Proteomic Analysis of Desiccation Tolerance and Its Re-Establishment in Different Embryo Axis Tissues of Germinated Pea Seeds

Author(s):  
Wei-Qing Wang ◽  
Yue Wang ◽  
Xian-Jun Song ◽  
Qi Zhang ◽  
Hong-Yan Cheng ◽  
...  
Botany ◽  
2021 ◽  
Author(s):  
Jiajin Li ◽  
Ganesh K. Jaganathan ◽  
Han Kang ◽  
Baolin Liu

In many -but not all- recalcitrant Quercus seeds, water loss during drying only occurs through the scar. Consequently, the embryo axis sitting on the opposite side of the scar is well protected from desiccation. However, whether such a mechanism is common throughout Fagaceae species is unexplored. Similarly, little is known about the desiccation response of other Fagaceae genera. Germination and desiccation tolerance of Castanopsis sclerophylla (Fagaceae) were studied by drying the seeds with silica gel. Fresh seeds had a moisture content (MC) of 36% and germinated to 92.5% when incubated at 15/20°C. Drying seeds to 22.5 and 20.7% MC decreased germination to 27 and 5%, respectively; indicating that seeds are recalcitrant. X-ray computed tomography and photomicrographs showed that the embryo axis of C. sclerophylla is located just below the scar. Regardless of drying occurring either through only scar or the whole pericarp, embryo drying was deemed unavoidable. Nevertheless, germination percentage during drying showed exceptional similarities with the other Fagaceae species.


1995 ◽  
Vol 5 (4) ◽  
pp. 185-193 ◽  
Author(s):  
Ellen H. Baker ◽  
Kent J. Bradford ◽  
John A. Bryant ◽  
Thomas L. Rost

AbstractDehydrin and QP47, proteins present in mature pea seeds (Pisum sativum), have been proposed to play protective roles during desiccation. To identify possible relationships between these proteins and desiccation tolerance, their tissue locations and patterns of synthesis and degradation have been examined during germination. Tissue locations were determined by immunocytochemistry using polyclonal antibodies raised against a conserved dehydrin amino acid sequence and against purified QP47. In embryonic axis and cotyledon cells, QP47 and dehydrin were distributed uniformly with no apparent nuclear or organellar specificity. Both proteins were present in 24 h-imbibed axes that had not initiated radicle growth but were completely absent from 24 h-imbibed axes that had begun to grow. The amounts of QP47 and dehydrin in embryonic axes decreased with time after the start of imbibition and were undetectable by 48 h. When germination was prevented by polyethylene glycol (PEG) or abscisic acid (ABA), both proteins remained at their original amounts. Thus, both QP47 and dehydrin disappeared coincidently with the beginning of growth and not simply as a function of the time after imbibition. QP47 persisted in cotyledons until at least 31 days into seedling growth, whereas dehydrin was not detectable in cotyledons after 7 days. Dehydrin, but not QP47, could be re-induced in pea shoots and cotyledons by dehydration. The timing of degradation of both proteins was correlated with the loss of desiccation tolerance during germination of pea axes.


2011 ◽  
Vol 144 (1) ◽  
pp. 20-34 ◽  
Author(s):  
Wei-Qing Wang ◽  
Hong-Yan Cheng ◽  
Ian M. Møller ◽  
Song-Quan Song

1995 ◽  
Vol 5 (2) ◽  
pp. 117-120 ◽  
Author(s):  
Robert J. Williams ◽  
A. Carl Leopold

AbstractAn element of storage stability of many orthodox seeds is that the embryo cytoplasm is vitreous at normal storage temperatures. That is, as drying proceeds during seed maturation, intracellular solutions become so concentrated and viscous that diffusional movement is all but eliminated (Williams and Leopold, 1989). In this report the relationship between desiccation tolerance and the ability to form the vitreous state as germination proceeds is examined. As pea seeds (Pisum sativum cv. Alaska) imbibed water up to 18 h, no change in the glass transition temperature was seen, and the embryos remained desiccation-tolerant. Between 18 and 44 h of imbibition, the axes lost the ability to exhibit a distinguishable vitreous transition, and the embryos had lost the ability to survive desiccation. After about 50 h, embryos again showed vitrification but only at markedly lower temperatures, as would be expected to accompany the loss of oligosaccharides (sucrose, raffinose, stachyose and verbascose) and their replacement by monosaccharides during early germination (Koster and Leopold, 1988). Thus, the loss of desiccation tolerance during germination in pea seeds appears to be associated with a loss of the high temperature oligosaccharide: water glass and a subsequent appearance of a new glass transition at a lower temperature resulting from the accumulation of monosacchrides.


2010 ◽  
Vol 9 (12) ◽  
pp. 6561-6577 ◽  
Author(s):  
Xiaonan Wang ◽  
Sixue Chen ◽  
Heng Zhang ◽  
Lei Shi ◽  
Fenglin Cao ◽  
...  

2000 ◽  
Vol 10 (3) ◽  
pp. 329-339 ◽  
Author(s):  
Françoise Corbineau ◽  
Mari Ange Picard ◽  
Jean-Albert Fougereux ◽  
Fabienne Ladonne ◽  
Daniel Côme

Germination and carbohydrate metabolism were studied in fresh developing pea (Pisum sativum L., cv Baccara) seeds and after artificial drying at 25°C and various relative humidities (20, 75 and 99% RH) to investigate whether the occurrence of desiccation tolerance was related to sucrose, raffinose and stachyose contents. Seeds became completely tolerant to fast drying at 25°C and 20% RH a few days after the end of reserve accumulation, i.e. when their moisture content dropped to approx. 50% (fresh weight basis). This acquisition of desiccation tolerance was associated with an accumulation of raffinose and stachyose, the latter being more abundant in the embryonic axis than in the cotyledons. The (raffinose+stachyose)/sucrose ratio increased during seed development and reached 1.1 in the axis and 0.2 in the cotyledons just before the onset of desiccation tolerance. When the natural acquisition of desiccation tolerance occurred on the mother plant, artificial drying of isolated seeds induced an increase in oligosaccharide content in the cotyledons. Immature seeds, the moisture content of which was higher than about 60% (fresh weight basis), did not tolerate fast drying (25°C and 20 or 75% RH). Such drying did not result in the synthesis of stachyose and induced an increase in electrolyte leakage, a decrease in the ability of seeds to convert 1-aminocyclopropane 1-carboxylic acid (ACC) to ethylene and an increase in ethane synthesis, thus indicating a deterioration of cell membrane properties and lipid peroxidation. In contrast, immature seeds tolerated drying either in the pods or at 25°C and 99% RH, and such drying induced a decrease in sucrose content, an increase in oligosaccharide content and a (raffinose+stachyose)/sucrose ratio higher than around 1. Soluble sugar contents of dried immature seeds depended on the conditions of dehydration. In cotyledons, the (raffinose+stachyose)/sucrose ratio reached 0.61 when seeds were dried at 25°C and 99% RH, whereas it was as low as 0.15 when drying was performed at 25°C and 20% RH. All the results obtained are consistent with the concept that oligosaccharides may well be involved in the protection of membranes during dehydration.


2007 ◽  
Vol 177 (4S) ◽  
pp. 297-297
Author(s):  
Kristina Schwamborn ◽  
Rene Krieg ◽  
Ruth Knüchel-Clarke ◽  
Joachim Grosse ◽  
Gerhard Jakse

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