Root Gravitropism in a Cultivar of Zea mays Whose Columella Cells Contain Starch-deficient Amyloplasts

Starch occupies 4.2 per cent of the volume of plastids in calyptrogencells in primary roots of Zea mays L. cv. vp-7 wild type. Plastidsin calyptrogen cells are distributed randomly around large,centrally located nuclei. The differentiation of calyptrogencells into columella cells is characterized by cellular enlargementand the sedimentation of plastids to the bottom of the cells.Although sedimented plastids in columella cells do not containsignificantly more starch than those in calyptrogen cells, primaryroots are graviresponsive. The onset of root gravicurvatureis not associated with a significant change in the distributionof plastids in columella cells. These results indicate thatin this cultivar of Z. mays (1) the sedimentation of plastidsin columella cells is not based upon their increased densityresulting from increased starch content alone, (2) starch-ladenamyloplasts need not be present in columella cells for rootsto be graviresponsive, and (3) the onset of root gravicurvaturedoes not require a major redistribution of plastids in columellacells. Columella cell, gravitropism (root), plastids, root cap, Zea mays     

Ultrastructural Aspects of the Glandular Cells from the Secretory Trichomes and from the Cell Suspension Cultures of Achillea millefolium L. ssp. millefolium

The ultrastructure of the glandular cells of the floret secretorytrichomes from Achillea millefolium L. ssp. millefolium (yarrow)was examined before and after anthesis and compared with theultrastructure of the cells from the cell suspension culturesobtained from the same plant. The profuse tubular structuresobserved in the plastids of the glandular cells of the trichomesduring the pre-secretory stage were much reduced in the secretorystage and showed an osmiophilic content. Some endoplasmic reticulumprofiles could be seen adjacent to the plastids. Later in thesecretory stage, the secretion appeared in the periplasmic spacebetween the cells of the upper tiers and in the sub-cuticularspace. Finally the secretion was released by rupture of thecuticle. At the lag phase, the cells from the cell suspensioncultures of yarrow were characterized by the presence or plastidswith tubular structures, similar to those observed in the plastidsof the trichomes in the pre-secretory stage. By the end of thelag phase accumulations of starch were observed inside the plastids.At the beginning of the exponential phase, the tubular structuresof the plastids started to show an osmiophilic content and theaccumulations of starch were still present. At the end of thisphase starch disappeared from the plastids and only osmiophilictubular structures were observed. Rough endoplasmic reticulumas well as smooth endoplasmic reticulum profiles were frequentlyin close association with plastids and mitochondria. At thestationary phase a very large vacuole filled the cells, andin the remaining cytoplasm some endoplasmic reticulum profilesand osmiophilic droplets were observed.Copyright 1994, 1999Academic Press Achillea millefolium L. spp. millefolium, yarrow, ultrastructure, trichomes, glandular cells, plant cell suspension cultures     

Studies on nucleic acids in plastids of the pigment mutant C-2A{acute} of Scenedesmus obliquus

Pigment mutant C-2A{acute} of Scenedesmus obliquus whose chlorophyllformation and chloroplast development are light dependent, wasstudied for the nucleic acid content of its plastids. The ribosomalRNA of plastids of the achlorophyllous or greened mutant C-2A{acute},did not show any difference from that of the wild type. Incorporationof [5-³H] uridine into mutant cells was partially inhibitedby rifampicin, indicating this part as being plastidial incorporation.Since there were no significant differences in the ribosomalRNA of plastids between the mutant and the wild type of Scenedesmus,the ribosomal system in the plastids of mutant C-2A' seemednot to be affected by the mutation. C_sCl gradient patterns ofScenedesmus mutant and wild-type DNA were almost identical withthose of Chlorella DNA. A peak at a buoyant density of 1.69g/cm³, the same as that of Chlorella chloroplast DNA, couldbe identified in Scenedesmus also as plastid DNA because itdisappeared after prolonged treatment with myxin and hybridizedwith rifampicin-sensitive pulse-labelled RNA. This peak waspresent to nearly the same degree in the mutant and the wildtype, indicating that a larger deficit of plastid DNA did notoccur in the mutant. Whether or not the mutation might be localizedin the plastid genome is discussed. (Received March 19, 1976; )     

Structure and Development of Plastids in Epidermal Cells of African Violet (Saintpaulia ionantha Wendl.) in Culture

The structure of plastids in epidermal cells of African violet(Saintpaulia ionantha Wendl.) ‘Marge Winters’ wasexamined using transmission electron microscopy before and afterplacement of leaf tissue in culture. The plastids from matureepidermal cells contained membrane-bound inclusion bodies andprolamellar bodies in various stages of development. Starchgrains and poorly developed granal stacks were observed in asmall number of plastids. After placement of the leaves on suitableculture medium, inclusion bodies decreased in size and the lamellarsystem became more organized. The plastids in the epidermaltissue are believed to be in an arrested state of developmentand are released from this state by placement on a medium inductiveto organogenesis. Saintpaulia ionantha Wendl., African violet, membrane-bound inclusion, tissue culture, plastid development     

Occurrence of Form PIIcf Sieve-element Plastids in Xyris Species (Xyridaceae)

Mature leaf fragments from eight species ofXyris from the Serrado Cipó, State of Minas Gerais, Brazil, were preparedby the usual methods for electron microscopy. Ultrastructuralanalysis of phloem shows the occurrence of nacreous walls witha polylamellate structure in the sieve-elements ofX. tortilisand plastids similar to P-plastids, form PIIcf in the sieve-elementsof all investigated species. Sieve-element plastids; monocotyledons; Xyris     

Ultrastructural Modifications of Plastids and Starch Metabolism during the Microsporogenesis of Ophrys lutea (Orchidaceae)

Ultrastructure of plastids has been studied throughout microsporogenesisof Ophrys lutea Cav. (Orchidaceae). A typical dedifferentiation/redifferentiationcycle of plastids was observed. At prophase I, plastids of pre-meiocytesgradually lost starch and separated the meiocytes through cytomicticchannels. At meiosis, plastids dedifferentiated to protoplastsand redifferentiated in young microspores. During pollen grainformation and maturation a cycle of starch accumulation/degradationoccurred; the mature pollen grain is starchless. Results arediscussed in terms of genetic inheritance following haploidnuclear state and in terms of carbohydrate metabolism. Plastids, starch, microsporogenesis, ultrastructure, Ophrys lutea, Orchidaceae     

The Formation of Pollenkitt in Apium nodiflorum (Apiaceae)

Apium nodiflorum produces a considerable amount of pollenkittwithin a secretory tapetum. ER and plastids (elaioplasts) participatein pollenkitt formation. Both organelles deposit precursorswithin vesicles, which finally fuse to form pollenkitt. Apium nodiflorum L., Apiaceaesecretory tapetum, pollenkitt, ER, plastids, elaioplasts     

Root Graviresponsiveness and Columella Cell Structure in Carotenoid-deficient Seedlings of Zea mays

Root graviresponsiveness in normal and carotenoid-deficientmutant seedlings of Zea mays was not significantly different.Columella cells in roots of mutant seedlings were characterizedby fewer, smaller, and a reduced relative volume of plastidsas compared to columella cells of normal seedlings. Plastidsin columella cells of mutant seedlings possessed reduced amountsof starch. Although approximately 10 per cent of the columellacells in mutant seedlings lacked starch, their plastids werelocated at the bottom of the cell. These results suggest that(i) carotenoids are not necessary for root gravitropism, (ii)graviresponsiveness is not necessarily proportional to the size,number, or relative volume of plastids in columella cells, and(iii) sedimentation of plastids in columella cells may not resultdirectly from their increased density due to starch content.Plastids in columella cells of normal and mutant seedlings wereassociated with bands of microtubule-like structures, suggestingthat these structures may be involved in ‘positioning’plastids in the cell. Zea mays, graviperception, graviresponsiveness, carotenoids, vp-9 mutant, columella cell, roots     

The distribution of protochlorophyllide and chlorophyll within seedlings of the lip1 mutant of Pea

The distribution of protochlorophyllide (Pchlide) and NADPH-Pchlideoxidoreductase (POR) was characterized in the epicotyls androots of wild-type pea (Pisum sativum L. cv. Alaska) and lip1,a mutant with light-independent photomorphogenesis caused bya mutation in the COP1 locus. The upper part of the dark-grownlip1 mutant epicotyls had a high Pchlide content that decreaseddownward the organ. The elevated Pchlide level in lip1 seedlingswas a result of the differentiation of more proplastids intoPchlide-containing plastids. The cortex cells in the lip1 epicotylwere filled with such plastids in contrast to the cortex cellsof wild-type seedlings. The mutant also developed Pchlide-containingplastids in the roots, indicating the suppressing effect ofthe COP1 locus on development of plastids in the correspondingtissues in dark-grown wild-type plants. The distribution ofPchlide-containing plastids in dark-grown lip1 mutant stem androot was similar to the distribution of chloroplasts in irradiatedwild-type plants. Both wild-type and lip1 epicotyls containedmostly short wavelength Pchlide fluorescing at 631 nm withonly a small shoulder at 654 nm, which was transformedto a minute amount of chlorophyllide (Chlide) by flash irradiation.In contrast, with continuous irradiation a considerable amountof Chlide was formed especially in the lip1 epicotyls. Immunoblotsindicated the presence of POR, as a 36 kDa band, in epicotylsof both dark-grown wild-type and lip1 mutant seedlings. However,lip1 stem tissue had a higher content of POR than the wild-typepea. The high content of POR was unexpected as lip1 lacked boththe 654 nm fluorescing Pchlide form and the regular PLBs.In light, a significant amount of chlorophyll was formed alsoin the roots of the lip1 seedlings. ³ Corresponding author: E-mail, mahdi.seyedi@molbio.gu.se; Fax,+46-31-773-2626.     

Structure of the Needles in the Early Phases of Development in Pinus ponderosa P. et C. Lawson with Special Reference to Plastids

Before they emerged from the fascicular sheath, the tissuesof young needles of Pinus ponderosa P. et C. Lawson alreadyshowed some characteristics typical of mature needles. The organelles,particularly the plastids, had undergone different development.The plastids in different types of cell varied in their ultrastructureand in association with the endoplasmic reticulum (ER). A sheathof ER was observed around the amoeboid plastids in epidermalcells, epithelial cells of resin ducts and maturing transfusiontracheids whereas there was no ER sheath around the young mesophyllchloroplasts, the fusiform chloroplasts in some transfusiontracheids and the proplastids in xylem and phloem cells. Thecontent of chlorophyll (a+b) was 0·85 g kg^-1 dry matterand chlorophyll a/b ratio was 2·70. The needles may becomephotosynthetically active whilst still within the fascicularsheaths.Copyright 1993, 1999 Academic Press Pinus ponderosa, ponderosa pine, needle structure, needle ontogeny, plastids, endoplasmic reticulum     

Effects of the Introduction of Agrobacterium tumefaciens T-DNA ipt Gene in Nicotiana tabacum L. cv. Petit Havana SR1 Plant Cells

Transformation of tobacco leaf discs with the ‘cytokinin’ipt gene yielded several transgenic callus tissue lines, respectiveto the kind of ipt construction present in the A. tumefacienscointegrates. Those calli containing an active ipt gene wereable to grow hormone-autotrophically and showed an increasedendogenous cytokinin level in comparison with controls. Analysisof endogenous IAA level did not allow any quantitative correlationwith the cytokinin content. However, a minimal level of auxinseems to be necessary to obtain hormone-autotrophic growth.Exogenously supplied NAA significantly reduced the endogenouscytokinin content without modifying growth characteristics. The varying chlorophyll content in the different callus lineselicited the study of the ultrastructure of the plastids. Thecontrols contained small plastids, often filled with starchor accumulated vesicles that did not allow observation of theinternal membrane system. The ‘Pssu-ipt’ line, havinga higher cytokinin content, showed plastids with an internalmembrane system consisting of stroma and grana thylakoids, butthis structure was lost during subculture. Swollen thylakoidsappeared, the amount of starch was reduced and vesicles wereaccumulating. (Received November 15, 1990; Accepted March 4, 1991)     

Cytochemical and Morphological Evidence for the Involvement of the Plasma Membrane and Plastids in Mucilage Secretion in Aloe arborescens

Most of the volume of Aloe arborescens leaves (volumetric density= 0.68±0.08) is occupied by a mucilage tissue. The mucilagesof Aloe species are glucomannans of great medical and pharmaceuticalimportance. An electron microscopical and histochemical studywas carried out, following the development of the tissue andsecretion processes. In contrast to other reports on polysaccharide secretion inplants, no observable activity was found in the Golgi apparatus.In the young stages of leaf development, positive histochemicalstaining for polysaccharides and structural changes were foundmainly in the plastids. In the mature leaves the mucilage cellsremain alive and intact and secretory activity appears to becentered in the plasma membrane. Aloe arborescens, cytochemistry, mucilage, plasma membrane, plastids, secretion     

Ultrastructure and Secretion of the Secretory Cells of Two Species ofFagoniaL. (Zygophyllaceae)

The ultrastructure and secretion of the secretory cells of theglandular trichomes ofFagonia mollisandF. glutinosawere studied.The most important finding of this study is that two speciesof the same genus produce the lipophilic component of the secretorymaterial in completely different ways and at different siteswithin the cell. In the early stages of development of secretorycells ofF. mollis,numerous mitochondria, containing myelin-likestructures, occur in the basal part of the cell. Above them,highly-elongate elements, which are suspected to develop frommitochondria with myelin-like structures, are present. Thesehave been termed ‘modified mitochondria’. It issuggested that the myelin-like structures are precursors ofthe lipophilic material ofF. mollis.InF. glutinosa,the lipophilicmaterial appears first in the plastids as plastoglobuli. Polysaccharidesappear to be produced by dictyosomes in both species. Secretionof the secretory substance to the outside of the protoplastappears to be granulocrine.Copyright 1998 Annals of Botany Company Fagonia mollis,Fagonia glutinosa,glandular trichomes, secretory cell, mitochondria, modified mitochondria, plastids, dictyosomes, lipophilic material, myelin-like structures, polysaccharides     

In situPCR on Plant Material with Sub-cellular Resolution

In situPCR and reverse transcribedin situPCR have been testedon leaves of sugar cane fixed in FAA, 4% PFA or 2% PFA+2.5%GA.In situPCR amplification of the gene coding for ribulose-1,5-bisphosphatecarboxylase/oxygenase (rbcL) was successfully performed followingall three fixation protocols. As expected the PCR product wasrestricted to the plastids of all cells. Reverse transcribedinsituPCR was performed onrbcL mRNA and in this case the PCR productwas restricted to the plastids of the bundle sheath cells. Thisis the first report ofin situPCR on plant material and onlythe second report ofin situPCR with sub-cellular resolution.InsituPCR onrbcL may prove to be a valuable positive control forfuturein situPCR studies on plant material.Copyright 1997 Annalsof Botany Company In situPCR; reversed transcribedin situPCR; rbcL; C₄-plants     

Effect of Chloramphenicol on Etiochloroplasts of Wild and Chlorophyll b-Less Barley Genotypes

Greening of etiolated seedlings of wild and Chl b-less barley(Hordeum vulgare L.) genotypes in the presence of D-threochloramphenicol(CAP) led to macrogranal arrangements accompanying the inhibitionof Chl synthesis and an enhancement of the total protein contentin differentiated etiochloroplasts. In treated mutant plastids,protein/Chl ratio reached up to 100. No light-dependent O₂ evolution was detected in CAP-treatedplastids which had deficiency in polypeptides belonging to thephotosystem II (PSII) centres. On the other hand, plastids displayeda high photosystem I (PSI) activity despite the absence of the92 kDa polypeptide linked to the PSI centre. The accumulationof polypeptides ranging from 16 to 20 kDa suggest that theycould originate from primary complexes consisting of few Chlmolecules, but they were sufficient to allow the activity ofthe reaction centres. No accumulation of the 25–27 kDapolypeptides linked to the PSII antenna was detected. The increase in the proportion of trans-₃hexadecenoic acid (16:1tr) in phosphatidylglycerol (PG) of etiochloroplasts from bothtypes after CAP treatment could indicate an alteration of theregulation process of 16:1 tr biosynthesis occurring in plastids.The formation of macrograna could optimize the energy transferin altered thylakoid membranes. The accumulation of PG-16:1tr molecules could be related to the formation of active primarycomplexes in thylakoid when Chl synthesis is altered. (Received March 30, 1988; Accepted June 1, 1988)     

Gibberellin-induced Changes in Ultrastructure of Lettuce Cotyledons

Seeds of lettuce (Lactuca saliva L. cv. Grand Rapids) were incubatedin water or in gibberellin A₃ (GA). Some ultrastructural differencesbetween the cotyledons of 145 hour-old seedlings resulting fromthese two treatments are reported. The cotyledons of GA-treatedseedlings contained many plastids with poorly developed grana,while the control cotyledons contained only well-developed plastids.The frequency of grana in developed chloroplasts was also reducedby the hormone treatment. Effects of GA on the nucleus includeda decrease in heterochromatin and an increase in nucleolar volume.After GA treatment, the nucleolar matrix had a largely fibrillarappearance in contrast to the predominantly granular structureof the control nucleoli. Ultrastructural changes are discussedin relation to the GA-induced variations in the biochemicalcomponents previously reported.     

Structure and Histochemistry of Stomata and Epidermal Cells in Five Species of Polypodiaceae

The epidermal structure of the five species of ferns, Arthromeriswallichiana (Spr.) Ching., Drymoglossum piloselloides (Prest.),Drynaria quercifolia (L.) J. Smith, Lepisorus nudus (Hook.)Ching. and Pyrrosia nuda (Gies.) Ching., has been investigated.Fifteen types of stomatal structures have been identified ofwhich copolo-desmocytic and coperi-desmocytic are new types.Four more possible stomatal structures: ccpolo-peri-, codesmo-polo-,codesmo-peri- and duplodesmocytic, are suggested. Localizationof starch, insoluble polysaccharides, protein and lipids hasbeen examined histochemically in the guard cells, subsidiarycells and epidermal cells. In Drynaria starch plastids and plastidscontaining both starch and protein are present in guard cells.Starch plastids are present in the subsidiary cells of all speciesexcept in Arthromeris, whereas, they are present in epidermalcells of only Drymoglossum and Lepisorus. Granular or amorphousinsoluble polysaccharides (other than starch) are present inguard cells of all the species, in the subsidiary cells of Arthromeris,Drynaria and Pyrrosia, and in the epidermal cells of Pyrrosia.Except in Pyrrosia lipids are present in the guard cells. Subsidiarycells of Drynaria and the epidermal cells of Arthromeris andDrynaria show lipid bodies. The presence of plasmodesmata andectodesmata is demonstrated in the epidermal cells of Drymoglossum.     

Chloroplast development in 4-thiouridine-cultured radish seedlings III. Photochemical activities in isolated plastids

Accumulation of chlorophyll, development of photosystem I andII activities and contents of chloroplastic components wereinvestigated in greening radish seedlings germinated and grownwith 4-thiouridine (4SU). The development of photosystem I activityprior to that of photosystem II was observed also in the 4SU-culturedgreening radish cotyledons in which chlorophyll accumulationwas inhibited up to 60–80% of that of the control. Photochemicalactivities expressed on a plastid protein basis decreased withthe increase of 4SU in the culture medium. In contrast to ferredoxinand ferredoxin-NADP reductase, which were present in significantamounts in the treated cotyledons, chloroplastic cytochromes(f, b₅₅₉ and b₆ decreased in the plastids from 4SU-culturedcotyledons. These results suggest that 4SU interferes in partwith protein synthesis in plastids and thereby with chloroplastdevelopment. (Received December 4, 1979; )     

Subcellular Localization of Adenylate Cyclase in the Shoot Apices of Bryum argenteum Hedw

Adenylate cyclase activity has been detected in the shoot apicesof Bryum argenteum at the ultrastructural level, using adenylylimidodiphosphate as substrate. Heavy deposits of the reactionproduct were observed along the plasma membrane, tonoplast andthe membranous system of developing plastids. No clear stainingwas associated with other subcellular membranes. Mosses, adenylate cyclase, Bryum, cyclic AMP     

Plastid Ontogeny in the Corolla Cells of Digitalis purpurea L. cv. Foxy

Initially the corolla plastids of Digitalis purpurea containsmall grana with negatively stained thylakoids. Degenerationof the grana, loss of chlorophyll and the transient accumulationof starch accompany corolla expansion Starch disappears by thetime the anthers dehisce and granular and amorphous phytoferrtindeposits become prominent in the stroma Concomitant with theseparation of the stigmatic lobes the thylakoid system is reducedto a central membranous network enveloping the phytofemtm aggregatesJust prior to corolla abscission the stroma becomes packed withplastoglobuh Although this developmental sequence closely resemblesthat for chromoplasts in yellow and red flowers, fruits andautumn leaves there is no synthesis of carotenoid pigments inthe corollas of Digitalis purpurea At maturity the plastidsare therefore best described as elaioplasts. Digitalis purpurea L., foxglove, corolla, plastids, elaioplasts, phytofemtin, ultrastructure, X-ray microanalysis