Can additional N fertiliser ameliorate the elevated CO2‐induced depression in grain and tissue N concentrations of wheat on a high soil N background?

Elevated CO₂ stimulates crop yields but leads to lower tissue and grain nitrogen concentrations [N], raising concerns about grain quality in cereals. To test whether N fertiliser application above optimum growth requirements can alleviate the decline in tissue [N], wheat was grown in a Free Air CO₂ Enrichment facility in a low‐rainfall cropping system on high soil N. Crops were grown with and without addition of 50–60 kg N/ha in 12 growing environments created by supplemental irrigation and two sowing dates over 3 years. Elevated CO₂ increased yield and biomass (on average by 25%) and decreased biomass [N] (3%–9%) and grain [N] (5%). Nitrogen uptake was greater (20%) in crops grown under elevated CO₂. Additional N supply had no effect on yield and biomass, confirming high soil N. Small increases in [N] with N addition were insufficient to offset declines in grain [N] under elevated CO₂. Instead, N application increased the [N] in straw and decreased N harvest index. The results suggest that conventional addition of N does not mitigate grain [N] depression under elevated CO₂, and lend support to hypotheses that link decreases in crop [N] with biochemical limitations rather than N supply.     

The effect of VRN1 genes on important agronomic traits in high‐yielding Canadian soft white spring wheat

For reproductive success, flowering time must synchronize with favourable environmental conditions. Vernalization genes play a major role in accelerating or delaying the time to flowering. We studied how different vernalization (VRN1) gene combinations alter days to flowering and maturity and consequently the effect on grain yield and other agronomic traits. The study focussed on the effect of the VRN1 gene series (Vrn‐A1, Vrn‐B1 and Vrn‐D1) and their combinations. The Vrn gene group Vrn‐A1a, Vrn‐B1, vrn‐D1 was the earliest to flower and mature, while Vrn‐A1b, Vrn‐B1, vrn‐D1 was the latest to flower. Spring wheat lines with vrn‐A1, Vrn‐B1, Vrn‐D1 were the highest yielding and matured at a similar time as those having vernalization genes Vrn‐A1a, Vrn‐B1 and Vrn‐D1. The findings of this study suggest that the presence of Vrn‐D1 has a direct or indirect role in producing higher grain yield. We therefore suggest the introduction of Vrn‐D1 allele into higher‐yielding classes within Canadian spring wheat germplasm.     

转基因水稻恢复系及其F1代Bt蛋白的时空表达分析

本研究以抗虫水稻恢复系9311(Bt)及其杂交种F1(Bt)为研究材料,以非转基因的9311为阴性对照,利用ELISA方法研究9311(Bt)及F1(Bt)各生育时期可溶性总蛋白和Bt蛋白的时空变化规律,为转Bt基因抗虫水稻的安全监管提供科学依据。结果表明：外源基因的导入没有引起水稻组织中可溶性总蛋白含量的明显变化;9311(Bt)的Bt蛋白表达量在整个生长周期的各个部位均高于相应的F1(Bt)植株;同一植株不同组织器官中Bt蛋白表达量为：叶片跃胚乳跃颖壳及茎秆跃根;同一植株不同发育期叶片Bt蛋白的测定结果整体表现为：营养生长阶段跃生殖生长阶段跃成熟衰老阶段。研究结果为转Bt基因抗虫水稻适宜检测时期的选择提供了一定的参考。     

猪圆环病毒2型间接ELISA方法的建立

为了猪圆环病毒2型（PCV2）抗体,本研究建立了快速、敏感的ELISA诊断方法。本研究应用原核表达的PCV2-Cap蛋白作为包被抗原,通过抗原最适包被浓度和兔抗猪IgG最佳稀释浓度的确定,待检血清稀释度的选择,阴阳性临界值的确定,然后进行特异性测定、重复性测定和符合率比较等,建立检测PCV2抗体的间接ELISA方法。结果显示,建立的间接ELISA方法只能检测出PCV2阳性血清;3次重复性试验的差异不显著;与韩国JBT公司的PCV2试剂盒的符合率达到了92.5%;对采集福建省内多个猪场204份血清样品进行检测,其阳性率达到了76.5%。实验表明,建立的检测PCV2抗体的间接ELISA方法具有特异性强、重复性和稳定性好的特点,可用于PCV2抗体的血清学诊断和流行病学调查。     

花生黄曲霉抗性与类受体蛋白激酶的相关性分析

LRR类受体激酶RH4基因在花生黄曲霉敏感品种发育种子的种皮中上调表达.基于这类受体激酶多由于序列的变异导致抗性的变异,笔者将数据库中花生抗黄曲霉和敏感品种相似基因编码的蛋白进行序列比较分析,发现抗性品种与敏感品种的类似蛋白序列有很大差别.用荧光定量PCR方法对抗性品种KB153与敏感品种JH1012发育中不同时期的果...     

大豆水溶性蛋白含量测定的不确定度评定

建立大豆水溶性蛋白含量测定（NY/T 1205-2006）不确定度评定的数学模型,对检测过程中带来的各个不确定度分量进行识别和量化,提出应用该方法检测的不确定度评定结果。     

农作物Pht1家族磷转运体蛋白的生物信息学分析

以AtPT1所编码的氨基酸序列做为检索序列,通过对GenBank NR数据库以及EMBI、DDBJ、PDB数据库进行检索,发现小麦、大麦、玉米、水稻和番茄等植物中具全长cDNA的33个Pht1家族磷转运体基因,包括马铃薯1个,苜蓿5个,辣椒3个,茄子2个,烟草2个,番茄2个,菜豆1个,玉米4个,大麦2个,小麦1个,水稻7个,大豆2个和木薯1个。利用生物信息学分析,首次将Pht1家族磷转运体基因保守特征序列确定为GGDYPLSATIMSE。对检索到的33个Pht1家族磷转运体蛋白进化关系分析表明,与AtPT1亲缘关系较近的双子叶植物磷转运体蛋白是木薯MePT1和GmPT2,关系较近的单子叶植物磷转运体蛋白是OsPHT8和OsPHT12。     

水稻OsABCC10基因的克隆及其功能分析

ABCC蛋白为ABC转运蛋白超家族中的一个亚家族,主要参与将各种分子从细胞质输出到外部介质或细胞器基质的过程。为了研究OsABCC10基因是否参与水稻Na+的运输,本研究从水稻基因组中克隆出OsABCC10基因,该基因cDNA全长4539 bp,编码1513个氨基酸。OsABCC10基因表达分析发现,其主要在水稻根中表达,表达量随盐处理浓度的升高及处理时间的延长而增强,表明OsABCC10基因的表达受盐胁迫的调控。亚细胞定位分析证实OsABCC10定位于液泡膜上。盐胁迫条件下,与野生型相比,osabcc10突变体表现出对盐更敏感,而且木质部汁液中Na+浓度升高。然而,当OsABCC10基因导入野生型酵母菌株BY4741表达时,与对照组实验相比,有OsABCC10表达的酵母细胞的生长受到了抑制。该结果与植物生理实验结果相反,这可能与OsABCC10蛋白在酵母中的定位有关。本研究初步推测OsABCC10基因参与水稻Na^+的转运,是一个新的耐盐基因。     

凯氏定氮法测定大米中蛋白质的不确定度分析

采用GB/T5009.5-2003第一法,凯氏定氮法测定大米中蛋白质的含量,其测量不确定度来源于样品称量、消化、定容、移取消化液、蒸馏及滴定等过程。通过对各个不确定度分量的计算合成,找出影响测量不确定度的因素,并对各个不确定度分量进行评估,最终分析出样品大米中蛋白质的标准不确定度及扩展不确定度并描述了影响大米蛋白质测定结果各分量对其不确定度的相对贡献。     

酶法改性大豆分离蛋白成膜条件的研究

以大豆分离蛋白为成膜主料,在一定条件下与交联剂(TG酶)、增塑剂(甘油)等共同作用,制备出可降解具有一定机械强度的大豆分离蛋白膜,可部分替代塑料用于食品包装领域,减少环境污染。结果表明,大豆分离蛋白膜的实验室制膜工艺参数为:质量分数为5.0%的大豆分离蛋白,2.0%的甘油,0.15%的TG酶、pH值8.0。