光敏核不育水稻农垦58S 41 kD蛋白质的N—端序列分析

光敏核不育性受1对或2对或3对隐性主基因控制,这反应了光敏核不育特性遗传机制的复杂性。张端品等用形态标记法将农垦58S光敏核不育基因定位于第5染色体。胡学应和万邦惠用同工酶法以农垦58S/02428 F_2群体为材料,将光敏核不育基因定位于第6和11染色体;Zhang等用RFLP法以32001S/明恢63 F_2群体为材料将不育基因定位于第3和7染色体。这三种方法所得到的定位结果完全不同,综合起来,第3、5、6、7和11染色体均有光敏核不育基因的位点,由此结果可得出两种解释:1.光敏核不育性由多对基因、至少5对基因控制;2.上述定位方法均是以不育(可育)性状在F_2群体中的分离模式为依据,育性划分界线的不同将会造成分离群体中单株表现值的差异,从而影响定位结果的精确性;再者不同实验室使用的材料不一致,已知不同遗传背景和光温条件影响光敏核不育基因的表达。因此,染色体定位结果有待确证。光敏核不育基因在染色体上定位的复杂性和不一致在某种程度上影响了基因克隆和光敏核不育分子机制的研究。无论光敏核不育性的遗传机制如何复杂,上述结果     

水稻感光性和光敏不育性的发育遗传关系

在人工气候室控制的光长与温度下,用光敏不育系7001S与早中熟粳稻(Oryza sativa ssp,japoni-ca)感光性弱的“秋光”、“有芒早粳”和“CPSLO-l7”3个品种分别杂交,分析了杂种F_1、F_2植株育性与感光性的表现,以及两者的关系。结果表明:这3个组合的恢复亲本均属于具两对光敏不育的恢复基因的品种。F_1植株均倾向晚熟亲本,说明控制感光性强的基因属于显性。F_2植株在长日照下表现为不育株的感光性均倾向感光性强的亲本;且有不少不育株为晚熟超亲;在少数弱感光性的植株中没有不育株。说明光敏不育基因与感光性基因关系密切,可能两者有连锁关系,光敏不育基因要在感光性基因表达的基础上才能表达。     

Rapid and efficientAgrobacterium-mediated transformation in rice

An improved protocol forAgrobacterium-mediated transformation of rice is described. The procedure permitted the regeneration of transgenic plants from callus in only two months.     

Gibberellin-induced elongation and osmoregulation in internodes of floating rice

Internodal elongation in floating rice ( Oryza sativa L. cv. Habiganj Aman II) is known to be enhanced by treatment with ethylene or gibberellic acid (GA₃) at high relative humidity (RH). However, ethylene-induced internodal elongation is inhibited at low RH. while GA₃-induced internodal elongation is hardly affected by humidity. We examined the possible involvement of osmoregulation in the stimulation by GA₃ of the elongation of internodes at low RH. Submergence and treatment with ethylene or GA3₃ at 100% RH increased the osmotic potential in internodes of excised stem segments, while GA₃ at 20% RH maintained the osmotic potential at a low level. In internodes of stem segments that had been treated with GA₃ at 20% RH, the activity of invertase and the level of soluble sugars were almost 2- and 1.5-fold higher, respectively, than those in internodes that had been treated with GA₃ at 100% RH. These results indicate that one of the possible mechanisms by which GA₃ promotes elongation of internodes at low RH involves the osmoregulation that is achieved by promotion of the synthesis of invertase.     

Isolation of endophytic diazotrophic bacteria from wetland rice

Endophytic nitrogen-fixing bacteria are believed to contribute substantial amounts of N to certain gramineous crops. We have been interested to find (a) a diazotroph(s) in rice which can aggressively and stably persist and fix nitrogen in interior tissues and (b) unique rice-diazotrophic endophyte combinations. To achieve these objectives, it has been essential to find an efficient method to surface sterilize rice tissues. The method described here consists of exposing tissues to 1% Chloramine T for 15 min followed by shaking with glass beads. It has proven very efficient since (a) surface bacterial populations on the root and culm were found to be reduced by more than 90%, (b) the number of the internal colonizers was found to be significantly higher than the number of surface bacteria, and (c) colonization of root but not subepidermal tissue by gusA-marked Herbaspirillum seropedicae Z67 bacteria was found to be virtually eliminated. Nitrogen-fixing putative endophytic populations (MPN g dry wt) in the root (7.94 × 10) and culm (2.57 × 10) on field-grown IR72 plants grown in the absence of N fertilizer was found to be significantly higher near heading stage. The corresponding total putative endophyte populations in the tissues of 25 highly diverse genotypes of rice and their relatives was found to range from 10–10and 10–10, in the roots and culms, respectively. Generally, the resident bacteria were found to be non-diazotrophic, although in isolated cases diazotrophs were found, for example in the roots and culm of IR72 rice plants, or the culm of Zizaniopsis villanensis plants. The size of populations of diazotrophic bacteria in different rice genotypes was found to be 10–10 for the roots and 10–10 for the culms, respectively. The rice genera-related plants Potamophila pariffora and Rhynchoryza subulata showed the highest levels.     

Effect of potassium nutrition of rice on rhizosphere redox status

With four soils differing in K supplying power and with four rice cultivars (Oryza sativa L.) differing in K uptake kinetic parameters, the relationship between K fertilizer application and soil redox status in rhizosphere and; the distribution of ferrous iron and other toxic substances on the root surface and in the rhizosphere; and the effect of K supply on uptake of reduced iron by rice plants have been studied.The results show that K application on K-deficient soils reduced the content of active reducing substances and ferrous iron in the soil, raised the soil redox potential in the rhizosphere, increased the Eh value of rice roots and lowered the content of iron in the rice plants. These effects of K varied with different rice cultivars. When no K fertilizer was applied, active reducing substances and ferrous iron in rhizosphere soils were decreased more by the rice cultivars absorbing K strongly (e.g. Shanyou 64) than by cultivars absorbing K weakly (e.g. Zhongguo 91). Therefore, the diminution of the toxic substances by K application in the weakly K-absorbing cultivars was more significant.The observation of a rhizobox separated by a nylon screen showed that appreciably more iron oxides, compared with the control, were deposited at or adjacent to the root surfaces of the rice plant supplied with K fertilizer, fully demonstrating the relationship between K nutrition and the total oxidizing power of rice plants. According to the distribution of active reducing substances and ferrous iron, the oxidizing range of the rice root extended in K application treatment a few centimeters away from the root plane. K application to rice affected the soil redox status in rhizosphere in many ways. The main effect was an increase of the oxidizing power of the rice root. As a result, the value of soil Eh was increased, the contents of active reducing substances and ferrous iron were lowered, as well as the number of oxygen consuming microorganisms.     

Effect of gas pressure in the root and stem base zone on methane transport through rice bodies

Ebullition of gas bubbles from the soil surface is, in some cases (e.g., in early growth stage of rice), one of the major pathways for methane transport from rice paddies to the atmosphere. However, the role of the gas phase (entrapped gas) in the paddy soil in plant-mediated methane transport, which is the major pathway for methane emission, has not been clarified. To clarify the effect of the gas phase below ground on the methane emission rate through rice plants, we partly exposed the root and stem base of hydroponically grown rice to a high concentration of methane gas at various gas pressures, and immersed the rest of the roots in a solution with a high methane concentration. The methane emission rate was measured from the top of the rice plant using a flow-through chamber method. The methane emission rate drastically increased with a small increase in gas pressure in the gas phase at the root and stem base zone, with about a 3 times larger emission rate being observed with 10 × 10^-3 atm of extra pressure (corresponding to 10 cm of standing water in rice paddy) compared to no extra pressure. However, when alginate was applied to the stem near the base to prevent contact with the gas phase, the methane emission rate did not increase with increasing gas pressure. On the other hand, from observations in the rice paddy, it was found that the gas is entrapped near the surface (e.g., at a depth of 1 cm) and the gas entrapped in the soil would come into direct contact with a part of the stem near the base of the rice plant. Thus, the gas entrapped in the soil could enter into the rice body directly from the part of the stem near the base which is beneath the soil surface due to gas pressure in the gas phase resulting from the pressure exerted by the standing water. Hence, this mechanism involving the entrapped gas could play an important role in methane emission from rice paddy by affecting the plant-mediated methane transport as well as ebullition of gas bubbles.     

The dependence of methane transport in rice plants on the root zone temperature

Large diurnal and seasonal variations in methane flux from rice paddies have been found in many studies. Although these variations are considered to result from changes in methane formation rates in the soil and the transport capacity (e.g. biomass, physiological activities, and so on) of rice plants, the real reasons for such variations are as yet unclear. This study was conducted to clarify the effects of temperature on the rate of methane transport from the root zone to the atmosphere using hydroponically grown rice plants. Methane emission rates from the top of the rice plants whose roots were soaked in a solution with a high methane concentration were measured using a flow-through chamber method with the top or root of the rice plants being kept at various temperatures. The methane emission rates and methane concentrations in solution were analyzed using a diffusion model which assumes that the methane emission from a rice paddy is driven by molecular diffusion through rice plants by a concentration gradient. In the experiment where the temperature around the root was changed, the conductance for methane diffusion was typically 2.0-2.2 times larger when the solution temperature was changed from 15 to 30 °C. When the air temperature surrounding the top of the rice plant was changed, the change in conductance was much less. In addition, from measurements of methane flux and methane concentration in soil water in a lysimeter rice paddy during the 2 growing seasons of rice, it was found that the conductance for methane transport was correlated with the soil temperature at 5 cm depth. These results suggest that the temperature around the root greatly affects the methane transport process in rice plants, and that the process of passing through the root is important in determining the rate of methane transport through rice plants.     

Physiological nitrogen efficiency in rice: Nitrogen utilization,photosynthesis, and yield potential

Characteristics of rice (Oryza sativa) as a crop plant are briefly introduced, and the relationship between formation of yield potential and nitrogen (N) nutrition is described on the basis of studies using 15N as a tracer. In addition, the relationship between the leaf photosynthetic capacity and leaf N, and the factors limiting leaf photosynthesis under different growth conditions are reviewed. Finally, targets for improving rice yield potential are discussed with a focus on the role of increased photosynthesis efficiency in relation to leaf N status and the photosynthetic components in the leaves.     

Phototropism of rice (Oryza sativa L.) coleoptiles: fluence-response relationships, kinetics and photogravitropic equilibrium

Phototropism of rice (Oryza sativa L.) coleoptiles induced by unilateral blue light was characterized using red-light-grown seedlings. Phototropic fluence-response relationships, investigated mainly with submerged coleoptiles, revealed three response types previously identified in oat and maize coleoptiles: two pulse-induced positive phototropisms and a phototropism that depended on stimulation time. The effective ranges of fluences and fluence rates were comparable to those reported for maize. Compared with oats and maize, however, curvature responses in rice were much smaller and coleoptiles straightened faster after establishing the maximal curvature. When stimulated continuously, submerged coleoptiles developed curvature slowly over a period of 6 h, whereas air-grown coleoptiles, which showed smaller phototropic responsiveness, established a photogravitropic equilibrium from about 4 h of stimulation. The plot of the equilibrium angle against log fluence rates yielded a bell-shaped optimum curve that spanned over a relatively wide fluence-rate range; a maximal curvature of 25° occurred at a fluence rate of 1 μmol · m⁻² · s⁻¹. This optimum curve apparently reflects the light sensitivity of the steady-state phototropic response. Received: 28 June 1996 / Accepted: 30 July 1996