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1.
Floral buds of the ‘False Horn’ plantain clonesMusa (AAB) ‘Harton Verde’, ‘Harton Negra’,and ‘Currare’ terminate in a large single floralstructure. The apices of these floral buds are here designatedas determinate since they have lost the ability to produce additionalfloral initials or buds. Terminal peduncle segments can be culturedin a modified Murashige and Skoog (1962) medium supplementedwith N6-benzyl-aminopurine (5 mg I–1). Under these conditions,this apparent inability to yield buds can be overcome as vegetativeshoot clusters form in the axils of the bracts. Rooted plantletsare obtainable by treating shoots with naphthaleneacetic acid(1 mg I–1) and activated charcoal (0.025%). The adventitiousorigin of the shoots has been established. Musa cultivars, plantains, floral bud, adventitious buds, tissue culture  相似文献   

2.
The metabolism of [3H]dihydrozeatin (DZ) in floral buds of threedevelopmental stages, and endogenous cytokinin (CK) levels inmature stamens were investigated in wild-type (WT) and a geniemale sterile (GMS) line of rapeseed (Brassica napus L.). Floralbuds were fed [3H]DZ and subsequently different metabolites,namely nucleotides, ribosides and glucosides, were analysedby 2DTLC and HPLC. The GMS buds exhibited a higher initial uptakeof [3]DZ than wild-type buds, but the total uptake after 12h was either similar or less in GMS buds. [3]Dihydrozeatin wasmetabolized more efficiently in WT than in GMS buds, as moreof [3]DZ was retained in the latter. This was especially thecase in stage 2 buds, when in GMS anthers microspores fail toseparate from tetrads, thereby causing sterility. [3H]Dihydrozeatinwas converted to dihydrozeatin nucleotide (DZNT), dihydrozeatinriboside and O-glucosides by both WT and GMS buds. However,all these metabolites were relatively low in GMS buds. The majordifference was in the reduced formation of DZNT by stage 2 GMSbuds. The GMS stamens also contained low levels of various cytokinins,including the nucleotides. These observations, along with earlierreports, suggest that low levels of endogenous CKs, and, inparticular, the reduced formation of CK nucleotides are partlyresponsible for the breakdown of microsporogenesis in GMS anthers. Key words: Cytokinin, metabolism, male sterility, rapeseed, Brassica napus  相似文献   

3.
Fragments of leaves, petioles and floral stalks of several speciesand varieties of Begonia have been cultured in vitro on dennedmedia. The presence of a cytokinin, adenine and an auxin wasfound necessary for optimum bud formation, especially on petiolesand floral stalks. Flower buds could be produced on leaves andfloral stalks, but not on petioles. They were of the male type. 1It is a real pleasure to express our gratitude to ProfessorDr. von DENFFER who gave the initial impetus for this pieceof research and granted a leave of absence to Dr. F. RINGE inorder to originate the in vitro culture of Begonia species inthe Laboratoire de Physiologie Pluricellulaire at Gif-sur-Yvette.  相似文献   

4.
The effects of various plant growth regulators and that of pHon the in vitro growth and development of young inflorescencesof Brassica napus L. cv. Westar were examined. A cytokinin wasrequired for normal maturation of floral buds, including thecompletion of microsporogenesis, and it stimulated the initiationof additional buds on the inflorescence axis. Benzylaminopurine(BAP) was the most effective of the cytokinins tested. Gibberellicacid (GA3) and naphthaleneacetic acid (NAA) alone were ineffective.In combination with BAP, both reduced the positive influenceof the cytokinin but GA3 was more inhibitory than NAA. At alow initial pH (3.9–4.6), the percentage of cultures whichproduced normal buds was significantly higher, especially inthe presence of 10-7 M or 5 ? 10-7 M BAP, in comparison to cultureswith a pH of 5.3-6.0, the standard range for plant tissue culture.  相似文献   

5.
In the sweet pea (Lathyrus odoratus L.) genes Dnl andDrh controlthe production of a graft-transmissible substance which delaysflowering and promotes outgrowth of basal laterals. Seed vernalizationpromotes flowering and reduces lateral outgrowth in intact plantsand grafted scions of genotype DniDnl, suggesting that vernalizationreduces output of the Dni system, possibly by disrupting therelationship between chronological and plastochronic age. Whenlateral outgrowth and floral abortion are used as indicatorsof inhibitor levels, it can be shown that vernalized Dni plantspossess more inhibitor but initiate flower buds at a lower nodethan unvernalized dn plants. This supports the suggestion thatin regard to floral initiation vernalization also alters thesensitivity of the shoot apex to the flowering hormone(s). InLathyrus odoratus an hormonally based vernalization responseof considerable magnitude can be shown for day-neutral (dndn)lines, supporting the suggestion that vernalization also influencesthe level of a flower promotor. Lathyrus odoratus L., sweet pea, vernalization, flowering, branching, genotype, grafting  相似文献   

6.
In Torenia stem segments cultured on a defined medium from whichammonium nitrate and growth regulators were omitted, adventitiousbuds were readily formed from epidermal tissue, with subsequentdifferentiation of floral buds. Using this plant material, thecorrelation between the time of application of various chemicalsand the time-course of floral bud differentiation was investigated.Histological examination showed that adventitious buds werevegetative during the first two weeks of the culture, and floralprimordia appeared after about three to four weeks of culture.We divided the flowering process in Torenia stem segments intothe following 3 phases: the first phase (first 2 weeks) duringwhich adventitious buds are formed, the second phase (3rd and4th weeks) during which floral buds are initiated and the thirdphase (5th to 12th weeks) during which floral buds develop.Then we added IAA, zeatin, ammonium nitrate or a high concentrationof sucrose to the medium during one, two or three of these phases.Ammonium nitrate added during the third phase suppressed floralbud development, but the high concentration of sucrose givenduring this phase stimulated it. These two chemicals influencedonly the development of floral buds previously initiated. Theapplication of IAA during the first phase promoted both theinitiation and development of floral buds. However, its applicationafter 2 weeks of culture failed to promote floral bud formation.Zeatin inhibited floral bud formation in a manner similar toammonium nitrate, but if it was added to the medium only duringthe first phase, it slightly promoted the initiation and developmentof floral buds. (Received July 7, 1981; Accepted October 12, 1981)  相似文献   

7.
The photoperiodic requirement for flowering in Impatiens balsaminachanges with the length of the photoperiod. Floral buds wereinitiated with two 8 hr but with four 15 hr photoperiods andflowers opened with four 8 hr but twenty-eight 15 hr photoperiods.A part of the photoperiodic requirement for floral inductionin this plant can be substituted by LDs containing 4 or morehours of darkness (10). It indicates the identical nature ofthe floral stimulus produced during the dark period, whetherit forms a part of the inductive or non-inductive cycles. Theeffect of these supplementary non-inductive photoperiodic cyclesin causing floral bud initiation also depends on the lengthof the first inductive obligatory cycle. More floral buds andflowers were produced on plants exposed to 15 hr than 8 hr photoperiods,probably due to the higher number of leaves that were producedunder the former condition of weaker induction. The shorterthe dark period in the photoperiodic cycle, the weaker the induction,the slower the rate of extension growth but the more differentiationof leaves. 1 Present address: Department of Biology, Guru Nanak Dev University,Amritsar-143005, India. (Received November 9, 1977; )  相似文献   

8.
NORRIS  I. B. 《Annals of botany》1985,56(3):317-322
Effects of temperature on floral initiation of ten white clovervarieties growing in controlled environments are described.Plants grown under long days (16 h) were subjected to constanttemperatures of 26, 18 and 10 °C. Relationships betweenmorphological and physiological traits and flowering were examined. Most plants flowered at the two higher temperatures but only10 per cent of plants flowered at 10 °C. Larger leaved typestended to produce more reproductive buds per stolon at the highertemperatures than did smaller leaved varieties. Of the floral characters studied, floret number was least affectedby temperature. Ovule number and peduncle length were greatestat 18 °C. Variation in, and absolute level of nectar secretionwas greatest at the highest temperature. Trifolium repens, white clover, flowering, temperature  相似文献   

9.
Pollen embryos and plantlets of Nicotiana tabacum cv. Samsunand Nicotiana rustica cv. Rustica were obtained through directpollen culture without prior treatment or prior culture of anthersor buds. Isolated pollen was cultured first in a medium withoutsucrose, then transferred into Nitsch's H medium containing2% sucrose and 5 mM glutamine. The optimum medium for the initialculture was water and the optimum period of culture was ca.6 days when binucleate pollen was used. 1 Present address: Friedrich Miescher Inst., P.O.B. 273, CH-4002Basel, Switzerland. (Received January 18, 1982; Accepted March 19, 1982)  相似文献   

10.
Levels of putrescine, spermidine and spermine increase whenvegetative or floral buds form in cultures derived from surfaceexplants of inflorescences of Nicotiana tabacum L. cv. Wisconsin-38.Concomitantly, the activity of arginine decarboxylase (ADC)rises and that of ornithine decarboxylase (ODC) declines. DL--Difluoromethylarginine(DFMA), a specific suicide inhibitor of ADC, inhibits bud initiation,while DL--difluoromethylornithine (DFMO), the analogous suicideinhibitor of ODC, does not. On the other hand, DFMO inhibitsthe subsequent development of newly regenerated floral buds,while DFMA does not. It thus appears that polyamines derivedthrough ADC may be involved in bud initiation, while polyaminesderived through ODC are required for subsequent growth and developmentof such buds. Especially large increases of spermidine are associatedwith floral bud differentiation, indicating a possible specialmorphogenetic role for that polyamine. 1Present address: Laboratori de Fisiologia Vegetal, Facultadde Farmacia, Universitat de Barcelona, 08028 Barcelona, Spain (Received April 25, 1988; Accepted August 12, 1988)  相似文献   

11.
12.
A series of myo-inositol phosphates including myo-inositol mono-to hexa-phosphates was observed during growth of cultured riceplant cells. We also found that 32Pi and myo-[2-3H] inositolwere incorporated into all these myo-inositol phosphates. myo-Inositolphosphorylating activity, which depended on ATP and Mg2+, wasdetected in the soluble fraction from the cells, and the reactionproduct was identified as myo-inositol-2-phosphate. (Received January 21, 1980; )  相似文献   

13.
During the course of characterizing fragments bound to an Arabidopsisfloral homeotic protein AGAMOUS in vivo, a gene encoding a putativeserine/threonine protein kinase was found on one of the fragments.The deduced 426 amino acid residues of the gene, named APK2a,are 65% identical to a previously reported Arabidopsisserine/threonineprotein kinase, APKla. The gene is composed of 6 exons and mapsat 10 cM from the upper end of chromosome 1. Northern hybridizationexperiments indicated that the gene is strongly expressed inleaves, moderately in roots, and very weakly in flowers. Furtherin situ analysis of the expression in floral buds showed thatthe APK2a gene is expressed at pedicels, is not expressed atthe floral organ primordia of wild type floral buds, but ismoderately expressed in the floral organ primordia of the agamousmutant. In vitro binding assay suggests that the AGAMOUS proteinbinds to a sequence similar to, but different from, the knownMADS-binding consensus sequences, the CArG box, located 3' downstreamof the APK2a gene. These results suggest that APK2a gene expressionis negatively regulated by the AG protein. A close homologue of the APK2a gene, named APK2b, was also isolatedfrom the Arabidopsis cDNA library. The expression pattern ofthe APK2b gene differs from that of APK2a. It is strongly expressedin leaves, moderately in flowers, and weakly in roots. 4Present address: Biomolecular Engineering Research Institute,6-2-3, Fruedai, Suita, Osaka, 565 Japan.  相似文献   

14.
Immature embryos of different sizes and ages from commercialvarieties of lychee (Litchi chinensis Sonn.) were cultured ina range of different media. Embryos as small as 3 mm could becultured using in vitro techniques and subsequently grown intoplants. MS solid medium with 2% sucrose supplemented with 150ml l–1 coconut water was most effective in stimulatingthe germination of immature lychee embryos. Embryos of lycheewere treated to induce adventitious buds from embryonic shootsas a means of achieving multiplication. The different varietiesexhibited differences in response, with Bengal embryonic shootsproducing 15 adventitious buds after pretreatment with 100 mgl–1 BAP for 3 h. Root formation was achieved in 65% ofadventitious shoots using MS medium supplemented with 0.5 mgl–1 NAA and activated charcoal. These plants were successfullydeflasked and grown on in the glasshouse. This technique providesof means of producing some multiple shoots from lychee embryosand has value for multiplication in a breeding program wherea method of micropropagation is unavailable. Litchi chinensis Sonn., lychee, embryo culture, multiple shoots, in vitro  相似文献   

15.
Zygotic embryos of Picea chihuahuana Martínez were cultivatedin vitro to determine the time of organogenic competence andto maximize adventitious bud induction. The induction mediumconsisted of modified B5 substrate supplemented with N6-benzyladenine(with or without naphthalene acetic acid) or kinetin (with orwithout 2-4, dichlorophenoxyacetic acid) at different concentrationsand induction times. The minimum induction time required forbud formation was 14 d with kinetin and 17 d with N6-benzyladenine.After induction embryos were transferred to the proliferationmedium (modified B5 substrate with 50% of its components andwithout growth regulators) for 30 d. The subsequent buds weretransferred every 15 d to Schenk and Hildebrandt medium at halfits concentration without growth regulators. The most effectivetreatments were 3 and 5 mg l-1kinetin or N6-benzyladenine whichproduced five to seven buds per embryo. The largest shoots weresubjected to rooting trials with pulses of different concentrationsof indole butyric acid resulting in only one bud developinga root. Histological analysis revealed clusters of three tofour cells that became more evident as induction time increased.Kinetin promoted the development of an organized structure priorto adventitious buds formation sooner than N6-benzyladenine.Copyright 2000 Annals of Botany Company Competence, plant tissue culture, micropropagation, Picea chihuahuana, endangered species, spruce  相似文献   

16.
Internodal segments of Torenia fournieri Lind. were culturedon various media to investigate chemical factors influencingin vitro flowering. The elimination or dilution of ammoniumnitrate from Murashige and Skoog's medium increased the formationof adventitious buds which subsequently differentiated floralbuds. The dilution of mineral salts in Murashige and Skoog'smedium enhanced adventitious bud formation, but did not influencethe ratio of cultures with floral buds to those with adventitiousbuds. Among various media tested, in vitro floral bud formationand development of Torenia was best on a medium having 1/5 ofthe mineral salts and no NH4NO3. Eighty-seven percent of thecultures produced floral buds on this medium. Using this medium,the effects of various sugars were also examined. Increasingthe concentration of sucrose in the medium (up to 60 g/liter)increased the rate of cultures with floral buds, and stimulatedthe development of floral buds led to anthesis. (Received January 17, 1981; Accepted February 21, 1981)  相似文献   

17.
Ethidium bromide (EB) inhibited growth of cells of the non-sulfurpurple photosynthetic bacterium Rhodopseudomonas spheroides.The inhibitory action of EB on the light-anaerobic culturedcells was stronger than on dark-aerobic cultured ones. EB alsosuppressed the induced synthesis of bacteriochlorophyll (Bchl)and carotenoids in the dark-aerobically grown cells incubatedwith gentle aeration under no-growth conditions, suggestingthat the target of the inhibitory action of EB on the photosyntheticgrowth of R. spheroides cells is chromatophore formation. EBdepressed the incorporation of 3H- or 14C-uracil into both RNAand DNA fractions from cells incubated with gentle aeration.In contrast, inhibition by EB of 3H-uracil incorporation intothe DNA fraction was not observed under vigorous aeration. Ourfindings seemed to favor the hypothesis described previously(10) that lowering the intracellular oxidation-reduction potentialmight bring about a unique synthesis or turnover of DNA responsiblefor chromatophore formation. (Received December 22, 1977; )  相似文献   

18.
A culture system of isolated mesophyll cells of Zinnia eleganswas used to examine the action of gibberellic acid (GA) on celldivision. Isolated Zinnia mesophyll cells cultured in a mediumcontaining auxin and cytokinin reinitiated cell division ina partly synchronized manner. When mesophyll cells isolatedfrom 21-day-old seedlings were used, GA added to the culturemedium at concentrations of 1 x 10–6 M or higher suppressedthe initial rise in the number of divided cells. Tracer experimentswith [3H]-dThd revealed that GA treatment inhibited the incorporationof [3H]-dThd into DNA in the nucleus without inhibiting theuptake of [3H]-dThd into the cells, indicating that GA inhibitedDNA synthesis. GA applied at 48 h inhibited the incorporationof [3H]-dThd into DNA during the following 24 h, but GA appliedat 72 h did not inhibit the incorporation during the subsequent24 h. This suggests that GA affects the process of reinitiationof DNA synthesis, but does not affect DNA synthesis once cellshave become proliferative. (Received January 14, 1986; Accepted March 31, 1986)  相似文献   

19.
The accumulation of endogenous cytokinins was studied in pedicelexplants of tobacco (Nicotiana tabacumL.) during regenerationof flower buds in vitro. Maximal bud formation was induced onmedia containing 1.0 mmol m–3 of benzyladenine or dihydrozeatin.No buds were formed in the absence of cytokinin. The levelsof dihydrozeatin, zeatin, and the corresponding ribosides weredetermined in explants cultured in the presence or absence ofcytokinin by means of a competitive ELISA technique. In explantsincubated without a cytokinin, only the dihydrozeatin concentrationincreased significantly during the first day of incubation anddecreased during the second day. No increase was observed inexplants incubated in the presence of benzyladenine. The concentrationof dihydrozeatin in these bud-forming explants was only 10 to15% of the concentration built up in explants cultured on dihydrozeatininstead of benzyladenine. This suggests that the endogenouscytokinins only play a minor role in the regeneration of flowerbuds in vitro. Key words: cytokinin, flower bud development, tissue culture, tobacco  相似文献   

20.
Impatiens balsamina L., a qualitative short day plant, requiresmore short days for the development of floral buds into flowersthan for their initiation. Phosfon D and cycocel reduce thenumber of short days required for flowering, increase the numberof floral buds and flowers and delay their reversion to vegetativegrowth when transferred to noninductive conditions. The effectof decapitation of the main shoot subsequent to the emergenceof floral buds resembles that of retardants indicating thatthe effect of the latter in flower promotion in this plant maybe by virtue of their effect on cessation of apical dominanceas a consequence of which reserve food materials may be channeledto axillary floral buds enabling them to develop into flowers. (Received January 9, 1969; )  相似文献   

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