Control of cocklebur seed germination by nitrogenous compounds : Nitrite, nitrate, hydroxylamine, thiourea, azide and cyanide

Germination of non-dormant upper cocklebur (Xanthium pinsylvanicumWallr.) seeds was stimulated by not only CS(NH₂)₂ but also NH₂OH,KCN and NaN₃. This stimulation was not via the enhancement ofaerobic C₂H₄ production. NH₂OH, KCN and NaN₃ in certain concentrationspromoted the initial growth of axial and/or cotyledonary parts,but the degree of growth promotion by NH₂OH, NaN₃ and KCN wasslight compared with that by CS(NH₂)₂. As in the case of CS(NH₂)₂,however, the germinationstimulating effect of NH₂OH disappearedrapidly as the preceding imbibition period was prolonged. Incontrast, KCN and NaN₃ were still effective in stimulating thegermination of aged seeds maintained on a water substratum,as previously seen with anaerobiosis. Anaerobic induction wasenhanced not only by NaN₃ and KCN but also by NH₂OH, KNO₃, KNO₂CO(NH₂)₂ and CS(NH₂)₂ applied during the anaerobic treatment,but without causing an increase in anaerobic production of C₂H₄.Furthermore, KCN and NaN₃, given prior to the anaerobic treatmentacted additively with anaerobic induction. The germination-stimulatingactions of nitrogenous compounds are discussed in comparisonwith those of C₂H₄ and anaerobiosis. (Received May 6, 1978; )     

Seed dormancy in red rice. X. A 13C-NMR study of the metabolism of dormancy-breaking chemicals

The metabolism of organic dormancy-breaking chemicals is poorly defined and may provide clues to their mode of action. Therefore, hydrated, dormant seeds of red rice ( Oryza sativa L.) were exposed to dormancy-breaking treatments of propionate-2-¹³C (22 m W ) or propanol-1-¹³C (75 m M ) for 24 h at 30°C. Embryo extracts were analyzed by ¹³C-nuclear magnetic resonance spectroscopy. Metabolism of propionate and propanol to 3-hydroxypropionate, an intermediate of the modified β-oxidation pathway, was detected after 2 and 4 h, respectively. This occurred prior to the onset of dormancy-breaking which required 12 h of chemical exposure. Accumulation of 3-hydroxypropionate was rapid and linear in the embryos of propionate-treated seeds. In the embryos of propanol-treated seeds, the level of 3-hydroxypropionate reached a plateau at 4 h. Following 24 h of contact with propionate, labeled citrate was detected in the embryos. The decrease in tissue pH associated with the dormancy-breaking process was fully accounted for by direct acid uptake and metabolic production of 3-hydroxypropionate.     

Seed dormancy in Acer: Endogenous germination inhibitors and dormancy in Acer pseudoplatanus L.

Summary Dormant seeds of Acer pseudoplatanus L. contain two zones of inhibition on paper chromatograms in 10:1:1 as detected by the lettuce and cress seed germination, and the wheat coleoptile bioassays. One zone at R_f 0.6–0.8 was partitioned into ethyl acetate at acid pH and was shown to contain ABA by its behaviour on GLC and isomerization under ultra-violet light. The other zone at R_f 0.9 was detected only in the germination bioassays and was partitioned into ethyl acetate over a range of pH indicating the presence of one or more neutral compounds.The inhibitors present in the embryo of dormant sycamore seeds inhibited the germination of non-dormant sycamore seeds at relatively low concentrations. A comparison with the effects of application of exogenous ABA indicated that endogenous ABA could not solely account for the inhibitory activity of seed extracts, which appeared to be due partly to the presence of ABA and partly to that of neutral compounds present in the embryo. Leaching treatments that removed dormancy led to a decrease in the level of inhibitors present mainly in the basic fraction. The exogenous application of kinetin to dormant sycamore seeds increased germination whereas gibberellic acid had no effect. Similar responses were obtained with lettuce seeds inhibited by the basic fraction of dormant sycamore seeds.It is suggested that an inhibitor-cytokinin interaction may be involved in the dormancy of sycamore seeds.     

Dormancy in red rice. IV. Response of unimbibed and imbibing seeds to nitrogen dioxide

Nitrogen dioxide at 4 to 8 ml 1⁻¹ breaks dormancy of dehulled, unimbibed seeds of red rice ( Oryza sativa L.) with minimum exposure times to the gas of 20 min or less. The response is independent of incubation medium pH following treatment. Germination is complete within 2 days but proceeds 4 to 6 h more slowly than non-dormant controls. The magnitude of response at a constant NO₂ dose is dependent upon initial seed moisture. There was less than 40% germination at 9.6% initial moisture while germination was 95% at 12% initial moisture. NO₂ treatment also breaks dormancy of imbibing, dehulled seeds, but the response is dependent upon the pH of the medium. Dormancy is broken at pHs close to the pK_a of nitrous acid. Intact, unimbibed or imbibing seeds respond to NO₂ treatment only if partially dry-afterripened prior to exposure.     

On the role of abscisic acid in seed dormancy of red rice

Abscisic acid (ABA) is commonly assumed to be the primary effector of seed dormancy, but conclusive evidence for this role is lacking. This paper reports on the relationships occurring in red rice between ABA and seed dormancy. Content of free ABA in dry and imbibed caryopses, both dormant and after-ripened, the effects of inhibitors, and the ability of applied ABA to revert dormancy breakage were considered. The results indicate: (i) no direct correlation of ABA content with the dormancy status of the seed, either dry or imbibed; (ii) different sensitivity to ABA of non-dormant seed and seed that was forced to germinate by fluridone; and (iii) an inability of exogenous ABA to reinstate dormancy in fluridone-treated seed, even though applied at a pH which favoured high ABA accumulation. These considerations suggest that ABA is involved in regulating the first steps of germination, but unidentified developmental effectors that are specific to dormancy appear to stimulate ABA synthesis and to enforce the responsiveness to this phytohormone. These primary effectors appear physiologically to modulate dormancy and via ABA they effect the growth of the embryo. Therefore, it is suggested that ABA plays a key role in integrating the dormancy-specific developmental signals with the control of growth.     

Hydrogen cyanide and embryonal dormancy in apple seeds

Embryos of apple ( Malus domestica Borh. cv. Antonówka) were treated with 1 m M gaseous HCN for 6 h and cultured under a 12 h photoperiod. HCN pretreatment stimulated germination, increased the length of hypocotyls, shortened the main root and decreased the percentages of seedlings with asymmetrically grown as well as with asymmetrically greened cotyledons. High activity of β-cyanoalanine synthase (EC 4.4.1.9) and a sharp increase in cyanogen content during embryo culture suggested very low levels of endogenous HCN. despite the activity of HCN releasing enzymes. The obtained data allow us to postulate an important role for cyanide in the regulatory complex controlling dormancy in apple seeds. Experiments with respiratory inhibitors indicated, however, that HCN pretreatment affected neither the alternative electron transport pathway nor residual respiration.     

Formate dehydrogenase. Subunit and mechanism of inhibition by cyanide and azide.

Formate dehydrogenase (EC 1.2.1.2) prepared from peas (Pisum sativum) was a two-subunit enzyme. The enzyme accelerated the formation of an NAD+-cyanide compound having an adsorption band at 330 nm. The enzyme was able to bind one NAD+ molecule per each subunit but only 1 mole of NAD+-cyanide compound was formed per two subunits. The complex of NAD+, cyanide, and the enzyme was very stable and had no catalytic activity. Azide inhibited the formate dehydrogenase reaction in two different ways. By incubation of the enzyme with azide in the presence of NAD+, half of its catalytic activity was lost. The remaining activity was also inhibited by azide but this inhibition was removed competively by formate. Contrary to the case of cyanide the inhibition by azide could be removed by dialysis and no spectral species due to the addition compound of NAD+ and azide could be observed. The data from double recipricol plots of the initial velocity and the formate concentration led to a conclusion that formate dehydrogenase has two sites with about equal catalytic activity. The Km for formate was different for the two catalytic sites (1.67 and 6.25 mM) but the difference was not noticeable in the case of the Km for NAD+.     

Ethylene production is associated with germination but not seed dormancy in red rice

BACKGROUND AND AIMS: The relationship between ethylene production and both seed dormancy and germination was investigated using red rice (weedy rice) as a model species. METHODS: Both fully dormant and after-ripened (non-dormant) naked caryopses were incubated with or without inhibitors of ethylene synthesis [aminoethoxyvinylglycine (AVG)] and perception [silver thiosulfate (STS)], or in the presence of the natural ethylene precursor 1-aminocyclopropane-1-carboxylic acid (ACC). The kinetics of ethylene emissions were measured with a sensitive laser-photoacoustic system. KEY RESULTS: Dormant red rice caryopses did not produce ethylene. In non-dormant caryopses, ethylene evolution never preceded the first visible stage of germination (pericarp splitting), and ethylene inhibitors completely blocked ethylene production, but not pericarp splitting. Accordingly, endogenous ACC appeared to be lacking before pericarp splitting. However, early seedling growth (radicle or coleoptile attaining the length of 1 mm) followed ethylene evolution and was delayed by the inhibitors. Wounding the dormant caryopses induced them to germinate and produce ethylene, but their germination was slow and pericarp splitting could be speeded up by ethylene. CONCLUSIONS: The findings suggest that, in red rice, endogenous ethylene stimulates the growth of the nascent seedling, but does not affect seed dormancy or germination inception. Correspondingly, this phytohormone does not play a role in the dormancy breakage induced by wounding, but accelerates germination after such breakage has occurred.     

Seed germination and dormancy responses to acetone condensation products

Acetone condensation products reported to have growth regulatingproperties were tested for their effects on seed germination.The active compounds—isoxylitones, isophorone, diacetonealcohol and phorone inhibited seed germination. The degree ofinhibition depends on the particular compound, its concentration,and the light and temperature environment of the imbibed seeds.Germination studies involving light quality, light energiesand temperature, and light microscope studies indicated little,if any, penetration of the chemicals into the seed but rathersurface effects. The results suggest that the chemicals inducedmembrane impermeability which was partially relieved by redlight and by a brief high-temperature treatment. (Received May 10, 1976; )     

Seed germination and dormancy: The classic story,new puzzles,and evolution

This review highlights recent progresses in seed germination and dormancy research.Research on the weakening of the endosperm during germination,which is almost a classic theme in seed biology,was resumed byα-xylosidase studies.Strong genetic evidence was presented to suggest that the quality control of xyloglucan biosynthesis in the endosperm(and the embryo)plays a critical role in germination.Further analyses on the endosperm and the adjace nt layers have suggested that the cutin coat in the endosperm-testa interphase negatively affects germination while the en dosperm-embryo in terphase produces a sheath that facilitates germination.These progresses significantly advanced our understanding of seed germination mechanisms.A breakthrough in dormancy research,on the other hand,revealed the unique abscisic acid signaling pathway that is regulated by DELAY OF GERMINATION1(DOG1).The detailed analysis of DOC1 expression uncovered the intriguing story of reciprocal regulation of the sensean tisense pair,which gen erated new questions.Recent studies also suggested that the DOG1 function is not limited to dormancy but extended through general seed maturation,which provokes questions about the evolution of DOG1 family proteins.Seed biology is becoming more exciting with the classic stories being revitalized and new puzzles emerging from the frontier.     

Polymer-supported silyl cyanide and silyl azide: useful reagents for solid-phase applications

The support of a delicate reagent on a solid matrix allows for better and safer handling of the reagent itself. Because we had an interest in silicon-based supported reagents(1) we turned our attention to a polymer-supported trialkylsilyl cyanide and trialkylsilyl azide starting from a commercially available trialkylsilane resin. The supported cyanide was obtained with excellent yield and proved to be shelf-stable. This supported reagent was reacted with a series of aldehydes and ketones yielding the corresponding polymer-supported cyanohydrins in good-to-excellent yields. A stability study on a model cyanohydrin demonstrated that these supported intermediates also can be stored for a prolonged time. For the last step, a cleavage strategy that could release either cyanohydrins or alpha-hydroxy esters was adopted. Finally, we prepared a polymer-supported trialkylsilyl azide, which also proved to be shelf-stable.     

Seed dormancy in relation to seed storage behaviour in Acer

Dormancy in seeds of Acer opalus is shown to be mainly caused by the seed coats, although a slight embryo dormancy exists in fresh seeds. The ability to germinate after drying indicates that seed storage behaviour is orthodox. Recalcitrant seeds were heavier than orthodox seeds not only within section Acer but also within the whole genus after statistical control of phylogeny, through a phylogenetic ANOVA with data from two different Acer phylogenies. An evolutionary change from orthodox to recalcitrant behaviour is postulated for genus Acer , but this change appears not to have been accompanied by a change in seed dormancy, at least in the taxonomic section in which Acer opalus belongs.  © 2004 The Linnean Society of London, Botanical Journal of the Linnean Society , 2004, 145 , 203–208.     

Seed dormancy in Rumex species in response to environmental factors

Abstract. Many Rumex species show similar seed dormancy characteristics but there is more information concerning R. crispus and R. obtusifolius than other species. These species respond positively to red or white light. Far-red light applied for short periods may promote or inhibit germination depending on the timing of the irradiation in relation to temperature change; but long periods of far-red inhibit germination. Seeds may also be stimulated to germinate in the dark by low-temperature stratification at 15°C or less providing the temperature of the seeds is subsequently raised to a minimum of about 15°C. Seeds can, however, germinate at lower temperatures providing they have received other appropriate stimulatory treatment. Seeds also respond to alternating temperatures. In a diurnal cycle the minimum upper temperature required is about 15°C and the maximum lower temperature is about 25°C. The optimum period spent at the upper temperature is about 8 h when it is 15–25°C but the optimum period decreases as the upper temperature is increased above this range so that at 45°C, for example, it is only about 30 min. The period spent at the lower temperature in a diurnal cycle is not critical. Providing these criteria are met, the percentage germination increases with the number and amplitude of the cycles. The warming part of the cycle is necessary for the response but so far there is no convincing evidence that cooling itself is important. Secondary dormancy is induced at constant temperatures at a rate dependent on temperature, but apparently only in the presence of oxygen. This feature affects the optimum timing of a temperature change or exposure to light. Strong positive interactions are shown between stimulatory temperature treatments and white or red light. Unlike many other weed species the seeds respond only slightly to nitrate ions. The implications of these responses are discussed in relation to field behaviour.     

Seed Dormancy in Red Rice : III. Response to Nitrite, Nitrate, and Ammonium Ions

Sodium nitrite at 10 millimolar breaks dormancy of dehulled red rice (Oryza sativa). While germination is light independent, low pH conditions (pH 3) are required for maximum response. Water and buffer controls at pH 3 remain dormant. The response to nitrite occurs at 25 and 30°C but is reduced at 20°C, although nondormant seeds germinate readily at this temperature. The contact time for response to nitrite is less than 2 h at the start of imbibition. Seeds imbibed first in water show reduced germination when subsequently transferred to nitrite. Dehulled seeds show little or no response to nitrate and ammonium ions.

Intact seeds remain dormant in the presence of nitrite or nitrate unless partially dry-afterripened. The pH dependence of nitrite sensitivity is reduced in intact, afterripening seeds. In highly dormant seeds, vacuum infiltration experiments suggest that the hull restricts uptake of nitrite.