C-Glycosylflavones in Gnetum gnemon

The relationship of the Gnetales to other gymnosperms is presently ill understood. The occurrence of C-glycosylflavones as the only detactable flav     

Stilbene derivatives from Gnetum gnemon Linn

Four stilbene derivatives, gnemonols K and L (resveratrol trimers), M (isorhapontigenin dimer), and gnemonoside K (glucoside of resveratrol trimer) together with eleven known stilbenoids and a lignan were isolated from the acetone, methanol and 70% methanol soluble parts of the root of Gnetum gnemon (Gnetaceae). The structures of the isolates were determined by spectral analysis. The antioxidant activity of the stilbenoids on lipid peroxide inhibition and super oxide scavenging activity were also investigated.     

Antioxidant activities of different parts of Gnetum gnemon L.

Analyses on biological activities of Gnetum gnemon were done to determine the total phenolic and antioxidants of the plant. Four parts of G. gnemon were used in this study, which were leaf, bark, twig, and seeds of the plant. All parts were extracted in methanol, ethanol, hexane, chloroform and hot water using reflux. The total phenolic content of the plant extracts were determined by using Folin-Ciocalteu method. The results demonstrated that the bark from hot water extract showed the highest total phenolic at 10.71?±?0.01 mg GAE/ FDW, while the lowest was chloroform extract of seed at 2.15?±?0.01 mg GAE/ FDW. The antioxidant activity of the plant extracts were determined by using DPPH and FRAP assays, respectively. The DPPH results showed that all plant extracts demonstrated weak free radical scavenging activity tested at the final concentration of 300 μg/ml. In contrast, the methanolic twig extract showed strong reducing power activity (FRAP) at 83.55?±?1.05%, while the hot water seed extract showed the least activity at 41.86?±?4.22% tested at the final concentration of 300 μg/ml. However, there were no correlation between total phenolics and both antioxidant assays tested.     

Development of gelatinous (reaction) fibers in stems of Gnetum gnemon (Gnetales)

In extraxylary tissues of the stem Gnetum gnemon produces gelatinous fibers that can also function as reaction or tension fibers. These gelatinous fibers occur in all axes in the outer cortex and in displaced axes progressively in the middle and inner cortex and finally in the secondary phloem. Early cell differentiation in the cortex produces initials of laticifers that are unique in gymnosperms. Subsequently narrow fibers differentiate from cells that undergo both extensive passive elongation, as a result of internodal elongation, together with their active apical intrusive growth. Outer fibers always complete secondary wall development and become an important mechanical component of stems. Differentiation of fiber initials continues in the middle and inner cortex, but secondary wall formation can only be determined by a gravimorphic stimulus that produces eccentric development of fibers. Further eccentric development of fibers then continues in the outer secondary phloem from dedifferentiated phloem parenchyma cells that initially undergo extensive intrusive growth. All such cells have characteristic features of tension fibers of angiosperms. They exhibit a pronounced purely cellulosic innermost layer of the secondary wall (Sg layer). In addition, fiber initials are coenocytic, including up to eight nuclei that become distributed uniformly throughout the length of the cell. Mature macerated fibers are markedly brittle, making accurate length measurements difficult. Although cytologically uniform, these fibers thus originate from two kinds of initial (primary and secondary). They also differ in their response to a gravimorphic stimulus determined by their times of inception and their eccentric location. These cells show a suite of positional and gravimorphic responses that illustrate the complexity of plant cell differentiation.     

Double Fertilization in Gnetum gnemon: The Relationship between the Cell Cycle and Sexual Reproduction

Gnetum gnemon, a nonflowering seed plant and member of the Gnetales, expresses a rudimentary pattern of double fertilization that results in the formation of two zygotes per pollen tube. The process of double fertilization in G. gnemon was examined with light and fluorescence microscopy, and the DNA content of various nuclei involved in sexual reproduction was quantified with 4[prime],6-diamidino-2-phenylindole microspectrofluorometry.Male and female gamete nuclei pass through the synthesis phase of the cell cycle and increase their DNA content from 1C to 2C before fertilization. Each of the two zygotes found in association with a pollen tube is diploid and contains the 4C quantity of DNA at inception. Based on these results as well as previous studies of nuclear DNA content in plant sperm, eggs, and zygotes, three fundamental and distinct patterns of gamete karyogamy among seed plants can be circumscribed: (1) G1 karyogamy, in which male and female gametes contain the 1C quantity of DNA throughout karyogamy and the zygote undergoes DNA replication; (2) S-phase karyogamy, in which gamete nuclei initiate fusion at 1C but pass through the S phase of the cell cycle before completely fusing; and (3) G2 karyogamy, in which male and female gamete nuclei pass through the S phase of the cell cycle before the onset of fertilization. Our results show definitively a pattern of G2 karyogamy in G. gnemon.     

Infrageneric variation in partner specificity: multiple ectomycorrhizal symbionts associate with Gnetum gnemon (Gnetophyta) in Papua New Guinea

Majority of autotrophic plants and fungi associate with multiple mycorrhizal partners, with notable exceptions being Gnetum africanum, Pisonia grandis, and Alnus spp from the phytobiont perspective. We hypothesized that an understorey tree species Gnetum gnemon hosts a narrow range of mycobionts as shown in G. africanum and suggested for South American species. Sampling and molecular analysis of G. gnemon root tips revealed that besides Scleroderma spp. this gymnosperm tree associates with several fungal species from unrelated lineages. However, all Scleroderma isolates that associate with Gnetum spp. belong to a narrow clade close to Scleroderma sinnamariense. Our results demonstrate for the first time that specificity for mycobionts may substantially differ within an ectomycorrhizal plant genus.     

Double fertilization in Gnetum gnemon (Gnetaceae): its bearing on the evolution of sexual reproduction within the Gnetales and the anthophyte clade

The fertilization process in Gnetum is critical to our understanding of the evolution of sexual reproduction within the Gnetales, a monophyletic group of nonfiowering seed plants that are the closest living relatives to flowering plants. Although much is known about the fertilization process in Ephedra, which is basal within the Gnetales, little is known about sexual reproduction in the derived sister groups Gnetum and Welwitschia. Ovules of Gnetum gnemon were collected at various stages after hand pollination and processed for light, fluorescence, and electron microscopy. Approximately 5 d after pollination, pollen tubes reach sexually mature female gametophytes, which are coenocytic. At that time, a binucleate sperm cell is found within each pollen tube. Within 7 d of pollination, double fertilization events occur when each of two sperm nuclei released from a pollen tube fuses with a separate, undifferentiated female nucleus within the free nuclear female gametophyte, which lacks differentiated egg cells. The products of double fertilization are two viable zygotes; endosperm is not formed. The lack of differentiated egg cells in Gnetum gnemon is unparalleled among land plants and the documentation of a regularly occurring process of double fertilization is congruent with the hypothesis that a rudimentary process of double fertilization evolved in a common ancestor of angiosperms and Gnetales.     

C-Glycosylflavones from Gnetum buchholzianum and Gnetum africanum

C-Glycosylflavones, including two new compounds 2″-xylosylisoswertisin and 2″-glucosylisoswertisin, were isolated from the leaves of Gnetum buchholzianum and G. africanum. The occurrence of apigenin 7-neohesperidoside distinguishes the latter from the first species.     

Stilbenes of Gnetum ula

Gnetin, a new stilbene isolated from Gnetum ula is assigned the structure 3,4-methylenedioxy-4′-methoxy-trans-stilbene, 3 on the basis of spectroscopic data and synthesis. The structure 3,3′,4-trihydroxy-2-methoxy-trans-stilbene, 1a earlier assigned to a trihydroxymonomethoxy stilbene is now revised to 3,4,5′-trihydroxy-3′-methoxy-trans-stilbene, 1b.     

Morphogenesis in Marsilea

An account is given of investigations on the development of sporelings of Marsilea using aseptic culture techniques. Special attention was paid to the heteroblastic leaf development and to the conditions leading to the origin of land or water forms. A study was made of the effects of changes in the composition and concentration of the culture medium. The substances tested included sugars, nitrogen compounds, metabolic inhibitors, auxins, gibberellic acid and kinetin.
It was concluded that the changes in leaf segmentation of Marsilea , or heteroplastic development, are correlated with changes in the size of the apical meristematic regions of the shoot, which in turn are influenced by the nutritional status of the plant. On the other hand, the differences between land and water forms are probably due to differences in the available concentration of dissolved carbohydrates in the growing parts. The results are discussed in relation to similar morphogenetic problems in other vascular plants.     

Stilbenoids from the lianas of Gnetum pendulum

Two stilbenoids, gnetupendin A and B, were isolated from the lianas of Gnetum pendulum C. Y. Cheng, together with four known compounds, resveratrol, isorhapontigenin, shegansu B and beta-daucosterol. Their structures were determined on the basis of analysis of spectral evidence, especially 2D NMR spectroscopic techniques.     

Ontogeny of the stomata in Gnetum ula Brongn.

The stomata in Gnetum ula Brongn. occur in large numbers on the abaxial surface of the leaves and are orientated in various directions. A few were seen in some preparations on the adaxial surface also, especially in the region of the midrib.
Stomatal development follows the syndetocheilic type of Florin. According to the terminology of ontogenetic types suggested by Pant, they may be described as mesogenous dolabrate; they are mesoparacytic (rubiaceous) and amphicyclic. In this respect, and in several details, the present findings support the observations of Takeda, and differ rather widely from those of Maheshwari & Vasil.
Twin stomata were also met with frequently, as well as several stomata lying together contiguously. The structural features of these are described and commented upon briefly in the paper.     

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.     

Ovule and seed ontogeny inGnetum gnemon L.

The ovule ofGnetum gnemon has three envelopes around the nucellus. The outer one forms two clear swellings at the lateral sides during the early developmental stages. The middle envelope also shows two swellings in many cases arranged decussately with respect to those of the outer one. All these swellings become obscure or disappear later. The inner envelope arises as an annular primordium and forms several manifest lobes at the stage of pollination. it develops two proliferating structures from its middle portion, viz., a flange and a micropyle-closing tissue. The three envelopes differentiatiate into the fleshy outer, sclerenchymatic middle and compressed inner layers of the seed coat, respectively. The inner one, however, remains restricted to the apical part of the seed owing to endochalazal growth. The outer envelope is derived from both dermal and subdermal cells of the ovule primordium and, therefore, is of dual origin. The middle and inner envelopes are subdermal in origin. The present study has cleared up some conflicting reports in the previous publications.     

Wood and bark anatomy of Gnetutn gnemon L.

Quantitative and qualitative data are presented for seven collections representing two varieties (unlike in habit) of Gnetum gnemon. Tracheids are present, but abundant and intermixed with them are septate fibre-tracheids rich in starch. Axial parenchyma has been reported only once previously for the species. Axial parenchyma is in strands of 4–10 cells, is rich in starch, is primarily vasicentric (paratracheal) in distribution, less commonly diffuse. About equally common are simple and compound perforation plates; the latter are composed of from two to about ten bordered foraminate perforations, the shape of which may be altered by crowding or coalescence, but is clearly still foraminate. Lateral walls of vessels bear pits that are vestured around pit cavities, not facing the pit membrane. Rays are composed mostly of procumbent cells; the tangential walls bear bordered pits. Crystals, present in ray cells and (rarely) axial parenchyma vary widely in size. Crystalliferous sclereids with layered walls, starch-rich parenchyma, and gelatinous secondary phloem fibres are the main components of bark. Early stages in origin of successive vascular cambia in bark are newly described. When representative conditions are derived from study of large numbers of slides, the classical view that Gnetum vessels are unlike those of angiosperms is supported. Features of Gnetum gnemon wood are discussed in the light of ecology and conductive physiology.