An ultrastructural study of Triticum monococcum cell suspension cultures during aging and after treatment with the herbicide Diclofop-methyl (methyl-2-(4-(2′,4′-dichlorophenoxy)phenoxy)propanoate)

1979 ◽  
Vol 57 (19) ◽  
pp. 2006-2020 ◽  
Author(s):  
David G. Davis ◽  
Aurelia Brezeanu

Cell suspensions from root-derived callus tissues of Triticum monococcum L. were examined during growth and senescence. The fine structure of control cultures was compared with the ultrastructural modifications in cultures treated with the compound, methyl-2-(4-(2′,4′-dichlorophenoxy)phenoxy)propanoate (Diclofop-methyl). The control cell suspensions were observed during the cell division phase, the log phase, and the early stationary phase of growth. Senescence is characterized by a loss of ribosomes, alteration of internal membranes of the plastids, vesiculation, formation of granular material in the cytoplasm, rupture of the tonoplast, and an increase in number of lipid bodies. Cells in advanced stages of senescence had few organelles, but rather the cytoplasm consisted almost exclusively of lipid bodies and vesicles. The fine structure of the nuclei and mitochondria was least affected during aging. The ultrastructural effects of herbicide treatment did not completely parallel those of senescing cells, although any distinctions were difficult to sort out. The intensity of herbicide damage depended on both concentration and time (and undoubtedly the physiological state of any particular cell at the time of treatment). Low concentrations (4 μM) at 12 h resulted in plastid damage (analogous to chloroplast damage in photosynthetic tissues treated with herbicides) and in the formation of some myelin figures. At 20 μM concentration for 12 h, very extensive formation of myelin figures was observed in all cells. By 70 h, cells treated with 4 μM herbicide ranged from those with little or no damage to cells with extensive vesicle formation. In contrast, all cells treated with 20 μM herbicide at 70 h were damaged greatly. Some nuclei were present, although the nuclear envelopes were altered. Most organelles were barely recognizable. Extensive vesiculation and lipid formation occurred. These effects were more pronounced in cells treated with 40 μM herbicide at 70 h than in cells treated with lesser concentrations for shorter times. In this case, some organelles were recognizable (plastids and mitochondria) but they were abnormal in that the contents were often granular with only remnants of membranes. Some cells appeared as though the physiological processes were stopped so rapidly that hydrolytic enzymes could not function totally.

2020 ◽  
Vol 115 (2) ◽  
pp. 369
Author(s):  
Esra KOÇ ◽  
Cemil İŞLEK ◽  
Belgizar KARAYİĞİT

This study examined the effects of different concentrations of spermine (Spm) and putrescine (Put) elicitors on capsaicin production at different times in cell suspension culture of peper (<em>Capsicum annuum </em>L‘Kahramanmaraş Hat-187’<em>.</em>), raised from pepper seeds. Callus was obtained from hypocotyl explants of pepper seedlings germinated <em>in vitro</em> conditions, and cell suspensions were prepared from calluses. Spm (0.1, 0.2 and 0.4 mg l<sup>-1</sup>) and Put (0.1, 0.2 and 0.4 mg l<sup>-1</sup>) elicitors were applied on cell suspensions, and control groups free from elicitor treatment were created. The amount of capsaicin in cells was found to be higher in the control groups and samples treated with Spm elicitors when compared to filtrates. The highest increase in the capsaicin amount in cells was determined on day 12 of elicitation with 0.2 mg l<sup>-1 </sup>Spm application. The highest capsaicin amount passing into the filtrate was determined as 0.1 mg l<sup>-1 </sup>Spm on day 8. The most effective Put concentration and time on capsaicin amount were found as 0.2 mg l<sup>-1 </sup>Put on day 12 in both cells and filtrates. The highest total capsaicin was also determined in the 0.2 mg l<sup>-1 </sup>Spm application on day 12with 312.747 ± 8.70 µg <sup> </sup>g<sup>-1</sup> of culture. Exogenous treatment of Spm and Put elicitors affected capsaicin accumulation.


1965 ◽  
Vol 25 (2) ◽  
pp. 141-157 ◽  
Author(s):  
David S. Maxwell ◽  
Lawrence Kruger

Normal and reactive astrocytes in the cerebral cortex of the rat have been studied with the electron microscope following focal alpha particle irradiation. The presence of glycogen and approximately 60-A fibrils identify astrocyte cytoplasm in formalin-perfused tissue. The glycogen particles facilitate the identification of small processes and subpial and perivascular end-feet. Both protoplasmic and fibrous astrocytes contain cytoplasmic fibrils and should be distinguished on the basis of the configuration of their processes and their distribution. Acutely reactive astrocytes are characterized by a marked increase in the number of glycogen granules and mitochondria from the first day after irradiation. These cells later hypertrophy and accumulate lipid bodies and increased numbers of cytoplasmic fibrils. The glial "scar" consists of a greatly expanded volume of astrocyte cytoplasm filled with fibrils and displays no signs of astrocyte death, reversion to primitive forms, or extensive multiplication.


1991 ◽  
Vol 69 (10) ◽  
pp. 2257-2260 ◽  
Author(s):  
Ann Francine Greer ◽  
Zohreh Tabaeizadeh

To produce calli for the establishment of a cell suspension, leaf, stem, and petiole explants of Lycopersicon chilense Dun., grown in vitro and in the soil, were cultured on media containing 15 different combinations of benzylaminopurine, kinetin, and indole acetic acid. Among the three types of tissues, leaf explants showed the best response. Cell suspension cultures of L. chilense were established from leaf callus derived from soil grown plants using Murashige and Skoog's medium supplemented with casein hydrolysate (250 mg/L), coconut water (5%), and 2,4-dichlorophenoxyacetic acid (2 mg/L). Once established, cell suspensions showed a rapid growth rate with no marked lag phase. Shooting via organogenesis occurred from callus derived from cell suspensions on medium containing 2 mg/L benzylaminopurine. Regenerated plants had the same morphology as the original plants. Key words: Lycopersicon chilense, tomato, tissue culture, cell suspensions, organogenesis, plant regeneration.


1986 ◽  
Vol 41 (4) ◽  
pp. 385-390 ◽  
Author(s):  
Karl-Heinz Pawelka ◽  
Joachim Stöckigt

Eleven main alkaloids were identified from cell suspension cultures of Rhazya stricta grown in 4X-medium for 15 days. The alkaloids comprised the five groups Corynanthe, Strychnos, Eburnan, Secodine, and Aspidosperma and can be regarded as being typical Rhazya alkaloids, although the Strychnos alkaloid akuammicine has been isolated for the first time from the genus Rhazya. The most abundant compound was ( + )-1,2-dehydroaspidospermidine (15 mg/l medium) whereas all other constituents were synthesized in about 5 - 10 times lower amounts. More than 15 further alkaloids were formed as minor components which have not yet been identified. Cultivated Rhazya cells have been shown to be one of the richest alkaloid sources from apocynaceous cell suspensions. The isolated compounds, because of their structural heterogeneity, cannot be presently arranged into a scheme with coherent biosynthetic sequences.


2000 ◽  
Vol 66 (7) ◽  
pp. 3004-3009 ◽  
Author(s):  
Udo Heyen ◽  
Jens Harder

ABSTRACT Monoterpenes with an unsaturated hydrocarbon structure are mineralized anaerobically by the denitrifying β-proteobacteriumAlcaligenes defragrans. Organic acids occurring in cells ofA. defragrans and culture medium were characterized to identify potential products of the monoterpene activation reaction. Geranic acid (E,E-3,7-dimethyl-2,6-octadienoic acid) accumulated to 0.5 mM in cells grown on α-phellandrene under nitrate limitation. Cell suspensions of A. defragrans65Phen synthesized geranic acid in the presence of β-myrcene, α-phellandrene, limonene, or α-pinene. Myrcene yielded the highest transformation rates. The alicyclic acid was consumed by cell suspensions during carbon limitation. Heat-labile substances present in cytosolic extracts catalyzed the formation of geranic acid from myrcene. These results indicated that a novel monoterpene degradation pathway must be present in A. defragrans.


In Vitro ◽  
1973 ◽  
Vol 8 (4) ◽  
pp. 301-306 ◽  
Author(s):  
G. Rappay ◽  
Angéla Gyévai ◽  
L. Kondics ◽  
E. Stark

Author(s):  
S. Y. Al-Mohanna ◽  
J. A. Nott ◽  
D. J. W. Lane

INTRODUCTIONIt is apparent, in a review on the decapod hepatopancreas (Gibson & Barker, 1979) that there is some consensus of opinion that the epithelium consists of E-, R-, F- and B-cells and M-cells (Al-Mohanna, Nott & Lane, 1985). Also, it is agreed that the gland produces enzymes and absorbs, digests and stores nutrients and excretes waste material. However, the apportionment of these functions to the different cells and the descriptions of the cytological processes involved are variously explained. Thus, the activity of proteases and amylases has been demonstrated in the secretion produced by the gland but the source of these enzymes is attributed to different cells and various modes of secretion are proposed. Also, no secretion granules of the zymogen type have been seen.There are probably two main reasons for the inconsistent interpretation of the activities of the cells. First, the different stages of the feeding and moult cycles are not taken into account and both these affect the cytology of the gland. Second, some of the functions have been deduced from observations of the fine structure without any experimental treatments to demonstrate more directly the processes involved. In the present work all the animals are taken at the same moult stage and observations are made throughout the feeding cycle. Also, aspects of the function are studied with markers which are administered in the diet and injected into the blood. The activities of hydrolytic enzymes associated with the different epithelial cells have been studied but these will be the subject of a separate publication dealing with the cytochemistry of the digestive processes.


2011 ◽  
Vol 57 (No. 1) ◽  
pp. 1-7 ◽  
Author(s):  
J. Malá ◽  
M. Hrubcová ◽  
P. Máchová ◽  
H. Cvrčková ◽  
O. Martincová ◽  
...  

We examined defence responses in embryogenic cell suspension cultures of Norway spruce (Picea abies [L.] Karst) elicited by intracellular protein and cell wall fractions (PF and WF, respectively) prepared from mycelia of the fungus Sirococcus strobilinus Preuss focusing on changes in (soluble and cell wall-bound) phenolic and stilbene concentrations. Treatment with both preparations induced an increase in the total contents of phenolic acids in Norway spruce cells and variations in the levels of stilbene glycosides. More rapid and intense induction of defence response was observed in cells after WF application. The contents of soluble phenolic acids (especially benzoic acid derivatives) and cell wall-bound phenolic acids (especially ferulic acid) started to increase (relative to controls) within 4 h after the addition of the WF preparation and remained high in elicited cells for 8&ndash;12 h. A moderate increase in phenolic acids in cells exposed to the PF preparation was observed within 8 h after application. However, after 24 h of WF treatment a decline of total phenolics was observed, while in PF elicited Norway spruce cells the phenolic content continued to increase. Significantly decreased concentrations of stilbene glycosides, isorhapontin, astringin and piceid, were determined in PF and WF treated Norway spruce cell cultures. The total content of stilbene glycosides decreased within 8 h after WF application to 68% of the amount determined in the control and within 12 h to 73% of the control in PF-treated cells. These results demonstrate that both PF and WF prepared from the Sirococcus strobilinus mycelium elicit changes in the metabolism of phenylpropanoids, which are involved in the defence responses of plants to pathogens.


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