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Presence of abscisic acid, a phytohormone, in the mammalian brain.

This paper reports the presence of abscisic acid, one of the most important phytohormones, in the central nervous system of pigs and rats. The identification of this hormone in brain was made after extensive purification by using a radioimmunoassay that is very specific for (+)-cis-abscisic acid. The final product of purification from mammalian brain has the same properties as authentic abscisic acid: it crossreacts in the radioimmunoassay for the phytohormone and it has the same retention properties and the same gas chromatography/mass spectrometry characteristics. Moreover, like (+)-cis-abscisic acid itself, the brain factor inhibits stomatal apertures of abaxial epidermis strips of Setcreasea purpurea Boom (Commelinaceae). The presence of abscisic acid conjugates that are present in plants has also been identified in brain.

Abscisic Acid↗

Aquaporin isoforms responsive to salt and water stresses and phytohormones in radish seedlings.

Aquaporins in the plasma and vacuolar membranes play a key role in the intercellular and intracellular water transport in plants. First, we quantitated the absolute amounts for mRNAs of eight aquaporin isoforms in hypocotyls of radish seedlings. Then, we investigated the effects of salt and water stresses (150 mM NaCl, 300 mM mannitol and 20% polyethylene glycol) and phytohormones (gibberellic acid, abscisic acid and brassinolide) on the mRNA and protein levels of aquaporins in the plasma membrane (RsPIP1-1, 1-2, 1-3, 2-1, 2-2 and 2-3) and vacuolar membrane (RsTIP1-1 and 2-1). The mRNA and protein levels of RsTIP1-1, RsTIP2-1, RsPIP1-1, RsPIP1-2 and RsPIP1-3 were comparatively constant. In contrast, mannitol treatment altered the mRNA levels of RsPIP2-1, RsPIP2-2 and RsPIP2-3 in roots. Immunoblot analysis showed that the RsPIP2-1 protein level was increased by NaCl treatment and decreased by treatment with mannitol and polyethylene glycol. Gibberellic acid and abscisic acid suppressed the levels of mRNAs of RsPIP2-1, RsPIP2-2 and RsPIP2-3 and the protein level of RsPIP2-1 in roots. On the other hand, the protein levels of RsPIP1-group members and RsTIPs were scarcely changed by these phytohormones. In the case of hypocotyls and cotyledons, the mRNA and protein levels of eight isoforms were not markedly affected by any treatment. These results indicate that aquaporins in the root, especially the RsPIP2 group, may be a stress responsive type of aquaporin at least in the protein level.

Abscisic Acid↗

Regulation of plant morphology by growth retardants: effects on phytohormone levels in soybean seedlings determined by immunoassay.

The effects of the growth retardants tetcyclacis, a norbornenodiazetine, and LAB 150 978, a dioxanylalkenyl triazole, on seedling growth and endogenous levels of phytohormone-like substances in Glycine max L. cv Maple Arrow were studied. The levels of phytohormone-like substances in the root and in the various shoot tissues were analyzed by immunoassay. After seed treatment with both compounds, shoot growth was reduced more intensively than root growth. Both compounds decreased, on a fresh weight basis, the amount of various immunoreactive gibberellins when compared with the levels in control plants, especially in the shoot tip. Likewise, the growth retardants lowered the levels of abscisic acid-like material, particularly in the primary leaf, the epicotyl and the root. In contrast, the levels of trans-zeatin-riboside and dihydrozeatin-riboside-type cytokinins were considerably elevated by the growth retardants, mainly in the primary leaf, epicotyl, and hypocotyl. On the other hand the level of isopentenyladenosine-like material was less influenced. In general, the immunoreactive 3-indoleacetic acid content in the different plant parts was changed only slightly. It is assumed that besides their effect on gibberellin content both compounds interfere directly or indirectly with the regulation of the endogenous levels of abscisic acid and cytokinins. This might be seen as an additional mode of action of growth retardants explaining some side effects on developmental processes of treated plants, e.g. delayed senescence and enhanced chlorophyll concentration in the leaves.

Journal Article↗

Phytohormonal responses in enod40-overexpressing plants of Medicago truncatula and rice.

Phytohormones are well-known regulators of the symbiotic Rhizobium-legume association in the plant host. The enod40 nodulin gene is associated with the earliest phases of the nodule organogenesis programme in the legume host and modifying its expression resulted in perturbations of nodule development in Medicago truncatula. Therefore in our pursuit to mimic the initial signal transduction steps of legume nodulation in the alien physiological set-up of a rice plant, we have expressed the Mtenod40 gene in rice. Molecular data confirm the stable integration, inheritance and transcription of the foreign gene in this non-legume. We have compared the phytohormonal responses of Mtenod40-overexpressing and control plants in a homologous legume background (M. truncatula) and in the non-legume rice. An enod40-mediated root growth response, induced by inhibition of ethylene biosynthesis, was observed in both plants. On the other hand, a significant differential effect of cytokinins was observed only in rice plants. This suggests that ethylene inhibits enod40 action both in legumes and non-legumes and reinforces that some of the early signal transduction steps of the nodule developmental programme may function in rice.

Journal Article↗

The influence of phytohormones on zeta potential and electrokinetic charges of winter wheat cells.

The zeta potential measurements of protoplasts obtained from winter wheat cell culture and phospholipid liposomes were performed to determine the electrokinetic charge in a medium containing various phytohormones (kinetin, 2,4-D and zearalenone) in absence and in presence of 2 x 10(-5) MCa2+. Calli were induced from immature inflorescences (inf) and embryos (emb) and cultured to obtain non-embryogenic (NE) and embryogenic (E) cell tissues. All investigated phytohormones indicate ability to adsorb to the negatively charged surfaces (latex, L88 - model negative adsorption site) both in water solutions and at the presence of mannitol and buffer (MES). In biological systems (protoplasts and liposomes - prepared from phospholipids of protoplasts) the electrokinetic charges were dependent on the phospholipid and protein composition of cells. The influence of protein groups on electrokinetic charge was calculated from charge values of protoplasts and liposomes, assuming additivity of surface charges. The comparison of calculated charges for protoplasts and liposomes indicate that 2,4-D is better adsorbed to the phospholipid and proteins of NE cells whereas kinetin is bound to the phospholipid and protein sites of E calli. This effect may be connected with embryogenesis process, where non-embryogenic culture of wheat requires 2,4-D in the medium, and embryogenic culture requires cytokinin rather. Zearalenone binding is especially dependent on the kind of explant.

Calcium↗

Synthesis of phytohormones by plant-associated bacteria.

The plant hormones, auxins and cytokinins, are involved in several stages of plant growth and development such as cell elongation, cell division, tissue differentiation, and apical dominance. The biosynthesis and the underlying mechanism of auxins and cytokinins action are subjects of intense investigation. Not only plants but also microorganisms can synthesize auxins and cytokinins. The role of phytohormone biosynthesis by microorganisms is not fully elucidated: in several cases of pathogenic fungi and bacteria these compounds are involved in pathogenesis on plants; auxin and cytokinin production may also be involved in root growth stimulation by beneficial bacteria and associative symbiosis. The genetic mechanism of auxin biosynthesis and regulation by Pseudomonas, Agrobacterium, Rhizobium, Bradyrhizobium, and Azospirillum, are well studied; in these bacteria several physiological effects have been correlated to the bacterial phytohormones biosynthesis. The pathogenic bacteria Pseudomonas and Agrobacterium produce indole-3-acetic acid via the indole-3-acetamide pathway, for which the genes are plasmid borne. However, they do possess also the indole-3-pyruvic acid pathway, which is chromosomally encoded. In addition, they have genes that can conjugate free auxins or hydrolyze conjugated forms of auxins and cytokinins. In Agrobacterium there are also several genes, located near the auxin and cytokinin biosynthetic genes, that are involved in the regulation of auxins and cytokinins sensibility of the transformed plant tissue. Symbiotic bacteria Rhizobium and Bradyrhizobium synthesize indole-3-acetic acid via indole-3-pyruvic acid; also the genetic determinants for the indole-3-acetamide pathway have been detected, but their activity has not been demonstrated. In the plant growth-promoting bacterium Azospirillum, as in Agrobacterium and Pseudomonas, both the indole-3-pyruvic acid and the indole-3-acetamide pathways are present, although in Azospirillum the indole-3-pyruvic acid pathway is of major significance. In addition, biochemical evidence for a tryptophan-independent indole-3-acetic acid pathway in Azospirillum has been presented.

Azospirillum↗

Somatic embryogenesis and ginsenoside production of Panax ginseng in phytohormone-free medium.

Embryogenic cultures of Panax ginseng were established without using phytohormones. Somatic embryos developed from the roots of an in vitro seedling and from excised leaf and petiole segments cultured in half-macro-salt strength Murashige and Skoog medium. Excised leaf and petiole segments were obtained from in vitro germinated seedlings. Plantlets were subsequently obtained from developing somatic embryos in phytohormone-free media. Shoot formation from somatic embryos was influenced by light intensity. The rate of growth and frequency of embryogenesis were improved when cut-up embryogenic tissues were inoculated into liquid media in the dark. The ginsenoside contents of a 4 year-old field-cultivated root, seedlings from zygotic embryos, somatic embryos and embryogenic tissues were determined and compared. Somatic embryos contained 1.7 times the amount of ginsenoside Rb1 and 2.3 times the amount of ginsenoside Re compared to seedlings from zygotic embryos. Ginsenoside Rd, which was absent in the seedlings derived from zygotic embryos, was detected in somatic embryos. Higher ginsenosides Rd and Rg1 levels were found in embryogenic tissues grown on solid media than in tissues grown in liquid media. The total ginsenoside yields, including the ginsenosides Rb1 and Rg1 levels, of cut-up embryogenic tissues, were higher than those of clump tissues.

Culture Media↗

Effect of phytohormones on the transmembrane translocation of protons in plasma membrane vesicles from tubers of Solanum tuberosum L.

Effects of phytohormones gibberellic acid (GA) and abscisic acid (ABA) on the ATP-dependent transmembrane transport of protons were studied in plasma membrane vesicles (PMVs) from non-dormant potato tubers. The uptake of H+ into PMVs was assessed by the fluorescence quenching of acridine orange (AO) after the addition of ATP to the incubation medium. Addition of ATP to the incubation medium led to the instantaneous rise of the AO fluorescence intensity followed by its decrease. The fluorescence quenching was not observed in the presence of either protonophore CCCP or inhibitors of the membrane-bound H+-ATPase. It is concluded that the ATP-induced quenching of the AO fluorescence resulted from the accumulation of protons in PMVs due to the function of the plasma membrane-bound H+-ATPase. Depending on their concentrations, GA and ABA either inhibited or stimulated the ATP-driven H+ translocation across the vesicle membrane. The growth-stimulating hormone GA at concentrations of 10(-9)-10(-5) M increased the initial rate of the fluorescence quenching, whereas 10(-4) M GA slightly inhibited the H+ translocation. The growth inhibitor ABA at a concentration of 10(-9) M slightly increased the rate of the proton accumulation in PMVs; at higher concentrations (10(-8)-10(-4) M), ABA inhibited the H+ translocation. Acetic acid, which has pK similar to pK of GA and ABA, did not influence the ATP-dependent H+ accumulation in PMVs, suggesting the hormone-specific action of GA and ABA on the H+-ATPase activity. In the presence of DCC, which completely inhibited the accumulation of H+, GA and ABA did not affect the passive proton efflux from PMVs. It is proposed that the mechanisms of the regulatory effects of phytohormones may involve modification of H+-ATPase activity leading to changes in the electrochemical gradient of H+ across the plasma membrane.

Abscisic Acid↗

Transcriptional regulation by light and phytohormones of the MGD gene in cucumber.

Monogalactosyldiacylglycerol (MGDG) synthase catalyses formation of MGDG, a major structural lipid of chloroplasts. We have already cloned a cDNA for the synthase from a cucumber cDNA library and shown that expression of this gene is regulated by light and a phytohormone, cytokinin. In the present study, we report the molecular basis for transcriptional regulation by light and cytokinin in detail. First, in terms of the enzyme activity, gradual increases in activity mediated by light and cytokinin treatments were observed. At the same time, however, the changes in the mRNA level showed different profiles, with a transient peak during the early stages of light and cytokinin treatment. The interval between the peak level of mRNA and enzyme activation implies the existence of a post-transcriptional regulatory system. In addition, a genomic clone of MGDG synthase isolated from a cucumber genome library was used for a motif search in databases, and this revealed that putative cis-acting elements for light and phytohormones exist in the 5'-upstream region of the MGD cucumber gene. Detailed analysis of this region for light- and cytokinin-responsive activity was performed using a -90 truncated 35 S minimal promoter/luciferase (LUC) reporter gene. It resulted in high levels of LUC expression in etiolated cucumber cotyledons in response to illumination and cytokinin treatment. These results indicate that this 5'-upstream region is involved in light- and cytokinin-enhanced MGD gene expression, and that light- and cytokinin-responsive enhancements of the MGDG synthase activity are regulated, at least in part, at the level of transcription.

Adenine↗

[Effect of phytohormones on the protein-synthesizing ability of rauwolfia serpentina benth. tissue culture].

The accumulation of intracellular protein by the callus culture of Rauwolfia serpentina Benth. was studied in a standard or phytohormone-containing medium. Changes in the concentration of total protein in cells induced by indolylacetic and naphthylacetic acids were shown to be associated with the effects of these phytohormones on the biosynthesis and degradation of intracellular protein.

Culture Techniques↗

[Influence of phytohormones on development of conidial inoculum of causative agents of the phlox and barley powdery mildew].

We studied the role of phytohormones: zeatin, kinetin, and abscisic acid, in the regulation of development of the conidial inoculum of Erysiphe cichoracearum DC. f. phlogis Jacz. and E. graminis DC. f. hordei Marchal. When the pathogen conidia were in direct contact with phytohormones, the intensity of their germination significantly increased. In the presence of cytokinins, the amount of normal appressoria decreased and that of abnormal growth tubes increased. On the phlox leaves treated with cytokinins, the intensity of germination of the conidia increased, as compared to the control, while abscisic acid exerted the opposite effect. The treatment of barley leaves with cytokinins did not affect markedly the development of conidial inoculum, as compared to the control, while abscisic acid significantly decreased the intensity of germination of the conidia. On the leaves of different Phlox species, the degree of germination of the conidial negative correlated with their resistance against the powdery mildew. The role of cytokinins in pathogenesis of biotrophic fungi is discussed.

Abscisic Acid↗

[Phytohormone interactions in the control of proton translocation activity of plant cell plasmalemma].

The effects of phytohormones (abscisic acid, gibberelic acid, and jasmonic acid) and ambiol (a synthetic growth regulator) on processes of H+ transport across the plasmalemma were studied in membrane vesicles isolated from the parenchyma of potato (Solanum tuberosum L.) tubers. Phytohormones and ambiol were tested either individually or in combinations. Each of the substances tested changed the initial rate of H+ uptake by the vesicles. Two signaling substances added to the incubation medium simultaneously modified the activity of each other. It is suggested that the interaction of a signaling substance with components of the plasmalemma alters the responses of the membrane to other signaling molecules.

Benzimidazoles↗

[The effect of pathogens and phytohormones on the rate of oxidation of phenols by oxalate oxidase in wheat seedlings].

We studied the effect of various fungal phytopathogens and exogenous phytohormones on the rate of o-phenylenediamine oxidation mediated by oxalate oxidase, which is one of protective proteins of wheat. The pattern of changes in o-phenylenediamine oxidation rate depended on pathogen type, cultivar resistance, and phytohormone class. This reaction is proposed as a model reaction for studying plant response to infection and effects of various physiologically active compounds.

Fungi↗

Effect of phytohormones on the growth dynamics and macromolecular contents of two extreme halophilic Cyanobacteria (Phormidium sps).

Two non-heterocystous, filamentous solar saltern extreme halophilic cyanobacteria viz., Phormidium tenue and Phormidium fragile were allowed to grow in different concentrations of phytohormones. Among the phytohormones, Indole-3 acetic acid and Indole-3-butyric acid at 0. l ppm concentration enhanced the growth, pigments and carbohydrate content in P. fragile. The phycobiliprotein production was found higher at 0. l ppm concentration of Indole-3-acetic acid in P. tenue, whereas Indole-3-butyric acid at 50 ppm and 0. 1 ppm concentrations proved to be inhibitory in the protein and carbohydrate contents in P. tenue.

Cyanobacteria↗

[Effects of phytohormones on growth and DHA production by Thraustochytrium roseum].

In this paper, effects of phytohormones on growth and DHA production by Thraustochytrium roseum MF2 were studied. Results showed that phytohormones had significant affect on growth and DHA production by T. roseum MF2. GA could promote the synthesis of DHA, and BA could accelerate the growth of T. roseum MF2, so the combination of GA and BA could increase DHA yield. The maximum DHA yield of 982mg/L was observed with 2mg/L GA and 3mg/L BA in medium.

Biomass↗

Growth, activity of phytohormones and inhibitors, and photosynthesis of dwarf pea mutants under different conditions of illumination.

A clear correlation was found between the growth of mutant forms of pea plants and the light intensity: With an increase in the latter the growth of the plants was inhibited and the rate of photosynthesis increased. The inhibitory action of light on stem growth affected not only tall pea plants, but also dwarf forms. A definite link was observed between the genetic apparatus and the balance of endogenous phytohormones and inhibitors. The content of bound forms of gibberellins was directly related to the growth intensity--the content of these substances was highest in the tall Torsdag pea plant, it was lower in the semidwarf K-29, and it was very low in the dwarf K-202. The content of quercetin glucosylcoumarate was lowest in Torsdag pea plants, in dwarf mutants the greater the amount of this compound the shorter the stem. The genetically determined ratio of phytohormones and inhibitors in the original tall and dwarf forms of pea plants is retained under all illumination conditions at various intensities.

Fabaceae↗

Effect of phytohormones on ATP-dependent accumulation of Ca2+ in plasma membrane vesicles from tubers of potato Solanum tuberosum L.

A membrane fraction enriched with plasmalemma vesicles was isolated from potato tubers using the polyethylene glycol 3550--dextran T-500 phase partitioning. As judged by the activities of enzyme markers of the inner plant cell membranes, the fraction consisted of plasmalemma vesicles with tonoplast vesicle contamination and contained no mitochondrial membranes, endoplasmic reticulum or Golgi apparatus. Under conditions of total inhibition of nitrate-sensitive ATPase of the tonoplast, the vesicles of the fraction obtained exhibited the ATP-dependent accumulation of Ca2+. It was inhibited to various extents by Na3VO4, dicyclohexyl carbodiimide (DCCD) and phytohormones--gibberellic acid (GA3), abscisic acid (ABA) and indoleacetic acid (IAA), whereas kinetin rendered a stimulating effect. The action of phytohormones on the accumulation of Ca2+ in the presence of DCCD or Na3VO4 suggests that GA3, ABA and kinetin affect the activity of Ca2+,Mg(2+)-ATPase, whereas IAA most probably stimulates the efflux of Ca2+ from the vesicles or the separation of membrane-bound Ca2+.

Adenosine Triphosphatases↗