum.     

In Vitro Phosphorylation of Proteins in IAA-Treated Mesocotyls in Zea mays

Five-mm sections of elongation zones of Zea mesocotyls wereincubated for designated periods with various concentrationsof IAA. In vitro protein phosphorylation in the soluble fraction(85,000 x g supernatant) prepared from the sections was analyzedby sodium dodecyl sulfate-polyacrylamide gel electrophoresis.The phosphorylation of proteins in the soluble fraction thathad been prepared from sections incubated for 20 min in thepresence of 10{small tilde}^s M IAA was greater than that inthe sections incubated for 20 min without IAA. The amount ofphosphorylation of proteins per protein became higher when higherconcentrations increased (10{small tilde}⁸—10{small tilde}⁵M).The growth of sections incubated in the presence of 10{smalltilde}⁸ M IAA or higher concentrations was greater than thatof sections incubated in the absence of IAA. The promotion ofgrowth by IAA was greater at higher concentrations of IAA. Proteinsin the soluble fraction, prepared from sections incubated for20 min in the presence of 10{small tilde}⁵ M IAA, were phosphorylatedin the presence of either 10 fM cAMP, 10 µM cGMP, 100µM W-7, 100 µM W-5, 20 µM H-7 or 20 µMHA1004. The calmodulin antagonist, W-7, and the inhibitor ofprotein kinase C, H-7, inhibited the phosphorylation of proteinsstimulated by incubation with IAA. These results suggest thatIAA promotes cell elongation via protein phosphorylation thatdepends on calmodulin-dependent protein kinase and protein kinaseC. (Received November 29, 1995; Accepted May 20, 1996)     

Ultrastructure, Origin, and Composition of the Protein Bodies in the Ligule of Isoetes lacustris L.

The basal cells in the ligule of Isoetes lacustris contain numerousprotein bodies, the contents of which can be digested enzymicallyby pronase and are stained red by treatment with ninhydrin Schiff'sreagent. Two types of protein bodies can be distinguished ultrastructurally:spherically-shaped bodies with granular contents and spindle-likebodies with fibrillar contents. Both are ensheathed by singlemembranes and do not show any solid inclusions within theirmatrix. The protein bodies probably arise from dilatation of the endoplasmicreticulum (ER) cisternae. This conclusion is based upon threeobservations: (a) The protein bodies occasionally show membranecontinuity with the ER; (b) ribosomes and polysomes are frequentlyattached to the protein-body membranes; (c) the contents ofthe protein bodies and of the dilated ER cisternae show similarultrastructural features. The dilatation of the ER cisternae is assumed to be a resultof protein accumulation in the intracisternal space. Based upon the results of polyacrylamide gel electrophoresis,it is likely that the spherically-shaped protein bodies storepredominately two proteins with molecular weights of 51300 and55800 D, while the spindle-like bodies store two proteins withmolecular weights of 92000 and 98000 D. The results presented do not permit a definite conclusion regardingthe function of the ligule of Isoetes lacustris but it is suggestedthat it may have a nutritive role. Isoetes lacustris L., ligule, protein bodies, endoplasmic reticulum, ultrastructure     

EXTRA-CAPSULAR YOLK BODIES IN THE EGG MASSES OF SOME TROPICAL OPISTHOBRANCHIA

Seventeen species of opisthobranch molluscs from Enewetak, MarshallIslands were found to deposit bodies of yolk within their gelatinousegg masses external to the capsules which surround the ova.These observations bring the total number of opisthobranch speciesin which extra-capsular yolk is known to 26. This study reviewsprevious reports of extra-capsular yolk and contributes newdata on the egg masses and developmental characteristics ofspecies in which it is known to occur. The various types ofyolk body found are detailed and categorized, and original observationson the deposition of yolk bodies and their fate during, andsubsequent to embryonic development presented. To date, extra-capsular yolk bodies have been found only withinthe egg masses of species of Chromodoris and Cadlinella (Nudibranchia:Chromodorididae), Elysia (Sacoglossa: Elysiidae), and Bosellia(Sacoglossa: Polybranchiidae). Three types of yolk body arerecognized: (1) cap-like yolk bodies associated with individualcapsules, (2) discrete yolk bodies strewn throughout the eggmass, and (3) continuous or discontinuous yolk strings. Direct consumption of yolk bodies by newlyhatched veligers ofChromodoris albopunctatus (Garrett) is described. In most otherspecies, the yolk disappears during the course of developmentand is probably of nutritive value to the embryos. The availabledata suggest that chromodorid species which utilize extra-capsularyolk during the course of development produce relatively largerlarvae than species with comparably sized ova that do not. (Received 25 November 1982;     

Generation of Seakale (Crambe maritima L.) Plantlets by Tissue Culture

When placed in shaken liquid culture in MS medium, callus derivedfrom petioles of seakale (Crambe maritima L.) failed to fragmentto produce a cell suspension culture. In the absence of 2,4-D,growth was very good, and hollow, dark green, trumpet-shapedbodies were produced, but in the presence of 2,4-D, solid, palergreen pear-shaped bodies were formed. When grown on filter paperbridges with White's medium, a small proportion of both typesof bodies underwent slow, partly-controlled development culminating,after several months, in the formation of plantlets. Seakale, Crambe maritima L., in vitro propagation, callus culture     

The Development of Mitochondria in Arum Spadix

Electron micrographs of Arum spadix cells prepared at four stagesof development all showed abundant sections of mitochondriawith tubular ingrowths (microvilli). At the earliest stage (whenthe spadix cells were still dividing) there was an average of9 sections of microvilli per mitochondrion. In later stagesof development, when the cells were growing by elongation, thenumber of microvilli rose to 22. It was reported earlier that the succinoxidase activity of themitochondria of Arum spadix increased as the spadix developed,and it is now shown that the rise in enzyme activity parallelsthe increase in length of microvilli.     

Immunocytochemical Localization of Wheat Storage Proteins in Endosperm Cells 30 Days After Anthesis

Antisera against seven different wheat (Triticum aestivum L.)storage protein subfractions were characterized using (1) ELISAwith gliadins and low- and high-molecular weight glutenin subunitsand (2) electrophoresis (SDS-PAGE and acidic buffer PAGE) andimmunoblotting. The specificities of these antisera (polyclonalantibodies) and 13 monoclonal antibodies covered various patternsof reactivity with alpha-, beta-, gamma- and omega-gliadinsand low- and high-molecular weight glutenins. The antisera andantibodies were applied to ultrathin sections of wheat endospermtissue, from kernels fixed 30 d after anthesis, and were detectedby secondary antibodies tagged with either 5 or 15 nm gold particlesusing transmission electron microscopy. Labelling was denserwhen the small gold particles were used but irrespective ofgold particle size, labelling of polyclonal antisera predominatedwhen the endosperm cells were subjected to both mono- and polyclonalantibodies. Each of the antisera and monoclonal antibodies thatlabelled the protein bodies, labelled them more or less uniformly.This indicates that only one kind of protein body, containingall gliadin and glutenin subfractions, exists during this stageof grain development. Electron-dense globular inclusions foundin many protein bodies were not labelled. Label was also foundon protein-like material present in the lumen of the rough endoplasmicreticulum and on vesicles of the Golgi apparatus. Thus concentrationof storage proteins takes place both at the site of synthesis,the lumen of the rough endoplasmic reticulum, and at the siteof processing and transport, the vesicles of the Golgi apparatus.Fusions between these proteinaceous materials give rise to largerprotein bodies and ultimately to the protein matrix. Key words: Wheat, immunocytochemistry, protein bodies, rough endoplasmic reticulum, Golgi apparatus     

Polyphosphate metabolism in the blue-green alga Microcystis aeru-ginosa

The uptake of inorganic phosphorus was studied in an axenicstrain of phosphorus-starved cells of the blue-green alga Microcystisaeruginosa, an organism often causing blooms in freshwater bodies.Rates of growth and of cellular polyphosphate content as a functionof initial orthophosphate in the medium indicate the operationof the ‘phosphorus overplus’ phenomenon in M. aeruginosa,accompanied by formation of volutin granules. The granules wereisolated by a non-aqueous centrifugation method, and identifiedas polyphosphate bodies.     

Calcium-Dependent Lamina Production of Nymphoides peltata (Gmel.) O. Kuntze (Menyanthaceae): Implications for Distribution

Nymphoides peltata (Gmel.) O. Kuntze, a nymphaeid macrophyte,occurs commonly in polder and fluviatile areas in large partsof Europe and Asia. In contrast to the nymphaeid macrophytesNymphaea alba L. and Nuphar lutea (L.) Sm., Nymphoides peltatais almost completely absent from poorly-buffered waters andis never found in acid water bodies. Transplantation experimentsin water bodies of varying alkalinity demonstrated that, irrespectiveof the sediment type, leaf production of Nymphoides did occurin poorly-buffered waters, but not in acid waters. Cultivation experiments showed that floating leaf developmentof Nymphoides peltata could only take place if sufficient calciumwas available in the water layer or in twice-demineralized water.Addition of calcium to an acid cultivation medium or to watercollected from an acid moorland pool resulted in leaf production.Growth of Nymphoides in acid waters is impossible due to insufficientcalcium concentrations in the water layer of such waters. Itis suggested that the absence of Nymphoides peltata in somepoorly-buffered water bodies is partly due to the spatial isolationfrom rivers and canals and the high frequence of desiccation.The restricted occurrence of Nymphoides peltata to well-bufferedalkaline waters is functionally more related to the calciumavailability than to the bicarbonate content. Key words: Aquatic macrophytes, distribution, Nymphoides peltata, leaf production, calcium, acid, poorly-buffered and alkaline water     

The Production of Plantlets from Tissue Cultures of Brussels Sprout (Brassica oleracea L. var gemmifera D.C.)

Shoots were induced on callus derived from sprout sections andpetiole slices of an inbred parent line of Brussels sprout (Brassicaoleracea L. var gemmifera D.C.). The shoots, when excised andtransferred to fresh medium, enlarged and formed roots. Theseplantlets could be transferred to soil or their number increasedby a multiplication process involving the production of newshoots from the dormant lateral buds. Some of the plantletsderived from sprout callus were grown to maturity in the fieldand their morphology and chromosome number compared to seedgrown plants. There were no significant differences in sproutsize and stem diameter but there were significant differencesin plant shape. None of the plants in the field experiment showedpolyploidy. Plants derived from callus possessed an enhanced ability toform callus and redifferentiate when sections from these plantswere placed back on to nutrient medium.