Phytochrome involvement in the induction of resistance to dark abscission by malformin

The active portion of the visible spectrum which is required for malformin to produce leaves which are resistant to dark abscission from cuttings of Phaseolus aureus is red light. Abscission resistance was partially to almost completely lost by far irradiation prior to dark incubation. Although Ethrel, an ethylene releasing compound, stimulated dark abscission of resistant and control leaves, resistance was not lost because control leaves always abscised at a greater rate. The participation of phytochrome in the induction of abscission resistance by malformin is indicated.Abbreviations Pfr far-red absorbing form of the phytochrome system - R red radiation - FR far-red radiation - D dark     

Ribonucleic acid synthesis by chromatin isolated from Phaseolus aureus Roxb.

Chromatin was isolated from the hypocotyls of Phaseolus aureus Roxb. and assayed for endogenous RNA polymerase (EC 2.7.7.6) activity in vitro. The molecular size of the RNA product, measured by polyacrylamide gel electrophoresis, was found to be much smaller than that known to be synthesised in vivo and was affected by the assay temperature. Although conventional enzyme assays provided no evidence for the presence of ribonuclease in chromatin, a more sensitive technique revealed sufficient ribonuclease activity to degrade high-molecular weight RNA to smaller fragments. The inclusion of unlabelled exogenous RNA in the media for chromatin preparation and RNA polymerase assay substantially increased the molecular-weight of the RNA products synthesised in vitro.Abbreviations TCA trichloroacetic acid - UTP uridine-5-triphosphate - UMP uridine-5-monophosphate - SOS sodium dodecyl sulphate     

Induction of resistance to dark abscission by malformin in white light

When cuttings or seedlings of Phaseolus aureus were treated proximally with malformin for 2 days in continuous white light, resistance to subsequent leaf abscission in the dark resulted. The amount of resistance diminished as the concentration of malformin decreased from 10 to 0.1 micromolar. Resistance to dark abscission persisted for 7 days in continuous light. Little resistance was obtained when cuttings were taken from seedlings grown under low irradiance and short photoperiods, but resistance gradually increased as the photoperiod increased. Resistance to dark abscission induced by malformin in light differs from inhibition of abscission by indoleacetic acid because when malformin is applied in the dark it stimulates abscission after distal or proximal application. Malformin induces resistance only in conjunction with light treatment.     

Effect of eucalyptus oil on germination and growth of Phaseolus aureus Roxb.

Crude oil from Eucalyptus globulus and E. citriodora was extracted and the rich components, cineole and limonene were fractionated. The vapours of these oils and fractions were adsorbed onto the soil in one set of germination trials while in the other set a vapour column of volatile oils was maintained above the oil-treated soil. In both sets seed germination, seedling growth, relative growth rate, water content, height and number of leaves of Phaseolus aureus var. ML-267 were compared to those of controls. All parameters were found to be significantly affected. The effect was more pronounced with a combination of eucalyptus oil onto soil and a vapour-rich air column. There was a strong correlation between the vapour concentration and its inhibitory effect.     

Effect of malformin on the major constituents of Phaseolus vulgaris

Malformin inhibits wet and dry weight, nitrogen accumulation,and cell wall, RNA, DNA and protein synthesis in Phaseolus vulgaris.The relative proportion of dry matter and nitrogen in malformedtissues is increased in the ethanol soluble fraction and decreasedin the residue remaining after hydrolysis with 0.5 N HCl. Inhibitionof cell wall and protein synthesis was generally greater thaninhibition of nitrogen accumulation and RNA and DNA synthesis.The effects of malformin on the composition of P. vulgaris aresimilar to alterations in composition reported for ethylene,and opposite to those reported for gibberellic acid. ¹This research was supported by grant GB-7158 from the NationalScience Foundation and grant E-146-F from the American CancerSociety. ²Journal Paper No. 3509 of the Purdue Agricultural ExperimentStation. (Received October 23, 1968; )     

Phytotoxicity of selected herbicides to mung bean (Phaseolus aureus Roxb.)

Mung bean (Phaseolus aureus Roxb.) is grown after harvest of wheat during the fallow period. Herbicides such as metsulfuron, atrazine and isoxaflutole are recommended to control weeds in wheat–rice cropping system including weeds of fallow crop. The effects of three herbicides with different modes of action—atrazine, photosystem II inhibitor; metsulfuron, acetolactate synthase inhibitor; and isoxaflutole, 4-hydroxyphenylpyruvatedioxygenase inhibitor—on shoot height, chlorophyll concentrations and cellular damage in herbicide-treated mung bean were studied. While isoxaflutole inhibited shoot growth and chlorophyll concentration of mung bean, atrazine and metsulfuron did not cause reduction in the shoot growth of mung bean. Metsulfuron (226, 452, 1356 and 2260 μg/kg soil) and isoxaflutole (452, 1356 and 2260 μg/kg soil) in soil reduced the concentration of leaf chlorophyll of mung bean compared to the control. Atrazine in soil did not affect the total chlorophyll concentration of mung bean leaves. Electron micrographs showed that untreated mung bean had elongated chloroplasts, thylakoids organized as intact grana, distinct starch grains and a small number of plastoglubuli. Mesophyll cells of atrazine-treated mung bean leaves had swollen chloroplasts and thylakoids with disorganized grana. Leaves of metsulfuron-treated mung bean had swollen chloroplasts with a large number of starch grains. Starch grains were not observed in leaves of mung bean treated with either atrazine or isoxaflutole. Complete disruption of thylakoids was observed in isoxaflutole-treated mung bean leaves. Leaves of atrazine-treated mung bean showed detached microfibrils along with distorted and degenerated secondary walls. Metsulfuron-treated mung bean leaves showed aggregated microfibrils with completely dissolved secondary walls, while isoxaflutole-treated leaves had completely degenerated secondary walls with complete loss of microfibrils. We conclude that isoxaflutole at higher doses, influence mung bean at the morphological, physiological and cellular levels.     

Age-dependent responses of Phaseolus aureus Roxb. to inorganic salts of mercury and cadmium

Phaseolus aureus Roxb. was exposed to Hg and Cd separately at different stages/ages of its development, viz. seed germination stage and seedling stages (4th and 6th day). The responses, besides being metal specific, were also age-dependent. The root growth study at germination stage treatment (GST) revealed Hg to be more toxic than Cd, but, in contrast, at seedling stage treatment (SST) with seedlings more than 5 days old, while Cd killed all the seedlings at 30 μM concentration, Hg did not even at 200 μM. Among the enzymes studied, catalase showed greater metal specific and age-dependent responses than the peroxidases. Both the metals significantly increased the levels of chlorophylls and carotenoids at GST (25 μM Hg/Cd) and 4th day SST (20 μM Hg/Cd), but not at 6th day SST (20 μM Hg/Cd). The photosynthetic O₂ evolution rate expressed as per unit chlorophyll (chl) decreased irrespective of the treatment stages, and also the metals; however, when expressed as per unit f. w., it was inhibited only at 6th day SST, exclusively by Cd. It seems that plants, unlike animals, are capable of facing challenges of metals more at younger than at older stages of their development, probably by mechanisms very different from those genetically controlled.     

RNA and protein metabolism during adventitious root formation in stem cuttings of Phaseolus aureus

Indole-3-butyric acid (IBA, 10⁻⁴ M ), spermine (7 × 10⁻⁵ M ) and vitamin D₂ (6.3 × 10⁻⁵ M ), all of which enhance rooting in mung bean cuttings ( Phaseolus aureus Roxb. cv. Berkin), influence RNA metabolism. Total and poly (A)⁺-RNA synthesis within the hypocotyl is inhibited by each of these chemicals within 24 h. These changes precede induced cell division and are therefore associated with the so-called inductive period of regeneration during which some cells in the hypocotyl undergo dedifferentiation. However, following subsequent transfer of cuttings to borate, which is an essential prerequisite for development of root primordia in these cuttings, RNA synthesis is enhanced by pretreatments with IBA, spermine or vitamin D₂. Furthermore, IBA inhibits synthesis and turnover of protein within the hypocotyl.     

Influence of IBA and Cordycepin on Rooting and RNA Synthesis in Stem Cuttings of Phaseolus aureus Roxb

Adventitious roots are initiated on stem cuttings of Phaseolusaureus Roxb. by treatment with IBA for 24 h, although subsequenttransfer to boric acid is essential for their development. Cordycepinenhances auxin-induced rooting when supplied for 4 h withinthe first twenty hours of IBA treatment, but not thereafter.Cordycepin alone does not enhance rooting. IBA treatment ofcuttings for 12 h results in a marked inhibition of RNA synthesis,including poly(A)-rich RNA, in the hypocotyl. After 24 h treatmentRNA synthesis is seen to increase, with a more marked recoveryin the synthesis of poly(A)+RNA relative to other RNAs. Subsequenttransfer to boric acid maintains this recovery. Cordycepin doesnot inhibit RNA synthesis below the level induced by IBA althoughon subsequent transfer to boric acid is seen to enhance synthesisand turnover of both polyadenylated and non-polyadenylated RNA. (Received August 28, 1982; Accepted November 25, 1982)     

Promotion of Growth in Mungbean (Phaseolus aureus Roxb.) by Selenium is Associated with Stimulation of Carbohydrate Metabolism

The mungbean plants were grown hydroponically in the absence (control) or presence of 0.1, 0.25, 0.50 and 0.75 ppm selenium (as sodium selenate) for 10 days. The growth of shoots and roots increased with application of selenium with greater extent in shoots. With 0.5 and 0.75 ppm Se levels, the shoot growth was stimulated by 24% to 27% over control, respectively, while the roots showed a corresponding increase of 18-19%, respectively. The shoot-to-root ratio was enhanced significantly with Se application and maximum effects occurred at 0.75 ppm Se. A significant increase was observed in chlorophyll and cellular respiration ability with 0.5 and 0.75 ppm selenium. The increase in growth by selenium was accompanied by elevation of starch, sucrose and reducing sugars. The activity of starch hydrolysing enzymes--amylases and sucrose hydrolysing enzyme--invertase was stimulated significantly with selenium. This was associated with elevation of activities of sucrose synthesising enzymes--sucrose synthase and sucrose phosphate synthase. It was concluded that increase in growth of shoots and roots by application of Se was possibly the result of up-regulation of enzymes of carbohydrate metabolism thus providing energy substrates for enhanced growth.     

White light requirements for stimulation of plant growth by malformin

Over a 3-day period, the minimum white fluorescent light intensity required for malformin-induced growth stimulation of etiolated and green cuttings of Phaseolus aureus was approximately 2.6 × 10³ and 0.4 × 10³ ergs/cm² · sec, respectively. High light intensities were unable to inhibit the ability of malformin to stimulate growth. Over 3 days, the minimum photoperiod for malformin-induced growth stimulation using etiolated and green cuttings and a light intensity of 13.5 × 10³ ergs/cm² · sec was 4 hours and 1 hour, respectively. Malformin must be present in the area of growth stimulation during the time of light treatment. Those changes induced by light and required for malformin-induced growth stimulation were estimated to undergo almost complete decay within 1 hour in the dark. By manipulating the experimental technique, it was possible to stimulate the growth of green cuttings with malformin with a 10-min light treatment (13.5 × 10³ ergs/cm² · sec). Although low light intensities and short photoperiods did not allow growth stimulation by malformin using etiolated cuttings, they prevented or alleviated growth inhibition induced by malformin in the dark.     

Cholinesterases from Plant Tissues: III. Distribution and Subcellular Localization in Phaseolus aureus Roxb

The distribution and localization of cholinesterase in Phaseolus aureus, Glycine max, and Pisum sativum is described. The enzyme is present in roots, leaves, stems, root callus tissue, root cells suspension cultures, and root nodules. Cholinesterase in roots is found primarily in the cell wall. In cell fractionation experiments, at least 95% of the cholinesterase activity is associated with cell wall material. The enzyme can be solubilized by salt solutions, whereas Triton X-100 and sodium deoxycholate solubilize relatively small amounts of the enzyme. Cytochemical techniques have been employed to show the presence of cholinesterase activity at the cell surface and in the cell wall of certain cells of the root.     

The influence of light quality on the phytochrome content of light grown Sinapis alba L. and Phaseolus aureus Roxb.

The effect on the phytochrome system of light regimes establishing a range of photoequilibria was studied in two light grown dicotyledonous plants, both of which were treated with the herbicide SAN 9789 to prevent chlorophyll accumulation. In Sinapis alba L. cotyledons the results are comparable with phytochrome behaviour in etiolated mustard seedlings; the level of Pfr becomes independent of wave-length whereas the total phytochrome level is wave-length dependent. Contrasting properties are exhibited in Phaseolus aureus Roxb. leaves in which total phytochrome is unaffected by light quality; consequently the Pfr level is dependent on wavelength. Nevertheless, the amount of phytochrome in mung leaves increased after transfer to darkness suggesting that light still has a profound influence on the phytochrome system, even though light quality during the light period and prior to darkness does not.Abbreviations FR far-red light - WL white light - PAR photosynthetically active radiation - Pfr far-red light absorbing form of phytochrome - Pr red light absorbing form of phytochrome - Ptot total phytochrome level (=Pr+Pfr) - Pfr/Pfr+Pr - SAN 9789 4-chloro-5-(methylamino) 2(,, trifluoro-m tolyl)-3(2H)-pyridazinone     

Studies on the abscission of blue lupin leaves

Summary The responses of three types of explants of blue lupin leaves are considered: pulvinar explants, consisting of the pulvinar region alone, petiolar explants, consisting of the pulvinar region plus petiole and laminar explants consisting of the pulvinar region plus leaflets. Abscission is accelerated by removal of the leaflets; removal of the petiole has much less effect. Pulvinar explants fail to abscise in darkness but are the first to abscise in the light. This is in accordance with previous evidence of high light sensitivity of the pulvinar region. Kinetin applied directly to the pulvinar region delays abscission, as does kinetin supplied via the transpiration stream. As shown by experiment, this is probably due to transported kinetin reaching the abscission zones of the pulvinar region. The effects of photoperiodic treatments on explants or whole leaves are described. Abscission in the whole leaf is delayed by short daily photoperiods; the delay reaches a maximum with 8 hours light per day. However, abscission is more rapid in continuous light than in darkness. Removal of the leaflets greatly accelerates abscission even in darkness. The pulvinar explant fails to abscise with photoperiods of 4 hours or less; although it appears to have a long day response, preliminary attempts failed to demonstrate that this is a true photoperiodic response (replacement of a long day by a short day together with a light break). The complex responses of leaves and explants to day length lend further support to the hypothesis that light has effects on abscission other than in photosynthesis.     

Caffeic acid affects early growth, and morphogenetic response of hypocotyl cuttings of mung bean (Phaseolus aureus)

Caffeic acid (CA) is one of the most common cinnamic acids ubiquitously present in plants and implicated in a variety of interactions including allelopathy among plants and microbes. This study investigated the possible interference of CA with root growth and the process of rhizogenesis in hypocotyl cuttings of mung bean (Phaseolus aureus=Vigna radiata). Results indicated that CA (0-1000 microM) significantly suppressed root growth of mung bean, and impaired adventitious root formation and root length in the mung bean hypocotyl cuttings. Further investigations into the role of CA in hampering root formation indicated its interference with the biochemical processes involved in rooting process at the three stages - root initiation (third day; RI), root expression (fifth day; RE), and post-expression (seventh day; PE) - of rhizogenesis. CA caused significant changes in the activities of proteases, peroxidases (PODs), and polyphenol oxidases (PPOs) during root development and decreased the content of total endogenous phenolics (TP) in the hypocotyl cuttings. The enhanced activity of PODs and PPOs, though, relates to lignification and/or phenolic metabolism during rhizogenesis; yet their protective role to CA-induced stress, especially during the PE phase, is not ruled out. At 1000 microM CA, where rooting was significantly affected, TP content was very high during the RI phase, thus indicating its non-utilization. The study concludes that CA interferes with the rooting potential of mung bean hypocotyl cuttings by altering the activities of PODs and PPOs and the endogenous TP content that play a key role in rhizogenesis.     

Sterol glucosylation by the plasma membrane from cotyledons of Phaseolus aureus

Membrane fractions were isolated from dark grown cotyledons of Phaseolus auneus by differential and sucrose density gradient centrifugation. Endoplasmic reticulum-, Golgi apparatus- and plasma membrane-rich fractions were identified by their respective enzymic activities and tested for their ability to transfer glucose from UDP-glucose to endogenous sterols to form steryl glucosides. The glucosyltransferase activity was shown to be located mainly at the plasma membrane.ABBREVIATIONS SG steryl glucoside - ASG acylated steryl glucoside - UDP-glc Uridine diphosphoglucose     

Changes in isoenzymes of soluble malate dehydrogenase during germination of mung bean (Phaseolus aureus Roxb.) under salt stress

Seeds of mung bean (Phaseolus aureus Roxb.) cv. Pusa Baisakhi were surface sterilized and sown both in Petri dishes and sand culture containing aqueous solutions of four different saltsviz. NaCl, KC1, Na₂SO₄ and K₂SO₄ each at 5 and 10 m ?^-1 cm^-1. Malate dehydrogenase (MDH) isoenzymes were studied in different plant parts of mung bean at suitable intervals during germination under four different salts. In cotyledons, 96 h after sowing only one isoenzyme was left in control as compared to three under salt treatment. In the embryo axis, 96 h after sowing, sulphate salts resulted in the disappearance of isoenzymes with R₁ 0.43 and 0.62, whereas isoenzyme with R₁ 0.62 was missing only at a higher concentration of chloride salts. Chloride salts also resulted in the disappearance of band with R₁ 0.15, both in the embryo axis and leaves. However, in the roots the isoenzymic pattern remains the same with all the salt treatments.     

Identification of chitinase mRNA in abscission zones from bean (Phaseolus vulgaris Red Kidney) during ethylene-induced abscission

Abstract. Total RNA was extracted from bean leaf abscission zones at different times after the induction of abscission by ethylene. The RNA was translated in the wheat germ system and the products analysed by SDS-PAGE. Products of molecular weight (raw) 42, 32 and 17 kD were seen to accumulate substantially during the induction. An attempt was made to establish that the mRNA species which produced the 32 kD product, which was coded for the ethylene-regulated enzyme chitinase. Mature chitinase (30 kD) was purifed from ethylene-treated abscission zones and used to raise monospecific antibodies in rabbits. These antibodies recognized the 32 kD product and mature chitinase. The 2 kD difference in molecular weight was due to the presence of the signal sequence which could be removed by microsomal membranes. Chitinase was also detected by enzymatic assay and immunoblotting of crude homogenates from ethylene-treated abscission zones. Chitinase appears to be ubiquitous in bean plants and probably does not have a direct role in abscission.     

大叶紫薇叶的化学成分研究

从大叶紫薇叶子中分离鉴定了4个化合物,分别为23-羟基熊果酸(1)、alphitolic acid(2)、熊果酸(3)和β-谷甾醇(4),这4个化合物均为首次从该植物中分离得到。