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1.
 为了探明水稻胚乳发育的过程和糊粉层形成的机理, 用光学显微镜和电子显微镜观察了水稻糊粉层细胞和内胚乳细胞在颖果发育过程中的结构变化,用能谱仪分析了胚乳细胞中元素的种类和相对含量。结果表明, 糊粉层细胞是由胚乳表层细胞转化而来的。糊粉层细胞中的P、K、Mg和Ca等矿质元素含量要明显高于内胚乳细胞。发育初期糊粉层细胞中富含线粒体、圆球体和小液泡;发育中后期小液泡积累蛋白质和矿质元素而形成糊粉粒。在发育中后期,内胚乳细胞随着细胞内淀粉体的充实,细胞核发生形变而衰亡;而糊粉层细胞的核在发育过程中不消亡。糊粉层的形成与表层细胞积聚矿质和脂类等“灌浆废物”(指非内胚乳细胞的贮藏物)有关。因而,转运灌浆物质多的胚乳背部,其糊粉层细胞的层数要比腹部和侧部多。谷物胚乳发育分为游离核期、细胞化期、分化期和成熟期四个时期。  相似文献   

2.
为直观揭示施氮对小麦籽粒灌浆的生理效应,以徐麦30(强筋小麦) 和扬麦13(弱筋小麦)为材料,采用树脂包埋样品进行半薄切片和Image Pro Plus图像分析软件从形态学角度研究了孕穗期施氮对小麦颖果腹部和背部胚乳细胞物质充实的影响。结果表明,施氮后颖果腹部和背部胚乳细胞蛋白体数目增加,花后11、15和19 d最显著,同时蛋白体的聚集方式发生改变,对照组(不施氮)胚乳细胞内以小蛋白体为主,呈散状分布,而施氮组胚乳细胞含有许多大蛋白体或蛋白聚积体,分布较为集中。徐麦30蛋白体发育对氮素的响应程度高于扬麦13。施氮后腹部胚乳细胞淀粉粒排列更为紧密,细胞充实率增加,且扬麦13的响应程度大于徐麦30。施氮也增加了徐麦30背部胚乳细胞充实率,而对扬麦13的影响表现相反。  相似文献   

3.
四个不同粒重水稻品种颖果发育的比较   总被引:2,自引:0,他引:2  
 以粒重差异较大的4个水稻品种为供试材料,采用树脂切片、酶解胚乳细胞和显微观察等方法,比较研究了品种间在颖果生长、胚乳细胞增殖、果皮和胚乳结构等方面的差异,探讨了影响颖果生长的因素。 大粒品种颖果发育时间较小粒品种长,其胚乳细胞数、胚乳干质量及单个胚乳细胞平均干质量均高于小粒品种。在粒重相近的情况下,籼稻颖果发育和淀粉积累快于粳稻。与小粒品种相比,大粒品种子房壁细胞中淀粉粒多,子房壁细胞生长的持续时间长,果皮及背部维管束衰亡迟。 小粒品种胚乳外层细胞在花后7 d已转化成糊粉层细胞,大粒品种胚乳外层细胞要在花后10 d才转化成糊粉层细胞。 大粒品种的库容大和生理活性期长是其颖果能显著增大的生理原因。  相似文献   

4.
小麦强弱势粒胚乳淀粉体和蛋白体发育及物质积累研究   总被引:1,自引:0,他引:1  
为探明小麦强弱势粒发育的差异,以大穗型小麦品种宁麦13为材料,采用半薄切片、组织染色和生理生化测定等方法比较研究了小麦强弱势粒胚乳淀粉体和蛋白体的发育及物质积累过程。结果表明,在小麦颖果发育过程中,强势粒的形态大小始终大于弱势粒,在花后3~11d表现尤为明显;与弱势粒相比,强势粒的胚乳尤其是背部胚乳中淀粉体和蛋白体的相对面积较大,充实度较高,胚乳质地更致密;强势粒的B型淀粉粒多于弱势粒,强、弱势粒的淀粉粒径分布均呈单峰型,强势粒中0~2μm的淀粉粒数显著高于弱势粒,在其他粒径范围两者无显著差异;与弱势粒相比,强势粒中总淀粉、蛋白质、醇溶蛋白、谷蛋白和支链淀粉含量均较高,而直链淀粉含量较低。由此可见,小麦弱势粒发育不良与胚乳淀粉体和蛋白体发育及物质积累密切相关。  相似文献   

5.
小麦胚乳发育过程中贮藏蛋白的积累和蛋白体的形成   总被引:3,自引:0,他引:3  
为给小麦品质育种提供参考,采用光学和电子显微镜技术系统观察了小麦品种扬麦12号胚乳发育过程中贮藏蛋白的积累和蛋白体的形成.结果表明,花后8 d的淀粉胚乳细胞开始出现贮藏蛋白颗粒.贮藏蛋白在粗内质网上合成后,有些经过高尔基体形成浓密小泡,有些直接在粗内质网腔中积累,脱离内质网形成蛋白体;浓密小泡和蛋白体进入蛋白贮藏液泡(PSV).早期的蛋白体较小,呈球状;随着胚乳发育,蛋白体可以相互融合,扩大体积.后期的蛋白体相互融合形成蛋白质基质,单个蛋白体不再存在;接近成熟期的胚乳,胚乳细胞被贮藏物质淀粉粒和蛋白质基质所充实,蛋白质基质分布在淀粉粒之间的空隙内.试验结果说明,贮藏蛋白从内质网到PSV的转运有两种途径:依赖高尔基体途径和内质网衍生出蛋白体途径.  相似文献   

6.
不同类型专用小麦品种胚乳发育的比较研究   总被引:1,自引:0,他引:1  
为揭示不同类型专用小麦品种胚乳发育的差异,以强筋小麦皖麦38和弱筋小麦扬麦9号为材料,比较了两者胚乳细胞游离核分裂状况、细胞数目的增殖变化、细胞体积的变化、糊粉层发育、淀粉体和蛋白质体发育等内容,主要结果如下:(1)皖麦38游离核有丝分裂所占比例较大,扬麦9号无丝分裂所占比例较大,且受温度影响较大;(2)胚乳细胞增殖均呈"S"型曲线变化,皖麦38胚乳细胞增殖较快,胚乳体积较大,最终粒重较高;(3)皖麦38胚乳细胞中大淀粉体数目多于扬麦9号,而小淀粉体数目表现却相反;(4)皖麦38与扬麦9号相比较,糊粉层出现时间较晚,而且糊粉层细胞壁较厚,被甲苯胺蓝染色更浓;(5)成熟籽粒中淀粉粒形状有饼形、椭圆形和近圆球形三种。皖麦38胚乳中饼形和椭圆形淀粉粒较多,且相互结合较紧密;扬麦9号饼形和近球形淀粉粒较多,胚乳结构疏松。  相似文献   

7.
小麦胚乳传递细胞发育的结构观察   总被引:1,自引:0,他引:1  
为从细胞学方面了解小麦产量和品质的形成机制,以扬麦5号为材料,利用光镜和透射电镜观察了小麦颖果发育过程中胚乳传递细胞的结构变化,并探讨了胚乳传递细胞的生理功能。结果表明:(1)胚乳传递细胞是胚乳发育过程中最早分化的细胞类型,它们发生在紧邻胚乳腔的胚乳表层,由位于外侧1~2层糊粉层传递细胞和位于内侧1~2层内胚乳传递细胞构成;(2)颖果发育成熟时,内胚乳传递细胞核衰亡,糊粉层传递细胞核依然完整;(3)胚乳传递细胞发育呈明显的极性,且具时空性;(4)糊粉层传递细胞胞质较浓,富含粗面内质网、线粒体、高尔基体和脂质体;质膜皱褶,在局部区域外翻,形成众多的原生质管;(5)内胚乳传递细胞胞质较稀,液泡化程度较高,富含淀粉体;(6)胚乳传递细胞未加厚以及未形成壁内突的壁区域分布有大量的胞间连丝;(7)胚乳传递细胞中线粒体呈极性分布,即质膜附近线粒体的密度较大。根据胚乳传递细胞的结构特点推测,经胚乳传递细胞的养分输送既可通过质外体途径又可通过共质体途径来完成。  相似文献   

8.
以农乐988和扬糯1号两个品种的玉米颖果为材料,利用树脂半薄切片、组织化学染色及生理测定等方法研究胚乳组织和细胞的发育过程。结果表明,两个玉米品种粒重及淀粉含量的变化呈S形生长曲线;可溶性糖变化呈单峰曲线,授粉后12 d含量最高;总蛋白含量在授粉后6 d较高。颖果粒重和总蛋白含量农乐988>扬糯1号;可溶性糖及淀粉含量扬糯1号>农乐988。授粉后0~2 d胚乳处在游离核期,授粉后3~5 d胚乳处在细胞化期,授粉6 d以后胚乳细胞开始分化,内胚乳细胞出现淀粉体和蛋白体。胚乳中淀粉的积累由颖果顶端向基部、由胚乳外层向中央推进。扬糯1号胚乳发育较提前,失活较晚;农乐988胚乳发育相对滞后,失活较早。玉米胚乳发育和颖果发育关系紧密,胚乳游离核期和细胞化期相当于颖果形成期,胚乳分化期相当于颖果乳熟期,胚乳成熟期相当于颖果蜡熟期与完熟期。  相似文献   

9.
植物最外层胚乳细胞在种子发育过程中分化为糊粉层细胞,其在形态和生理功能上均显著区别于内胚乳细胞。与淀粉胚乳不同,糊粉层富含蛋白质、脂类、维生素、膳食纤维、矿质元素和抗氧化物等多种营养物质。同时,在种子萌发过程中,糊粉层细胞能够分泌淀粉酶和蛋白酶分解种子内积累的储藏物质,为种子萌发提供能量。目前利用突变体材料,克隆了一些控制糊粉层细胞分化的关键基因,相关研究极大深化了我们对糊粉层细胞命运决定的认识。同时,由于糊粉层富含各种营养物质,增加糊粉层细胞层数可以作为改良谷物营养品质的一个重要手段。本文主要以水稻及其他谷类作物为例,系统介绍了糊粉层细胞分化和发育的过程,并对其遗传调控机制进行总结梳理,同时对利用糊粉层相关性状进行稻米品质改良可能存在的问题及其对策进行了探讨。  相似文献   

10.
 利用荧光显微术观察,发现同源四倍体水稻与其二倍体原种的糊粉层细胞壁纤维素物质都存在一个“充实”的过程。授粉后5~6 d,糊粉层开始分化形成,此时其细胞壁上未观察到纤维素物质;授粉后6~8 d,糊粉层细胞壁上开始积累纤维素物质;授粉后8~9 d,糊粉层细胞壁积累了大量的纤维素物质。胚乳淀粉的积累存在一个变化的过程:初生胚乳核周围可见一些淀粉体,随着胚乳游离核的增多,游离核周围淀粉体的数量逐渐减少,胚乳细胞化后,胚乳细胞内开始大量形成淀粉体。利用苯胺蓝染色连续切片荧光观察,发现同源四倍体水稻及其二倍体原种胚乳发育过程中,在珠心表皮和内珠被之间存在一层胼胝质物质,围绕着胚囊并包裹住珠心呈“套”状。这个结构的形成变化过程为:授粉后30 min在珠孔端珠心表皮细胞与内珠被之间开始积累少量的胼胝质,之后胼胝质逐渐增多并向合点端扩展延伸;授粉后1~2 d包裹着整个胚囊外的珠心而仅在维管束处断开;授粉后9~13 d,胼胝质“套”消失。该结构可能与胚和胚乳在发育期间的水分和养分的调节等有密切关系。同源四倍体水稻还存在糊粉层细胞壁发育不同步、糊粉层细胞壁结构异常以及胼胝质“套”不消失等异常现象。这些现象有可能会影响同源四倍体水稻的结实率。  相似文献   

11.
The development of pericarp, seed coat, starchy endosperm and aleurone of the rice caryopsis was investigated, histochemically and structurally, from the time of flowering to maturity. The results showed that during its growth, the maximum length of the caryopsis was attained first, followed by width and then thickness. Histochemical examination of the caryopsis showed that starch was mainly accumulated in the endosperm, but the endosperm showed no metabolic activity, while embryo and pericarp contained a few starch grains, and embryo and aleurone were strongly active. Aleuronic cells contained many aleurone grains and spherosomes, and aleurone in the dorsal region developed earlier and contained more layers of cells. Amyloplasts in endosperm contained many starch granules and were spherical at early stages but polyhedric at late stages. The protein bodies appeared later than amyloplasts, and the number of protein bodies in subaleurone was greater than those in the starchy endosperm. The white-belly portion of endosperm might be relative to the status of amyloplast development.  相似文献   

12.
鸟苷酸激酶OsGK1对水稻种子发育至关重要   总被引:1,自引:1,他引:0  
【目的】对水稻粉质皱缩突变体fse2进行表型分析及基因克隆,为阐明水稻淀粉合成机制以及胚的发育奠定基础。【方法】fse2来自粳稻品种滇粳优1号的MNU(N-甲基-N-亚硝基脲)诱变突变体库。本研究考查了突变体fse2籽粒的理化性状,利用扫描电镜和半薄切片观察了淀粉颗粒的结构;构建了fse2与N22的F2群体,通过图位克隆及转基因互补验证确定目标基因;通过qRT-PCR以及GUS活性染色对FSE2进行组织表达分析;免疫印迹分析了突变体中淀粉合成相关基因以及线粒体基因的蛋白变化。【结果】fse2籽粒粉质皱缩,千粒重显著下降;胚乳中淀粉颗粒变小变圆,排列松散,不能形成正常的复合淀粉颗粒;突变体中总淀粉、直链淀粉含量均显著下降,脂肪含量显著上升,突变体淀粉的糊化特性发生明显改变。FSE2编码一个线粒体和质体双定位的鸟苷酸激酶(guanylate kinase),命名为OsGK1。OsGK1在各器官中组成型表达,并在花后6 d的胚乳中表达水平最高。突变体胚乳中淀粉合成相关蛋白水平显著降低,尤其是AGPS2b和PHOI。此外,突变体fse2的胚发育严重受损,导致种子纯合致死;线粒体定位的AOX积累显著增强,而野生型中几乎检测不到,表明线粒体呼吸途径受损。【结论】由于OsGK1的功能缺陷,导致水稻种子中线粒体和造粉体发育异常,进而产生了胚致死以及胚乳粉质皱缩的表型,因此OsGK1对水稻种子的发育至关重要。  相似文献   

13.
14.
The starchy endosperm of the mature wheat grain comprises three major cell types, namely sub-aleurone cells, prismatic cells and central cells, which differ in their contents of functional components: gluten proteins, starch, cell wall polysaccharides (dietary fibre) and lipids. Gradients are established during grain development but may be modified during grain maturation and are affected by plant nutrition, particularly nitrogen application, and environmental factors. Although the molecular controls of their formation are unknown, the high content of protein and low content of starch of sub-aleurone cells, compared to the other starchy endosperm cells types, may result from differences in developmental programming related to the cells having a separate origin (from anticlinal division of the aleurone cells). The gradients within the grain may be reflected in differences in the compositions of mill streams, particularly those streams enriched in the central and outer cells of the starchy endosperm, respectively, allowing the production of specialist flours for specific end uses.  相似文献   

15.
Rice oil bodies enclosed by unique structural proteins, oleosins, are found in the embryo and the aleurone layer, but not the starchy endosperm where starch and storage proteins are accumulated. To examine oleosin promoter specificity, a sesame storage protein, 2S albumin, was expressed in transgenic rice seeds under the control of a rice oleosin promoter. In all transgenic rice seeds, the sesame 2S albumin was found exclusively in the bran fraction after milling. Immunological staining revealed that the sesame 2S albumin was also located in the embryo and the outermost cells of the starchy endosperm. Furthermore, immunogold labeling showed that the transgenic 2S albumin was deposited in both type-I and type-II protein bodies of the outermost cells of the endosperm as well as in the type-II protein bodies of the embryo. The methionine and cysteine contents in the bran from four homozygous transgenic lines were elevated by 24–38 and 50–62%, respectively, compared with those of wild-type plants. The results suggest that the rice oleosin promoter is bran-specific and could be used to add value to rice bran, an abundant by-product of rice polishing, by genetic engineering.  相似文献   

16.
【Objective】Aminoacyl-tRNA synthetases (aaRSs) are closely related to the transmission of genetic information. Besides translation, aaRSs in plants participate in gametogenesis and embryo development, early plastid development, immune signal perception and disease defense. In this study, we used a rice endosperm defective mutant to analyze the function of tryptophanyl-tRNA synthase (WRS1) during seed development, proving that WRS1 gene encodes a key factor affecting rice endosperm development. 【Method】In this study, a stably-inherited rice floury endosperm mutant (wrs1) was screened from the mutant library of indica cultivar N22 (Oryza sativa subsp. indica) induced by ethyl methane sulfonate (EMS). Map-based cloning and complementation test identified the target gene. Morphological observation and starch physicochemical properties of wrs1 mature seeds were analyzed. Semi-thin sections were prepared to observe the developing endosperm structure with a scanning electron microscope. qRT-PCR and GUS staining were performed to analyze the expression of WRS1. The expression of starch synthesis related genes in the endosperm at 12 days after flowering was determined by qRT-PCR, and these protein expression levels in mature seed were detected by immunoblotting. The free amino acid contents of mature seeds were measured with a fully automatic amino acid analyzer. 【Result】The seedlings of wrs1 were featured by obvious delay in development and finally withered and died. The floury grains isolated from the heterozygous mutant (WRS1wrs1) showed shrunken belly, decreased grain thickness and thousand-grain weight. Total starch contents, the peak viscosity and breakdown viscosity of pasting starch were lower in wrs1. The compound starch granules in developing endosperm of wrs1 were smaller and loosely arranged. WRS1 was restricted to the 183 kb region of the long arm of chromosome 12. Sequencing revealed a single base substitution in exon 6 of the tryptophanyl-tRNA synthetase gene (WRS1), resulting in a substitution of methionine. The expression of most starch synthesis-related genes in wrs1 was down-regulated, while these proteins showed different accumulation levels. The contents of proteins in wrs1 grains were decreased, while free amino acids contents were significantly increased. 【Conclusion】WRS1 encodes tryptophanyl-tRNA synthase. Mutation of this gene affects amino acid homeostasis and protein synthesis in rice endosperm, resulting in abnormal expression of the genes in starch synthesis pathway which affects starch synthesis and accumulation, and eventually lead to seed development defects.  相似文献   

17.
【目的】水稻种子主要以淀粉形式储藏能量。淀粉合成需要多种酶类和调控因子参与,机制较为复杂。本研究利用水稻胚乳发育缺陷突变体,克隆和鉴定新的调控淀粉合成相关基因,旨在为研究淀粉合成及其调控提供理论依据。【方法】从化学诱变剂甲基亚硝基脲(1-methyl-1-nitroso-urea, MNU)处理的宁粳3号(Ningjing 3, WT)突变体库中筛选到一个能稳定遗传的胚乳粉质皱缩突变体,命名为fse4 (floury and shrunken 4 )。与籼稻品种Dular杂交获得F1种子(F2),通过图位克隆的策略确定FSE4候选基因。利用杂合植株(FSE4fse4)分离出的粉质种子,观察形态学特征,分析其理化性质。使用扫描电镜和半薄切片技术观察胚乳结构。使用qRT-PCR和免疫印迹分析淀粉合成相关基因表达模式和淀粉合成相关酶类的蛋白积累量。利用全自动氨基酸分析仪测定成熟胚乳各氨基酸含量。【结果】突变体fse4籽粒宽度、厚度以及千粒重显著下降,同时胚乳中总淀粉、总蛋白、直链淀粉含量亦显著下降,而脂肪含量显著上升;淀粉黏度、崩解值和消减值显著低于野生型。突变体fse4中多为单粒型淀粉颗粒,且排列分散。FSE4定位于第5染色体长臂约252 kb的区间内,测序发现编码Δ1-吡咯啉-5-羧酸合成酶基因 (Delta 1-pyrroline-5-carboxylate synthetase, P5CS)第1外显子上发生单碱基替换,导致一保守的氨基酸发生变异。突变体fse4中大部分淀粉合成相关基因表达量下调,多种淀粉合成相关蛋白积累量减少。突变体fse4米粉中多种氨基酸含量发生显著变化,游离氨基酸含量是其野生型的3.6倍。此外,外源喷施脯氨酸能部分恢复突变体fse4种子萌发缺陷表型。【结论】FSE4编码脯氨酸合成关键限速酶P5CS,该基因对胚乳中氨基酸的合成及代谢起重要的调控作用,并影响淀粉的合成与积累。  相似文献   

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