Growth Inhibition of Intact Plants and In Vitro Cultures of Tobacco by Culture Filtrates of Fusarium oxysporum f.sp. nicotianae

The culture filtrate of Fusarium oxysporum was able to induceseveral symptoms on tobacco plants that appeared during theactual pathological condition. Positive correlations were establishedfor the degree of culture-filtrate-induced symptoms developedin a range of tobacco cultivars and those caused by the livepathogen after inoculation into the same cultivars. Effectsof culture filtrate on the growth of intact plants, anthers,leaf discs and cell suspensions were examined to assist in understandingthe cellular basis of pathogenicity. The culture filtrate above25 % (v/v) was found inhibitory to the growth of leaf-disesand plated cell suspensions. No growth occurred above the 50%(v/v) level of the filtrate. Similarly, wilt symptoms were observedon the whole plants when the culture filtrate exceeded 25% (v/v).In vitro androgenesis was inhibited at a much lower concentration(12.5% v/v) of culture filtrate. Fusarium oxysporum f.sp, nicotianae, Nicotiana tabacum, fungal culture filtrate, will disease     

Experimentally Synthesized Plant Chimeras 2. A Comparison of In vitro and In vivo Techniques for the Production of Interspecific Nicotiana Chimeras

In vitro and in vivo techniques were compared for synthesizingchimeras between Nicotiana glauca Grahm and N tabacum L Interspecificchimeral callus, produced from mixed callus cultures in vitro,was placed on media which favoured only N tabacum shoot formationNone of the 474 regenerated N tabacum shoots incorporated Nglauca cells into their meristems When chimeral callus was regeneratedunder hormonal conditions favouring simultaneous organogenesis,of 397 shoots, only non-chimeral shoots of both species aroseIn vivo, reciprocal splice grafts between species were decapitatedjust above the graft union and treated with or without auxin—lanolinpastes Auxin increased callus formation but inhibited adventitiousshoot formation Three of 209 adventitious shoots arising fromthe graft union were interspecific mericlinal chimeras whichwere later stabilized as periclinal chimeras All three chimerasformed when N glauca was the understock Two of the chimerasarose on untreated shoots which produced no visible callus,indicating that excessive callus formation may be unnecessaryfor multiple cell origin of adventitious shoots to occur Chimeras, tobacco, Nicotiana glauca, Nicotiana tabacum, tissue culture, graft chimeras, callus cultures     

Ethylene and Ethane Production in 2,4-D Treated and Salt Treated Tobacco Tissue Cultures

Gas chromatography was used to measure ethylene (ethene) andethane production by tobacco (Nicotiana tabacum cv. Wisconsinno. 38) callus tissues grown on media containing inorganic saltsaccording to Murashige and Skoog (1962), sucrose, myo-inositol,thiamine-HCl kinetic according to Linsmaier and Skoog (1965),and either 2,4-dichiorophenoxyacetic acid (2,4-D) in the range0–100 mgl^–1 or 2 mgl^–1 indoi-3-ylacetic acidplus NaCl in the range 0–200 Meq l^–1. Ethylene productionrates were high (> 500 nl h^–1 g^1– fresh weight)initially in all treatments. Subsequently, ethylene productiondeclined in rapidly growing cultures but remained high in moderatelyand severely 2,4-D (> 0·5 mgl^–1) stressed andin severely NaCl (150 Meql^–1) stressed cultures. Highinitial rates of ethane production (> 200 nl h^–1 g^–1fresh weight) were obtained under conditions of severe stresscaused by 2,4-D or NaCl but not in control or moderately inhibitedcultures. With further incubation ethane production declinedin the severely stressed cultures. It is concluded that ethyleneproduction can be used as an index of moderate 2,4-D stressand severe NaCl stress by virtue of the high persisting ratesof ethylene production in stressed cultures. Ethane productioncan be used as an early index of severe stress caused by either2,4-D or NaCl in vitro. Nicotiana tabacum L., tobacco, ethylene, ethenen, ethane, 2,4-dichlorophenoxyacetic acid, auxin, stress, callus tissue     

The involvement of ethylene in in vitro maturation of mid-binucleate pollen of Nicotiana tabacum

The role of ethylene during in vitro maturation of Nicotianatabacum pollen from the mld-binucleate (MB) stage was analysedby the addition of aminooxyacetic acid (AOA), aminoethoxyvinylglycine(AVG), CoCl₂ and AgNO₃ to the maturation medium (AMGLu). Anincrease in ethylene production was obtained in both isolatedpollen and pollen surrounded by sporophytic tissue during insitu maturation. in vitro maturation of pollen was inhibitedby AOA and AVG; ACC and ethrel were able to overcome this inhibitoryeffect. Cyclohexylamine (CHA) reverted the inhibition provokedby both Ag⁺ and Co²⁺ The results reported in this paper indicatethat ethylene is one of the factors implicated in in vitro maturationof MB pollen of Nicotiana tabacum. Key words: Nicotiana tabacum, maturation, germination, pollen, ethylene     

Studies on the Growth in Culture of Plant Cells: VIII. THE PRODUCTION OF ETHYLENE BY SUSPENSION CULTURES OF ACER PSEUDOPLATANUS, L.

Sycamore cell suspension cultures in a synthetic medium releaseethylene; during a 24-day incubation period a single culture(initial volume 70 ml) produces c. 4 µ moles. There isa very sharp peak of ethylene production between day 10 andday 14 of culture; at the peak of production c. 2 nmoles ethyleneare released per million cells in 24 h. Evidence is presentedthat 2,4-D enhances ethylene production independently of itseffects on culture growth. Under the standard conditions of culture (250-ml Erlenmeyerflasks closed with aluminium foil and containing 70 ml cellsuspension) the concentration of ethylene in the gas phase ofthe cultures rises above 10 ppm. No evidence was obtained thatthis ethylene is inhibitory to culture growth or that a criticallevel of ethylene is necessary to initiate cell division incultures at a critically low cell density. The low rate of ethylene release by stationary phase culturesis temporarily enhanced by the addition of various solutes andfurther depressed by dilution with water.     

The Role of Glucose on Flower Bud Formation in Thin-Layer Tissue 12Nicotiana tabacum L.

The effect of glucose on flower bud formation was studied inthin-layer tissue cultures of epidermal strips from flower stalksof Nicotiana tabacum L. cv. Samsun. A minimum concentration of 30 mol m^–3 glucose in the MS-mediumcontaining 1.0 mmol m^–3 of both NAA and BA was necessaryfor flower bud formation. With 150 mol m^–3 glucose a minimumstay of 10 d was required for optimal flower bud formation. Withholding glucose for a limited period at different time intervalsafter the onset of culture caused a delay in flower bud formationand did not affect previous development on glucose. The resultsindicated that competence for flower bud initiation is not restrictedto the early stage of culture. The process may start at anytime later at the appropriate glucose concentration. However,for both optimal initiation and further development of flowerbuds the presence of a metabolizable sugar is required. Incubationof the tissue on glucose is associated with higher respirationrate. Key words: Flower formation, Glucose, mannitol, Nicotiana tabacum, Respiration, tissue culture     

Ventilation in Plant Tissue Cultures and Effects of Poor Aeration on Ethylene and Carbon Dioxide Accumulation, Oxygen Depletion and Explant Development

A simple technique for comparing and quantifying the ventilationcapacity of vessels used for plant tissue culture is described.Ethylene was injected into culture vessels and its rate of lossmonitored by gas chromatography. From the resulting exponentialdecay curves, the time in hours for half the ethylene to belost (t₅₀) was calculated and used to compare different containersand sealing methods. Cultures of Ficus lyrata Warb. and Gerberajamesonii Bolus grown for up to 28 d in plastic vessels sufficientlywell-sealed to generate t₅₀ values of approx. 16 h, accumulatedethylene and carbon dioxide in association with depleted oxygen.The relationship between carbon dioxide accumulation and oxygendepletion within culture vessels indicated little if any anaerobicrespiration. Gerbera explants did not appear to be affectedby these gaseous environments. However, in Ficus, leaf expansionwas approximately halved, although fresh and dry mass of wholeshoots was not decreased. The smaller leaf size is attributedto the action of accumulated ethylene, because when the gaswas absorbed with 'Ethysorb' granules or its action inhibitedby 2,5–norbornadiene, leaf growth was normal. The removalof carbon dioxide with potassium hydroxide did not enhance theethylene effect, indicating little if any antagonism of ethyleneaction by carbon dioxide. Shoots of potato (Solanum tuberosumL. cv. Red Craig's Royal) were shortened in sealed culture vessels,in association with swelling, diageotropism and miniaturizationof the leaves. When tuber production was induced by decreasingthe photoperiod, increasing the sucrose concentration and includingcytokinin in the medium, partial sealing promoted conspicuoushypertrophy of the lenticels. These responses of potato wereprevented if the ethylene absorbant mercuric perchlorate wasenclosed together with the cultures. Plant tissue culture, poor aeration, ethylene, leaf expansion, Ficus lyrata Warb., Gerbera jamesonii Bolus, Solanum tuberosum L. cv. Red Craig's Royal     

Effect of Light on Alkaloid Accumulation in Cell Cultures of Nicotiana Species

The effect of light on alkaloid accumulation in a range of cellcultures of tobacco was determined. Cell suspension culturesof Nicoriana rabacwn L. cv. Wisconsin-38 with differing degreesof photosynthetic activity, callus cultures of N. glauca Graham,root cultures of N. rustica L. and shoot cultures of N. tabacumwere used. The alkaloid content of green illuminated cultureswas greatly reduced compared with non-green cultures grown inthe dark, but decreased accumulation did not correlate withincreasing photosynthetic activity. The accumulation of allof the major alkaloids was affected, regardless of the speciesof tobacco used. Transfer of N. glauca callus from the darkinto the light caused a decrease in alkaloid accumulation, whilemoving cultures from the light into the dark resulted in anincrease in alkaloid content. In root cultures light causeda reduction in growth, which affected alkaloid synthesis. Inshoot cultures there were only traces of alkaloid detectable,regardless of whether or not cultures were illuminated. Lightappeared to cause a non-photosynthetic suppression of alkaloidaccumulation in visibly undifferentiated cultures, and thiseffect was modified in visibly differentiated cultures. Key words: Nicoriana spp, tobacco, alkaloid accumulation, cell culture     

Inhibition of Somatic Embryogenesis in Tissue 2Medicago sativa by Aminoethoxyvinylglycine, Amino-oxyacetic acid, 2, 4-Dinitrophenol and Salicylic Acid at Concentrations which do not Inhibit Ethylene Biosynthesis and Growth

Meijer, E. G. M. and Brown, D. C. W. 1988. Inhibition of somaticembryogenesis in tissue cultures of Medicago sativa by aminoethoxyvinylglycine,amino-oxyacetic acid, 2, 4-dinitrophenol and salicylic acidat concentrations which do not inhibit ethylene biosynthesisand growth. J. exp. Bot. 39: 263–270. The effects of aminoethoxyvinyglycine (AVG), amino-oxyaceticacid (AOA), 2, 4-dinitrophenol (DNP) and salicylic acid (SA)on ethylene production, tissue proliferation and somatic embryo-genesisin a recently developed rapid in vitro regeneration system ofMedicago sativa L. were examined. Contrary to numerous publications,AVG, AOA and DNP did not affect the rate of ethylene biosynthesis,while SA even caused an increase in ethylene production. Allfour compounds were, however, potent inhibitors of somatic embryoformation in the M. sativa tissue cultures, even at concentrationswhich did not affect tissue growth. Generally, a 5-d exposureto the inhibitors reduced the number and quality of somaticembryos obtained. It is suggested that the inhibitors may notreach the site of action of enzymes involved in ethylene biosynthesisand may possibly block other biosynthetic pathways which areof crucial importance to somatic embryo development. The resultsindicate that a delicate differentiation process like somaticembryogenesis is very sensitive to metabolic perturbances. Theresults are also discussed in the light of other known effectsof these four compounds on higher plants. Key words: Ethylene, Medicago sativa, somatic embryogenesis, tissue culture     

The Development of Male and Female Regenerants by In Vitro Androgenesis in Dioecious Plant Melandrium album

We examined induced androgenesis in vitro in the dioecious plantMelandrium album and aimed to produce complete plants from culturedimmature microspores. Flow cytometric analysis of nuclear DNAcontent was used to screen ploidy levels in regenerated plantsand to estimate the nuclear genome size in plants differingin sex. Haploid and spontaneous dihaploid (polyhaploid) femalesdominated among androgenic regenerants. Androgenic males occurredsporadically. They were exclusively dihaploid and geneticallysupermales (AAYY). The progenies obtained as a result of thecrosses between supermales and standard females contained onlymales. This is the first report on complete androgenesis inM. album from the microspores carrying the Y chromosome.Copyright1994, 1999 Academic Press Melandrium album (Miller) Garcke, pollen androgenesis, sex, female, male, supermale, flow-cytometry, nuclear genome size     

Atmospheric Ozone Interacts with Stress Ethylene Formation by Plants to Cause Visible Plant Injury

Ozone toxicity was studied in peas, beans, and tobacco (BelB and Bel W3). These experiments showed that ozone toxicitywas related to the rates of ethylene biosynthesis. Sensitivityto ozone was reduced if ethylene biosynthesis was inhibitedafter treatment with aminoethoxyvinylglycine (AVG). Similarly,plants that were able to reduce or prevent stress ethylene formationwere less sensitive after both short- and long-term exposureto ozone. Plants conditioned by longer exposures to ozone havelow rates of ethylene formation and this may be why brief ozoneexposures may be more phytotoxic than prolonged fumigations. Key words: Nicotiana tabacum, Phaseolus vulgaris, Pisum sativum, lipid peroxidation, peas, Pinto beans, tobacco     

Developmental Aspects of Ethylene Biosynthesis during Somatic Embryogenesis in Tissue 4Medicago sativa

Rates of ethylene production were determined in highly embryogenicand virtually non-embryogenic tissue cultures of Medicago sativassp. falcata during a 10-d induction period on medium containing2, 4, -dichlorophenoxyacetic acid and kinetin, and during thefirst 10 d of somatic embryo formation on growth regulator-freemedium. In cultures of both genotypes, ethylene production increasedrapidly, peaked after 10 d and then declined again rapidly.This fall in ethylene production rate also occurred when thecultures were kept on the growth regulator-containing medium,but it was more pronounced in cultures which were transferredto growth regulator-free medium, i.e. under conditions favouringsomatic embryo formation. There were only minor differencesin the rates of ethylene production between the two genotypes,mainly after transfer to growth regulator-free medium. Cobaltand nickel ions strongly inhibited ethylene biosynthesis throughoutthe culture period under investigation. They did not, however,affect embryo induction, but exerted strongly inhibitory effectson somatic embryo formation. Amino-oxyacetic acid and aminoethoxyvinylglycinehad no effect on ethylene production during the inductive period.It is concluded from these experiments that the high rates ofethylene production during embryo induction are not essentialfor subsequent embryo differentiation. Key words: auxin, ethylene, Medicago sativa, somatic embryogenesis, tissue culture     

A Nicotiana Gametosomatic Hybrid and its Progenies

A Nicotiana gametosomatic hybrid between N. tabacum and N. glutinosawas studied. It was shown to have a stable somatic chromosomecomplement of 2n=5x=60. Karyotypes and measures of DNA contentshow that there have been no major changes in the parental chromosomenumbers or morphology accompanying hybridization. Forty-eightchromosomes are derived from N. tabacum (2n=4x=48); 12 fromN. glutinosa (2n=2x=24). Homologous pairs of N. tabacum chromosomesusually pair normally at meiosis. Trivalents incorporating aglutinosa chromosome do occur but usually these remain as univalents. The fertility of the hybrid is low but some products of self-pollinationwere obtained. These carry the complete N. tabacum genome witha few glutinosa chromosomes, some of which form supplementarybivalents at meiosis. All derivatives studied were mixoploidbut progressive selfing reduces the extent of abnormality ofmitotic divisions. The study of morphological and developmentaltraits indicates that the addition of even a few chromosomesof N. glutinosa to the N. tabacum complement can modify thetabacum phenotype substantially. There is considerable variationamong the derivatives and scope for fixing desirable qualitiesthrough selection. The presence of only a haploid set of glutinosachromosomes in the original hybrid makes the return to a desirablegenotype more efficient than that achieved through more conventionalbreeding methods. Key words: Nicotiana, gametosomatic hybrid, selfed progeny, cytology     

Characterization and expression of an mRNA encoding a wound-induced (Win) protein from ethylene-treated tomato leaf abscission zone tissue

A cDNA clone (TAB7) encoding a putative woundinduced (Win) proteinhas been isolated from a tomato (Lycopersicon esculentum Mill.cv. Ailsa Craig) leaf abscission zone cDNA library using a differentialscreening strategy. The clone has a high degree of homologyat the amino acid level to both the potato win1 and 2 genes,Hevea brasiliensis hevein and Nicotiana tabacum PR-4a and PR-4bproteins. The mRNA encoded by TAB7 is up-regulated within 12h of exposure to ethylene (10µl l^–1) and its expressionincreases steadily within the cells comprising the leaf abscissionzone and to a lesser extent in the adjacent non-zone tissue.This rise precedes the onset of cell separation. Southern analysisindicates that the mRNA is encoded by either a single gene ora small gene family. The role of the protein during abscissionis discussed. Key words: Lycopersicon esculentum, abscission zone, ethylene, tomato, wound-induced proteins     

Guar gum as a gelling agent for plant tissue culture media

Summary Guar gum, a galactomannan derived from the endosperms of Cyamposis tetragonoloba, has been successfully used as a sole gelling agent for plant tissue culture media. Its suitability as a gelling agent was demonstrated by using guar gumgelled media for in vitro seed germination of Linum usitatissimum and Brassica juncea, in vitro axillary shoot proliferation in nodal explants of Crataeva nurvala, rooting of regenerated shoots of the same, in vitro androgenesis in anther cultures of Nicotiana tabacum, and somatic embryogenesis in callus cultures of Calliandra tweedii. The media used for these were gelled with either guar gum (2, 3, or 4%) or agar (0.9%). Guar gum-gelled media, like agar media, supported all these morphogenic responses. Rather, axillary shoot proliferation, rhizogenic and embryogenic responses were better on guar gum-gelled media than on agar media.     

Development of Jobacco Carpel Primordia in vitro

The state of determination of the two emergent carpel primordiaof Nicotiana tabacum was tested. Carpel rudiments were excisedand cultured singly or in pairs. The basal medium was that ofLinsmaier and Skoog, supplemented with 1.0 mg 1^–1 kinetin.Over the ensuing 4 week period, whole differentiated pistilsformed from the pairs and half pistils grew from the singlecarpels. It is concluded that these emergent organs show a certaindegree of autonomy and that they may have been determined atthe time of isolation. Nicotiana tabacum L, tobacco, carpel, organ determination, tissue culture, morphogenesis     

Anther Culture in Nicotiana tabacum: The Role of the Culture Vessel Atmosphere in Pollen Embryo Induction and Growth

A comparison of four volumes of culture vessel atmosphere revealedthat this variable greatly influenced the induction and growthof pollen embryos from anthers of Nicotiana tabacum. The optimumfrequency of anthers producing embryos and plantlets was foundwith a culture atmosphere of 15 ml per anther, whereas the optimumnumber of plantlets was found with 5.5 ml per anther. A smallvolume (0.5 ml per anther) almost completely suppressed embryoinduction. Removal of specific components of the culture atmosphere(ethylene, carbon dioxide, oxygen) influenced the response ofthe anthers but did not produce a satisfactory explanation ofthe inhibition of pollen embryogenesis by the small cultureatmosphere volume. In particular, the influence of ethyleneabsorption on embryo induction and growth depended both on theculture atmosphere volume and on the stage of development ofthe pollen at the start of culture. Using anthers containingpollen at a stage after the first pollen grain mitosis. ethyleneabsorption was found to increase the survival of induced embryos.Treatment of anthers for 3 d with silver nitrate, a known antagonistof ethylene action, was not an efficient means of increasingthe yield of pollen plantlets.     

Novel 'homeotic' CMS patterns generated in Nicotiana via cybridization with Hyoscyamus and Scopolia

Cytoplasmic hybrids (cybrids) that contain nuclear genetic materialfrom Nicotiana tabacum and cytoplasms from Hyoscyamus nigeror Scopolia carniolica were constructed by protoplast fusions.Both types of hybrids exhibited cytoplasmic male sterility (CMS).Furthermore, unusual floral morphogenesis marked by ‘greenflowers’ deprived of corolla and stamens occurred in themajority of the lines. Backcrosses of these plants with wild-typetobacco demonstrated a maternal inheritance of the ‘greenflower’ trait. After repeated transfer of cytoplasm (‘donor-recipientfusion’) from cytoplasmic hybrid N. tabacum (+H. niger)to albino plastome mutant N. tabacum DSR A15, male sterile tobaccoplants with two types of flowers were recovered (‘greenflowers’ and corolla-containing flowers with transformedstamens). RFLP analysis confirmed that N. tabacum (+ H. niger)and N. tabacum (+S. carniollca) as well as their sexual progeniescontained plastids from H. niger and S. carniolica, respectively.Mitochondrial DNA within the hybrids N. tabacum (+H. niger)originated from H. niger, but was obviously altered. Repeatedparasexual transmission, cybrids in the combination of N. tabacum+N.tabacum (+H. niger), reflected similar characteristics. Cybrids,N. tabacum (+S. carniolica) and their sexual progeny, whichresulted after pollination with wild-type tobacco, containeda modified mtDNA generally originating from tobacco. Furtherhistological analysis established the dramatic difference inthe composition of ‘green flowers’ and flowers ofwild-type tobacco. Therefore, the construction of tobacco cybridswith foreign cytoplasms provides a functional method for thede nova generation of alternative CMS types. Key words: Nicotiana, Hyoscyamus, Scopolia, cybrids, CMS, homeotic patterns     

Stages in the Initiation of Root and Shoot Organogenesis in Cultured Leaf Explants of Nicotiana tabacum cv. Xanthi nc.

Reciprocal transfers of Nicotiana tabacum cv. Xanthi nc. leafexplants were made daily between root inducing medium (RIM)and shoot inducing medium (SIM), SIM and a basal medium containingno growth regulators (BM), and RIM and BM. It was found thatthe explants became determined for shoot production after 6d, while roots were produced after only 1 d on RIM before transferto BM. The competence of the explant to produce roots was greatlyreduced by culture on BM prior to culture on RIM. There wasfar less reduction in shoot numbers with preculture on BM. Explantswere found to be only weakly canalized for both caulogenesisand rhizogenesis for the first 2 d after determination. Thereafterthey became strongly canalized. Transfers were also made fromBM to SIM and back to BM, which revealed that the explants becamecompetent for caulogenesis in the absence of cytokinins priorto determination. The period for which SIM is required can bereduced to only 1 d. Key words: Nicotiana tabacum, in vitro, organogenesis, competence, determination     

Developmental Pattern of Root and Shoot Organogenesis in Cultured Leaf Explants of Nicotiana tabacum cv. Xanthi nc.

Caulogenesis and rhizogenesis were studied in cultured leafexplants of Nicotiana tabacum cv. Xanthi nc. using both lightand scanning electron microscopy. The timing of organ appearancewas also recorded. The patterns of development seen were comparedto each other and to that in explants grown on growth regulator-freemedium. Shoots first appeared after 12 d in culture and rootsafter 7 d. In caulogenesis nodules appear at the explant edgeand from these the shoots arise. The nodules are mainly derivedfrom palisade mesophyll cells, along with some spongy mesophylland bundle-sheath cells. The nodules form a continuous row alongthe edge of the explant and their initiation appears to be centredon veins. Shoots are produced indirectly. Roots are produceddirectly from bundle-sheath and vein parenchyma cells. Withoutplant growth regulators bundle-sheath cells still divide, althoughonly a few divisions were seen. Key words: Nicotiana tabacum, in vitro, caulogenesis, rhizogenesis