Culture of Mesophyll Protoplasts and Stem Segments of Antirrhinum majus (Snapdragon): Growth and Organization of Embryoids

Protoplasts isolated enzymatically from the leaves of Antirrhinummajus L. were cultured on a synthetic medium and their growthand development were followed in vitro. Cultured protoplastsincreased in size, regenerated cell walls, divided and formedsmall colonies and embryoids. Cell wall formation and cell divisionrequired both auxin and cytokinin in the medium. Isolated stemsegments of the same species, when cu1tured on a synthetic mediumwith an added auxin, yielded rapidly growing callus tissuesin which differentiation of embryoids occurred.     

Graft Formation in Sitka Spruce: A Scanning Electron Microscope Study

Low-temperature and conventional scanning electron microscopyhave been used to examine the callus formed at the graft interfacein Picea sitchensis (Bong.) Carr. Callus cells are producedby both cambium and ray parenchyma dedifferentiation and redifferentiationin scion and stock. Adhesion between the cells derived fromscion and rootstock is thought to be my means of pectinaceousbeads at the surface of the callus cells, preceding a more generalfusion of cell walls. The cambia of the two graft componentsare prevented from growing towards each other by the presenceof callus. Instead, the differentiation of new cambium withinthe callus, in the vicinity of the cambia exposed at the preparedsurfaces of the scion and rootstock, links them to form a continuouscambial layer around the combined stem. Callus, cambium, differentiation, grafting, Picea sitchensis     

Radiation-induced Organogenesis and Isoenzyme Patterns in Long-term Callus Cultures of Datura innoxia

Effect of gamma irradiation on growth, shoot organogenesis andenzyme activities and isoenzyme patterns of -amylase and peroxidaseduring differentiation in long-term calluses of Datura innoxiahave been investigated. Radiation in doses of 0.2 and 1.0 kRstimulated the shoot regeneration frequency as well as the numberof shoots per regenerating callus. The 0.2 kR dose could induceshoot organogenesis even in calluses incubated in the dark oncallusing medium, although with less frequency. Such cultures,however, showed profuse shoot regeneration when sub-culturedonto regeneration medium under light conditions. A higher radiationdose (5.0 kR) was lethal to both growth and shoot differentiation.Prior to shoot regeneration, -amylase and peroxidase specificactivities increased to four- to fivefold and 7–24-fold,respectively. While the amylase isoenzyme pattern remained unchanged,specific changes in the isoperoxidase pattern were observedduring shoot differentiation in callus cultures. The most significantchange was the appearance of fast-moving anodic bands priorto visible shoot differentiation. Thus, such isoperoxidasesprovide useful biochemical markers for shoot differentiation. Datura innoxia, shoot organogenesis, isoenzyme pattern, gamma-radiation, growth regulators     

Levels of {beta}-Glucan and Lignin in Elongating Internodes of Deepwater Rice

Partial submergence or treatment with either ethylene or gibberellicacid (GA₃ induces rapid growth in deepwater rice (Oryza sativaL.). We correlated the synthesis of two cell wall componentswith two phases of internodal elongation, namely (13,14)-ß-glucanformation with cell elongation and lignification with differentiationof the secondary cell wall and cessation of growth. The contentof ß-glucan was highest in the zone of cell elongationin internodes of air-grown plants and plants that were inducedto grow rapidly by submergence. In the intercalary meristemand in the differentiation zone of the internode, ß-glucanlevels were ca. 70% lower than in the zone of cell elongation.The outer cell layers, enriched in epidermis, contained moreß-glucan in submerged, rapidly growing internodesthan in air-grown, control internodes. The ß-glucancontent of the inner, parenchymal tissue was unaffected or slightlylowered by submergence. The epidermis appears to be the growth-limitingstructure of rapidly growing rice internodes. We hypothesizethat elevated levels of ß-glucan contribute to elongationgrowth by increasing the extensibility of the cell wall. Lignificationwas monitored by measuring the content of lignin and the activitiesof two enzymes of the lignin biosynthetic pathway, coniferylalcohol dehydrogenase (CAD) and phenylalanine ammonia-lyase(PAL), in growing and non-growing regions of the internode.Using submerged whole plants and GA₃-treated excised stem segments,we showed that lignin content and CAD activity were up to sixfoldlower in newly formed internodal tissue of rapidly growing ricethan in slowly growing tissue. No differences were observedin parts of the internode that had been formed prior to inductionof growth. PAL activity was reduced throughout the internodeof submerged plants. We conclude that lignification is one ofthe processes that is suppressed to permit rapid growth. ¹ This work was supported by the National Science Foundationthrough grants No. DCB-8718873 and DCB-9103747 and by the Departmentof Energy through grant No. DE-FGO2-90ER20021. M.S. was therecipient of a fellowship from the Max Kade Foundation.     

Root, Callus, and Cell Suspension Cultures, from Atropa belladonna, L. and Atropa belladonna, Cultivar lutea Doll

Root, callus, and cell suspension cultures have been establishedfrom seedlings of Atropa belladonna, L. and Atropa belladonna,cultivar lutea Döll. The growth of these cultures is described.Callus cultures transferred to auxin (-naphthaleneacetic acid)-freemedium initiated roots and shoots. Excised root cultures havebeen established from such roots and plants from such shoots.Extracts of the cultures have been submitted to the Vitali—Morinreaction and following chromatography, to the Dragendorff reaction.Cultured excised roots and plants raised from shoots initiatedon cultured callus were shown to contain atropine (hyoscyamine)and reactive substances corresponding in Rf to hyoscine andcuscohygrine. These alkaloids were absent from cultured callusand cultured cell suspensions and from leaves when initiatedwithout roots on callus. The cultured calluses and cell suspensionscontained choline (0.022–0.027 g per 100 g dry weightof root callus). The growth of cell suspension cultures wasnot inhibited by incorporating atropine sulphate, L-hyoscyamine,L-hyoscine hydrobromide, or DL-scopoline nitrate in the culturemedium at 250 mg/I. These alkaloids were absorbed by the cells,a high proportion of the added alkaloid could be recovered fromthe cultures even after 4 weeks' growth and no evidence wasobtained of the presence of degradation products of the alkaloids.The suppression of alkaloid formation in actively growing callusand cell suspension cultures is discussed.     

Cell wall invertases from apex and callus tissues of sugar cane

Calluses were obtained from the stalk apex of sugar cane. Boththe stalk apex and callus tissues possessed firmly bound cellwall invertases. The invertases of each tissue were characterizedon the basis of their Km, optimum pH and the action of variousinhibitors. According to this characterization, the two tissuespossess different isoenzymes. Taking into account the presentisoenzymes and the known cell wall invertases from stalk tissue,we postulated a different pattern of isoenzymes for each organof the sugar cane. These differences suggest that the cell wallinvertases might be used as markers in studies of tissue differentiation. (Received May 27, 1980; )     

Cell wall invertases from apex and callus tissues of sugar cane

Calluses were obtained from the stalk apex of sugar cane. Boththe stalk apex and callus tissues possessed firmly bound cellwall invertases. The invertases of each tissue were characterizedon the basis of their Km, optimum pH and the action of variousinhibitors. According to this characterization, the two tissuespossess different isoenzymes. Taking into account the presentisoenzymes and the known cell wall invertases from stalk tissue,we postulated a different pattern of isoenzymes for each organof the sugar cane. These differences suggest that the cell wallinvertases might be used as markers in studies of tissue differentiation. (Received May 27, 1980; )     

Graft establishment between compatible and incompatible Prunus spp

Graft compatibility has been studied in apricot (prunus armeniacaL.) grafted on Prunus cerasifera Ehrh. Two apricot cultivars,one compatible and one incompatible on this rootstock, wereselected for this study. In these species incompatibility isonly manifested by tree breakdown at a late phase of the tree'slife. The process of graft union formation was observed forthe first month following grafting. No differences were foundeither in the process of healing or in its kinetics. Thus, callusproliferation, callus differentiation and vascular connectionsare established in the same way and at the same time in bothcompatible and incompatible grafts. However, clear differencesexist in the level of differentiation of the callus produced.While in compatible grafts, callus quickly differentiates intocambium and vascular tissue, in incompatible grafts this differentiationis not complete and a portion of the tissue evolves into a parenchymatoustissue that coexists with the differentiated vascular tissue. Key words: Graft, Prunus, compatibility     

Regulation of a Sub-sexual Life Cycle in a Moss: Evidence for the Occurrence of a Factor for Apogamy in Physcomitrium

As demonstrated in our earlier studies, the differentiationof apogamous sporophytes on the secondary protonema of the mossPhyscomitrium pyriforme Brid. requires an exogenous supply ofsucrose in the medium. In the present work, similar differentiationwas observed in the leaf cells of aged gametophytes. The experimentsindicate an accumulation in the leaves of a sporophytic factorwhich initiates a de novo differentiation of sporophytes fromleaf cells without the intervention of sexual reproduction.In the absence of sucrose, the factor for apogamy was not present.Highlight intensity (5000–6000 lx) also inhibited itsproduction. There was no evidence that its presence interferedwith or inhibited production of gameto-phores. Growth regulatorssuch as IAA and kinetin altered only the effectiveness of thissporophytic factor, demonstrating that it was endogenous. Sporogenesisin the apogamous sporophytes took place without orthodox meiosis. Results obtained by using different exogenous environments forthe in vitro differentiation of callus into gametophytes orsporophytes are also reported. These support our contentionthat there is an accumulation of a sporophytic factor in thegametophytic callus cells, which is diluted during the processof differentiation. The morpho-regulatory influence of lightin the differentiation of apical cells with three cutting facesfrom unorganized callus is also considered.     

Tracheary Element Differentiation Induced in Isolated Cylinders of Lettuce Pith: a Bipolar Gradient Technique

To study the influence of morphogenetic gradients on vasculardifferentiation patterns, a new technique was developed whichallows different substances to be applied at opposite ends ofa tissue block. It yielded information on the mobility of particularmorphogens and on the dependence of callus formation and trachearyelement differentiation on their presence. Application of indol-3ylacetic acid (1AA) (10 mg l^–1), zeatin (0.1 mg l^–1)and sucrose (3 per cent, w/v) in various combinations to theends of cylindrical explants of lettuce pith (Lactuca sativaL.) showed that (a) callus formation was stimulated by IAA,whereas induction of tracheary elements required both IAA andzeatin; (b) callus was confined to a few millimetres at theends of the explants, and tracheary elements occurred mainlywithin the callus; (c) sucrose or its metabolic products diffusedthe 10 mm length of the explants, while IAA and zeatin wereeffective only close to the application site; and (d) some callusand tracheary elements formed when no sucrose was applied, butboth increased with sucrose application, though inhibition oftracheary elements formation occurred with high sucrose concentrations. differentiation, pith explant, tissue culture, xylogenesis, indol-3yl acetic acid, sucrose, zeatin, lettuce, Lactuca sativa     

Fine Structure of Parenchymatous and Differentiated Pinus radiata Callus

The fine structure of Pinus radiata D. Don callus before andafter differentiation into stem-like tissues has been examinedwith the electron microscope. In callus prior to differentiation(here called parenchymatous callus) the cells accumulate tanninsas they age and are quite distinct from the cells of differentiatedcallus. In the latter, cambium, phloem and xylem cells may beidentified by their general morphology and by their ultrastructuralfeatures. Differentiation into a true stem-like structure is,however, incomplete in that the tissues are not uniformly oriented,and parenchyma cells of the rays and phloem contain chloroplasts.The tracheids also show unusual differentiation in that borderedpits form over their entire surface and may be of two types.The reasons for these variations are discussed.     

Fine Structure of Established Callus Cultures of Taraxacum officinale Weber

The nodular, brown callus cultures of Taraxacum officinale growslowly on a modified White's medium. A section of nodule revealsa meristematic layer bounded both internally and externallyby parenchymatous tissue. No other types of tissue occur withinthe callus. The cells of the inner parenchyma are often compressedand senescing, whereas in the outer tissue localized de-differentiationapparently contributes to the development of new nodules duringcallus growth. Fine-structural observations of both meristematic and parenchymatoustissues show the normal complement of higher plant cell organellesexcept for the apparent absence of cytoplasmic microtubules.The rough endoplasmic reticulum cisternae are often alignedparallel to the cell wall or in whorls and may show pores, thusresembling annulate lamellae. Numerous lipid bodies, up to 7µm wide, occur and these are sometimes invested by arraysof apparently membranous material. The mitochondria are frequentlyhighly branched and often show a scalariform arrangement ofcristae. The plastids show few internal membranes despite cultureof the callus under continuous illumination. Lomasomes are very common in all cells and in the parenchymatissue membranous wall bodies also occur. The latter bodiesare much larger than lomasomes and consist of wall overgrowthsin which vesicular, myelin-like or isolated membranous elementsare enmeshed in fibrillar material. It is suggested that membranouswall bodies may originate from the amalgamation and subsequentproliferation of several adjacent lomasomes. Taraxacum officinale Weber, dandelion callus cultures, fine structure     

Callus Initiation and Organized Development from Zamia pumila Embryo Explants

Explants derived from Zamia pumila embryos were cultured ona Murashige and Skoog basal medium supplemented with naphthaleneaceticacid (NAA), N⁴-benzylaminopurine (BAP), or combinations of thetwo at 27 °C in darkness. NAA was invariably required forcallus initiation, and its minimal effective concentration was0.1 mg l^–1. BAP was not always required, and dependingon the explant type and NAA concentration, BAP either enhanced,suppressed, or had little effect on the frequency of callusinitiation. High frequency of callus initiation occurred with1.0 mg l^–1 NAA combined with 0.01 or 1.0 mg l^–1BAP. When the concentration of NAA was high relative to thatof BAP, friable callus was produced. As the relative BAP concentrationwas increased, a more compact callus formed. Compact-nodularcallus developed at equal concentrations of NAA and BAP overa wide range of absolute concentrations. Friable callus formedroots only. Compact-nodular callus formed roots, shoots andembryo-like structures. Root and shoot formation predominatedand were of nearly equal frequency. Formation of embryo-likestructures was infrequent. Zamia pumila, callus differentiation, callus formation, embryo culture, naphthaleneacetic acid, N⁴-benzylaminopurine     

Studies on the cell wall of Chlorella I. Quantitative changes in cell wall polysaccharides during the cell cycle of Chlorella ellipsoidea

1. 1. The cell wall of Chlorella ellipsoidea was fractionated intotwo components, alkali-soluble hemicellulose and alkali-insoluble"rigid wall". The former was composed of several neutral sugars,i.e. rhamnose, xylose, arabinose, mannose and galactose, andthe latter had glucosamine as a main constituent sugar.
2. 2.Quantitative changes in both hemicellulose and "rigid wall"contents during the cell cycle were followed using synchronouslygrown cells. The two cell wall components showed markedly differentchanges. Hemicellulose increased in proportion to the enlargementof the cell surface area in the growing phase, while the "rigidwall" remained almost constant in this phase. The "rigid wall"increased only in the reproduction phase—the time of autosporeformation.

(Received September 26, 1977; )     

Morphogenic Potential of Cultured Explants of Crocus chrysanthus Herbert. cv. E. P. Bowles

Explants of leaves, basal plates, petals, anthers and ovariesof young growing corms of Crocus chrysanthus var. E. P. Bowleswere cultured on MS basal media with 20 different combinationsof either kinetin and NAA or BAP and 2, 4-D in the dark. Nomajor change was observed except on ovary explants. The ovaryexplants produced callus at 5.0 mg 1^–1 and 10 mg^–1BAP and subsequently stigma-like structures formed on the surfaceof the callus. Transfer to light resulted in the stigma-likestructures developing a yellow pigmentation whereupon they cameto resemble the naturally-grown stigmas. Corm formation andshoot regeneration was obtained from the callus when the ovaryexplants were cultured on media containing 5.0 and 10 mg I^–1BAP with 0.5 mg 1^–1 2, 4-D. Increasing the level of 2,4-D markedly reduced the number of shoots produced per explant. Key words: Crocus chrysanthus, callus, ovary explants     

The Structure and Composition of Bead-like Projections on Sitka Spruce Callus Cells Formed during Grafting and in Culture

Projections at the cell wall surface in callus formed at thegraft interface and in vitro in Picea sitchensis (Bong.) Carrhave been examined using light and electron microscopy. Thesestructures range in size from 1 to 5 µm in diameter, andconsist of a homogeneous matrix enclosing one or more fibrillar/vesicularcores. Histochemical and cytochemical studies have shown thatthe homogeneous matrix is made up of a mixture of pectins, carbohydrate,protein and fatty acids, while the fibrillar/vesicular componentis mainly carbohydrate and pectins. The possible functions ofthese structures are discussed on the bases of their composition.Copyright1993, 1999 Academic Press Picea sitchensis, callus, cell-wall projections, histochemistry, cytochemistry     

Effects of Monochromatic Radiations on Growth of Pelargonium Callus Tissue

Pith callus tissues were grown under continuous blue (450 mµ),green (545 mµ), red (650 mµ), and ‘white’(full-spectrum) light, and in the dark for 22 days at 27±2°C at energy levels of 15,000 ergs cm^–2 sec^–1. Mean increases in fresh weight of tissues grown under ‘white’and blue light were significantly greater than those of tissuesgrown in green and red light and in the dark. Tissues grownin the dark yielded mean fresh weight increases significantlylower than tissues grown under blue, red, and ‘white’light. No significant differences were shown between blue and‘white’, red and green, and green and dark treatmentsrespectively. Cell differentiation occurred in all treatmentsonly to the extent of vessel element formation. There were nodifferences in degree of differentiation between treatments. It was proposed that the high-energy reaction of photomorphogenesiswas in operation in the Pelargonium callus tissue. The resultsindicated the presence in the tissue of high-energy photoreceptor(s).The use of high-intensity, incandescent illumination for experimentalprocedures approximating natural conditions of irradiation wasindicated as desirable for pith callus tissues of Pelargoniumzonale var. Enchantress Fiat.     

Morphogenetic Responses of Browallia Leaf Sections and Callus

Leaf sections of Browallia viscosa and B. speciosa were placedon Murashige and Skoog (1962) salts and vitamins medium (MS)containing auxins and cytokinins, singly or in combination,to elicit morphogenetic responses. B. viscosa developed extensiveroots in 4 weeks on media supplemented with indolebutyric acid(IBA), indol-3-yl acetic acid (IAA) or naphthalene acetic acid(NAA) (0·01, 0·1, 1·0, 5·0 and 10·0mg^–1), but with 2, 4-D (0·1 mg^–1) only lightyellow friable callus was obtained. Shoot initiation and elongationoccurred consistently in 4–6 weeks on leaf sections inthe presence of 6---dimethylallyl amino purine (2iP). Similarly,shoot regeneration from leaf-derived callus, initiated and sub-culturedon MS + benzyladenine (BA) + NAA only induced callus on leafexplants of both species. B. speciosa did not respond exceptfor moderate and prolific callus formation on MS + BA + NAAand Uchimiya and Murashige (1974) media respectively. Browallia viscosa, Browallia speciosa, tissue culture, regeneration, morphogenetic potential     

Growth and Organogenesis in Moth Bean Callus as Affected by Paclobutrazol

Addition of relatively low concentrations (1.7 to 6.8 µM)of paclobutrazol to the culture medium decreased in vitro growthof Vigna aconitifolia (Jacqu.) Marechal cv. Jaadia (moth bean)callus. Presence of paclobutrazol increased the content of sugarsand total soluble protein in the callus. Addition of paclobutrazolto a regeneration medium reduced the differentiation of rootsand shoots in vitro. (Received October 11, 1988; Accepted May 30, 1989)     

Stress relaxation properties of the cell wall of growing intact plants

The cell wall of dark-grown Avena coleoptiles and the epidermisof light-grown mungbean hypocotyls was subjected to stress-relaxationanalysis and the following results were obtained. 1. Actively growing apical regions of the organs, either coleoptilesor hypocotyls, had certain threshold values of minimum stress-relaxationtime, T_O, 0.04 sec for coleoptile cell wall and 0.03 sec forthe epidermal cell wall of hypocotyls. The cell wall of thebasal region of the organs, which were mature and not growing,had a higher value of To. 2. When the apical regions of the organs, either coleoptilesor hypocotyls, ceased to grow, their cell walls showed T_O valuesabove these thresholds. 3. The relaxation rate, b, was small in the cell wall of activelygrowing regions of the organs, compared with that of non-growingregions. 4. The maximum relaxation time, T_m, was variable and no significantrelationship with growth capacity was found. 5. The extensibility, mm/gr, was large not only in activelygrowing regions of the organs but also in fully grown regions,suggesting that the value represents complex properties of thecell wall including the history of cell wall extension. From these results, we concluded that biochemical modificationsoccur in the cell wall matrix of actively growing organs ofeither monocots or dicots, and these are the bases of the capacityof the cell wall to extend and are represented chiefly by T_oand possibly by b. (Received August 12, 1974; )