In vitro regeneration patterns of Platycerium bifurcatum leaf cell suspension culture

A simple suspension culture system of Platycerium bifurcatum was developed where sporophytes could be regenerated directly from leaf cells or indirectly through an aposporous gametophyte stage under the same culture conditions. Single cells and aggregates of up to 100 cells developed aposporous gametophytes which later gave rise to sporophytes. Such gametophytes started apogamy when they were mostly less than 0.7 mm in length, bearing only rhizoids. In most cases, only one sporophyte was regenerated from one gametophyte. Aggregates of 500–1000 or more cells, on the other hand, regenerated sporophytes directly. Intercellular interaction was considered to be the physiological cause, and the separation of leaf cells to a certain degree drove the cells to embark on different regeneration paths. It is suggested that the possible existence of a threshold size of cell aggregates separates the two regeneration patterns. Received: 3 March 1997 / Revision received: 11 April 1997 / Accepted: 3 June 1997     

鹿角蕨化学成分的研究

从鹿角蕨（Platycerium wallichii Hook.)的干燥叶中分离得到七个成分,利用UV、IR、^13C-NMR、^1H-NMR、MS等光谱方法鉴定出它们的结构,分别为β－谷甾醇（I）、谷甾醇β-D-吡喃葡萄糖苷（Ⅱ）、2－propenoic acid,3-[2,3-dihydro-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-7-methoxy-5-benzofuramyl]-(Ⅲ）、松脂素（Ⅳ）、松脂素－4′－O－β－D－葡萄糖苷（Ⅴ）、2,5－二羟基苯甲酸甲酯（Ⅵ）、槲皮素3－O－β－吡喃半乳糖苷（Ⅶ）。七个成分均为首次从该种植物中获得。     

Ammonium and nitrate uptake and nitrate reductase activity of photoautotrophic callus cultures of the fernPlatycerium coronarium (Koenig) DESV

Summary The uptake of nitrate and ammonium by callus ofPlatycerium coronarium from the culture medium was examined. Nitrate reductase activity of photoautotrophic callus cultures under CO₂ enrichment was significantly lower compared to the cultures without CO₂ enrichment, but higher than that of heterotrophic callus cultured on medium with 2% (wt/vol) sucrose. When sucrose concentration of the heterotrophic culture was lowered to 0.2%, nitrate reductase activity increased. The level of nitrate reductase activity increased by about 25% in the heterotrophic callus with an increase in 2,4-D from 2 μM to 10 μM, despite a decline in fresh weight gain. However, photoautotrophic cultures with 1% CO₂ enrichment showed 20% decline in nitrate reductase activity and 45% decline in fresh weight gain with a similar increase in 2,4-D level. The rate of uptake of nitrate from the culture medium was unrelated to the level of nitrate reductase activity in the callus. For photoautotrophic callus under CO₂ enrichment, the presence of 1% (vol/vol) CO₂ generally resulted in the highest rate of nitrate uptake. The rate of uptake of ammonium was higher for callus cultured on 2 μM 2,4-D compared to that on 10 μM 2,4-D.     

Morphogenetic plasticity of callus reinitiated from cell suspension cultures of the fern Platycerium coronarium

Cell suspension cultures were initiated from gametophyte-derived callus of the fern Platycerium coronarium. Two distinct types of callus masses, distinguished by their colouration, were obtained when the cells from suspension culture were plated on semisolid Murashige and Skoog (MS) medium containing 10 M kinetin. The two types of callus masses had distinct morphogenetic capacities despite their common origin. Morphogenesis into either gametophytes or sporophytes occurred when these callus masses were cultured on phytohormone-free MS medium depending on the type of callus used. The dark-green gametophytic callus showed a faster rate of growth and morphogenesis as compared to the pale-green sporophytic callus. Total chlorophyll content and autofluorescence and size of chloroplasts of the sporophytic callus and cell suspension cultures were lower than that of the gametophytic callus. Observations from confocal laser scanning microscopy were in agreement with the physiological parameters measured. The availability of cell cultures of the same ploidy level, but with two distinct pathways of development will be useful for comparative studies of developmental plasticity.     

Ribulose-1,5-bisphosphate carboxylase and phosphoenolpyruvate carboxylase activities of photoautotrophic callus of Platycerium coronarium (Koenig ex O.F. Muell.) Desv. under CO2 enrichment

The in vitro activities of ribulose-1,5-bisphosphate carboxylase/oxygenase (Rubisco) and phosphoenolpyruvate carboxylase (PEPC) were measured in cell-free extracts of Platycerium coronarium callus cultured for up to 42 days under photoautotrophic conditions with CO₂ enrichment. With an increase in CO₂ in the culture environment to 10% (v/v) at low light, the apparent photoautotrophic fixation of CO₂ by Rubisco declined, whereas the non-photoautotrophic CO₂ fixation by PEPC activity was enhanced. Hence, photosynthesis appears to play a lesser role in providing carbon skeletons and energy with prolonged culture in a CO₂-enriched environment. Instead, the anaplerotic supply of C-skeletons by PEPC may be important under such a situation. Short-term H¹⁴CO₃-fixation experiments indicated that photoautotrophic callus cultured for 3 weeks with 10% CO₂ enrichment assimilated less ¹⁴CO₂ than the control (0.03% CO₂). Analyses of ¹⁴C-metabolites indicated that about 50% of the total soluble ¹⁴CO₂ fixed was in the organic acid fraction and 35% in the amino acid fraction. Despite the changes in the in vitro Rubisco/PEPC activity-ratio, no significant change in the ¹⁴C distribution pattern was apparent in response to increasing sucrose or CO₂ concentrations. The suppression of Rubisco activity and total chlorophyll content in high sucrose or elevated CO₂ concentrations suggests an inhibition of the capacity for photoautotrophic callus growth under these conditions. This revised version was published online in June 2006 with corrections to the Cover Date.     

Characterisation of a new species of Pythium isolated from a wheat field in northern France and its antagonism towards Botrytis cinerea causing the grey mould disease of the grapevine

A new species, Pythium bifurcatum, isolated from soil samples taken from a wheat field in Lille in northern France is described here. The oomycete occurred thrice out of 50 samples. The type specimen is F-91, which is a slow-growing saprophyte living on vegetable debris and which can be recognised by its antheridial as well as oogonial characteristics, which are different from other known species of Pythium. When grown together with Botrytis cinerea, the causal agent of the grey mould disease of the grapevine, Pythium bifurcatum shows a pronounced antagonism and suppresses its growth. Morphological features of this new species, its antagonism to B. cinerea, the sequences of the ITS region of its nuclear ribosomal DNA, and its comparison with related species are discussed in this article.     

Development of mantle leaves inPlatycerium bifurcatum (Polypodiaceae)

InPlatycerium bifurcatum the leaf primordia emerge alternately right and left below the shoot apical cell on the dorsal surface of the rhizome. They arise from groups of small cells, a single large cell becoming the initial of the leaf apical cell. The longitudinal axis of the leaf apical cell is at a right angle to the rhizome axis and the leaf primordia are arranged longitudinally in two rows. The leaf apical cell gives rise to marginal initials which are responsible for leaf growth in one plain. Early marginal cells are crescent-shaped while the later ones are wedge-shaped. Hairy marginal cells appear in the very early stages of development. The interpretation of these cells as a promeristem and as initials are discussed.     

二歧鹿角蕨组织培养的研究

在二歧鹿角蕨孢子体的组织培养中,通过适宜的培养基诱导形成绿色球状体(GGB),再采用添加植物生长调节物质以及恰当的选材,可促进GGB的生长和芽分化,经生根培养、炼苗和移栽可获得大量种苗。     

Jasmonic acid promotes division of fern protoplasts, elongation of rhizoids and early development of gametophytes

The effects of jasmonic acid (JA) on spore germination, early gametophyte development and sporophytic protoplast culture of the fern Platycerium bifurcalum (Cav.) C. Chr. were investigated. JA and no influence on spore germination and primary rhizoid initiation, but significantly promoted early gametophyte development, which was evident from the longer primary rhizoids as well as the higher number of rhizoids and cells per gametophyte. Jasmonic acid (1 μ M ) also promoted the transition of gametophytes from a filamentous to a planar growth. Optimal primary rhizoid elongation and highest cell division activities in the gametophytes were observed at 0.01–1 μ M JA, while the highest number of rhizoids on gametophytes was obtained at 0.1–1 μ M JA. Jasmonic acid (0.01 μ M ) also stimulated initial protoplast divisions. Except for the experiment in which the effect of JA on germination was tested. JA concentrations exceeding 1 μ M did not promote cell elongation or cell division but were instead inhibitory. On the basis of these findings, we propose that JA may be involved in early stages of P. bifurcatum development.     

The impact of a pulse treatment of penicillin-G and streptomycin sulfate on sporophyte regeneration of Platycerium bifurcatum

 This study was aimed at investigating the impact of antibiotic pulse treatment (APT) of penicillin-G and streptomycin sulfate at a concentration of 1000 mg/l each on the regeneration ability of leaf and shoot-base explants and homogenized sporophytes of Platycerium bifurcatum. The reaction of the plant to APT, as measured by changes in sporophyte regeneration and morphology, was considered to be a stress response. Cell's susceptibility to APT was graded as: tissue homogenized prior to treatment>tissue homogenized after treatment>leaf and shoot-base explants. Biphasic inhibition in sporophyte regeneration was observed in homogenized sporophytes; a sharper decrease occurred with 20–60 min of the APT, followed by a slower decline for up to 180 min. No significant impact on the regeneration ability of leaf and shoot-base explants was found. Morphologically, APT caused leaf cleavage, mesophyll damage and hyperhydricity in some sporophytes. Except for the hyperhydric sporophytes, regenerants were able to continue their growth in soil, and no carry-over effect was found in the next generation. Received: 9 October 1998 / Revision received: 10 May 1999 / Accepted: 31 May 1999