Iridoid glycosides from Gmelina arborea

Three iridoid glycosides 6-O-(3'-O-benzoyl)-alpha-l-rhamnopyranosylcatalpol (1a), 6-O-(3'-O-trans-cinnamoyl)-alpha-l-rhamnopyranosylcatalpol (2a) and 6-O-(3'-O-cis-cinnamoyl)-alpha-l-rhamnopyranosylcatalpol (3a) were isolated from aerial parts of Gmelina arborea and structures were elucidated by spectral analysis. Additionally a known iridoid 6-O-(3', 4'-O-dibenzoyl)-alpha-l-rhamnopyranosylcatalpol (4) was also isolated and identified.     

Provenance- and subculture-dependent variation during micropropagation of Gmelina arborea

Axillary shoot elongation, formation of multiple shoots and rooting of shoots were compared in nodal segment cultures of Gmelina arborea Roxb. from seedlings obtained from six provenances, over several subcultures. Provenance-dependent variation was observed with respect to these parameters. In addition, a subculture-dependent decrease was observed in multiple shoot formation and root induction. Seventy percent of the rooted plantlets were successfully hardened and transferred to soil. A transient decrease in photochemical efficiency was observed during the early stages of hardening, whereas ribulose-1,5-bisphosphate carboxylase (EC 4.1.1.39) levels increased gradually as the plants acclimatized to photoautotrophic growth.     

Acylated iridoid glycosides and acylated rhamnopyranoses from Gmelina arborea flowers

Nine acylated iridoid glycosides (1–9), five acylated rhamnopyranoses (10–14) and verbascoside (15) were isolated from Gmelina arborea flowers, including 5 new compounds (1, 2, and 10–12). The cytoprotective activity of 11 selected compounds (1–8, 10, 11, and 15) against CCl₄-induced cytotoxicity on liver was determined. Compounds 1, 2, 4, 7, 8 and 15 displayed hepatoprotective activity. 6-O-α-l-(2″, 3″-di-O-trans-p-hydroxycinnamoyl)rhamnopyranosylcatalpol (2) exhibited the most potent cytoprotective effect with an EC₅₀ value of 42.5 μM (SI = 19.3) compared with biphenyldimethylesterate (DDB, EC₅₀ = 277.3 μM, SI = 9.8) and bicylo-ethanol (EC₅₀ = 279.2 μM, SI = 12.2). Among the acylated iridoid glycosides, the compounds (2 and 8) containing phenolic hydroxy groups were more active than were those lacking them.     

The influence of soil drought and partial waterlogging on water relations of Gmelina arborea seedlings

Summary Stomatal conductance of unstrossed, soil drought, and previously drought (predrought) Gmelina arborea seedlings increased in the morning and decreased before or immediately after midday. In the unstressed and predrought seedlings, leaf water potential decreased with increases in transpiration. In soil drought seedlings, there was some evidence of decreased hydraulic conductivity from soil to the plant, as indicated by the shape in the slope of the water potential/transpiration relationship. Root growth of drought plants was greater than in their unstressed counterparts at the lowest soil segment of a pot. The partial recovery of predrought seedlings was attributed to this subtantial root growth in the lowest soil segment.In the second experiment, Gmelina arborea seedlings were partially waterlogged, by flooding the polyethylene bag to half its length, for a period of 23 days. Waterlogging induced stomatal closure and reduction in leaf water potential but there was some evidence of tolerance to waterlogging towards the end of treatment. Root growth, shoot and root dry weights were slightly reduced below those of controls. After 9 days of waterlogging, adventitious roots began to form which correlated with depletion of soluble sugars in the shoot but with an increase in the roots.It is suggested that the tolerance of Gmelina plants to either soil drought or waterlogging may partly be due to partitioning of the soluble sugars from shoot to roots for production of roots and formation of adventitious roots respectively which are likely to enhance the flow of water from the soils to the plant. Therefore the plant response is very similar under conditions of increased deficits and surplus of soil water.     

P-Protein in sieve elements

Summary The ultrastructure of P1 and P2 proteins in the sieve elements of Heracleum mantegazzianum is described. P1-protein tubules are closely associated with stacks of membranes, are often linked by short cross-bridges, and occasionally display a hexagonal packing. Incubation with the alkaloids vinblastine and colchicine had no discernible effects on the ultrastructure of the sieve elements at various stages during differentiation. Evidence for and against any similarities between P1-protein tubules and cytoplasmic microtubules is discussed.     

Pollen limitation and seed set associated with year-to-year variation in flowering of Gmelina arborea in a natural tropical forest

The year-to-year variations in flowering, pollen and fruit production in ten Gmelina arborea individuals in a natural forest were observed over a period of five years, 2009?2013, and pollinator visits were observed closely over two years, 2011 and 2012. A pollen supplementation experiment was also undertaken in two years (2011 and 2012) of contrasting flowering levels. Considerable year-to-year variations were observed in flower, pollen and fruit production. The observed variation represented a normal sequence of good-year and poor-year cycling which is most parsimoniously attributed to resource allocation. The average level of pollen production per individual tree in good flowering years oscillated between 6.6 and 9.62 × 10⁸, which in the poor flowering years was between 1.92 and 3.07 × 10⁸. The magnitude of pollen limitation across years was highly significant (p < 0.0001). Fruit set through supplemental pollination was 73% and 96% greater than that of the open-pollinated branches in the year 2011 and 2012, respectively. Pollen limitation, irrespective of the arrival of outcross pollen, can reduce annual seed set in predominantly bee-pollinated trees. However, various other factors may cause flower abortion in addition to pollen limitation. The results of this study would be very valuable to the seed orchard managers and the silviculturists to manage the seed production areas (SPAs) of G. arborea. The study ultimately recommends supplemental pollination in seed orchards of G. arborea for better genetic gain and good seed yield.     

Proteomic approach to study leaf proteins in a fast-growing tree species, Gmelina arborea Linn. Roxb

Foliar proteome studies have become highly significant for a comprehensive understanding of complex processes associated with plant growth and development. In the present study, we present a proteomic approach to analyze leaf proteins in an important timber-yielding and fast-growing forest tree species, Gmelina arborea Linn. Roxb. (Verbanaceae). Foliar protein analysis involved protein extraction, two-dimensional electrophoresis (2-DE) and matrix-assisted laser desorption/ionization time of flight (MALDI–TOF–TOF). From the 2-DE protein profile of Gmelina leaves, we identified and isolated 150 well-separated protein spots; among these, 64 protein spots were identified by mass spectrometric (MS/MS) analysis. These proteins were classified according to their involvement in basic biological functions, such as photosynthesis, amino acid metabolism, cytoskeleton, cell wall metabolism, stress-related proteins, redox maintenance, electron transport chain, phytohormone metabolism and protein translation and folding. Analytical variance was determined for the protein spots of samples from different plants. The present study is believed to provide a foundation for the use of leaf proteomics in addressing fundamental physiological and biochemical processes associated with growth and productivity of tree species such as Gmelina arborea.     

Seasonal variation in antioxidant enzymes and the sprouting response of Gmelina arborea Roxb. nodal sectors cultured in vitro

Nodal sector explants of Gmelina arborea Roxb. showed seasonal variation in the sprouting of axillary buds in vitro. Explants from mature trees showed only 20% sprouting in summer, while those from seedlings and young trees showed over 85% sprouting in this season. In winter, there was a significant decrease in the sprouting response of explants from young and mature trees but not in that of seedling explants. We have attempted to correlate the sprouting response of the explants with their antioxidant status. Activities of three enzymes, namely ascorbate peroxidase, superoxide dismutase and guaiacol-dependent peroxidase which form a part of the antioxidant defense system of plants, were studied in the excised nodal sectors before and after placing them on culture medium. Prior to culture, higher activities of ascorbate peroxidase, superoxide dismutase and guaiacol-dependent peroxidase were observed during winter than during summer. During the culture period, ascorbate peroxidase, superoxide dismutase and guaiacol-dependent peroxidase showed variation depending on the season in which the explants were isolated, and the age of the donor. Axillary bud sprouting in vitro appeared to depend more on the physiological state of the donor, than on the oxidative stress generated during culture. This revised version was published online in June 2006 with corrections to the Cover Date.     

Effect of aluminium toxicity on growth responses and antioxidant activities in Gmelina arborea Roxb. inoculated with AM fungi

Arbuscular mycorrhizal fungi alleviating the adverse Aluminium effects on growth and antioxidant activity was tested in Gmelina plants. Under greenhouse and aluminium stress condition, the mycorrhizal Gmelina plants showed good growth as compared to non mycorrhizal Gmelina plants. Mycorrhizal colonization in Gmelina was found not to be significantly influenced by aluminium concentrations. Results also indicate that symbiotic association was successfully established between Glomus intraradices and Gmelina plants and mycorrhizal colonization consequently increased the biomass of Gmelina. The root proline accumulation was found to increase in mycorrhizal Gmelina plants for osmotic adjustment of stress tissues under first and second level of Aluminium stress. It was observed that Mycorrhizal colonization increased the shoot root Peroxidase and Superoxide dismutase activities in mycorrhizal Gmelina under second level of Aluminium stress. Mycorrhizal fungi play a major role in phytostabilization by secreting one of the glycoprotein, i.e., Glomalin, which stabilizes the Aluminium in soil as well as in the roots of Gmelina plants.     

Growth,biomass, carbon storage and nutrient distribution in Gmelina arborea Roxb. stands on red lateritic soils in central India

Growth, biomass, carbon storage and nutrient (N, P and K) variations in 1 to 6-year-old chronosequence plantations of Gmelina arborea were studied in three degraded red lateritic sites in central India. Growth parameters (dbh, total height and number of branches) varied significantly due to difference in age and site quality, but tree density showed non-significant variation. Stand biomass ranged from 3.94 (1-year-old) to 53.67 Mgha(-1) (6-year-old) and stand carbon in 6-year-old plantations ranged from 24.12 to 31.12 Mgha(-1) at different sites. Among the tree components, the stem wood accounted for maximum C (56.25% at site 1) followed by branches (19.8% at site 3), roots (18.51% at site 2) and foliage (7.01% at site 3). Mean annual C accretion at 6 years age of plantation was highest in site 3 and it was 0.35, 2.66, 0.965 and 0.87 Mgha(-1) for leaf, stem, branches and roots, respectively. Quantity of nutrients increased with age. Total nitrogen accumulation in 6-year-old stands at the three sites ranged from 212.9 to 279.5 kgha(-1) with a mean annual storage of 238.43 kgha(-1) and total K ranged from 170.8 to 220.5 kgha(-1) with a mean annual storage of 189.93 kgha(-1). Phosphorous accumulation was lowest with a mean storage of 16.75 kgha(-1). The organic carbon and nutrients in the soils improved significantly after 6 years of G. arborea planting. Soil organic carbon increased from 8.46 to 14.02 Mgha(-1) within 6 years. At soil depths 0-20 cm, 21-40 cm and 41-60 cm, available N enhanced by 14.85%, 11.98% and 11.25%, K by 10%, 9.13% and 10.63%, whereas phosphorous declined by 26%, 23% and 20%, respectively. At 6 years, G. arborea stands sequestered 31.37 Mgha(-1) carbon. The nutrient management strategies in relation to carbon accretion in G. arborea stands on degraded lateritic sites are discussed.     

Displacement of an herbaceous plant species community by mycorrhizal and non-mycorrhizal Gmelina arborea, an exotic tree, grown in a microcosm experiment

Gmelina arborea Roxb. (Gmelina, Yemane) is a fast growing tree, native from India and considered as a potentially invasive woody plant in West Africa. Mycorrhizal inoculation of seedlings with Glomus intraradices was performed to study (1) the effect on the growth of G. arborea, (2) the impact on the catabolic diversity of soil microbial communities and (3) the influence on the structure of herbaceous plant species communities in microcosms. Treatments consisted of control plants, pre-planting fertilizer application and arbuscular mycorrhizal (AM) inoculation. After 4 months’ culture in autoclaved soil, G. arborea seedlings were either harvested for growth measurement or transferred into containers filled with the same soil but not sterilized. Other containers were kept without G. arborea seedlings. After 12 months’ further culture, effects of fertilizer amendment and AM inoculation on the growth of G. arborea seedlings were recorded. AM colonization was significantly and positively correlated with plant diversity. The substrate-induced respiration response to carboxylic acids was significantly higher in the absence of G. arborea and in the presence of G. intraradices as compared to the other treatments. The influence of AM symbiosis on plant coexistence and on allelopathic processes of invasive plants are discussed.     

The distribution of P-Protein in mature sieve elements of celery

Summary The extent of blocking of sieve-plate pores caused by release of cell turgor was investigated by fixing and processing for electron microscopy a long length of celery (Apium graveolens L.) phloem. Differences in distribution of P-protein within the pores were observed between those cells near the two cut ends, and the central cells.To assess the effect of chemical fixation on the distribution of P-protein, strands of celery phloem (fixed or unfixed, and not treated with cryoprotectants) were frozen in Freon 12 and then freeze-substituted. In sieve elements from unfixed tissue there were a greater number of sieve plates displaying partially open pores.Direct freezing of unprotected phloem tissue in Freon 12 resulted in the formation of ice crystals within the lumen of the sieve elements. Freezing of tissue at rates fast enough to avoid the formation of damaging ice crystals resulted in sieve-plate pores having an unoccluded central channel with a peripheral lining of P-protein. In the lumen of the sieve elements the P-protein filaments occurred as discrete bundles ca. 0.5 m in diameter, and as a parietal layer varying in thickness from 0.1 to 0.5 m.     

Iridoid glycosides from Gmelina philippensis

Six new iridoids, 6-O-alpha-L-(2"-O-, 3"-O-, 4"-O-tribenzoyl)rhamnopyranosylcatalpol, 6-O-alpha-L-(2"-O-, 3"-O-dibenzoyl, 4"-O-cis-p-coumaroyl)rhamnopyranosylcatalpol, 6-O-alpha-L-(2"-O-, 3"-O-dibenzoyl, 4"-O-trans-p-coumaroyl)rhamnopyranosylcatalpol, 6-O-alpha-L-(2"-O-benzoyl, 3"-O-trans-p-coumaroyl)rhamnopyranosylcatalpol, 6-O-alpha-L-(2"-O-, 3"-O-dibenzoyl)rhamnopyranosylcatalpol, and gmephiloside as well as five known monoacyl and diacyl rhamnopyranosylcatalpol derivatives were isolated from the aerial parts of Gmelina philippensis. Their structures were established by spectroscopic means. Additionally, the known iridoids catalpol, geniposidic acid, gardoside, and 8-epi-loganic acid were identified and quantified by GC and GC-MS. The taxonomic significance of rhamnopyranosylcatalpol derivatives and iridoid acids as chemical characters is discussed.     

Micropropagation ofGmelina arborea

Multiple shoots were obtained from single node explants of matureGmelina arborea Roxb. on MS medium supplemented with 6-benzyladenine (BA). Seven to nine shoots were formed whenin vitro-derived single node explants were subcultured on MS medium supplemented with 1.1 M BA. For root initiation the cut ends of microshoots were pulsed for 5 min with 246 M indole-3-butyric acid and transferred to a plastic cup containing sterile vermiculite. The shoots were covered with polyethylene bag and maintained in a culture room. After hardening, plantlets were transferred to earthen pots containing a mixture of garden soil: compost and have been established in the field.     

Diarylheptanoids from Myrica arborea

Investigations of the stem and root bark of Myrica arborea (Myricaceae) have yielded two novel diarylheptanoids, myricarborin and 11-O-beta-D-xylopyranosylmyricanol along with the known myricanol and 5-O-beta-D-glucopyranosylmyricanol. The structures of the novel compounds were determined by spectroscopic methods.     

A flavone glycoside from the stem of Ixora arborea

A new flavone glycoside isolated from the stem of Ixora arborea has been characterized as chrysin 5-O-β-D-xylopyranoside on the basis of spectral data, colour reactions and degradation studies.