On the Origin,Development and Ultrastructure of the Orbicuies and Pollenkitt in the Tapetum of Anemarrhena Asphodeloides (Liliaceae)

Anemarrhena asphodeloides Bunge is a monotypic genus of Liliaceae, growing in China and Korea. The pro‐orbicules are derived from the cisternae of rough endoplasmic reticulum. There are prominent aggregates of orbicuies in Anemarrhena. The first sign of the formation of pollenkitt is that the proplastids begin to differentiate into elaioplasts in the tapetum, and then the elaioplasts become the main source of pollenkitt. Alternatively, cytoplasmic vesicles derived from RER are probably the other way pollenkitt is synthesed in this species.     

The Transfer of Pollenkitt in Smyrnium perfoliatum (Apiaceae)

In Smyrnium perfoliatum the formation of pollenkitt within asecretory tapetum, and the subsequent breakdown of the cellorganelles, is followed by the transformation of pollenkittlumps into pollenkitt droplets. These droplets move within alocular fluid towards the pollen exine, where they enter theexine cavities after passing a fibrillar layer (remnants ofthe primexine-matrix) in between the tectum elements. This isfollowed by the fusion of pollenkitt droplets, forming a distinctlayer at the bottom of the exine cavities. Smyrnium perfoliatum L., Apiaceae, tapetum, pollenkitt formation, organelle disintegration, transformation, pollenkitt deposition, primexine matrix     

The Formation of Pollenkitt in Apium nodiflorum (Apiaceae)

Apium nodiflorum produces a considerable amount of pollenkittwithin a secretory tapetum. ER and plastids (elaioplasts) participatein pollenkitt formation. Both organelles deposit precursorswithin vesicles, which finally fuse to form pollenkitt. Apium nodiflorum L., Apiaceaesecretory tapetum, pollenkitt, ER, plastids, elaioplasts     

Entwicklungsgeschichte und Ultrastruktur des Pollenkitts beiTilia (Tiliaceae)

The pollenkitt ofTilia platyphyllos andT. tomentosa is produced during the tetrade-stage by the tapetum plastides. After tapetum degeneration pollenkitt and accompanying substances are deposited predominantly in the intrabacular spaces of the exine, and only in small quantities on the surface of the exine itself.

     

Pollenkitt is lacking inGnetatae:Ephedra andWelwitschia; further proof for its restriction to the angiosperms

Three members of theGnetatae (Ephedra campylopoda, E. americana, Welwitschia mirabilis) were investigated by TEM and SEM with respect to their anther tapetum and pollen development. In all three species pollenkitt is lacking. The pretended pollen stickiness thus does not depend on pollenkitt. Considering former observations one can now clearly state that pollenkitt is missing in all recent gymnosperm classes (both anemophilous and ± entomophilous). Pollenkitt thus is restricted and ± omnipresent within the angiosperms, where it represents one of the most important components of the entomophily syndrome. This can be regarded as important proof for the hypothesis that the angiosperms are a single coherent phylogenetic group.     

Pollenkitt is lacking inGnetum gnemon (Gnetaceae)

The anther tapetum of the gymnospermGnetum gnemon produces no lipid osmiophilous droplets as pollenkitt forerunners. Thus—in contrast to entomophilous and anemophilous angiosperms—no pollenkitt is produced at all. From lack of pollenkitt in other gymnosperms, it appears to be restricted to angiosperms. This can be considered as new and additional proof for the hypothesis that the angiosperms are one coherent phylogenetic group, and that the development of pollenkitt in their ancestors was one of the main prerequisites for the adaptive switch to entomophily.     

Can Pollen Headspace Volatiles and Pollenkitt Lipids Serve as Reliable Chemical Cues for Bee Pollinators?

Chemical analysis of putative contact chemical cues for pollinators from pollen of two plant species, Ranunculus bulbosus (Ranunculaceae) and Campanula rapunculoides (Campanulaceae), showed high consistency in the qualitative and quantitative composition of pollenkitt surface lipids in all samples analyzed per species. The pollenkitt lipids of R. bulbosus included an aldehyde, fatty acid amides, saturated and unsaturated hydrocarbons, and secondary alcohols; the lipids of C. rapunculoides consisted of an aldehyde, monoketones, and β-diketones. In marked contrast, the pollen headspace volatiles showed a wide qualitative and quantitative variability among all samples per species, whereby the variability was more pronounced in R. bulbosus. Hence, the highly species-specific pollenkitt lipids may provide pollinators with more reliable information on pollen identity.     

Developmental stages of the pollen wall and tapetum in some Crocus species

The developmental stages of the pollen wall and tapetum, together with exine morphology were studied in a number of Crocus species, by light and scanning electron microscopy. Gametogenesis was characterized by: 1) development of a thick intine, 2) single mitosis, and 3) terminal amylolysis. The tapetum was of the secretory type. In C. cartwrightianus cv. albus, abnormal sporogenesis and gametogenesis produced vacuolate pollen grains with a reduced-or no intine layer, and rich with starch granules; the tapetum was either of the parietal-or amoeboid type. The exine was echinate and the pollen grains had different types of aperture: furrows, colpi or pores. The ornamentation varied from microreticulate to irregularly perforate. The exine framework was overlaid by a pellicle resistant to chloroform-carbon disulphide, on which a layer of pollenkitt was deposited. The results are discussed from both cytological and evolutionary viewpoints.     

“Pollen Buds” in Ophiorrhiza (Rubiaceae) and their Role in Pollenkitt Release

Pollen buds are apertural protrusions formed by the ectintine. In their wall unesterified and methyl-esterified pectins are detected by immunogold labeling. During pollenkitt formation pollen buds become adpressed and connected to the tapetum wall. The following expansion of the endothecium causes the mechanical rupture of the tapetum at the binding sites of the pollen buds. These events are accompanied by the release of the pollenkitt.     

The tapetum: Its form,function, and possible phylogeny inEmbryophyta

It appears that the tapetum is universally present in land plants, even though it is sometimes difficult to recognize, because it serves mostly as a tissue for meiocyte/spore nutrition. In addition to this main function, the tapetum has other functions, namely the production of the locular fluid, the production and release of callase, the conveying of P.A.S. positive material towards the loculus, the formation of exine precursors, viscin threads and orbicules (= Ubisch bodies), the production of sporophytic proteins and enzymes, and of pollenkitt/tryphine. Not all these functions are present in all land plants:Embryophyta. Two main tapetal types are usually distinguished in theSpermatophyta: the secretory or parietal type and the amoeboid or periplasmodial type; in lower groups, however, other types may be recognized, with greater or lesser differences. A hypothetical phylogenesis of the tapetum is proposed on the basis of its morphological appearance and of the nutritional relations with meiocytes/spores. The evolutionary trends of the tapeta tend towards a more and more intimate and increasingly greater contact with the spores/pollen grains. Three evolutionary trends can be recognized: 1) an intrusion of the tapetal cells between the spores, 2) a loss of tapetal cell walls, and 3) increasing nutrition through direct contact in narrow anthers.     

Knockdown of FIBRILLIN4 Gene Expression in Apple Decreases Plastoglobule Plastoquinone Content

Fibrillin4 (FBN4) is a protein component of plastoglobules, which are antioxidant-rich sub-compartments attached to the chloroplast thylakoid membranes. FBN4 is required for normal plant biotic and abiotic stress resistance, including bacterial pathogens, herbicide, high light intensity, and ozone; FBN4 is also required for the accumulation of osmiophilic material inside plastoglobules. In this study, the contribution of FBN4 to plastoglobule lipid composition was examined using cultivated apple trees in which FBN4 gene expression was knocked down using RNA interference. Chloroplasts and plastoglobules were isolated from leaves of wild-type and fbn4 knock-down trees. Total lipids were extracted from chloroplasts and plastoglobules separately, and analyzed using liquid chromatography-mass spectrometry (LC–MS). Three lipids were consistently present at lower levels in the plastoglobules from fbn4 knock-down apple leaves compared to the wild-type as determined by LC-MS multiple ion monitoring. One of these species had a molecular mass and fragmentation pattern that identified it as plastoquinone, a known major component of plastoglobules. The plastoquinone level in fbn4 knock-down plastoglobules was less than 10% of that in wild-type plastoglobules. In contrast, plastoquinone was present at similar levels in the lipid extracts of whole chloroplasts from leaves of wild-type and fbn4 knock-down trees. These results suggest that the partitioning of plastoquinone between the plastoglobules and the rest of the chloroplast is disrupted in fbn4 knock-down leaves. These results indicate that FBN4 is required for high-level accumulation of plastoquinone and some other lipids in the plastoglobule. The dramatic decrease in plastoquinone content in fbn4 knock-down plastoglobules is consistent with the decreased plastoglobule osmiophilicity previously described for fbn4 knock-down plastoglobules. Failure to accumulate the antioxidant plastoquinone in the fbn4 knock-down plastoglobules might contribute to the increased stress sensitivity of fbn4 knock-down trees.     

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.

     

Effect of the <Emphasis Type="Italic">desA</Emphasis> gene encoding Δ12 acyl-lipid desaturase on the chloroplast structure and tolerance to hypothermia of potato plants

Effects of the desA gene from the cyanobacterium Synechocystis sp. encoding Δ12 acyl-lipid desaturase and increasing the level of unsaturated fatty acids (linoleic acid (18:2) primarily) in membrane lipids, which was inserted into potato (Solanum tuberosum L., cv. Desnitsa) plants, on chloroplast ultrastructure and plant tolerance to low temperatures were studied. The main attention was focused on modifications in the chloroplast structure and their possible relation to potato plant tolerance to oxidative and low-temperature stresses under the influence to their transformation with the Δ12 acyl-lipid desaturase gene from cyanobacterium (desA-licBM3-plants). Morphometric analysis showed that, in comparison with wild-type (WT) plants, in desA-licBM3-plants the number of grana in chloroplasts increased substantially. The total number of thylakoids in transformant chloroplasts was almost twice higher than in WT plants. The number of plastoglobules per chloroplast of transformed plants increased by 25%. A marked increase in the number of grana, total number of thylakoids, and the number of plastoglobules in chloroplasts of desA-licBM3-plants indicates their more intense lipid metabolism, as compared with WT plants, and this resulted in the conservation of some part of lipids in plastoglobules. In addition, the expression of heterological desA gene encoding Δ12 acyl-lipid desaturase positively influenced stabilization of not only structure but also functioning of chloroplast membranes, thus preventing a transfer of electrons from the ETR to oxygen and subsequent ROS generation at hypothermia. This was confirmed by the analysis of the rate of superoxide anion generation in tested genotypes.     

Pollen and Tapetum Development in Male Fertile Rosmarinus Officinalis L. (Lamiaceae)

The development of microspores/pollen grains and tapetum was studied in fertile Rosmarinus officinalis L. (Lamiaceae). Most parts of the cell walls of the secretory anther tapetum undergo modifications before and during meiosis: the inner tangential and radial cell walls, and often also the outer tangential and radial wall, acquire a fibrous appearance; these walls become later transformed into a thin poly-saccharidic film, which is finally dissolved after microspore mitosis. Electron opaque granules found within the fibrous/lamellated tapetal walls consist of sporopollenin-like material, but cannot be interpreted as Ubisch bodies. The middle lamella and the primary wall of the outer tangential and radial tapetal walls remain unmodified, but get covered by an electron opaque, sporopollenin-like layer. Pollenkitt is formed only by lipid droplets from the ground plasma and/or ER profiles, the plastids do not form pollenkitt precursor lipids. Tapetum maturation (“degeneration”) does not take place before late vacuolate stage.

The apertures are determined during meiosis by vesicles or membrane stacks on the surface of the plasma membrane. The procolumellae are conical, but at maturity the columellae are more cylindrical in shape. The columellar bases often fuse, but a genuine foot layer is lacking. The formation of the endexine starts with sporopollenin-accumulating white lines adjacent to the columellar bases. Later, the endexine grows more irregularly by the accumulation of sporopollenin globules. In mature pollen the intine is clearly bilayered.

Generative cells (GCs) and sperm cells contain a comparatively large amount of cytoplasm, and organelles like mitochondria, dictyosomes, ER, and multi-vesicular bodies, but no plastids; GCs and sperms are separated from the vegetative cell only by two plasma membranes.     

Pollen Ontogeny in Catananche caerulea L. (Compositae: Lactuceae) II. Free Microspore Stage to the Formation of the Male Germ Unit

The development of Catananche caerulea pollen grains from theearly free microspore stage to the formation of the male germunit has been studied using the scanning electron microscope.The differentiation of the elaborate ectexine from primexineand the accompanying cytoplasmic changes in the microsporesare described. Changes in the tapetum, reflecting first theformation of sporopollenin precursors and then of pollenkitt,are also described. The origin of taxonomically important featuresis discussed. Catananche caerulea, Compositae: Lactuceae, microspore mitosis, male germ unit, ontogeny, primexine differentiation, scanning electron microscopy     

Tunable nano‐oleosomes derived from engineered Yarrowia lipolytica

Oleosomes are discrete organelles filled with neutral lipids surrounded by a protein‐embedded phospholipid monolayer. Their simple yet robust structure, as well as their amenability to biological, chemical, and physical processing, can be exploited for various biotechnology applications. In this study, we report facile biosynthesis of functionalized oleosomes within oleaginous yeast Yarrowia lipolytica, through expression of oleosin fusion proteins. By fusing a cDNA clone of a sesame oleosin with either the coding sequence of a red fluorescent protein mCherry or a cellulosomal scaffolding protein cohesin from Clostridium cellulolyticum, these oleosin‐fusion proteins were efficiently expressed and specifically targeted to and anchored on the surface of the oleosomes within the Y. lipolytica cells. The engineered oleosomes can be easily separated from the Y. lipolytica cell extract via floating centrifugation and both mCherry and cohesin domains are shown to be functional. Upon sonication, the engineered Yarrowia oleosomes exhibit a mean diameter of 200–300 nm and are found to be highly stable. The feasibility of co‐displaying multiple proteins on the Yarrowia oleosomes was demonstrated by incubating cohesin‐displaying oleosomes with different dockerin‐fusion proteins. Based on this strategy, engineered oleosomes with both cell‐targeting and reporting activities were created and shown to be functional. Taken together, the Yarrowia oleosome surface display system in which oleosin serves as an efficient membrane anchor motif shows great promise as a simple platform for creating tunable nanoparticles. Biotechnol. Bioeng. 2013; 110: 702–710. © 2012 Wiley Periodicals, Inc.     

Pollenkitt of some monocotyledons: lipid composition and implications for pollen germination

• The composition of pollenkitt and its role in the progamic phase of reproduction are poorly understood. With the aim of extending knowledge on these topics, we chose to study two monocotyledons rich in pollenkitt, with bi‐celled and long‐lived pollen and dry‐type stigma: Crocus vernus Hill subsp. vernus and Narcissus poeticus L.
• Fatty acids of pollenkitt were assayed with gas chromatography. Germination tests were performed in vivo by pollinating the stigmas with a beard hair under a stereomicroscope, and in vitro in liquid culture medium using pollen, either treated or not, with carbon disulphide to remove pollenkitt. The pollen tube percentages were evaluated using fluorescence microscopy techniques. Scanning electron microscopy was used to examine pollen and to follow the early post‐pollination stages.
• Pollenkitt forms bridges between pollen grains but not between grains and stigma papillae. It consists of a mixture of 25 fatty acids, most with long and unsaturated chains, among which are some omega acids. The same acids with different percentages persist on the peritapetal membrane. After its removal, the pollen loses adhesiveness and dries quickly, but retains full capacity for germination on the papillae and can even trigger germination in contiguous pollen grains that do not touch the papillae.
• The results, while confirming the key role of pollenkitt in protecting pollen and favouring pollination, suggest secondary roles in the progamic phase, and highlight the interactive ability of the pollen regardless of lipid shell. The predominance of fatty acids with 18:3 and 16:0, as already noted in Brassica napus pollenkitt, suggests their hierarchy independent of plant species.

     

A Comparison of Anther Tissue Development in Male Sterile Aloe vera and Male Fertile Aloe ciliaris

Cytological differences between the anther development of amale sterile and a male fertile Aloe species are used to explaininteractions between anther tissues. Some deviations in thelayers of the locule wall and the microspores of the male sterileanther are related to each other and their biological functionsare discussed. The cytological development of the male sterility,which can be observed shortly after meiosis, seems to be restrictedto the locular cavity. The tapetal development and breakdownare normal, apart from the size of some orbicules. However,the pollenkitt is not transported to the pollengrains, whichstrongly supports our theory that this process is mechanicallypollen-controlled. The development of the epidermal and endothecialcells is normal, except in a part of the anthers where thesecells do not expand, after which dehiscence is incomplete. Thelatter process is discussed in relation to the deviations insidethe locular cavity. Aloe vera (L.) Burm. fil., Aloe ciliaris Haw., Liliaceae, male sterility, tapetum, pollenkitt, endothecium, anther dehiscence     

Anther, pollen and tapetum development in safflower, Carthamus tinctorius L

In safflower, the anther wall at maturity consists of a single epidermis, an endothecium, a middle layer and the tapetum. The tapetum consists mainly of a single layer of cells. However, this single-layer appearance is punctuated by loci having ‘two-celled’ groupings due to additional periclinal divisions in some tapetal cells. Meiotic division in microsporocytes gives rise to tetrads of microspores. The primexine is formed around the protoplasts of microspores while they are still enveloped within the callose wall. Just prior to microgametogenesis, the microspores enlarge through the process of vacuolation, and the exine wall pattern becomes established. Microgametogenesis results in the formation of 3-celled pollen grains. The two elongated sperm cells appear to be connected. The exine wall is highly sculptured with a distinct tectum, columellae, a foot layer, an endexine and a thin intine. Similar to other members of the Asteraceae family, the tapetum is of the invasive type. The most novel finding of this study is that in addition to the presence of invasive tapetal cells, a small population of ‘non-invasive’ tapetal cells is also present. The tapetal cells next to the anther locules in direct contact with the microspores become invasive and start to grow into the space between developing microspores. These tapetal cells synthesize tryphine and eventually degenerate at the time of gametogenesis releasing their content into the anther locules. A smaller population of non-invasive tapetal cells is formed as a result of periclinal divisions at the time of tapetum differentiation. These cells are not exposed to the anther locules until the degeneration of the invasive tapetal cells. The non-invasive tapetal cells have a different cell fate as they synthesize pollenkitt. This material is responsible for allowing some pollen grains to adhere to each other and to the anther wall after anther dehiscence. This observation explains the out-crossing ability of Carthamus species and varieties in nature.     

Composition of lipids produced by some strains ofCandida species. Production of single-cell oil in a chemostat culture

Fatty acid composition of the lipids produced by four strains ofCandida species was studied. Oleic acid was the principal fatty acid. Cellular lipids ofCandida sp. andC. pulcherima were rich in palmitic acid. Lipids fromC. lipolytica contained a significant amount of palmitoleic acid, whereasC. farinosa produced oil rich in stearis and α-linolenic acid. Analysis of cellular lipids ofCandida sp. andC. pulcherima during growth on a nitrogen-limited medium showed that oils accumulated in the exponential growth phase were more unsaturated than those accumulated in the decelerating and stationary phases. In a chemostat culture,Candida sp. accumulated about 40% of lipid. The specific rate of lipid formation, at a dilution rate ofD=0.09/h, was 35 mg of lipid per g of biomass per h and the yield of lipid on glucose was 11.4%.