Surface carbohydrates and cell wall structure of in vitro-induced uredospore infection structures ofUromyces viciae-fabae before and after treatment with enzymes and alkali

Summary Uredospores ofUromyces viciae-fabae differentiate to form germ tubes, appressoria, infection hyphae and haustorial mother cells on oil-containing collodion membranes. The cell walls of these infection structures were studied with the electron microscope and with FITC-labeled lectins before and after treatment with enzymes and inorganic solvents. Binding of the FITC-labeled lectins was measured with a microscope photometer. The enzymes pronase E, laminarinase, chitinase and lipase had different effects on each infection structure. Pronase treatment uncovered the chitin of germ tubes, appressoria and haustorial mother cells, but not of substomatal vesicles and infection hyphae. A mixture of - and -1,3-glucanase which also contained chitinase activity dissolved germ tubes and appressoria completely, but not infection pegs, substomatal vesicles, infection hyphae and haustorial mother cells. After treatment with laminarinase or lipase, an additional layer, which is especially obvious over the substomatal vesicle, infection hypha and haustorial mother cell, bound to LCA-FITC. In the wall of the haustorial mother cell, a ring, which surrounds the presumed infection peg, had strong affinity for WGA after protease and sodium hydroxide treatment. The infection structures have a fibrillar skeleton. The main constituent seems to be chitin. This skeleton is more dense or has a higher chitin content in the walls of appressoria and haustorial mother cells. The fibrils of the skeleton extend throughout the cell wall of the germ tube and appressorium. They are embedded within amorphous material of complex chemical composition (-1,3-glucan, -1,3-glucan, glycoprotein). The chitin of the infection peg, substomatal vesicle, infection hypha and haustorial mother cell is covered completely with this amorphous material. These results show, that each infection structure has distinct surface and wall characteristics. They may reflect the different tasks of the infection structures during host recognition and leaf penetration.Abbreviations AP appressorium - FITC fluorescein isothiocyanate - GT germ tube - HC haustorial mother cell - IH infection hypha - IP infection peg - LCA Lens culinaris agglutinin - n nucleus - neu neuramic acid - p pyranoside - R ring - s septum - SV substomatal vesicle - WGA wheat germ agglutinin     

Cell structure and reproduction process in the Blue-Green algaChamaesiphon

Ultrathin sections were studied in 2 strains and 2 samples from the nature of the genusChamaesiphon, representing 4 different species. Thylakoids are distributed mainly on the periphery of the cells, the cell-wall is probably 2-layered, and variable multilayered mucilaginous envelopes are developed around the cells. The cell division starts, as well as in otherCyanophyceae, by the invagination of the cytoplasmic membrane and of cell-wall layers into the protoplast; the mucilaginous envelopes—pseudovaginae—do not participate in this process but they form only the firm sheaths around the cells. The way of reproduction is, therefore, essentially the same as that described in other chroococcal Blue-Green algae (e.g.,Synechococcus), and the main difference is the polarized growth of theChamaesiphon cells. The taxonomical position of chamaesiphonoid algae is not as isolated as it was earlier supposed, the similarity withEntophysalidaceae is evident.     

Ribeiroia marini: Surface ultrastructure of redia,cercaria, and adult

Rediae, cercariae, and adults of Ribeiroia marini were examined using a scanning electron microscope to determine the types of tegumental sensory structures and their locations. Sensory structures were observed among numerous tegumental folds in the area immediately surrounding the mouth of the rediae. These sensory structures are similar in appearance, location and fine structure to sensory structures described from the anterior tips of rediae known to be predacious on the sporocysts of Schistosoma mansoni. These uniciliated structures may function as chemoreceptors to aid the redia in migration through snail tissue. Five types of sensory structures bearing one, two, or multiple cilia were distinguishable on the cercariae. These structures were located on and around the oral sucker, dorsal and ventral body surfaces and on the tail. They may be used by the cercariae to locate the intermediate host fish and to find suitable sites within the lateral line scales for encystment. The ventral surface of the adult fluke is covered with spines and shows an absence of sensory structures on the general body surface. Sensory structures were seen in the area surrounding the oral and ventral suckers. The extended cirrus organ has a folded tegument, but lacks spines or sensory structures.     

In vitro initiation of adventitious structures in relation to the abscission zone in needle explants of Picea abies: anatomical considerations

A comparison of the regeneration potential of needles of different ages in Picea abies emphasized the importance of taking into account the manner of explantation as well as the state of differentiation of the abscission zone. Generally, response in terms of initiation of adventitious structures decreased progressively not only with needle age (5 to 10 to 15 mm long) but also with the distance from the abscission zone towards the tip, that is, distally. On a bud-induction medium adventitious shoot but primordia were produced proximally and distally (except for the very tip) of the weakly-developed abscission zone in needles ca. 5 mm and shorter. In needles between 5 and 10 mm long the various cell types of the abscission zone commenced differentiation, and adventitious structures (shoot bud and other primordia) were formed proximal and immediately distal to it. In needles ca. 15 mm long, in which the abscission zone's hyaline, separation and protective layers became well-developed and where senescence of the distal part commenced, response was limited to proximal tissues. Divisions giving rise to adventitious primordia distal to the abscission zone arose from epidermal cells proper and, in a more acropetal position, also from subsidiary cells of the stomata. Cells of the hypodermis contributed only in the near-distal region of the abscission zone in younger needles, and before commencing differentiation into fibres.
When excised carefully, the explant consists of a leaf plus a peg-like cushion of axillary, meristematic tissue proximal to the abscission zone and capable of ready regeneration. In view of the apparent relationship between age and the stage of development of the abscission zone, it was concluded that there exists a critical needle length which should not be exceeded when attempting in vitro induction of organ primordia.     

CHARACTERIZATION OF MICROBIALITE-FORMING CYANOBACTERIA IN A TROPICAL LAGOON: TIKEHAU ATOLL, TUAMOTU, FRENCH POLYNESIA

Natural populations of benthic cyanobacteria in the lagoon of Tikehau Atoll in French Polynesia were studied using a polyphasic approach that combined field observations, LM, culturing, and molecular sequencing. The approach assessed their phenotypic (morphotypic and ecological) and genotypic diversity. Partial sequences (approximately 450 bp long) of the PCR-amplified 16S rRNA gene were obtained from both natural and cultured populations using cyanobacteria-specific primers. The sequences obtained clustered into six separate phylogenetic clusters in relation to the complete set of 16S rRNA sequences available in public databases. Phylogenetic clustering correlated in many cases with some morphological characteristics. For example, Spirulina subsalsa could be identified to the morphospecies level using both molecular and microscopic approaches. Morphotypes identified as Symploca hydnoides (Kütz. ex Gomont) TK22, Phormidium sp. TK1, and P. laysanense (Lemmerman) TK14 formed a distinct cluster. The morphogenus Hydrocoleum (Blennothrix) clustered interestingly close to the morphologically similar, but planktonic, marine cyanobacterium Trichodesmium , suggesting a relationship. Other sequences belonging to morphotaxa with very narrow trichomes were found to be polyphyletic. Enrichment cultures, with inoculum obtained from field populations, were followed over a period of 18 months. Dominance in all cultures shifted over time in favor of a set of cyanobacterial strains with narrow trichomes, which were phenotypically and phylogenetically different from natural populations dominating the original samples. Sequences from strains enriched by cultivation clustered into two well-defined phylogenetic groups, possibly identifying new taxa. These clusters may represent a niche of opportunistic species, evolved to exploit short-term nutrient spikes in the environment.     

Reproductive morphology in relation to alternative male reproductive tactics in Scartella cristata

The relationship between reproductive morphology and reproductive tactics was examined in Scartella cristata , a combtooth blenny, which exhibits three behaviourally distinct mature male types: nesters, big males that care for eggs; hole-dwellers, medium-sized, non-reproducing males that are site-attached to a hole; sneakers, small, vagrant males that release sperm in the nests of the big males. The anal fin gland was a densely folded, mucous-secreting structure probably involved in pheromone synthesis. It was relatively larger in nesters than hole-dwellers, and altogether rudimentary in sneakers. Sneakers invested more in sperm production than nesters or hole-dwellers, suggesting adaptation to sperm competition. Approximately half of the testes of nesters and hole-dwellers was comprised of a highly developed efferent duct system or 'testicular gland', but this was extremely reduced in sneakers. In nesters the gland was characterized by many large vacuoles. A pair of secretory blind pouches was present in nesters and hole-dwellers, but barely visible in sneakers. In nesters, the sperm duct walls were thickened and highly secretory containing sperm dispersed in a granular matrix. In sneakers they were thin-walled and packed with concentrated sperm. Such differences probably represent different priorities for sperm production in relation to sperm competition and sperm economy. Thus it appears the accessory structures are traits developed specifically for a nesting tactic, whereas the gonad of sneakers is simply organized to produce as much sperm as possible.     

Rhodium aryloxide complexes containing terdentate nitrogen ligands, C-O bond formation, hydrogen bonding with phenol and oxidative addition reactions. Molecular structure of an Rh(III)-acetyl complex

The new rhodium(I) phenoxide complexes [Rh(OPh) (2,6-(CH=R²)₂C₅H₃N)] (R² = i-Pr(3), t-Bu(4)) containing strongly electrondonating N-N′-N ligands, have been prepared by a metathesis reaction of [RhCl(2,6-(CH=R²)₂C₅H₃N)] (R² = i-Pr (1), t-Bu (2)) with NaOPh. These rhodium(I) phenoxide complexes 3 and 4, which are very sensitive to O₂ but stable towards H₂O, give with phenol the adducts [Rh(OPh) (2,6-(CH=NR²)₂C₅H₃N)] · HOPh (R2 = i-Pr (5), t-Bu (6)), which contain strong O-HO hydrogen bonds. The hydrogen bonded phenol could not be extracted with diethyl ether, while no exchange of the hydrogen bonded phenol and the phenoxide ligand in 4 is observed on the NMR time scale. However, a small excess of phenol results in exchange of the hydrogen bonded phenol, the coordinated phenoxide ligand and free phenol on the NMR time scale. Reaction of 3 and 4 with p-nitrophenol afforded [Rh(OC₆H₄-(NO₂-4))(2,6-(CH=R²)₂C₅H₃N)] · HOPh (R² = i-Pr (7), t-Bu (8)) in which the formed phenol is hydrogen bonded to the Rh(I)-OC₆H₄-(NO₂-4) moiety. The O-HO bond is less strong than in 5 and 6, as the hydrogen bonded phenol could be removed by diethyl ether.Treatment of 3 with acetyl chloride and benzoyl chloride in benzene at room temperature gave phenylacetate and RhCl₂(C(O)C₆H₃) (2,6(C(H)=N-i-Pr)₂C₅H₃N)] (15), and phenylbenzoate and [RhCl₂(C(O)Ph) (2,6-(C(H)=N-i-Pr)₂C₅H₃N)] (19), respectively. Complex 15 and the analogous complex [RhCl₂(C(O)CH₃) (2,6-(C(H)=N-t-Bu)₂C₅H₃N)] (16) could also be prepared directly from acetyl chloride and 1 or 2, respectively. The single crystal X-ray determination of complex 16, monoclinic, space group P2₁/_c, a = 10.0477(5), b= 11.7268(6), c= 19.2336(9) Å, β = 92.041(4)°, Z = 4, R₁ = 0.0281, shows that the acetyl group occupies an axial position, while the N-N′-N ligand is positioned equatorially. In solution this geometry remains unchanged as was shown by variable temperature ¹H NMR measurements. When the oxidative addition of acetyl chloride to 3 was carried out at −78°C in toluene the intermediate complex [RhCl(OPh) (C(O)Me) (2,6-(C(H)=N-i-Pr)₂C₅H₃N)] (11) could be isolated, which at room temperature reductively eliminates phenylacetate with formation of 1. Oxidative addition of acetyl chlori de to 4 at room temperature gives [RhCl(OPh) (C(O)Me) (2,6-(C(H)=Nt-Bu)₂C₅H₃N)] (12) which yields phenylacetate and 2 at 70°C in benzene by inductive elimination. Treatment of 3 with two equivalents of benzyl chloride afforded a mixture of [RhCl(OPh) (CH₂Ph) (2,6-(C(H)=N-i-Pr)₂C₅H₃N)] (13) and [RhCl₂(CH₂Ph) (2,6-(C(H)=N-i-Pr)₂C₅H₃N)] (17) and some non-characterizable organic products, while 4 only yielded [RhCl(OPh) (CH₂Ph) (2,6-(C(H)=N-tBu)₂C₅H₃N)] (14).     

Synthesis, characterization, and reactivity of organometallic Zr(IV) carboxylate complexes

A series of zirconium(IV) complexes, [ZrX₂(XDK)], where XDK is the constrained carboxylate ligand m-xylylenediamine bis(Kemp's triacid imide), were prepared and structurally characterized. The solid state structure of the mononuclear carboxylate alkyl complex [Zr(CH₂Ph)₂(XDK)] reveals that one benzyl group is bonded in an η²-fashion to the metal center. The reactivity of [Zr(CH₂Ph)₂(XDK)] displays its electrophilic character toward nucleophiles strong enough to displace the η²-benzyl group. Thus, weak sigma donor ligands such as CO, alkynes and anilines do not react, whereas strong sigma donors, such as pyridines and isocyanides, rapidly form the monoadduct [Zr(CH₂Ph)₂(4-tert-butylpyridine)(XDK)] and [Zr{η²-2,6-Me₂PhNCCH₂Ph}₂(XDK)], an η²-iminoacyl derivative, respectively. Attempts to prepare zirconium amido complexes with H₂XDK generally afforded the eight-coordinate [Zr(XDK)₂] complex but use of the small amido ligand precursorZr(NMe₂)₄ allowed [Zr(NMe₂)₂(4-tert-butylpyridine)(XDK)] to be isolated in good yield.