Interaction of growth retardants,daylength, and gibberellins A19, A20, and A1 on shoot elongation in birch and alder

Gibberellins A₁₉, A₂₀, and A₁ were applied to seedlings of birch (Betula pubescens Ehrh.) and alder (Alnus glutinosa (L.) Gaertn.) in order to test their ability to counteract growth inhibition induced by growth retardants (ancymidol and BX-112) or short day (SD, 12 h) photoperiod. Ancymidol inhibits early and BX-112 inhibits late steps in gibberellin biosynthesis. BX-112 inhibited stem elongation in both species while ancymidol, applied as a soil drench, was effective in alder only. Growth retardants affected stem elongation mainly by inhibiting elongation of internodes. All three gibberellins were equally active when applied to seedlings treated with ancymidol; however, only GA₁ was able to counteract the growth inhibition induced by BX-112. SD-induced cessation of elongation growth in birch was counteracted by GA₁, and to some degree, by GA₂₀, while GA₁₉ was inactive. SD treatment did not induce cessation of apical growth in alder. These results are consistent with the hypothesis that of gibberellins belonging to the early C-13 hydroxylation pathway, GA₁ is the only active gibberellin for stem elongation.     

The role of endogenous gibberellin-like substances and inhibitors in the growth of pea internodes

Third internodes or whole stems of 7-days old etiolated pea plants were extracted and the content of gibberellin-like substances and inhibitors has been determined. Extracts were found to contain four or five different gibberellin-like substances, some of which are chromatographically similar to GA₃. The content of gibberellins has been high in young internodes and decreased along with the internodes elongation. Brief red light irradiation brings about quantitative changes in gibberellin content, depending also on the length of internodes. The extracts contain acidic and neutral inhibitors which interfere with the response to GA₃. The content of the inhibitors does not seem to be affected by the ageing of internodes or by the light treatment.     

Gibberellins in developing fruits of Pisum sativum cv. Alaska: Studies on their role in pod growth and seed development

Gibberellins A₁, A₈, A₂₀ and A₂₉ were identified by capillary gas chromatography-mass spectrometry in the pods and seeds from 5-d-old pollinated ovaries of pea (Pisum sativum cv. Alaska). These gibberellins were also identified in 4-d-old non-developing, parthenocarpic and pollinated ovaries. The level of gibberellin A₁ within these ovary types was correlated with pod size. Gibberellin A₁, applied to emasculated ovaries cultured in vitro, was three to five times more active than gibberellin A₂₀. Using pollinated ovary explants cultured in vitro, the effects of inhibitors of gibberellin biosynthesis on pod growth and seed development were examined. The inhibitors retarded pod growth during the first 7 d after anthesis, and this inhibition was reversed by simultaneous application of gibberellin A₃. In contrast, the inhibitors, when supplied to 4-d-old pollinated ovaries for 16 d, had little effect on seed fresh weight although they reduced the levels of endogenous gibberellins A₂₀ and A₂₉ in the enlarging seeds to almost zero. Paclobutrazol, which was one of the inhibitors used, is xylem-mobile and it efficiently reduced the level of seed gibberellins without being taken up into the seed. In intact fruits the pod may therefore be a source of precursors for gibberellin biosynthesis in the seed. Overall, the results indicate that gibberellin A₁, present in parthenocarpic and pollinated fruits early in development, regulates pod growth. In contrast the high levels of gibberellins A₂₀ and A₂₉, which accumulate during seed enlargement, appear to be unnecessary for normal seed development or for subsequent germination.Abbreviations GA_(a) gibberellin A_n - GC-MS combined gas chromatography-mass spectrometry - HPLC high-performance liquid chromatography - PFK perfluorokerosene - PVP polyvinylpyrrolidone     

Changes in Gibberellin-Like Substances and Indole-3-Acetic Acid in Picea abies during the Period of Shoot Elongation

Grafted clones of Picea abies (L.) Karst. were used for the study. A very rapid and conspicuous rise in the content of gibberellin-like substances chromatographically similar to gibberellin A₁, and of indole-3-acetic acid, occurred during the brief period of most rapid shoot elongation. A few days later, when the shoot growth had terminated, very small amounts of both compounds could be detected. The changes in the qualitative pattern of gibberellin-like substances were consistent with a suggested interconversion pathway leading from non-polar to increasingly polar compounds     

Endogenous Gibberellins and Growth of Tobacco Callus Cultures

Tobacco callus grown under a range of conditions for different lengths of time contained various levels of gibberellin-like substances. Culture conditions, viz: light versus darkness and the quantity of cytokinin in the medium, affected the amount of gibberellins found in the tissue. These culture conditions were also important in controlling growth rate of the callus and modified the ability of the tissue to respond to exogenous gibberellins. Furthermore, substances which are known to inhibit gibberellin biosynthesis and also thought to block gibberellin action in some cases, were found to reduce the rate of growth. These data support the idea that endogenous gibberellins may be important in the control of the normal growth of tobacco cells in culture.     

Metabolism of Steviol and Its Derivatives by Gibberella fujikuroi

Steviol (ent-13-hydroxykaur-16-en-19-oic acid)* is metabolized by Gibberella fujikuroi in the presence of inhibitors of gibberellin biosynthesis, such as quaternary ammonium salt-type growth retardants, to afford 7β-Miydroxy- and 6β,7β-dihydroxysteviol, gibberelhns A₁, A₁₈, A₁₉, A₅₃ and 7β,13-dihydroxykaurenolide. Steviol acetate (ent-13-acetoxykaur-16-en-19-oic acid) is also metabolized to the 6β,7β-dihydroxy-derivative and to the 13-acetyl derivatives of gibberellins A₁₇ and A₂₀ and steviol methyl ester (methyl ent-13-hydroxykaur-16-en-19-oate) into the monohydroxy-, dihydroxy- and hydroxyoxo-derivatives. These results indicate a low substrate specificity of the enzymes in the fungus and provide a useful preparative methodology of several important plant gibberellins carrying the 13-hydroxyl group.     

Ein Beitrag zur Analyse der Gibberelline in Samen von Pisum sativum L.

Summary Unripe seeds of Pisum sativum were analyses for gibberellins and gibberellin-like substances. Forty kg of seeds were extracted with methanol, the methanol was evaporated and the residue distributed between water and ethylacetate, and between water and butanol at different pH-values. The acidic ethylacetate and the butanol fractions were separated by thin layer chromatography. In the acidic ethylacetate fraction a new substance tentatively named gibberellin A_x was isolated by preparative thin layer chromatography. In different solvent mixtures this substance migrates closely behind gibberellin A₃. It is biological active in a dwarf pea and in dwarf maize mutant bioassays. IR and fluorescense spectra point to a gibban structure. Furthermore gibberellin A₅ was found to be the main gibberellin in pea seeds. It was identified by its R_f-values and the R_f-values of its methylester in different solvent systems as well as by its characteristic relative biological activity in three biological test systems. Most probably gibberellin A₆ is also present in the pea seeds, but because the amounts detected were small, no clear evidence can be presented.In the butanol phase two gibberellin-like substances could be separated by thin layer chromatography.

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Mit Hilfe der Deutschen Forschungsgemeinschaft.     

The growth promoting effect of red light on internode elongation of Progress seedlings

Red light increased elongation of the apical 10 mm of epicotylsexcised from 7-day-old dark grown Progress seedlings. Removalof the basal portion of the plant appears to render the tissueinsensitive to the inhibitory influences of light. Additionof gibberellins A₁, A₃ or A₅ further increased elongation. Thered light growth response was independent of the gibberellinresponse; therefore, it was considered to be unrelated to anincrease in gibberellin biosynthesis. A study of the time course of growth in the presence of thegibberellins revealed that a 6–8 hr lag period was requiredbefore A₁ and A₅ became effective, while no lag period was associatedwith A₃. It was suggested that A₁ and A₅ were converted to anA₃-like gibberellin. (Received July 29, 1972; )     

Gibberellins and the Legume-Rhizobium Symbiosis : I. Endogenous Gibberellins of Lima Bean (Phaseolus lunatus L.) Stems and Nodules

The content of gibberellin-like substances in nodules formed by Bradyrhizobium species strain 127E14 on roots of lima bean (Phaseolus lunatus L.) has been previously found to be relatively high. The objectives of the present study were to purify and identify the endogenous gibberellins from the stems and nodules of lima bean. By sequential silica gel partition column chromatography, C₁₈ reverse-phase high performance liquid chromatography, and combined gas chromatography-mass spectrometry, the gibberellins A₁, A₃, A₁₉, A₂₀, A₂₉, and A₄₄ were identified from root nodules. Gibberellins A₁, A₃, A₁₉, A₂₀, and A₄₄ were also identified from lima bean stem tissue. These data provide the first mass spectral-based evidence that gibberellins are present in leguminous root nodules. The presence of the gibberellins identified indicates that the early 13-hydroxylation gibberellin biosynthetic pathway predominates in stem and nodule tissue. However, it is not known if the gibberellins within the nodules are produced in situ, or if they are imported from some remote host plant tissue.     

Site of production of gibberellin-like substances in germinating barley embryos

Summary It has been shown that gibberellin-like substances are produced in the scutellum of barley embryos during the first two days of germination (at 25°). This production is not stimulated by mevalonic acid or sugar, but it is inhibited by CCC. On the third day the activity of the scutellum ceases and the axis probably commences to produce gibberellins. Both gibberellic acid and gibberellin A₁ appear to be present, the latter predominating.     

Structure Elucidation of Gibberellin A32 and Its Acetonide

The structures of two gibberellin-like substances isolated from the immature seeds of Prunus persica, tentatively named PG–I and PG–II, were elucidated. PG–I was an ammonium salt of a novel gibberellin, ent-3α,10,12β,13,15α-pentahydroxy-20-norgibberella-l,16-diene-7,19-dioic-19,10-lactone (1), to which gibberellin number A₃₂ was allocated. PG–II was shown to be gibberellin A₃₂ acetonide (7), and concluded to be an artifact produced from gibberellin A₃₂ in the isolation process.     

Endogenous Gibberellins in Floating Plants and Turions of Wolffiella floridana

Endogenous gibberellins from floating plants and in vitro induced turions of Wolffiella floridana (Lemnaceae) were extracted and partially purified. Gibberellin-like activity was detected in two zones of the chromatogram corresponding to Rf 0-0.1 and Rf 0.4-0.5 by dwarf pea bioassay. The active compounds in the two zones have been referred to in this paper as factor I and factor II respectively. There were quantitative differences in the gibberellin-like substances of floating plants and turions. The floating plants contained more of factor I but less of factor II as compared to the turions. The chromatographic behavior of factor I was similar to either gibberellin A₁ and A₃ while the identity of factor II was uncertain.     

Physiological Roles of Brassinosteroids in Early Growth of <Emphasis Type="Italic">Arabidopsis:</Emphasis> Brassinosteroids Have a Synergistic Relationship with Gibberellin as well as Auxin in Light-Grown Hypocotyl Elongation

We examined the physiological effects of brassinosteroids (BRs) on early growth of Arabidopsis. Brassinazole (Brz), a BR biosynthesis inhibitor, was used to elucidate the significance of endogenous BRs. It inhibited growth of roots, hypocotyls, and cotyledonous leaf blades dose-dependently and independent of light conditions. This fact suggests that endogenous BRs are necessary for normal growth of individual organs of Arabidopsis in both photomorphogenetic and skotomorphogenetic programs. Exogenous brassinolide (BL) promoted hypocotyl elongation remarkably in light-grown seedlings. Cytological observation disclosed that BL-induced hypocotyl elongation was achieved through cell enlargement rather than cell division. Furthermore, a serial experiment with hormone inhibitors showed that BL induced hypocotyl elongation not through gibberellin and auxin actions. However, a synergistic relationship of BL with gibberellin A₃ (GA₃) and indole-3-acetic acid (IAA) was observed on elongation growth in light-grown hypocotyls, even though gibberellins have been reported to be additive to BR action in other plants. Taken together, our results show that BRs play an important role in the juvenile growth of Arabidopsis; moreover, BRs act on light-grown hypocotyl elongation independent of, but cooperatively with, gibberellins and auxin.     

Involvement of Abscisic Acid and Indole-3-acetic Acid in the Flowering of Pharbitis nil

The involvement of abscisic acid (ABA) and indole-3-acetic acid (IAA) in the regulation of flowering of Pharbitis nil was investigated through exogenous applications and analyses of endogenous levels. Both hormones inhibited the flowering of P. nil when they were applied before or after a single 15-h dark treatment. The inhibitory effect of ABA and IAA was significant when they were applied before the dark treatment, and the application to plumules was more effective than that to cotyledons. In all applications, the inhibitory effect of IAA was stronger than that of ABA. Endogenous levels of ABA and IAA in the plumules were compared between flower-inductive (15-h dark treatment) and noninductive (continuous light) light conditions. There was no significant difference in the ABA level between light and dark conditions, whereas the level of IAA was decreased by the dark treatment. These results suggest that biosynthesis and/or catabolism of IAA is affected by the light treatment and therefore may be involved in the regulation of early flowering processes in the apex. The inhibitory effects of ABA and IAA were reversed by an application of gibberellin A₃, indicating that gibberellin A₃ counteracts the flowering processes affected by ABA and IAA. Application of aminoethoxyvinylglycine restored the flowering response inhibited by IAA, which suggests the possibility that the inhibitory effect of IAA is the result of enhanced ethylene biosynthesis. Received November 22, 1996; accepted February 17, 1997     

Plant growth regulation with triazoles of the dioxanyl type

The plant growth retarding activities of several dioxanylalkyl and dioxanylalkenyl triazoles were determined in seedlings of barley, rice, and oilseed rape. Out of these groups some substances proved to be among the most efficient growth retardants known. The compound 1-(4-trifluormethyl)-2-(1,2,4-triazolyl-(1))-3-(5-methyl-1,3-dioxan-5-yl)-propen-3-ol was investigated more closely. Shoot growth is reduced more intensively than root growth by this compound. At lower dosages root growth may even be stimulated. The action of this retardant can be antagonized by gibberellin A₃ and byent-kaurenoic acid. It is suggested that its main biochemical action is to block the reactions that lead froment-kaurene toent-kaurenoic acid in the course of gibberellin biosynthesis.     

The Gibberellins of Developing Bean Seeds

Properties of gibberellin-like substances extracted from Frenchbean seeds during their development were studied. Two zonesof gibberellin-like activity were detected on paper chromatograms. Changes in activity of one of the zones correlated with changesin growth-rate of the seed. From considerations of Rf on paperchromatograms, and differential activity on dwarf peas, dwarf-1and dwarf-5 corn, it was deduced that activity of this zonewas due to substances resembling gibberellin A₁ and gibberellinA₅. Gibberellin A₅-like activity was highest in young seedsand disappeared after cell division in the cotyledons had ceased.Gibberellin A₁-like activity rose to its highest level duringthe period of rapid cell expansion in the cotyledons, afterthe disappearance of gibberellin A₅-like activity. The second zone of gibberellin-like activity was due mainlyto a non-acidic substance, which disappeared at the time GAj-likeactivity was rising to its highest level. A non-acidic substance that stimulated lateral bud growth ofdwarf peas also was detected in the extracts. It is presumedto be a cytokinin.     

Gibberellins in Relation to Flowering and Stem Elongation in the Long Day Plant Silene armeria

Two long days induced some flowering and 4 or more long days caused 100% flowering in Silene armeria. On long days microscopically detectable flower primordia were first seen after 6 days, which is at least 1 day before the start of stem elongation. Both gibberellin A₃ and A₇ caused flowering on short days, but the results were variable and flowering was never 100%. Three different gibberellins were detected in Silene extracts. The pattern of gibberellins extracted from plants on short and long days was qualitatively the same, but on long days gibberellin content was up to 100% higher than on short days. Only small amounts of diffusible gibberellins were obtained from Silene shoot tips (including very young leaves) on short days. However, on long days the diffusible gibberellins increased by as much as 10-fold after 4 to 6 long days but then declined somewhat after 10 long days. The gibberellins extracted from the shoot tips at the completion of the diffusion period also increased under long days, although the increase was not as large as for the diffusible gibberellins. An A₅-like gibberellin present in extracts was not detected in diffusates.     

3-hydroxylation of gibberelin A,12-aldehyde in Gibberella fujikuroi strain rec-193A

When grown on PDL medium for 11 days the strain REC-193A of Gibberella fujikuroi produces the usual range of gibberellins and ent-kaurenoid metabolites. After 3–5 days under the same conditions of culture, this slow growing strain produces virtually none of these metabolites. These short term cultures were found to convert gibberellin A₁₂-aldehyde into gibberellins A₁₂ (8.3 % A₁₄ (45%), A₄ (ca. 17%) and A₇ (ca. 6%). Under identical conditions of culture gibberellin A₁₂ was largely unmetabolised. These results show that 3-hydroxylation is the first step in the conversion of gibberellin A₁₂-aldehyde into gibberellins A₁₄, A₄ and A₇.     

Light-Stimulated Gibberellin Biosynthesis in Gibberella fujikuroi

Gibberellins (GAs) are a group of plant growth hormones that were first isolated from the fungus Gibberella fujikuroi. The biosynthesis of GA in liquid cultures of the fungus has been examined using high-performance liquid chromatography and combined gas chromatography-mass spectrometry. GA₃ was the predominant GA in well-aerated cultures. GA₄ and GA₇, intermediates in GA₃ biosynthesis, accumulated in cultures with low levels of dissolved oxygen, but were not detectable in more highly aerated cultures. Light stimulated the production of GA₃ in G. fujikuroi cultures grown from young stock cultures. Cell-free enzyme studies revealed a significant stimulation in the levels of kaurenoic acid oxidation in cultures grown in the light in comparison with those grown in the dark. However, measurements of the relative rates of [¹⁴C]mevalonic acid incorporation into kaurene showed no effect of light on this early part of the pathway. Preliminary experiments indicated that blue light is most effective in enhancing kaurenoic acid oxidation.     

Regulation of Medicago sativa L. somatic embryogenesis by gibberellins

The influence of exogenous gibberellic acid (GA₃) andpaclobutrazol, an inhibitor of gibberellin biosynthesis, on growth of callusandsomatic embryogenesis in petiole-derived tissue cultures of Medicagosativa L. has been investigated. GA₃ (0.5–500M) or paclobutrazol(5–100 M) were added to either an induction (with 2,4 Dand kinetin) or a differentiation medium (without plant growth regulators).Gibberellin A₃, applied during the induction as well as thedifferentiation stage, reduced the weight of callus and increased the number ofsomatic embryos in Medicago sativa L. tissue cultures.Somatic embryo production was increased more by the presence of exogenousGA₃ in the differentiation than induction medium. The inclusion ofpaclobutrazol in the induction or differentiation medium caused the inhibitionof callus growth and embryo production. Callus growth was much less affectedthan embryogenesis. These results indicate that gibberellins are beneficial forboth embryoinduction and formation. The level of endogenous gibberellins is presumablysufficient for callus induction and growth. However, it seems not optimal forthe induction and particularly for the differentiation of embryos.