Fine structure of the differentiating sieve elements of Vicia faba

1969 ◽  
Vol 17 (3) ◽  
pp. 441 ◽  
Author(s):  
S Zee

The fine structure of the sieve elements of the primary phloem of the epicotyl of Vicia faba is described. The cytoplasm of the young sieve element contains four distinct forms of "slime" body: amorphous, crystalline, tubular (each tubule measuring about 140 Å in diameter), and short fibrillar (each fibril measuring about 350 Å in diameter). At the very early stages of differentiation, polysome helices are prevalent often in close association with the amorphous but not the other forms of "slime" bodies. At the early stages of development of the sieve element the tubular form of "slime" is closely associated with the endoplasmic reticulum, which suggests their possible origin. The plastids of the sieve element lack a well-developed internal membrane system but contain two characteristic types of inclusion bodies, starch granules and crystalloids identical to those revorted for the secondarv vhloem of the root of Pisum sativum. Mitochondria - remain apparently unchanged throughout sieve element development. Microtubules are present during the early stages of sieve element development but become scarce at later stages. Dictyosomes, coated vesicles, ribosomes, polysomes, and nucleus disappear as the sieve element matures. The fine structure of the sieve plate pore initial is complex. It consists of an outer electron-dense ring ("desmotubule") which encloses a central dark core. The developmental pattern of the sieve plate pore has been traced from the very young to the mature stages.

1967 ◽  
Vol 34 (3) ◽  
pp. 801-815 ◽  
Author(s):  
James Cronshaw ◽  
Katherine Esau

An ontogenetic study of the sieve element protoplast of Nicotiana tabacum L. by light and electron microscopy has shown that the P-protein component (slime) arises as small groups of tubules in the cytoplasm. These subsequently enlarge to form comparatively large compact masses of 231 ± 2.5 (SE)A (n = 121) tubules, the P-protein bodies. During subsequent differentiation of the sieve element, the P-protein body disaggregates and the tubules become dispersed throughout the cell. This disaggregation occurs at about the same stage of differentiation of the sieve elements as the breakdown of the tonoplast and nucleus. Later, the tubules of P-protein are reorganized into smaller striated 149 ± 4.5 (SE)A (n = 43) fibrils which are characteristic of the mature sieve elements. The tubular P-protein component has been designated P1-protein and the striated fibrillar component P2-protein. In fixed material, the sieve-plate pores of mature sieve elements are filled with proteinaceous material which frays out into the cytoplasm as striated fibrils of P2-protein. Our observations are compatible with the view that the contents of contiguous mature sieve elements, including the P-protein, are continuous through the sieve-plate pores and that fixing solutions denature the proteins in the pores. They are converted into the electron-opaque material filling the pores.


1965 ◽  
Vol 13 (2) ◽  
pp. 185
Author(s):  
MC Wark

The companion cells of the secondary phloem of Pisum contain all the organelles characteristic of cells possessing an active metabolism. The cytoplasm of the companion cells shows little change during ontogeny. Complex plasmodesmata connect the sieve elements and companion cells. These are the only connections observed between the sieve elements and other phloem cells. New wall structures of the companion cells are described. These structures are here tentatively called trabeculae; they intrude into the cytoplasm, but never completely cross the cell. The trabeculae alter in appearance at the time when the sieve element nucleus and tonoplast disappear. The phloem parenchyma cells are large vacuolated cells wider in diameter but shorter in length than the sieve elements. They contain all the organelles found in normal photosynthetic tissue. The cytoplasm of the phloem parenchyma shows little change during ontogeny. Plasmodesmata of well-developed pit fields connect the phloem parenchyma with the companion cells. The phloem parenchyma does not communicate with the sieve elements.


1983 ◽  
Vol 64 (1) ◽  
pp. 37-47
Author(s):  
J. Thorsch ◽  
K. Esau

Nuclear crystalloids have been found in sieve elements of several Boraginaceae. Nuclei of differentiating sieve elements of Echium and other genera except Amsinckia contain one or more crystalloids composed of thin rods densely packed in parallel arrangement. After the nuclei disintegrate in the maturing sieve element the crystalloids are released into the cell lumen where they persist intact. In Amsinckia the crystalloid consists of two components: a dense component, similar to the crystalloid in the other genera and a loosely arranged paracrystalline component. The proteinaceous nature of the nuclear crystalloids and their possible similarity to P-protein was investigated by enzyme digestion techniques. Three proteolytic enzymes were employed in this study: protease, pepsin and trypsin. Successful digestion of the dense crystalloid in both Echium and Amsinckia was obtained with each enzyme tested. P-protein plugging the sieve plate pores was also digested. The loose component in Amsinckia and the aggregated and dispersed P-protein were not affected by the enzyme digestion procedures. These results seemed to indicate that the density or compactness of the proteinaceous inclusions may play a role in the differential response.


1979 ◽  
Vol 38 (1) ◽  
pp. 11-22
Author(s):  
K. Esau ◽  
A.C. Magyarosy

The compounds crystalloids formed in sieve element nuclei of Amsinckia douglasiana A. DC. (Boraginaceae) during differentiation of the cell become disaggregated during the nuclear breakdown characteristic of a maturing sieve element. The phenomenon occurs in both healthy and virus-infected plants. The crystalloid component termed cy, which is loosely aggregated, separates from the densely aggregated component termed cx and disperses. The cx component may become fragmented, or broken into large pieces, or remain intact after the cell matures. After their release from the nucleus both crystalloid components become spatially associated with the dispersed P-protein originating in the cytoplasm, but remain distinguishable from it. The component tubules of P-protein are hexagonal in transections and are somewhat wider than the 6-sided cy tubules. The cx tubules are much narrower than the P-protein or the cy tubules and have square transections. Both the P-protein and the products of disintegrated crystalloids accumulate at sieve plates in sieve elements subjected to sudden release of hydrostatic pressure by cutting the phloem. The question of categorizing the tubular components of the nuclear crystalloid of a sieve element with reference to the concept of P-protein is discussed.


1984 ◽  
Vol 23 (10) ◽  
pp. 2169-2171 ◽  
Author(s):  
P.M. Dey ◽  
M.G. Jones ◽  
S. Naik ◽  
J.B. Pridham

Observations on the development of the sieve-plate pores of Acer pseudoplatanus have enabled five stages in the differentiation of the cell to be recognized. The functional relationships of the endoplasmic reticulum to the formation of the sieve plate and its close association with other organelles of the cell during development have been described in detail. During differentiation slime bodies are formed and these disaggregate to form the fibrillar material present in the lumen of the mature cell. It is probable that the fibres found in the slime body arise from granular bodies which may consist of ribosomes, seen within the organelles. The granules are thought to form the fibrils which are linear subunits of the fibres of the slime body and the sieve-plate pores. An account is given of the degeneration of the nucleus and the changes in the fine structure of the mitochondria and plastids which accompany the differentiation of a cambial initial into a mature sieve element. The formation of laminar material and other inclusions found in the mature cell is also described. Autoradiographic techniques have been used to show the function of the Golgi bodies and their associated vesicles in the development of the cell wall and also to indicate that some of the callose formed at the sieve plate is deposited after the general formation of wall material. This latter observation lends support to the view that callose is deposited at the sieve plate in response to wounding of the tissue.


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