Membrane phospholipid composition during maturation of seeds of Acer platanoides and Acer pseudoplatanus in relation to desiccation tolerance

1999 ◽  
Vol 21 (2) ◽  
pp. 109-115 ◽  
Author(s):  
Stanisława Pukacka
1991 ◽  
Vol 1 (3) ◽  
pp. 149-162 ◽  
Author(s):  
J. B. Dickie ◽  
K. May ◽  
S. V. A. Morris ◽  
S. E. Titley

AbstractMature seeds of Norway maple (Acer platanoides L.) are tolerant of desiccation, at least to moisture contents of about 7% (fresh weight basis), but those of sycamore (Acer pseudoplatanus) are killed by drying below about 45% moisture content. Sycamore seeds are thus recalcitrant; while the classification of those of Norway maple as orthodox is confirmed by the fact that between 19% and 7.5% moisture content their longevity is increased in a predictable way by reduction of seed moisturecontent. However, the period of useful storage of the latter in seed banks may be much less than for many crop species. The rates of water loss to a dry environment of both fruits and seeds of sycamore are much less than those of Norway maple, suggesting a degree of desiccationavoidance in the desiccation-intolerant species. Seed physiological maturity (maximum dry weight) occurred 2–3 weeks earlier in Norway maple than insycamore, but in both species this occurred about 150–160 days after peak flowering. Tetrazolium staining is a good indicator of embryo viability in both species, correlating well with germination test results. In Norway maple both methods of viability testing indicated that whole-seed desiccation tolerance coincided with the attainment of maximum dry weight. Tetrazolium staining indicated the development of desiccation tolerance in the radicles/hypocotyls of both species approximately 2–4 weeks before physiological maturity. Possible correlation between changes in the level of embryo dormancy during development and the acquisition of desiccation tolerance are discussed.


1994 ◽  
Vol 124 (3) ◽  
pp. 273-287 ◽  
Author(s):  
TP McGee ◽  
HB Skinner ◽  
EA Whitters ◽  
SA Henry ◽  
VA Bankaitis

SEC14p is required for protein transport from the yeast Golgi complex. We describe a quantitative analysis of yeast bulk membrane and Golgi membrane phospholipid composition under conditions where Golgi secretory function has been uncoupled from its usual SEC14p requirement. The data demonstrate that SEC14p specifically functions to maintain a reduced phosphatidylcholine content in Golgi membranes and indicate that overproduction of SEC14p markedly reduces the apparent rate of phosphatidylcholine biosynthesis via the CDP-choline pathway in vivo. We suggest that SEC14p serves as a sensor of Golgi membrane phospholipid composition through which the activity of the CDP-choline pathway in Golgi membranes is regulated such that a phosphatidylcholine content that is compatible with the essential secretory function of these membranes is maintained.


2021 ◽  
Vol 1863 (1) ◽  
pp. 183482
Author(s):  
Estelle Deschamps ◽  
Annick Schaumann ◽  
Isabelle Schmitz-Afonso ◽  
Carlos Afonso ◽  
Emmanuelle Dé ◽  
...  

2007 ◽  
Vol 34 (7) ◽  
pp. 601 ◽  
Author(s):  
Stanislawa Pukacka ◽  
Ewelina Ratajczak

The ascorbate–glutathione system was studied during development and desiccation of seeds of two Acer species differing in desiccation tolerance: Norway maple (Acer platanoides L., orthodox) and sycamore (Acer pseudoplatanus L., recalcitrant). The results showed remarkable differences in the concentration and redox balance of ascorbate and glutathione between these two kinds of seeds during development, and a significant dependence between glutathione content and acquisition of desiccation tolerance in Norway maple seeds. There were relatively small differences between the species in the activities of enzymes of the ascorbate–glutathione cycle: ascorbate peroxidase (APX, EC 1.11.1.11), monodehydroascorbate reductase (MR, EC 1.6.5.4), dehydroascorbate reductase (DHAR, EC 1.8.5.1), and glutathione reductase (GR, EC 1.6.4.2). At the end of seed maturation, ascorbic acid content and the activities of the above enzymes was about the same in both species The electrophoretic pattern of APX isoenzymes was also similar for both species, and the intensity of the bands decreased at the end of seed maturation in both species. When sycamore seeds were desiccated to a moisture content of less than 26%, there was a marked decrease in seed viability and an increase in the production of reactive oxygen species. During desiccation, Norway maple seeds had a more active defence system, which was reflected in a higher glutathione content, a higher glutathione redox status, a higher ascorbate redox status, and higher activities of APX, MR, DHAR, GR and GPX (glutathione peroxidase). During desiccation, sulfhydryl-to-disulfide transition into proteins was more intense in Norway maple seeds than sycamore seeds. All of these results suggest that, in orthodox seeds, the ascorbate–glutathione cycle plays an important role in the acquisition of tolerance to desiccation, in protein maturation, and in protection from reactive oxygen species.


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