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  • Articles  (9)
  • Microsporogenesis  (5)
  • Plasma membrane  (4)
  • 1
    Electronic Resource
    Electronic Resource
    A model for the pattern of deposition of microfibrils in the cell wall of Glaucocystis (1978)
    Springer
    Planta 141 (1978), S. 51-58 
    Details
    ISSN: 1432-2048
    Keywords: Cell wall ; Cellulose ; Freeze-etching ; Glaucocystis ; Microfibrils (cellulose) ; Morphogenesis ; Plasma membrane
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Freeze-fracturing of Glaucocystis nostochinearum Itzigsohn cells during cell-wall microfibril deposition indicates that unidirectionally polarized microfibril ends are localized in a “zone of synthesis” covering about 30% of the sarface area of the plasma membrane. Within this zone there are about 6 microfibril ends/μm2 cell surface. It is proposed that microfibrils are generated by the passage of their tips over the cell surface and that the pattern of microfibril organization at the poles of the cells, in which microfibrils of alternate layers are interconnected at 3 “rotation centres”, results directly from the pattern of this translation of microfibril tips. In a model of the deposition pattern it is proposed that the zone of synthesis may split into 3 sub-zones as the poles are approached, each sub-zone being responsible for the generation of one rotation centre. It is demonstrated that the microfibrillar component of the entire wall could be generated by the steady translation of the microfibril tips (at which synthesis is presumed to occur) over the cell surface at a rate of 0.25–0.5 μm min-1. Microcinematography indicates that the protoplast rotates during cell-wall deposition, and it is proposed that this rotation may play a role in the generation of the microfibril deposition pattern.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00387744
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  • 2
    Electronic Resource
    Electronic Resource
    Nuclear cytoplasmic domains, microtubules and organelles in microsporocytes of the slipper orchid Cypripedium californicum A. Gray dividing by simultaneous cytokinesis (1996)
    Springer
    Sexual plant reproduction 9 (1996), S. 145-152 
    Details
    ISSN: 1432-2145
    Keywords: Cytokinesis ; Microtubules ; Microsporogenesis ; Orchids ; Phragmoplast ; Pollen
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Microsporocytes of the slipper orchidCypripedium californicum A. Gray divide simultaneously after second meiosis. The organization and apportionment of the cytoplasm throughout meiosis are functions of nuclear-based radial microtubule systems (RMSs) that define domains of cytoplasm - a single sporocyte domain before meiosis, dyad domains within the undivided cytoplasm after first meiosis, and four spore domains after second meiosis. Organelles migrate to the interface of dyad domains in the undivided cytoplasm after first meiotic division, and second meiotic division takes place simultaneously on both sides of the equatorial organelle band. Microtubules emanating from the telophase II nuclei interact to form columnar arrrays that interconnect all four nuclei, non-sister as well as sister. Cell plates are initiated in these columns of microtubules and expand centrifugally along the interface of opposing RMSs, coalescing in the center of the sporocyte and joining with the original sporocyte wall at the periphery to form the tetrad of microspores. Organelles are distributed into the spore domains in conjunction with RMSs. These data, demonstrating that cytokinesis in microsporogenesis can occur in the absence of both components of the typical cytokinetic apparatus (the preprophase band of microtubules which predicts the division site and the phragmoplast which controls cell-plate deposition), suggest that plant nuclei have an inherent ability to establish a domain of cytoplasm via radial microtubule systems and to regulate wall deposition independently of the more complex cytokinetic apparatus of vegetative cells.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02221394
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  • 3
    Electronic Resource
    Electronic Resource
    Nuclear cytoplasmic domains, microtubules and organelles in microsporocytes of the slipper orchid Cypripedium californicum A. Gray dividing by simultaneous cytokinesis (1996)
    Springer
    Sexual plant reproduction 9 (1996), S. 145-152 
    Details
    ISSN: 1432-2145
    Keywords: Key words Cytokinesis ; Microtubules ; Microsporogenesis ; Orchids ; Phragmoplast ; Pollen
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract  Microsporocytes of the slipper orchid Cypripedium californicum A. Gray divide simultaneously after second meiosis. The organization and apportionment of the cytoplasm throughout meiosis are functions of nuclear-based radial microtubule systems (RMSs) that define domains of cytoplasm – a single sporocyte domain before meiosis, dyad domains within the undivided cytoplasm after first meiosis, and four spore domains after second meiosis. Organelles migrate to the interface of dyad domains in the undivided cytoplasm after first meiotic division, and second meiotic division takes place simultaneously on both sides of the equatorial organelle band. Microtubules emanating from the telophase II nuclei interact to form columnar arrrays that interconnect all four nuclei, non-sister as well as sister. Cell plates are initiated in these columns of microtubules and expand centrifugally along the interface of opposing RMSs, coalescing in the center of the sporocyte and joining with the original sporocyte wall at the periphery to form the tetrad of microspores. Organelles are distributed into the spore domains in conjunction with RMSs. These data, demonstrating that cytokinesis in microsporogenesis can occur in the absence of both components of the typical cytokinetic apparatus (the preprophase band of microtubules which predicts the division site and the phragmoplast which controls cell-plate deposition), suggest that plant nuclei have an inherent ability to establish a domain of cytoplasm via radial microtubule systems and to regulate wall deposition independently of the more complex cytokinetic apparatus of vegetative cells.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/s004970050024
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  • 4
    Electronic Resource
    Electronic Resource
    Further evidence from sectioned material in support of the existence of a linear terminal complex in cellulose synthesis (1987)
    Springer
    Protoplasma 136 (1987), S. 96-103 
    Details
    ISSN: 1615-6102
    Keywords: Boergesenia forbesii ; Microfibrils ; Microtubules ; Plasma membrane ; Sectioned material ; Terminal complexes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Transmembrane linear terminal complexes considered to be involved in the synthesis of cellulose microfibrils have been described in the plasma membrane ofBoergesenia forbesii. Evidence for the existence of these structures has been obtained almost exlusively using the freeze etching technique. In the present study an attempt has been made to complete these studies using conventional fixation, staining, and sectioning procedures. In developing cells ofBoergesenia forbesii, strongly stained structures traversing the plasma membrane and averaging 598.9 nm ± 171.3 nm in length, 28.7 nm ± 4.2 nm in width, and 35.2 nm ± 6.6 nm in depth have been demonstrated. These structures are considered to be linear terminal complexes. At their distal (cell wall) surface, they appear to be closely associated with cellulose microfibrils. At the proximal (cytoplasmic) surface, they are associated with microtubules and polysomes. A model of the possible interrelation of the terminal complexes and microtubules leading to the generation of cell wall microfibrils is proposed.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF01276358
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  • 5
    Electronic Resource
    Electronic Resource
    Plastid polarity and meiotic spindle development in microsporogenesis ofSelaginella (1991)
    Springer
    Protoplasma 161 (1991), S. 168-180 
    Details
    ISSN: 1615-6102
    Keywords: Microsporogenesis ; Microtubules ; Mitotic apparatus ; Plastid polarity ; Selaginella
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Microsporogenesis inSelaginella was studied by fluorescence light microscopy and transmission electron microscopy. As in other examples of monoplastidic meiosis the plastids are involved in determination of division polarity and organization of microtubules. However, there are important differences: (1) the meiotic spindle develops from a unique prophase microtubule system associated with two plastids rather than from a typical quadripolar microtubule system associated with four plastids; (2) the division axes for first and second meiotic division are established sequentially, whereas as in all other cases the poles of second division are established before those of first division; and (3) the plastids remain in close contact with the nucleus throughout meiotic prophase and provide clues to the early determination of spindle orientation. In early prophase the single plastid divides in the plane of the future division and the two daughter plastids rotate apart until they lie on opposite sides of the nucleus. The procytokinetic plate (PCP) forms in association with the two slender plastids; it consists of two spindle-shaped microtubule arrays focused on the plastid tips with a plate of vesicles at the equatorial region and a picket row of microtubules around one side of the nucleus. Second plastid division occurs just before metaphase and the daughter plastids remain together at the spindle poles during first meiotic division. The meiotic spindle develops from merger of the component arrays of the PCP and additional microtubules emanating from the pair of plastid tips located at the poles. After inframeiotic interphase the plastids migrate to tetrahedral arrangement where they serve as poles of second division.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF01322729
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  • 6
    Electronic Resource
    Electronic Resource
    Pollen development in orchids (1991)
    Springer
    Protoplasma 165 (1991), S. 155-166 
    Details
    ISSN: 1615-6102
    Keywords: Cytokinesis ; F-actin ; Microsporogenesis ; Microtubules ; Orchids ; Phragmoplast
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Cytokinesis in microsporocytes of moth orchids is unusual in that it occurs simultaneously after meiosis, the cytoplasm does not infurrow in the division planes, and cell plates are deposited in association with centrifugal expansion of phragmoplasts. Microtubules radiating from the nuclear envelopes appear to be of fundamental importance in establishment of division planes. Primary interzonal spindles develop between sister nuclei and interaction of radial microtubules triggers development of secondary interzonal spindles between non-sister nuclei. From three to six or more phragmoplasts, depending upon the arrangement of nuclei in the coenocyte, develop from these postmeiotic arrays. The phragmoplasts consist of co-aligned microtubules and F-actin organized into bundles that are broad proximal to the mid-plane and taper distally. Ultrastructure of the phragmoplast/cell plate reveals that abundant ER is associated with vesicle aggregation and coalescence. Cell plates are deposited in association with phragmoplasts as they expand centrifugally to join the parental wall and/or fuse with one another in the interior of the cell.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF01322286
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  • 7
    Electronic Resource
    Electronic Resource
    A new putative cellulose-synthesizing complex ofColeochaete scutata (1992)
    Springer
    Protoplasma 168 (1992), S. 51-63 
    Details
    ISSN: 1615-6102
    Keywords: Cellulose microfibril formation ; Chlorophyta ; Coleochaete scutata ; Freeze fracture ; Plasma membrane ; Terminal complex
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Cells of the charophycean alga,Coleochaete scutata active in cell wall formation were freeze fractured in the search for cellulose synthesizing complexes (TCs) since this alga is considered to be among the most advanced and a progenitor to land plant evolution. We have found a new TC which consists of two geometrically distinctive particle complexes complementary to one another in the plasma membrane and occasionally associated with microfibril impressions. In the E-fracture face is found a cluster of 8–50 closely packed particles, each with a diameter of 5–17 nm. Most of these particles are confined within an 80 nm circle. In the P-fracture face is found an 8-fold symmetrical arrangement of 10 nm particles circumferentially arranged around a 28 nm central particle. The TCs ofC. scutata are quite distinctive from the rosette/globule TCs of land plants. The 5.5×3.1 nm microfibril inC. scutata is also distinctive from the 3.5×3.5 nm microfibril typical of land plants. The phylogenetic implications of this unique TC in land plant evolution are discussed.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF01332650
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  • 8
    Electronic Resource
    Electronic Resource
    Pollen development in orchids 1. Cytoskeleton and the control of division plane in irregular patterns of cytokinesis (1991)
    Springer
    Protoplasma 163 (1991), S. 9-18 
    Details
    ISSN: 1615-6102
    Keywords: Meiotic cytokinesis ; Microsporogenesis ; Microtubules ; Orchids ; Phragmoplast
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The cytokinetic apparatus in microsporogenesis lacks a preprophase band of microtubules and the selection of cytokinetic planes is dependent upon disposition of nuclei which define cytoplasmic domains via post-meiotic radial systems of microtubules. Meiotic cytokinesis was investigated in hybrid moth orchids (Phalaenopsis) exhibiting irregular patterns of cytokinesis. In these polliniate orchids, spindle orientation is imprecise, and the tetrad nuclei (therefore the microspores) may be in rhomboidal, tetrahedral or linear arrangement. The hybrid “Sabine Queen” (section Phalaenopsis) regularly undergoes simultaneous cytokinesis, as is common in orchids. The hybrid “Vista Rainbow” (section Amboinenses) produces either a complete dyad wall, a partial wall, or no wall after first nuclear division. In all cases, a first division phragmoplast is initiated in the interzonal region and expands centrifugally into the peripheral cytoplasm. Fluorescence microscopy shows that the phragmoplast consists of fusiform bundles of microtubules and Factin bisected by a non-fluorescent zone. If a cell plate fails to form, a band of organelles polarized in the equatorial region effectively divides the cell into two domains. The organelles disperse when a dyad wall is complete, but tend to remain polarized around an incomplete wall. In four-nucleate coenocytes, the usual interzonal microtubules between sister nuclei (primary) form slightly in advance of secondary arrays between non-sister nuclei. Phragmoplasts are initiated in sites defined by the post-meiotic microtubule arrays.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF01323402
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  • 9
    Electronic Resource
    Electronic Resource
    Effects of 2,6-dichlorobenzonitrile and Tinopal LPW on the structure of the cellulose synthesizing complexes ofVaucheria hamata (1992)
    Springer
    Protoplasma 166 (1992), S. 200-207 
    Details
    ISSN: 1615-6102
    Keywords: Cellulose formation ; 2,6-Dichlorobenzonitrile ; Freeze etching ; Plasma membrane ; Cellulose synthesizing enzyme complex ; Tinopal LPW ; Vaucheria hamata
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The effects of 2,6-dichlorobenzonitrile (DCB, a known inhibitor of cellulose synthesis) and Tinopal LPW (TPL, an agent which disrupts glucan crystallization) on the structure of cellulose synthesizing complexes (terminal complexes, TCs) in the xanthophycean algaVaucheria hamata were investigated. DCB (10 μM) inhibits nascent fibril formation from the TC subunit (based on the absence of impressions) although it does not alter the overall shape of the rectangular TC during the short treatment of 20 min. With a prolonged treatment (60 min), the arrangement of TC subunits becomes disordered, and particles generally exhibited as doublets of subunits are released from each other. DCB also interferes with the formation of the overall shape of the TC although it does not disturb the conversion into TC rows of the subunits (the zymogenic precursor of the TC) packed in the globules. A 15 min treatment with TPL (1 mM) destroys the TC integrity by reducing the subunits into small fragments or particulate aggregates. The particulate rows of the TC are interrupted at many points, and fragments and particulate aggregates are dispersed by prolonged treatment (45 min) with TPL. Unlike DCB, TPL inhibits the conversion of globule subunits into TC rows. New insights on the structural characteristics necessary for cellulose microfibril assembly and possible mechanisms for the biogenesis of theVaucheria TC come from these data.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF01322782
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