Inclusions in seed protein bodies in members of the Compositae and Anacardiaceae: comparison with other dicotyledonous families

1978 ◽  
Vol 56 (17) ◽  
pp. 2062-2071 ◽  
Author(s):  
Mark S. Buttrose ◽  
John N. A. Lott
Keyword(s):  
Crystal Size ◽  
Freeze Fracture ◽  
Protein Body ◽  
Protein Bodies ◽  
Body Structure ◽  
Thin Sections ◽  
Edx Analyses ◽  
Pistachio Nut ◽  
Taxonomic Grouping ◽  
Helichrysum Bracteatum

Thin sections, freeze-fracture replicas, energy dispersive x-ray (EDX) analyses, and chemical analyses of cotyledon tissue from seeds of sunflower (Helianthus annuus), golden everlasting daisy (Helichrysum bracteatum), cashew (Anacardium occidentale), and pistachio nut (Pistacia vera) showed that in all four species the protein bodies consisted of a proteinaceous matrix surrounding numerous globoid crystals. Some variation in globoid crystal size did occur, but they were generally small in relation to the size of the protein body. No protein crystalloids were found in the cotyledon protein bodies of these four species. EDX analysis results were consistent with the globoid crystals being phytin rich. Results of this study, combined with an evaluation of protein body structure in other dicot embryos that have been studied, support the theory that protein body structure is related to taxonomic grouping.

Thin-section, freeze-fracture, and energy dispersive x-ray analysis studies of the protein bodies of tomato seeds

1980 ◽  
Vol 58 (6) ◽  
pp. 699-711 ◽  
Author(s):  
Ernest Spitzer ◽  
John N. A. Lott
Keyword(s):  
Freeze Fracture ◽  
Protein Body ◽  
Cell Types ◽  
Energy Dispersive ◽  
Protein Bodies ◽  
Elemental Content ◽  
Tomato Seed ◽  
Endosperm Tissue ◽  
X Ray ◽  
Edx Analysis

Protein bodies of dry seeds of tomato (Lycopersicon esculentum) from radicle, hypocotyl, cotyledon, and endosperm tissue were extensively studied using thin-sectioning, freeze-fracturing and energy dispersive x-ray (EDX) analysis. Protein bodies varied in size, were oval to circular in section, and generally consisted of a proteinaceous matrix, globoid crystal, and protein crystalloid components. Size, shape, and arrangements of globoid crystals and protein crystalloids varied even within the same cell. Globoid crystals were generally oval to circular in section. They were always surrounded by a proteinaceous matrix. In a given protein body the number present ranged from a few to numerous. A protein body generally contained only one protein crystalloid. In section, protein crystalloids were irregular or angular in shape. They were composed of substructural particles which formed lattice planes. EDX analysis of tomato seed globoid crystals revealed the presence of P, K, and Mg in all cases, a fact that is consistent with globoid crystals being phytin-rich. Rarely, small amounts of calcium were found along with P, K, and Mg in globoid crystals of each of the tissue regions considered. The distribution pattern of cells with Ca containing globoid crystals was random. Small amounts of Fe and Mn were also found in the globoid crystals of protein bodies from certain cell types. These two elements, unlike calcium, were specific in terms of their distribution. Globoid crystals from the protodermal cells often contained Mn and Fe. The globoid crystals from provascular tissue of radicle, hypocotyl, and cotyledon regions often contained Fe while globoid crystals in the first layer of large cells surrounding these provascular areas always contained Fe. Results from EDX analysis of the proteinaceous material from the protein bodies are presented and discussed as are variations in elemental content due to different fixations.

Studies of mature seeds of eleven Pinus species differing in seed weight. II. Subcellular structure and localization of elements

1993 ◽  
Vol 71 (4) ◽  
pp. 577-585 ◽  
Author(s):  
M. M. West ◽  
J. N. A. Lott
Keyword(s):  
Seed Weight ◽  
Female Gametophyte ◽  
Protein Body ◽  
Energy Dispersive ◽  
Protein Bodies ◽  
Body Structure ◽  
X Ray ◽  
Tissue Weight ◽  
Membrane Bound ◽  
Mature Seeds

Seed tissues of 11 species of Pinus, varying greatly in seed weight, all contained protein bodies with one or more protein crystalloids and (or) one or more globoid crystals. Protein body structure and the types of elements stored in globoid crystals of protein bodies were similar between female gametophytes and their embryos. Energy dispersive X-ray analysis of globoid crystals revealed the presence of P, K, and Mg, a finding consistent with their being phytate rich. Traces of Ca and Fe were also detected in globoid crystals of some tissues. The P and Mg levels in globoid crystals of embryo and female gametophyte tissues decreased as interspecific seed tissue weight increased. High levels of Fe and significant levels of P, K, and Mg were detected in small, often ≤ 0.33 μm, naturally electron-dense particles distributed in all tissues of the embryo and female gametophyte. Unlike conventional phytate-rich globoid crystals, these Fe-rich particles were not contained in typical protein bodies but were contained within membrane-bound structures that may be plastids. Iron levels of the Fe-rich particles of Pinus seed tissues decreased as seed tissue weight increased. Key words: Pinus, seed weight, energy dispersive X-ray analysis, globoid crystals, Fe-rich particles.

Thin sectioning, freeze fracturing, energy dispersive x-ray analysis, and chemical analysis in the study of inclusions in seed protein bodies: almond, Brazil nut, and quandong

1978 ◽  
Vol 56 (17) ◽  
pp. 2050-2061 ◽  
Author(s):  
John N. A. Lott ◽  
Mark S. Buttrose
Keyword(s):  
Chemical Analysis ◽  
Freeze Fracture ◽  
Prunus Dulcis ◽  
Energy Dispersive ◽  
Protein Bodies ◽  
Brazil Nut ◽  
Fixed Tissue ◽  
Thin Sections ◽  
X Ray ◽  
Freeze Dried

Protein bodies from almond (Prunus dulcis), Brazil nut (Bertholletia excelsa), and quandong (Santalum acuminatum) have been studied in thin sections of fixed and embedded tissue, in freeze-fracture replicas of unfixed tissue, by chemical analysis of tissue for P, K, Mg, and Ca, and by energy dispersive x-ray (EDX) analysis of both sections of glutaraldehyde-fixed tissue and freeze-dried tissue powders. The protein bodies in all three species contained globoid crystals, protein crystalloids, and proteinaceous matrix regions. Results of EDX analyses were consistent with globoid crystals being rich in phytin. Variation in both the structure and the elemental composition of globoids was common. In almond some globoids were lobed rather than spherical, and large globoid crystals often contained considerable calcium whereas small globoid crystals contained little if any calcium. The globoid crystals of Brazil nut often contained barium in addition to P, K, Ca, and Mg. Protein crystalloids of Brazil nut were compound crystals. Protein bodies of quandong seed, which is largely endosperm rather than embryo, were unexceptional.

Calcium oxalate druse crystals and other inclusions in seed protein bodies: Eucalyptus and jojoba

1978 ◽  
Vol 56 (17) ◽  
pp. 2083-2091 ◽  
Author(s):  
Mark S. Buttrose ◽  
John N. A. Lott
Keyword(s):  
Calcium Oxalate ◽  
Structural Variation ◽  
Seed Protein ◽  
Freeze Fracture ◽  
Protein Body ◽  
Protein Bodies ◽  
X Ray ◽  
Edx Analysis ◽  
Plant Seeds ◽  
Freeze Dried

Druse crystals of calcium oxalate are known to occur in some protein bodies of some plant seeds. This paper reports observations on crystals, and other contents, of protein bodies of Eucalyptus erythrocorys and Simmondsia chinensis (jojoba). Results are presented from thin section studies of glutaraldehyde–OsO4 fixed, dehydrated, and embedded tissue; freeze-fracture studies; energy dispersive x-ray (EDX) analysis studies of freeze-dried tissue powders (Eucalyptus only); and chemical analysis studies of P, Mg, K, and Ca content (Eucalyptus only). Many Eucalyptus protein bodies contained large druse crystals rich in Ca but devoid of P, K, and Mg, and an occasional protein body from jojoba contained some dispersed crystals. Eucalyptus seeds were exceptionally high in Ca content. EDX analysis results provide evidence favouring the phytin-rich nature of globoid crystals in the two species. Structural variation in the globoid crystals was great, especially in jojoba. Eucalyptus, whose protein bodies contained very large globoid crystals rich in P, Mg, and K, was found to have higher levels of these elements than most species investigated to date.

Gap junctions in the prothoracic glands of the tobacco hornworm, Manduca sexta

1992 ◽  
Vol 50 (1) ◽  
pp. 706-707
Author(s):  
Ji-da Dai ◽  
M. Joseph Costello ◽  
Lawrence I. Gilbert
Keyword(s):  
Gap Junctions ◽  
Small Molecules ◽  
Manduca Sexta ◽  
Freeze Fracture ◽  
Cell Communication ◽  
Cellular Level ◽  
Thin Sections ◽  
Prothoracic Glands ◽  
Polyhydroxylated Steroids ◽  
Stimulation Of

Insect molting and metamorphosis are elicited by a class of polyhydroxylated steroids, ecdysteroids, that originate in the prothoracic glands (PGs). Prothoracicotropic hormone stimulation of steroidogenesis by the PGs at the cellular level involves both calcium and cAMP. Cell-to-cell communication mediated by gap junctions may play a key role in regulating signal transduction by controlling the transmission of small molecules and ions between adjacent cells. This is the first report of gap junctions in the PGs, the evidence obtained by means of SEM, thin sections and freeze-fracture replicas.

Where is the prolamine located in rice endosperm?

1990 ◽  
Vol 48 (3) ◽  
pp. 696-697
Author(s):  
Hsin-Kan Wu ◽  
Mei-Chu Chung
Keyword(s):  
Storage Protein ◽  
Sodium Phosphate ◽  
Recent Experiment ◽  
Protein A ◽  
Uranyl Acetate ◽  
Protein Bodies ◽  
Lead Citrate ◽  
Thin Sections ◽  
Rice Endosperm ◽  
Ethanol Series

In one of our earlier papers (Wu et al. 1978), we suggested that glutelin is the major composition of the round storage protein bodies although they also contain relatively more prolamine than the angular one does. Immunochemical studies of Krishnan et al. (1986) later showed the presence of glutelin in the irregularly-shaped (angular) protein bodies while the prolamines were found in the round ones. Our recent experiment using protein A-gold technique found that prolamine is mainly deposited into the angular protein bodies.Small blocks (1 mm3) of 7 DAF (days after flowering) caryopsis of Orvza perennis were fixed with 3% paraformaldehyde and 3% glutaraldehyde in 0.1M sodium phosphate, pH7.4, dehydrated in a graded ethanol series and infiltrated with Spurr’s resin. Thin sections, after gold labeling, were stained with uranyl acetate and lead citrate. Rabbit antibodies were raised against purified prolamine. Protein A-gold sol complex was prepared based on the technique of Horisberger et al. (1977).

Membranes in lupin root nodules. II. Preparation and properties of peribacteroid membranes and bacteroid envelope inner membranes from developing lupin nodules

1978 ◽  
Vol 30 (1) ◽  
pp. 151-174
Author(s):  
J.G. Robertson ◽  
M.P. Warburton ◽  
P. Lyttleton ◽  
A.M. Fordyce ◽  
S. Bullivant
Keyword(s):  
Sucrose Gradient ◽  
Phosphotungstic Acid ◽  
Nadh Oxidase ◽  
Osmotic Shock ◽  
Root Nodules ◽  
Freeze Fracture ◽  
Electrophoretic Analysis ◽  
Thin Sections ◽  
Peribacteroid Space ◽  
Gradient Fractionation

Peribacteroid membranes and bacteroid envelope inner membranes have been isolated from developing lupin nodules. Isolation of the peribacteroid membranes was achieved by first preparing membrane-enclosed bacteroids free from other plant organelles or membranes. The peribacteroid membranes were then released by osmotic shock and purified by centrifugation to equilibrium on sucrose gradients. The bacteroids were broken in a pressure cell and the bacteroid envelope inner membranes were isolated using sucrose gradient fractionation of the bacteroid total envelope preparation. The density of the peribacteroid membranes decreased during the period of development of N2-fixation in lupin nodules from 1.148 g/ml for nodules from 12-day plants to 1.137 g/ml for nodules from 18-day plants. The density of the bacteroid envelope inner membranes from nodules from 18-day plants was 1–153 g/ml. The identity and homogeneity of the isolated membranes was established, by comparison with membranes in intact nodules, using phosphotungstic acid and silver staining of thin sections and particle densitites on faces of freeze-fracture replicas of the membranes. Analyses for NADH oxidase and succinate dehydrogenase, spectral analyses and gel-electrophoretic analysis of proteins were also used to characterize the membrane and soluble protein fractions from the nodules. The ratio of lipid to protein was 6.1 for the peribacteroid membranes and 2.5 for the bacteroid envelope inner membranes. Leghaemoglobin was localized in the plant cytoplasm in lupin nodules and not in the peribacteroid space.

Structural cross-bridges between microtubules and mitochondria in central axons of an insect (Periplaneta americana)

1977 ◽  
Vol 27 (1) ◽  
pp. 255-272
Author(s):  
D.S. Smith ◽  
U. Jarlfors ◽  
M.L. Cayer
Keyword(s):  
Electron Micrographs ◽  
Mitochondrial Membrane ◽  
Periplaneta Americana ◽  
Freeze Fracture ◽  
Outer Mitochondrial Membrane ◽  
Thin Sections ◽  
Cross Bridge ◽  
Multiple Association ◽  
Random Models ◽  
Cross Bridges

The distribution of microtubules and mitochondria in central axons of an insect (Periplaneta americana) is assessed by comparison between counts on micrographs and computed axon random ‘models’. These studies show that the observed multiple association of microtubules with individual mitochondria is statistically highly significant. Electron micrographs of thin sections show that linkage is effected by physical cross-bridge, possibly comprising components from the microtubule and mitochondrion. Linear particle arrays are described on the outer mitochondrial membrane in freeze-fracture replicas, and tentatively related to the bridges seen in thin sections. The results are discussed in terms of proposed roles of microtubules in neurons and other cells.

Stages in the assembly of pleated and smooth septate junctions in developing insect embryos

1982 ◽  
Vol 56 (1) ◽  
pp. 245-262 ◽  
Author(s):  
N.J. Lane ◽  
L.S. Swales
Keyword(s):  
Embryonic Development ◽  
Freeze Fracture ◽  
Organizational Capacity ◽  
Intramembranous Particle ◽  
Septate Junctions ◽  
Thin Sections ◽  
Intramembranous Particles ◽  
Initial Event ◽  
Random Arrays ◽  
Insect Embryos

The stages that occur during the assembly of both pleated and smooth septate junctions in developing insect tissues have been examined. The oesophagus and mid-gut of the embryonic moth, and the oesophagus and central nervous system (CNS) of the locust embryo, have been investigated in thin sections and by freeze-fracture during the course of membrane biogenesis. The smooth septate junctions developing between the lateral borders of the mid-gut exhibit, in the early stages, individual intramembranous particles becoming aligned into short ridges. These ultimately migrate over the membrane face and fuse into longer arrays, which become stacked in parallel with other ridges to form the characteristic mature form of the junction just before hatching. Pleated septate junctions occur between the cells both of the oesophagus and of the perineurium, which ensheathes the neurones and the neuroglial cells in the locust CNS; these are also fully formed by the end of embryonic development. The pleated junctions appear to be assembled during the later stages of CNS or gut differentiation, arising first in embryos about two-thirds of the way through development. During their maturation, the initial event seems to be a membrane depression in the P face, which occurs in patches over the presumptive junctional membrane. Into these depressed regions or ‘formation-plaque’ areas, 8–10 nm particles appear to be inserted intramembranously in apparently random arrays. These particles are the most common elements but larger particles are also present; the former ultimately become aligned in a row. With time, other intramembranous particles come to lie in rows parallel to the original one. By hatching, the typical undulating stacks of parallel intramembranous particle rows are fully formed. Gap junctions also form between the same perineurial or oesophageal cells, usually before, but in some cases at the same time, or just after, the septate junctions have been assembled. Tricellular associations between cells also appear around the same time in embryonic development. The simultaneous assembly of these different junctions reflects a high degree of organizational capacity at the membrane level.

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