Effect of plant growth substances on the growth of axillary buds in cultured stem segments of Phaseolus vulgaris L.

The hormonal control of axillary bud growth was investigated in cultured stem segments of Phaseolus vulgaris L. When the stem explants were excised and implanted with their apical end in a solid nutrient medium, outgrowth of the axillary buds-located at the midline of the segment-was induced. However, if indoleacetic acid (IAA) or naphthaleneacetic acid (NAA) was included in the medium, bud growth was inhibited. The exposure of the apical end to IAA also caused bud abscission and prevented the appearance of new lateral buds.In contrast to apically inserted segments, those implanted in the control medium with their basal end showed much less bud growth. In these segments, the auxin added to the medium either had no effect or caused a slight stimulation of bud growth.The IAA transport inhibitor N-1-naphthylphthalamic acid (NPA) relieved bud growth inhibition by IAA. This suggests that the effect of IAA applied at the apical end requires the transport of IAA itself rather than a second factor. With the apical end of the segment inserted into the IAA-containing medium, simultaneous basal application of IAA relieved to some extent the inhibitory effect of the apical IAA treatment. These results, together with data presented in a related article [Lim R and Tamas I (1989) Plant Growth Regul 8: 151–164], show that the polarity of IAA transport is a critical factor in the control of axillary bud growth.Of the IAA conjugates tested for their effect on axillary bud growth, indoleacetyl alanine, indoleacetic acid ethyl ester, indoleacetyl-myo-inositol and indoleacetyl glucopyranose were strongly inhibitory when they were applied to the apical end of the stem explants. There was a modest reduction of growth by indoleacetyl glycine and indoleacetyl phenylalanine. Indoleacetyl aspartic acid and indoleglyoxylic acid had no effect.In addition to IAA and its conjugates, a number of other plant growth substances also affected axillary bud growth when applied to the apical end of stem segments. Myo-inositol caused some increase in the rate of growth, but it slightly enhanced the inhibitory effect of IAA when the two substances were added together. Gibberellic acid (GA₃) caused some stimulation of bud growth when the explants were from younger, rather than older plants. The presence of abscisic acid (ABA) in the medium had no effect on axillary bud growth. Both kinetin and zeatin caused some inhibition of axillary buds from younger plants but had the opposite effect on buds from older ones. Kinetin also enhanced the inhibitory effect of IAA when the two were applied together.In conclusion, axillary buds of cultured stem segments showed great sensitivity to auxins and certain other substances. Their growth responded to polarity effects and the interaction among different substances. Therefore, the use of cultured stem segments seems to offer a convenient, sensitive and versatile test system for the study of axillary bud growth regulation.     

Effect of Morphactin, Gibberellic Acid and Auxin and on Growth and Development of Bryophyllum tubiflorum

six month old LD- and SD- grown plants of Bryophyllum tubiflorum were treated with morphactin (n-buty1-9-hydroxy-fluorene-(9)-carboxylate), singly and in combination with GA₃ and IAA. Morphactin and IAA decreased stem elongation and number of leaves, the effect increasing with concentration concentation. Morphactin also caused lateral buds to develop into branches and the fusion of upper leaves to form structures of different shapes. GA₃ enhanced stem elongation, increased leaf number and induced floral buds under SD conditions. It reversed the inhibitory effect of morphactin on stem elongation, leaf number and leaf fusion and also restored apical dominance when applied simultaneously with morphactin. The stimulaneous application of IAA also reversed the morphactin effects on leaf fusion and on apical dominance. The results have been discussed in the light of literature available on the subject.     

Effect of Abscisic Acid and Other Plant Hormones on Growth of Apical and Lateral Buds of Seedlings

The effect of abscisic acid (AbA) on the growth of lateral and apical buds was studied in seedlings of Pisum sativum and some other species. The hormone was applied in three different ways: 1) directly to the lateral bud on the second node of decapitated pea seedlings as 5 μI droplets in an ethanolic solution; 2) to the cut surface of decapitated seedlings: 3) to the apical bud of intact plants. AbA directly applied in amounts of 5 to 0.1 μg to the lateral bud of the second node of decapitated seedlings had a strong inhibitory effect on the bud. Application to the cut surface of seedlings decapitated about 5 mm above the second node resulted in slight inhibition of the lateral bud on the second node and in growth promotion of the bud on the first node. When AbA at 10 to 0.1 μg was applied to the apical bud of intact seedlings, the growth of this bud was inhibited but the lateral buds grew out. It is concluded that the release of the lateral buds from apícal dominance is the result of the inhibitory effect of AbA on growth of the apical bud and of low transport of AbA. This conclusion is supported by application of GA₃ and IAA, individually and each combined with AbA.     

Kinetin Transport to Axillary Buds of Dwarf Pea (Pisum sativum L.)

Decapitation resulted in the transport of significant amountsof ¹⁴C to the axillary buds from either point of application,but pretreatment of the cut internode surface of decapitatedplants with IAA (alone or in combination with unlabelled kinetin)inhibited the transport of label to the axillary buds and resultedin its accumulation in the IAA-treated region of the stem. Inintact plants to which labelled kinetin was applied to the apicalbud there was little movement of ¹⁴C beyond the internode subtendingthis bud; when labelled kinetin was applied to the roots ofintact plants, ¹⁴C accumulated in the stem and apical bud butwas not transported to the axillary buds. A considerable proportionof the applied radioactivity became incorporated into ethanol-insoluble/NaOH-solublecompounds in the apical bud of intact plants, in internodestreated with IAA, and in axillary buds released from dominanceby removal of the apical bud. The results are discussed in relation to the possible role ofhormone-directed transport of cytokinins m the regulation ofaxillary bud growth.     

Changes of endogenous hormones in lateral buds of chrysanthemum during their outgrowth

The character of branching for two chrysanthemum (Chrysanthemum × morifolium) cvs. Jinghai and Jingyun was observed, and the changes of endogenous hormones in apical and lateral buds were investigated to determine the relationship between the pattern of hormone distribution, apical dominance, and lateral bud outgrowth. The growth rate of Jinghai lateral buds was higher than that of Jingyun. In vegetative growth stage, IAA level in apical buds of Jingyun was significantly higher than in Jinghai. After flower induction, IAA level in apical buds of two cultivars decreased remarkably, but the IAA level decreased in Jingyun faster than in Jinghai. These results showed that the higher was the IAA level in apical buds the stronger was inhibition of lateral bud outgrowth. An increase in IAA and iP/iPA and a decrease in ABA concentrations were closely associated with lateral bud growth alterations in chrysanthemum.     

Changes in the level of endogenous gibberellins and auxins in apical buds ofChenopodium rubrum L. after application of growth substances reversing the effect of (2-chlorethyl)-trimethylammonium chloride (CCC) on flowering

The application of CCC at concentrations inhibiting flowering ofChenopodium rubrum reduces the level of endogenous gibberellins in the apical buds of the plants. The effect of CCC may be reversed by appropriate concentrations of gibberellin (GA-), indole acetic acid (IAA) or kinetin. Kinetin applied to the apical bud during floral induction reduced the level of endogenous gibberellins similarly as CCC and if both CCC and kinetin were applied simultaneously their action was additive. On the other hand IAA applied under the same conditions increased the level of endogenous gibberellins and after joint application of CCC and IAA their level was the same as in untreated control plants. After application of CCC during floral induction the level of endogenous auxins did not change markedly but an active substance “x” appeared on the chromatograms of indole compounds. This substance was found also after simultaneous application of GA- and CCC but not after joint application of CCC and kinetin. If follows from our results that the same morphological phenomenon (flowering) can take place in plants considerably differing as to their level of endogenous growth substances. The ratio of different growth substances is obviously more important than the actual level of the single substances.     

Factors Influencing the Distribution of Growth Between Stem and Axillary Buds in Decapitated Bean Plants

Phaseolus multiflorus plants at three stages of developmentwere decapitated either immediately below the apical bud orlower down at a point 1 cm above the insertion of the primaryleaves. Growth regulators in lanolin were applied to the cutstem surface. IAA always inhibited axillary bud elongation anddry-matter accumulation, and enhanced internode dry weight butnot elongation. GA₃ applied below the apical bud greatly increasedinternode elongation and dry weight, but simultaneously reducedbud elongation and dry-weight increase. Application of GA₃ 1cm above the buds had no effect on bud elongation in the youngestplants, but enhanced their elongation in the two older groups.IAA always antagonized GA₃-enhancement of internode extensiongrowth, whereas its effects on GA₃-enhanced dry-matter accumulationdepended on the stage of internode development. Bud elongationwas greater in plants treated with GA₃+IAA than in plants treatedonly with IAA, except in the youngest plants decapitated immediatelybelow the apical bud, where GA₃ caused a slight increase inIAA-induced bud inhibition. GA₃ increased inhibition of buddry weight by IAA in the two youngest groups of plants, butslightly reduced it in the oldest plants. No simple compensatorygrowth relationship existed between internode and buds. It wasconcluded that, (1) auxin appears to be the principal growthhormone concerned in correlative inhibition, and (2) availabilityof gibberellin to internode and buds is of importance as a modifyingfactor in auxin-regulated apical dominance by virtue of itslocal effects on growth in the internode and in the buds.     

Correlative integration in dormant tubers of circaea intermedia

The apical dominance in dormant tubers ofCircaea intermedia preventing the extension of lateral buds under favourable conditions differs from the apically directed growth inhibition inducing true dormancy in the tubers. This acropetal inhibition affects the tuber tip more strongly than its lateral buds, which develop into long stolon-like shoots after the tuber decapitation. The local supply of ABA shows no tuberizing effect, but enhances the dormancy of the tuber top. MH interrupts the correlation between the tuber laterals tuberizing without previous stolon formation. The uppermost leaf structures participate in the apical dominance, inhibiting their own axillaries on intact tubers. Mature scales disclose this correlative influence only on decapitated or dissected tubers on which IAA or BA release their inhibitory effect, but ABA increases it. Two scale pairs occurring regularly at the top of dormant tubers and seen later at the erect base of the stem are involved in the initiation of foliage leaves for the next-year growth period. BA applied to an axil at the top of the tuber provokes its sylleptic branching.     

Localization of Stem Elongation Control in Cucumis sativus L

Reciprocal grafts, and applications of gibberellin (GA) and indoleacetic acid (IAA) were used to localize the site of control for stem elongation in cucumber (Cucumis sativus L.). Dwarf and tall plants were reciprocally grafted to determine influence of stems and roots on stem elongation. At 21 days there were no significant differences in length between stems grafted to their own roots and those grafted to roots of the other type. GA₃, GA₄₊₇, and IAA were applied to seedlings with and without live apical buds. Seedlings with live apical buds responded to level of added GA, but not to added IAA. GA₄₊₇ was more effective than GA₃. Hypocotyls of tall plants responded more to both GA treatments than did those of the dwarves when both types had live apical buds. When either GA₄₊₇ or IAA was applied to seedlings with dead apical buds, elongation of the hypocotyl responded to level of the growth regulator, but there was no difference in response between the dwarf and tall plants.     

STUDIES ON THE FLORAL HISTOGENESIS AND PHYSIOLOGY OF PERILLA. III. EFFECTS OF INDOLEACETIC ACID ON THE FLOWERING OF APICAL BUDS AND EXPLANTS IN CULTURE

Raghavan , V. (Princeton U., Princeton, N. J.) Studies on the floral histogenesis and physiology of Perilla. III. Effects of indoleacetic acid on the flowering of apical buds and explants in culture. Amer. Jour. Bot. 48(10): 870–876. Illus. 1961.—The responses of apical buds and explants of a short-day plant, Perilla frutescens (L.) Britt. var. 'Tall Late,' when grown in vitro in White's medium supplemented with indoleacetic acid (IAA) and subjected to short-days (SD) or long-days (LD), are described. Additions of varying concentrations of IAA to the medium inhibited the flowering of the photoinduced apical buds in 2 ways. There was a progressive delay in the appearance of the first signs at the apex and a gradual transition from the more flower-like structures in lower concentrations of IAA (0.1 mg/liter) to sterile cones in higher doses. The sterile cones had florets with well-developed calyx and corolla lobes, but lacked the sporogenous tissues. When subjected to LD, visible signs were observed only in buds grown in 0.1 and 1.0 mg/liter IAA, the pronounced effect of the auxin being in the step-wise inhibition in the formation of the non-sporogenous tissues of the differentiating florets. Flowering of the explants with the 1st pair of unfolded leaves was also inhibited by IAA in either SD or LD, but the 1st signs appeared relatively faster than in apical buds. When photoinduced, explants with the 1st and 2nd pairs of unfolded leaves flowered in all concentrations of IAA tried (up to 100 mg/liter) while those kept in LD remained entirely vegetative.     

Abscisic acid and apical dominance in Phaseolus coccineus L.

Abscisic acid (ABA) in lanolin, applied to the internode of decapitated runner bean plants enhances the outgrowth of lateral buds. The optimum concentration of the paste is 10^-5 M. The effect of ABA is counteracted by indoleacetic acid (IAA) but not by gibberellic acid (GA₃). There is no effect when ABA is applied to the apical bud or lateral buds of intact plants. However, 13.2 ng given to the lateral buds of decapitated plants stimulate their growth, whereas higher concentrations are inhibitory. Consequently, ABA enhances growth of lateral buds directly, but only when apical dominance is already weakened. The growth of the decapitated 2^nd internode was not affected by ABA. Radioactivity from [2-¹⁴C] ABA, applied to nonelongating 2^nd internode stumps of decapitated runner bean plants moves to the lateral buds, whereas [1-¹⁴C]IAA-and [³H]GA₁-translocation is much weaker. ABA transport is inhibited if IAA or [³H]GA₁ is applied simultaneously. In elongating internodes [¹⁴C]ABA is almost completely immobile. [¹⁴C]IAA-and [³H]GA₁-translocation is not affected by ABA. The amount of radioactivity from labelled ABA, translocated to the lateral buds, is highest during the early stages of bud outgrowth.Abbreviations ABA 2,4-cis, trans-(+)-abscisic acid - GA gibberellic acid - IAA indoleacetic acid - p.l. plain lanolin     

THE ROLE OF AUXINS AND CYTOKININS IN THE RELEASE OF BUDS FROM DOMINANCE

The paper deals with the general problem of the physiological basis of branching, and the roles of known and unexplored factors in sensitivity to apical dominance. It is shown that when pea seedling shoots are completely or partially inhibited by other shoots on the same plant auxin can promote their elongation, even though it does not have this effect on inhibited buds. This influence of auxin is only exerted on internodal elongation and not on apical growth. When kinetin in a solution of alcohol and carbowax is applied directly to the lateral buds of pea seedlings, it releases them from inhibition by the growing apex. It is shown that the role of alcohol in this solution is to act as a surfactant, permitting good contact with the buds, while that of carbowax, being hygroscopic, is to maintain a thin film of solution over the buds. Buds thus released from apical dominance by kinetin do not elongate as much as do uninhibited control buds. Such kinetin-treated buds can, however, be made to elongate normally by the application of auxin locally to their apices. It is concluded that growing shoots are relatively insensitive to correlative inhibition because they synthesize two types of growth substances, namely, auxin, which antagonizes the inhibitory effect on internodal elongation, and cytokinins, which permit the apex itself to develop. In the discussion it is brought out that many cases of branching, which appear at first to bear little relation to one another, can be understood on the basis of two principles, namely: (1) Any reduction in the growth rate of a dominant apex reduces its inhibitory effect on other apices, and (2) once an apex starts growing it becomes less sensitive to inhibition by other apices These generalizations and the experimental results are tentatively interpreted in terms of an interaction between the syntheses of auxin and of cytoldnin.     

Stimulatory effect of cytokinins and interaction with IAA on the release of lateral buds of pea plants from apical dominance

Lateral buds of pea plants can be released from apical dominance and even be transformed into dominant shoots when repeatedly treated with synthetic exogenous cytokinins (CKs). The mechanism of the effect of CKs, however, is not clear. The results in this work showed that the stimulatory effects of CKs on the growth of lateral buds and the increase in their fresh weights in pea plants depended on the structure and concentration of the CKs used. The effect of N-(2-chloro-4-pyridyl)-N'-phenylurea (CPPU) was stronger than that of 6-benzylaminopurine (6-BA). Indoleacetic acid (IAA) concentration in shoot, IAA export out of the treated apex and basipetal transport in stems were markedly increased after the application of CPPU or 6-BA to the apex or the second node of pea plant. This increase was positively correlated with the increased concentration of the applied CKs. These results suggest that the increased IAA synthesis and export induced by CKs application might be responsible for the growth of lateral shoots in intact pea plants.     

Role of mineral nutrients and growth regulators in the apical dominance in Solanum sisymbrifolium

Summary The lower axillary buds of intact plants of Solanum sisymbrifolium are released from complete inhibition by supplying high doses of potassium to the soil while complete apical dominance is shown by plants grown at low, but not deficiency levels of K. Nitrate and phosphate supplied alone or together are ineffective but when either of them is supplied with K, the effect of the latter on the growth of axillary buds is somewhat enhanced. The buds thus released from inhibition elongate further only when supplied with gibberellin A₃ (GA₃). Indoleacetic acid (IAA) alone has a considerably weaker effect but when supplied with GA₃ the stimulatory effect is greater than is caused by the latter alone. The completely inhibited buds of low-K plants can be released from inhibition by supplying kinetin. In such buds IAA promotes further extension but GA₃ does not. The partially inhibited buds of the high-K plants, on the other hand, are not affected by exogenous kinetin.Dedicated to Professor H. D. Wulff on the occasion of his 60th birthday.     

Growth Regulators and Wood Formation in Pinus silvestris

The formation of new xylem in the spring is preceded by bud development. In decapitated pine stem the formation of xylem is arrested until the outgrowth of interfascicular buds takes place. When indole-3yl-acetic acid (IAA) is applied to the cut surfaces of decapitated stems it induces the formation of a xylem ring on the whole length of 5-ycar old trees. Naphthaleneacetic acid (NAA) causes the formation of xylem; however, the width of the growth ring is several times broader at the point of application than at the base of the leader. Cis- and trans-cinnamic acids, coumarin, L-tryptophan, kinetin (Kin), benzylaminopurine (BAP) and gibberellic acid (GA) alone do not induce cambial divisions; however, GA and the cytokinins given jointly with IAA or NAA accelerated the basipetal stimulus which has been induced by the auxins, resulting in normal xylem formation. 2,3,5-Triiodobonzoic acid (TIBA) given jointly with IAA-induced formation of compression wood in the apical part of the stem and narrow diameter tracheids at the base. When carboxyl labelled IAA or NAA are applied to pine segments it is found that the basipetal movement of IAA is much quicker than that of NAA. GA and the cytokinins increase the rate of transport of both auxins, whereas TIBA arrests the bulk of auxin in the apical part of the stem.     

Release of lateral buds from apical dominance by glyphosate in soybean and pea seedlings

Application of a sublethal dose of glyphosate (N-[phosphonomethyl]glycine) to the seedlings of soybean (Glycine max L. Merr. cv. Evans) and pea (Pisum sativum L. cv. Alaska) promoted growth of the cotyledonary and other lateral buds. The pattern of the glyphosate-induced lateral bud growth was different from that induced by decapitation. Under the experimental condition, glyphosate did not kill the apical buds. Feeding stem sections of the seedlings with radiolabeled indole-3-acetic acid ([2¹⁴C]IAA) and subsequent analysis of free [2-¹⁴C]IAA and metabolite fractions revealed that the glyphosate-treated plants had higher rates of IAA metabolism than the control plants. The treated pea plants metabolized 75% of [2-¹⁴C]IAA taken up in the 4-h incubation period compared to 46.5% for the control, an increase of 61%. The increase was small but consistent in soybean seedlings. As a result, the glyphosate-treated plants had less free IAA and ethylene than the control plants. The increase of IAA metabolism induced by glyphosate is likely to change the auxin-cytokinin balance and contribute to the release of lateral buds from apical dominance in these plants.     

Effects of Indol-3yl acetic Acid on Floral Induction and Apical Differentiation in Chenopodium rubrum L.

Indol-3yl acetic acid (10^–4M) was applied to the plumulesof Chenopodium rubrum. Effects on the anatomical structure andthe growth pattern in the apical meristem, as well as DNA synthesisand nucleolus size were investigated. When auxin is applied before or during photoperiodic inductionit inhibits DNA synthesis and meristematic activity. The axillarymeristem (i.e. a group of cells in the axils of the leaf primordia)is most affected. A similar inhibition of the axillary meristemwas also observed in non-induced control plants grown in continuouslight. Auxin applied simultaneously with photoperiodic inductioncounteracts the reduction of apical dominance in the apex andthus inhibits the onset of floral differentiation. Auxin appliedfollowing induction inhibits the previously-formed buds andmakes possible a more complete development of the apical flower. The dual effect of IAA on flowering, inhibitory and stimulatory,manifests itself as a growth response at different stages ofthe changing shoot apex.     

A Note on the Manipulation of Flower Symmetry inAntirrhinum majus

Treatments consisting of maceration of the centre of the shootapical meristem or localized application of the plant hormone,indoleacetic acid (IAA), to apical flower buds or the estimatedcentre of the shoot apex were made to test their effect, ifany, on flower shape or symmetry. Both types of treatment affectedflower symmetry. IAA treatment was most successful, but it alsoaffected the completeness of the flower, producing a small numberof reduced flowers. Alteration of symmetry was, however, themain response to treatment.Copyright 1999 Annals of Botany Company Antirrhinum majusL., flower symmetry mutants, microsurgical and microhormonal treatments, apical meristem, flower buds.     

The Mechanism of Apical Dominance in Coleus

The development of lateral buds in isolated stems of Coleus blumei is inhibited by low concentrations of indoleacetic acid or other auxins, just as in other plants. The inhibition can be fully reversed by kinetin, about 3 times as much kinetin as IAA being needed. However, the outgrowth of the same lateral buds on intact Coleus plants is sensitive to environmental conditions, well-nourished plants in full daylight often showing little inhibition by applied auxin. It is shown that (a) the solvent used for IAA, (b) the light intensity and (c) the nitrogen and phosphorus nutrition, all control the sensitivity of the buds to auxin inhibition. Using water instead of lanolin, lowering the light intensity or decreasing the supply of either nitrogen or phosphorus all increase the degree of apical dominance.     

Einfluß von Pasten mit verschiedenen Indolylessigsäure-Konzentrationen auf den Transport von 32P in dekapitierten Erbsenepikotylen

Summary Either a 0.25% or a 0.007% IAA paste was smeared on the apical cut surface of decapitated pea epicotyls and simultaneously ³²P was added to the roots. When subsequently the radioactivity of the apical segment of the epicotyls was measured at different time intervals following the addition of ³²P, no significant differences between the effect of 0.25 and 0.007% IAA paste on ³²P transport were found. Because the 0.25% IAA paste completely retards the growth of cotylary buds whereas the 0.007% paste supports this growth, it might appear that the effect of 0.25% IAA paste on the transport of nutrient substances plays a decisive role in the apical dominance. More probably 0.25% IAA paste imitates the apical dominance only by means of its toxic effect, which, however, requires a detailed investigation.