Osmotic regulation of assimilate unloading from seed coats of Vicia faba. Role of turgor and identification of turgor-dependent fluxes

1993 ◽  
Vol 89 (1) ◽  
pp. 87-96 ◽  
Author(s):  
J. W. Patrick
2021 ◽  
Vol 22 (12) ◽  
pp. 6557
Author(s):  
Li-Ying Ren ◽  
Heng Zhao ◽  
Xiao-Ling Liu ◽  
Tong-Kai Zong ◽  
Min Qiao ◽  
...  

Gastrodia elata is a well-known medicinal and heterotrophic orchid. Its germination, limited by the impermeability of seed coat lignin and inhibition by abscisic acid (ABA), is triggered by symbiosis with fungi such as Mycena spp. However, the molecular mechanisms of lignin degradation by Mycena and ABA biosynthesis and signaling in G. elata remain unclear. In order to gain insights into these two processes, this study analyzed the transcriptomes of these organisms during their dynamic symbiosis. Among the 25 lignin-modifying enzyme genes in Mycena, two ligninolytic class II peroxidases and two laccases were significantly upregulated, most likely enabling Mycena hyphae to break through the lignin seed coats of G. elata. Genes related to reduced virulence and loss of pathogenicity in Mycena accounted for more than half of annotated genes, presumably contributing to symbiosis. After coculture, upregulated genes outnumbered downregulated genes in G. elata seeds, suggesting slightly increased biological activity, while Mycena hyphae had fewer upregulated than downregulated genes, indicating decreased biological activity. ABA biosynthesis in G. elata was reduced by the downregulated expression of 9-cis-epoxycarotenoid dioxygenase (NCED-2), and ABA signaling was blocked by the downregulated expression of a receptor protein (PYL12-like). This is the first report to describe the role of NCED-2 and PYL12-like in breaking G. elata seed dormancy by reducing the synthesis and blocking the signaling of the germination inhibitor ABA. This study provides a theoretical basis for screening germination fungi to identify effective symbionts and for reducing ABA inhibition of G. elata seed germination.


1962 ◽  
Vol 2 (3-4) ◽  
pp. 189-194 ◽  
Author(s):  
E.J. Hall ◽  
L.G. Lajtha ◽  
F.A.L. Clowes
Keyword(s):  

2021 ◽  
Author(s):  
Samaneh Roudgarnejad ◽  
Morteza Samdeliri ◽  
Amirabas Mousavi Mirkalaei ◽  
Mojtaba Nasheai Moghaddam

2009 ◽  
Vol 19 (1) ◽  
pp. 3-13 ◽  
Author(s):  
K.M.G. Gehan Jayasuriya ◽  
Jerry M. Baskin ◽  
Carol C. Baskin

AbstractCycling of physically dormant (PY) seeds between states insensitive and sensitive to dormancy-breaking factors in the environment has recently been demonstrated inFabaceaeandConvolvulaceae, and it may be a common phenomenon in seeds with water-impermeable seed coats. In contrast to seeds of many species with physiological dormancy (PD), those with PY cannot cycle between dormancy and non-dormancy (ND). In this paper, we evaluate the role of sensitivity cycling in controlling the timing of germination of seeds with PY in nature, and show that sensitivity cycling in seeds with PY serves the same ecological role as dormancy cycling in seeds with PD. Thus, sensitivity cycling in seeds with PY ensures that germination in nature occurs only at (a) time(s) of the year when environmental conditions for growth are, and are likely to remain, suitable long enough for the plant to complete its life cycle or to form a perennating structure. Further, we describe the experimental procedures necessary to determine whether sensitivity cycling is occurring, and discuss briefly the possible relevance of sensitivity cycling to dormancy classification.


2005 ◽  
Vol 143 (1) ◽  
pp. 43-55 ◽  
Author(s):  
L. W. ZENG ◽  
P. S. COCKS ◽  
S. G. KAILIS ◽  
J. KUO

Changes in the seed coat morphology of 12 annual legumes were studied using environmental scanning electron microscopy (ESEM). The seeds of Biserrula pelecinus L. cv. Casbah, Ornithopus sativus cv. Cadiz, Trifolium clypeatum L., T. spumosum L., T. subterraneum L. cv. Bacchus Marsh, Trigonella balansae Boiss. & Reuter., Trigonella monspeliaca L. and Vicia sativa subsp. amphicarpa Dorthes (morthes.) were examined by ESEM after exposure to field conditions for 6 months, while those of Medicago polymorpha L. cv. Circle Valley, Trifolium clypeatum L., T. glanduliferum Boiss., T. lappaceum L., T. spumosum L., and T. subterraneum L. cv. Dalkeith, were examined after 2 years' exposure. The entry of water into seeds was followed by covering various parts of the seed coat with petroleum jelly and soaking the treated seeds in dyes.As the seeds softened over time, more and larger fractures appeared on the seed coat. Water entered the seed either through fractures, over the seed coat as a whole or through the lens. It is hypothesized that the formation of fractures occurs after physicochemical changes in the seed coat, probably associated with changes in the amount and nature of seed coat lipids.The newly matured whole seeds of M. polymorpha cv. Circle Valley, T. clypeatum, T. glanduliferum, T. lappaceum, T. spumosum, and T. subterraneum cv. Dalkeith were analysed for lipid content in 1997. The seed coats of T. subterraneum cv. Dalkeith and T. spumosum were separated from the cotyledons and examined in detail for lipid content.The lipid content of whole seeds ranged from 48 (T. lappaceum) to 167 mg/g (T. subterraneum cv. Dalkeith). Total lipid of the whole seeds of T. subterraneum cv. Dalkeith and T. glanduliferum declined by about 9 mg/g over 2 years, while in T. spumosum it declined by about 17 mg/g.In contrast, the major fatty acids in the seed coat declined by 0·67 mg/g over the 2 years. Change in seed coat lipids showed a marked similarity to changes in hardseededness for both T. subterraneum cv. Dalkeith and T. spumosum. The results strongly suggest that seed softening is associated with loss of lipids in the seed coat, because lipids have physical characteristics that are altered at temperatures experienced in the field.


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